Next Article in Journal
Relationship between Diet Quality and Maternal Stool Microbiota in the MUMS Australian Pregnancy Cohort
Previous Article in Journal
Understanding NAFLD: From Case Identification to Interventions, Outcomes, and Future Perspectives
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Sun Exposure Score and Vitamin D Levels in Moroccan Women of Childbearing Age

1
Cluster of Competence Environment and Health, Faculty of Sciences, Moulay Ismail University, Meknes 50000, Morocco
2
Higher Institute of Nursing Professions and Health Techniques, Meknes 50000, Morocco
3
Health and Environment Unit, Faculty of Medicine, KU Leuven, 3000 Leuven, Belgium
4
IDEWE, External Service for Prevention and Protection at Work, 3001 Heverlee, Belgium
5
Statistic Unit, Louvain School of Management, University Catholique of Louvain, 1348 Louvain-la-Neuve, Belgium
6
Faculty of Sciences and Techniques Errachidia, Moulay Ismail University of Meknes, Errachidia 52000, Morocco
7
Department of Pharmacology and Physiology, Faculty of Medicine, University of Montreal, Montreal, QC H3C 3J7, Canada
8
BASE Laboratory, Faculty of Sciences and Techniques Errachidia, Moulay Ismail University, Meknes 50000, Morocco
*
Author to whom correspondence should be addressed.
Nutrients 2023, 15(3), 688; https://doi.org/10.3390/nu15030688
Submission received: 14 December 2022 / Revised: 22 January 2023 / Accepted: 23 January 2023 / Published: 29 January 2023
(This article belongs to the Section Lipids)

Abstract

:
Sunlight exposure is an essential source of vitamin D for many humans. However, hypovitaminosis D is a global public health problem. This study aimed to develop and validate a sun exposure score (SES) and correlate it with serum 25-hydroxyvitamin D levels in women of childbearing age. One hundred and sixty women aged 18 to 45 years residing in Meknes, Morocco, were included. A questionnaire estimating the sun exposure score and blood analysis of serum 25-OHD concentration were performed. The questionnaire’s reliability and construct validity were evaluated using Cronbach’s alpha and factor analysis. Spearman’s test was used to assess the correlation between SES and 25-OHD levels. The score’s reliability and construct validity were good, with Cronbach’s alpha values >0.70 and factorial saturation ranging from 0.696 to 0.948. Serum 25-OHD levels were significantly associated with the total sun exposure score, and all SES domains (Rho was 0.615 (p < 0.0001), 0.307 (p < 0.0001), 0.605 (p < 0.0001), and 0.424 (p < 0.0001) for total SES, indoor exposure domain, outdoor exposure domain, and sun protection practice domain, respectively). In addition, median 25-OHD levels increased significantly when sun exposure was changed from insufficient to sufficient (p < 0.0001). The results suggest that the sun exposure score could be used as a clinical tool to assess vitamin D levels in women of childbearing age.

1. Introduction

Hypovitaminosis D is a worldwide health problem affecting growth and development with insidious health consequences, including increased risk of musculoskeletal disorders, falls, osteoporosis-induced fractures, chronic inflammatory diseases, cardiovascular problems, increased risk of cancers, respiratory infections, type 1 and type 2 diabetes, autoimmune diseases, and neurological and psychiatric disorders [1,2,3,4,5,6,7,8,9,10,11]. Recently, vitamin D has been implicated in reproductive health and pregnancy outcomes [12,13]. Clinical studies have shown that vitamin D supplementation can lower androgen levels, lower anti-Mullerian hormone (AMH) levels [14,15], normalize the metabolic profile, and regularize periods in women with polycystic ovarian syndrome (PCOS) [16,17]. In fact, low serum 25(OH)D concentrations have been linked to problems of infertility [18,19], endometriosis [20], polycystic ovary syndrome (PCOS) [16,17,21,22], as well as adverse pregnancy outcomes, including spontaneous abortions [23], gestational diabetes [24,25], bacterial vaginosis [26], preeclampsia [27,28], neonatal hypocalcemia [29], prematurity, and low birth weight [30], as well as fetal and infant growth disorders [31].
The World Medical Association estimates that nearly one-third of the population has a low serum vitamin D concentration below 30 ng/mL [32]. In Morocco, vitamin D deficiency is widespread, with a prevalence of 76.6 to more than 90%, especially in women over 50 years of age [33,34,35], and is becoming increasingly common among women of reproductive age. A study in Marrakech showed that 100% of participants aged 18–45 years had hypovitaminosis D (<30 ng/mL) [36]. Similarly, a recent national nutrition survey (NNS 2019) published in 2022 found that 78% of women of childbearing age have 25(OH)D levels below 20 ng/mL [37]. This situation is confusing because Morocco is one of the sunniest countries in the world [38]. The explanation for this phenomenon may be the lack of sun exposure [33], increased rates of obesity [37], sedentary lifestyles [13], and restrictive clothing habits [39].
The skin, through solar radiation, provides up to 90% of the body’s vitamin D needs [40,41,42], as only a few foodstuffs contain it (e.g., oily fish, eggs, meat, offal, mushrooms), and dietary intake of this vitamin is generally insufficient to cover requirements [43,44]. Cutaneous exposure to ultraviolet radiation with a wavelength between 290 and 315 nm induces the transformation of epidermic 7-dehydrocholesterol (7-DHC) into previtamin D3, which undergoes isomerization, giving rise to cholecalciferol or vitamin D3 [45,46]. However, this process is conditioned by a complex set of variables, including the solar zenith angle (number of available UVB photons), timing and mode of exposure, skin pigment, aging, exposed skin surface, and sun protection habits (sunscreen, clothing).
Latitude, altitude, season, weather, or time of day significantly affect the solar zenith angle (SZA) and, consequently, the amount of cutaneous vitamin D synthesis [45,47,48,49,50,51]. Thus, above and below latitudes of about 33° to 35°, cutaneous synthesis of vitamin D3 is very low or absent for most of the winter. This is also why very little or no vitamin D is synthesized in the skin during sun exposure before 10 a.m. and after 3 p.m., even in summer [49,50,51,52].
Personal characteristics such as age and skin pigmentation are also limiting factors. Vitamin D synthesis decreases with increasing age due to a drop in 7−dehydrocholesterol levels and in changes in skin morphology, resulting in a 50% decrease in the formation of previtamin D3 in the elderly compared to the young [49,53,54]. In the case of skin pigmentation, darker skin has more melanin, acting as a filter for ultraviolet radiation (UVR); research shows that type II skin converts epidermal 7-DHC to provitamin D3 approximately 5–10 times more efficiently than pigmented type V skin [45,55,56,57].
Sun protection behavior, such as shading out from the sun, lack of physical activity in open environments [58], clothing type [59,60,61,62], and sunscreen use [49,61], can affect UVB-7-dehydrocholesterol interactions by blocking, absorbing, reflecting, or scattering incident UV radiation.
Previously, sun exposure was measured using dosimeters or a brief sunlight diary. However, these tools have some limitations. Dosimeters are prohibitively expensive and require sensitive equipment and expertise; moreover, these devices cannot record the use of certain sun protection behaviors. A questionnaire or self-reported measures assessing sun exposure found in the literature estimate the duration and frequency of outdoor sun exposure with little or no consideration of covariates that could influence vitamin D photosynthesis, such as skin phototype, exposed body surface, and sun protection practices (type of clothing, use of sunscreens, etc.). In addition, the rating scales generally used were Likert-type (e.g., never to always) or rating scales measuring the consistency of use (e.g., always, often, sometimes, rarely, never). To our knowledge, only one study has developed a scoring algorithm for estimating outdoor sun exposure [63], but no questionnaire has assessed the sun exposure of individuals inside their homes. Indeed, lying down in a place where the horizon is flat, one receives a much higher dose of UV than walking in the street, where the body is often in the shade, and only a tiny amount of UV radiation is accessible [50]. In this sense, the household is the best place where homeowners can uncover their bodies for personal comfort and expose themselves to adequate sunlight on the terrace, backyard, patio, balcony, or garden. In the literature, a small number of studies evaluating exposure to natural sunlight in the home, Reid et al. [64] and Okan et al. [65] found that 25(OH)D increased significantly in people who sat for 15 or 30 min a day under the verandah or garden of the nursing home. In Morocco, traditional houses have a design centered on a courtyard or patio that allows natural sunlight to pass through and a roof terrace that serves as a solarium for sunbathing [66,67]. In addition, several countries in the world, including Morocco, tend to adopt a bioclimatic architectural design of housing according to the local climate to maximize the sunlight hours of the buildings and ensure thermal comfort [68,69].
The objective of this study was to develop and validate a sun exposure scale to assess the numerous factors influencing indoor and outdoor sun exposure, as well as the different sun protection techniques used, and correlate it with 25(OH)D levels in women of childbearing age living in Meknes, Morocco.

2. Methods

The aim of this study was to develop and validate a score to measure sun exposure and correlate it with 25(OH)D levels. The methodology for developing and validating the score included three steps: (1) literature review and Sun Exposure Score (SES) development, (2) participant recruitment and data collection, and (3) construct validity and reliability of SES (Figure 1).

2.1. Step 1: Development of the Sun Exposure Score (SES)

2.1.1. Literature Review and Sun Exposure Score (SES) Development

We developed a scale to estimate women’s sun exposure by considering all factors related to sun exposure that affect vitamin D levels, including phototype, weather, time and frequency of sun exposure, body parts exposed, and different sun protection behaviors. This score was developed from an extensive literature review of questionnaires assessing sun exposure in correlation or not with vitamin D levels [63,70,71,72,73,74,75,76,77]. A unique feature of our questionnaire is the inclusion of indoor exposure as a significant determinant of sun exposure, considering the specificity of Moroccan culture and home architecture that favor adequate indoor sun exposure.
This instrument is a questionnaire with two variables assessing weekly sun exposure: the first is composed of modifiable factors influencing sun exposure (duration, time slot, frequency of exposure, body part exposed, and sun protection behaviors). This variable contains 15 items, divided into three domains: indoor sun exposure, outdoor sun exposure, including work or routine activities, and outdoor recreation or leisure activities, and the third domain concerning sun protection practices. Each item is scored on a response option scale of 0 to 4 (e.g., for frequency of exposure: 0 if never; 1 if once/week; 2 if two to three times/week; 3 if four to five times/week; and 4 if more than five times/week). The second is an adjustment variable with two elements involving non-modifiable factors, the first being skin phototype based on Fitzpatrick’s skin type [78], namely: (I) white skin that always burns and never tans; (II) fair skin that burns easily and tans hardly; (III) fair to medium skin that burns moderately and always tans gradually; (IV) medium skin that burns little and tans easily; (V) brown skin that rarely burns and always tans darkly; and (VI) black, heavily pigmented skin that never burns and tans very easily. This item was scaled from 0 to 1 (0.25 if type V and VI, 0.5 if type III and VI, 0.75 if type II, and 1 if type I). The second item is the inside weather conditions, scored from 0 to 1 (0 if rainy, 0.25 if cloudy/lightly rainy, 0.5 if cloudy, 0.75 if sunny/lightly cloudy, and 1 if sunny).
The score attributed to each domain of the first variable corresponds to the sum of the scores of its different items multiplied by the scores of the second variable. The total score of sun exposure was classified according to four levels of satisfaction: insufficient, moderately sufficient, sufficient, and very sufficient or high. The sun exposure is considered insufficient if the total score is less than 7.5; moderate if it is between (7.5–15); sufficient if it is between (15–30); and very sufficient or high if it is greater than 30. Adequate sun exposure means sufficient scores in the indoor and outdoor SES domains and insufficient scores in the sun protection practices domain. Appendix A shows the different domains included in the score.

2.1.2. Pretest of SES

A questionnaire pretest was conducted with 30 university students not included in the study to verify the questionnaire’s simplicity, fluidity, and comprehensibility. The questions were then readjusted based on the pretest results.

2.2. Step 2: Participant Recruitment and Data Collection

2.2.1. Study Population

It is a cross-sectional study conducted in the prefecture of Meknes in north-central Morocco (coordinates 5° 32’ 26.628’’ W, 33° 52’ 22.8576’’ N, sea level), with an average daily maximum UV index in spring of 8, and an average of 08 h of sunlight per day in spring.
The sample size (n0) was set concerning Cochran’s formula [79]: n0 = z2pq/e2; where z is the value from the standard normal distribution reflecting the confidence level (Z = 1.96 for 95%); p is the estimated prevalence of hypovitaminosis D in Moroccan women of reproductive age (limited to studies defining hypovitaminosis D as a circulating level of 25(OH)D less than 30 ng/mL); p is calculated based on the mean prevalence of hypovitaminosis D in premenopausal and reproductive age women reported by Allali et al. [33] and Baki et al. [36], respectively, (p = 90%); q is 1 − p, and e is the desired level of precision set at 5%. Thus, 138 women were required to obtain statistically representative data.
A total of 160 healthy women of childbearing age (18 to 45 years) were included during medical and outreach campaigns conducted by the midwifery association in spring 2019. Exclusion criteria included participants with malabsorptive, hepatic, and renal conditions; pregnant or lactating women; vitamin D supplementation in the past three months; and women on corticosteroid therapy or other drugs known to alter vitamin D metabolism.
This study was conducted following the guidelines outlined in the Declaration of Helsinki, and all procedures involving human subjects were approved by the Ethics Committee for Biomedical Research of the Moulay Ismail University of Meknes (CERB-UMI protocol codes 201901 (January 2019)). All participants were recruited after obtaining written informed consent.

2.2.2. Data Collection

The score questionnaire was conducted in a face-to-face interview and was complimented by a demographic questionnaire. In addition, a physical examination was performed to detect possible diseases that would prohibit participation in the study and to collect the participant’s medical history and anthropometric data.
Serum 25-hydroxyvitamin D (25(OH)D) concentrations were determined from blood samples collected from the non-fasting participant in a red dry tube; the blood was centrifuged at 3000 rpm for 15 min at room temperature. Serum samples were immediately stored in aliquots at −80 °C until use. The serum samples were analyzed at the clinical laboratory of Mohamed V Hospital in Meknes, Morocco. Serum 25(OH)D determination was performed using an electrochemiluminescence (Cobas E411 immunoassay analyzer, Sterifil, casablaca, Morocco) measuring a range of 3–100 ng/mL or 7.5–250 nmol/L. Based on the thresholds of 25(OH)D levels proposed by the Research Group on Information on Osteoporosis (GRIO) and adopted by the Moroccan Society of Rheumatology to define a vitamin D deficiency or insufficiency, women were classified as sufficient (>30 ng/mL), insufficient (10 to 29.9 ng/mL), and deficient (<10 ng/mL) [80,81].

2.3. Step 3: SES Validation

Test of Construct Validity and Reliability of SES

The final questionnaire was interviewer-administered to the sample population. The reliability of the first variable of the questionnaire was assessed by internal consistency using Cronbach’s alpha. The scores below 5 were considered unacceptable, while those ranging from 0.50 to 0.59 were considered poor, 0.60 to 0.69 questionable, 0.70 to 0.79 acceptable, 0.80 to 0.89 good, and those >0.90 were rated as excellent [82,83].
The construct validity of the sun exposure questionnaire was assessed by adopting principal component analysis (PCA) with varimax rotation. The adequacy of factorial analysis models was checked using the Kaiser–Meyer–Olkin (KMO) test [84], and the Bartlett test for sphericity; the sampling was considered adequate at a KMO value greater than 0.6 and when Bartlett’s sphericity test was significant (p < 0.05). Based on the eigenvalues, total variance explained, and the scree plot, factors with eigenvalues >1 were selected, and a varimax rotation of the variance with Kaiser Normalization was performed. Thus, items with factor loadings values greater than or equal to 0.40 were grouped into a particular domain [85].

2.4. Statistical Analyses

The Shapiro–Wilk test was used to evaluate the normality of the quantitative data. Variables with a normal distribution were represented as mean values ± standard deviation (SD). For a non-normal distribution, data are expressed as median with an interquartile range (IQR). Categorical variables are represented as counts or frequencies. Kruskal-Wallis, one-way ANOVA, and chi-square tests for categorical and quantitative variables were used to compare participants’ demographic characteristics with the different domains and classes of the sun exposure score. The Spearman rank correlation coefficient was a non-parametric test to determine the association between SES scores and 25-OHD levels. Results were considered statistically significant at p-values < 0.05. All statistical analyses were realized using the statistical software R (version 4.0.4. R Foundation for Statistical Computing).

3. Results

A total of 160 women were included in the present study, with a median age of 25 years (18–45). A total of 63.7% were residents in urban areas and 58% lived in traditional houses, compared to 42% who lived in apartments. As for occupation, 50% of the participants were housewives, 35% were students, and 15% were officials/salaried.

3.1. Validation of the Sun Exposure Score

As shown in Table 1, the KMO test = 0.755 is more significant than the minimum acceptable value of 0.6, and the Bartlett test shows a chi-square value of 1882.232 and p < 0.0001, indicating that there is sufficient correlation between the variables and that the data can be factorized. Thus, a principal component analysis with the varimax rotation method and Kaiser Normalization was performed to evaluate the construct validity of the sun exposure score.
The scree plot (Figure 2) indicates that four factors have an eigenvalue more significant than one and result in four common factors, which contribute to the cumulative variance of 79.37% of the 15 variables deemed sufficient in terms of total variance explained (Table 2). The four factors were entitled: (1) indoor sun exposure consisting of four items, (2) outdoor work or routine activities grouping four items, (3) outdoor recreational activities including four items, and (4) sun protection practices comprising three items. Regarding the validity or quality of the items that make up each factor, Table 2 shows that the 15 items have a saturation ranging from 0.699 to 0.948.
The internal consistency coefficients for each of the four factors are, respectively, 0.909, 0.923, 0.835 and 0.787 (Table 2). The variables forming the same factor have good internal consistency since the minimum recommended value of Cronbach’s alpha is 0.70. This consistency in internal coherence is further evidence of the reproducibility of the results over time.

3.2. Participants’ Sun Exposure Score and Vitamin D Levels

Figure 3 shows that about 57% of the women surveyed had a sufficient score of sun exposure between 7.5–15; due to the smaller sample size of the high score (n = 2), they were fused with the sufficient score. In contrast, 36% and 7% of the participants had moderate and insufficient sun exposure, respectively.
As presented in Table 3, the mean ±SD exposure score was 15.82 ± 5.64. Primiparous women, officials/salaried women, participants living in rural areas, and participants residing in houses had the highest mean of SES (19.46, 18.02, 17.72, and 17.03, respectively). Participants with insufficient and moderate sun exposure were predominantly obese women, participants living in apartments, and students.
Table 4 indicates that women living in rural areas and houses had a higher median score for indoor exposure, which explains their sufficient exposure compared to those living in urban areas and apartments (p < 0.0001). Regarding outdoor exposure, officials/salaried women and those with a normal weight had a higher median score compared to others (10.96, p = 0.007 and 10.13, p < 0.0001, respectively).
Table 5 shows that the median [IQR] for indoor exposure, outdoor exposure, and sun protection practice SES domains were 4.78 [3.00], 7.88 [6.19], and 3.38 [3.18], respectively. Women with moderate scores were exposed more indoors than outdoors, whereas those with sufficient scores had higher outdoor than indoor scores. Women insufficiently sun exposed had higher sun protection practice scores than those sufficiently exposed to the sun.
As reported in Table 6, serum 25-OHD levels were significantly associated with the total sun exposure score and all SES domains (Spearman’s Rho was 0.615 (p < 0.0001), 0.307 (p < 0.0001), 0.605 (p < 0.0001), and 0.424 (p < 0.0001) for total SES, indoor exposure domain, outdoor exposure domain, and sun protection practice domain, respectively).
Table 7 reveals that all participants had hypovitaminosis D (<30 ng/mL), with a median of 8.42. Nevertheless, the medians of 25-OHD levels increased significantly when sun exposure progressed from insufficient to sufficient (4.78 and 10.47, respectively; p < 0.0001). In addition, most women (87%) with insufficient or moderately sufficient sun exposure had vitamin D deficiency (<10 ng/mL), whereas women with vitamin D insufficiency (10–30 ng/mL) had an adequate sun exposure score (19.88).

4. Discussion

Endogenous synthesis of vitamin D requires occasional exposure to UV radiation from the sun. Most experts consider the recommendation of daily exposure of 25% of the unprotected skin surface for 5 to 15 min between 10:00 a.m. and 3:00 p.m. in the fall, spring, and summer to be generally sufficient for people with skin types II or III. People with skin type V require more prolonged sun exposure of 25 to 40 min [45,47,55,56,57,86]. Such exposure increases vitamin D levels to a level semblable to an oral dose of 1000 IU [87,88].
This research is the first study to develop and validate a sun exposure score (SES) correlated with 25(OH)D levels for women of childbearing age in Meknes, Morocco. The questionnaire score was designed to estimate overall sun exposure according to skin phototype, and outside weather, encompassing indoor exposure, outdoor exposure, and habitual sun protection practices in the week prior to the survey. The one-week SES was adopted to provide participants with an accurate recall and account of sun exposure behavior. However, some studies have examined longer periods, ranging from a few weeks to several years, allowing a more reliable estimate of sun exposure for people who rarely expose themselves [63,71,76,77,89]. Furthermore, the SES was administered only once since exposure behavior constantly changes depending on heat preferences, sun protection measures [90], individual needs, and habits. In addition, leisure activities depend more on weather conditions such as temperature, humidity, and sun duration than routine activities [91].
Our results indicate that the SES is valid for classifying study participants according to their level of weekly sun exposure; this is based on the questionnaire’s good validity and reliability results. In addition, we found a significant association between the SES and serum 25 (OH) D concentrations (Rho = 0.615 (p < 0.0001).
The score questionnaires were evaluated for construct validity and reliability. The construct validity of our score questionnaire was satisfactory. Factor analysis identified a four-factor solution that accounted for 79.3% of the total variance, namely: indoor sun exposure, outdoor work or routine activities grouping, outdoor recreational activities including four items, and sun protection practices. All items had high loadings ranging from 0.699 to 0.948. This analysis indicated that no items needed to be excluded from our sun exposure score.
SES has also revealed good to excellent internal consistency for all four factors, illustrated by a high Cronbach’s alpha exceeding the required minimum threshold of 0.70 [82,83]. This high index suggests a substantial homogeneity of the items of the score [92]. However, very few studies on sun exposure have validated their measurement questionnaires. In China, a questionnaire on lifetime sun exposure revealed two factors with factor loadings ranging from 0.616 to 0.908 [76]. In Spain, a principal component analysis of the CHACES questionnaire on knowledge, attitudes, and habits related to sun exposure in young adults showed that two components accounted for more than 50% of the total variance. The reliability of the CHACES questionnaire was proven with a Cronbach’s coefficient between 0.45 and 0.8 for all components, except knowledge (0.335) and test-retest reliability (absolute agreement > 60%) [93]. Another questionnaire of the Sun Exposure Protection Index (SEPI), developed in Sweden and Australia, showed that an internal consistency as reflected by Cronbach’s alpha was found to be slightly below the desired value of >0.70 [71]. In contrast, Yu et al. [77] validated an urban Filipino adult sun exposure questionnaire (SEQ) by grouping items with similar factor loadings into three domains, even with a lower value than recommended for factor analysis (0.4) [85]. Furthermore, they based the validation of the SEQ on a sufficient content validity index of at least 0.86 and satisfactory internal consistency with an overall Cronbach alpha of 0.80.
Our results revealed sufficient sun exposure in 57% of the participants, with an average of 15.82. The median indoor exposure, outdoor exposure, and sun protection practices were 4.78, 7.88, and 3.38, respectively. Women insufficiently sun-exposed had higher sun protection practice scores than those sufficiently exposed to the sun. These results are consistent with other findings in the literature [39,63,94], in contrast to Abda et al. [95], who found that the prevalence of sun exposure is high in Morocco (52.1%) and that sun protection practices are often inadequate.
Moreover, our SES showed that women living in rural areas and houses had a higher median score explained by high indoor sun exposure compared to those living in urban areas and/or apartments. In this context, the total sun exposure score of women inside their homes in the yard or on the terrace, especially in rural areas, may be more important than the self-reported frequency and time spent outdoors. This can also be explained by the fact that the outdoor activities of the rural participants begin early in the morning, before 10:00 a.m., whether it is raising livestock, collecting water, or gathering wood.
In our results, the sun exposure score was negatively correlated with BMI; obese women had a lower score than others, as did students, who had a lower mean score of 13.56 than housewives (16.73) and official/salaried women (18.02). Comparable results were reported by Dadda et al. [39] who showed that high vitamin D levels can be linked to outdoor activities with greater exposure to the sun.
Despite sufficient sun exposure in 57% of women, all participants had hypovitaminosis D < 30 ng/mL, with a median of 8.42 ng/mL. Baki et al. [36] and the national nutrition survey (ENN 2019) [37] confirms the high prevalence of hypovitaminosis D in women of childbearing age in Morocco. Nevertheless, the findings indicated a significant increase in 25-OHD levels as sun exposure progressed from insufficient to sufficient (4.78 and 10.47, respectively; p < 0.0001). Similar results were found by Mansibang et al. [94], who reported that the mean 25-OHD levels of the different groups increased significantly when sun exposure moved from low to high (p < 0.001). Humayun et al. [63] observed that the mean serum 25-OHD concentration was lower in all sun exposure groups. Similarly, in Morocco, the national nutrition survey (ENN 2019) [37] reported that the duration of exposure to sunlight has a large impact on vitamin D status, with significantly less vitamin D deficiency in women who were exposed to the sun for more than 20 min/d than those who were exposed to the sun for less than 20 min/d or who were not exposed to the sun (27.6%). In the same sense, Dadda et al. [39] explain the high prevalence of hypovitaminosis D (94%) in the Draa-Tafilalet region by restrictive clothing habits and low daily sun exposure.
In this study, serum 25-OHD levels were significantly associated with total sun exposure score and all SES domains (Rho = 0.615, 0.307, 0.605 and 0.424; p < 0.0001, for total SES, indoor exposure domain, outdoor exposure domain, and sun protection practice domain, respectively). The results of our study are consistent with previous research. Hanwell et al. [72] in Italy demonstrated a significant correlation between weekly sun exposure score and 25(OH)D concentrations during summer (Rho = 0.59, p = 0.003). Humayun et al. [63] in Pakistan showed a moderate correlation between self-reported SEQ and serum 25-OHD (short-term SEQ (Rho = 0.36, p = 0.01) and long-term SEQ (Rho = 0.43, p = 0.01)) in summers and 0,48 (p = 0,01) in winters. In Philippines, Yu et al. [77] reported a moderate correlation between 25-OHD levels and SEQ (r = 0.396, p < 0.001). Similarly, in Morocco, Dadda et al. [39] indicated a positive correlation of vitamin D levels with daily sun exposure (r = 0.308, p < 0.001). Conversely, in a study by Cargill et al. [70] in Australia and Sham et al. [96] in Canada, there was no significant correlation between questionnaire measures of time outdoors on weekdays, weekends, or cumulative time and 25-OHD concentration.
Our study showed that 43% of women of childbearing age had an insufficient to moderate sun exposure score, and all had a hypovitaminosis D below 30 ng/mL. This may be related to factors other than sun exposure that are not accounted for in the questionnaire score, such as pollution and daily dietary vitamin D intake. Another limitation was the short estimation period of sun exposure limited to one week, which could be more susceptible to reflect effects specific to the situation of rarely exposed women but could be counterproductive for those with frequent sun exposure.

5. Conclusions

The main objective of this research is to adopt an appropriate and simple tool to measure sun exposure, which is an essential determinant of vitamin D levels. The SES developed in this study had good construct validity and reliability for estimating and classifying sun exposure in female participants of reproductive age. Furthermore, the SES showed a significant positive correlation with 25(OH)D levels. Therefore, it could be a valuable clinical tool to evaluate sun exposure and identify individuals at risk for vitamin D deficiency and associated diseases. However, we recognize that because of limitations in participant size and the spring study period, the predictive value of the current score needs to be validated in other experimental conditions with a larger population (women and men) at different latitudes/altitudes and seasons of the year.

Author Contributions

Conceptualization, I.L., N.Z. and A.M.; methodology, I.L.; data collection and processing, I.L. and N.Z.; statistical processing, I.L. and Y.F.-Z.; writing—original draft preparation, I.L.; scientific supervision, A.E.M., L.G. and Y.F.-Z.; supervision of the study and validation of the manuscript A.E.M., L.G., Y.F.-Z., M.-P.K. and S.E.J. All authors have read and agreed to the published version of the manuscript.

Funding

This research was supported by the Institutional University Cooperation Program with Moulay Ismail University, which is funded by the VLIR-UOS (Phase I: 2017–2021; Contract n°MA2017IUC038A104) and by the Research and Development Project “SEBIO” (Morocco, PDR-MA-SEBIO (2017–2022).

Institutional Review Board Statement

This study was conducted in accordance with the guidelines set out in the Declaration of Helsinki and all procedures involving human subjects were approved by the Ethics Committee for Biomedical Research of Moulay Ismail University of Meknes (CERB-UMI protocol codes 201901 (January 2019). The written consent of all subjects has been obtained.

Informed Consent Statement

Informed consent was obtained from all subjects involved in the study.

Data Availability Statement

The data used to support the findings of this study are available from Prof. Filali-Zegzouti Younes upon request.

Conflicts of Interest

The authors declare no conflict of interest.

Appendix A

Sun Exposure Score (SES)
Variable Sun Exposure Domains:
Items:01234
Indoor sun exposure Frequency of indoor sun exposure (in terrace, balcony, courtyard)Never1 time/week2 to 3 times/week4 to 5 times/weekMore than 5 times/week
Indoor exposed body part FaceFace, handFace, armFace, arm, leg
Indoor duration sun exposureLess than 5 min5 to 15 min15 to 30 min30 to 60 minMore than 60 min
Indoor sun exposure time slotBefore 7 a.m.7 a.m. to 9 a.m.9 a.m. to 11 a.m./5 p.m. to 19 p.m.11 a.m. to 1 p.m.1 p.m. to 5 p.m.
Outdoor sun exposure Frequency of professional or routine outdoor activitiesNever1 time/week2 to 3 times/week4 to 5 times/weekMore than 5 times/week
A time slot for professional or routine outdoor activitiesBefore 7 a.m.7 a.m. to 9 a.m.9 a.m. to 11 a.m./5 p.m. to 19 p.m.11 a.m. to 1 p.m.1 p.m. to 5 p.m.
Duration of professional or routine outdoor activitiesLess than 5 min5 to 15 min15 to 30 min30 to 60 minMore than 60 min
Outdoor exposed body part FaceFace, handFace, armFace, arm, leg
Practice outdoor activities (sports, hiking, walking, camping, swimming, etc.)Never1 time/week2 to 3 times/week4 to 5 times weekMore than 5 times/week
Duration outdoor activitiesLess than 5 min5 to 15 min15 to 30 min30 to 60 minMore than 60 min
Time slot for sun exposure in the open airBefore 7 a.m.7 a.m. to 9 a.m.9 a.m. to 11 a.m./5 p.m. to 19 p.m.11 a.m. to 1 p.m.1 p.m. to 5 p.m.
Part of the body exposed in the open air FaceFace, handFace, armFace, arm, leg
Sun protection practices Staying out of the sunUsed shade of tree/building/ parasol etc.Market in the shadeCar/bus/van smoked window/ofCar/bus/van glass windows upNo protection
Type of sunscreen usedSPF sunscreen of 50 and +SPF sunscreen from 30 to 50Sunscreen SPF from 15 to 30Other creams and lotions without knowledge of the FPS or SPF 6 to 10No sunscreen
Type of clothing usually usedUsual clothes with long sleeves/long pants/heavy/tight clothes with dark colorantsUsual clothes with long sleeves/long pants/loose with dark colorantsLong loose clothing with light coloring.Short sleeve/pants/shortsShort no shirt /bikini
Adjustment variable
Items:00.250.50.751
Phototype Type V & VIType III & IVType IIType I
Weather outsiderainycloudy/light rainycloudysunny/light cloudysunny
TotalSun exposure score = the sum of the domain scores x phototype score x outdoor weather score.
The score is considered insufficient if the score is below 7.5, moderate if the score is between 7.5–15, sufficient if the score is between 15–30, and as very sufficient or high if the score is above 30. Indoor sun exposure is considered insufficient if the score is below 4, moderately sufficient if the score is between 4 and 8, sufficient if the score is between 8 and 12, and high for a total above 12. For outdoor sun exposure, it is considered insufficient if the total is less than 8, moderately sufficient if the total is between 8 and 16, sufficient if the score is between 16 and 24, and high for a total greater than 24. Finally, for sun protection practices, this subscale has an inverse relationship with sun exposure: a score below 3 is considered high and considered sufficient from 3 to 6, moderately sufficient if the score is between 6 and 9, and insufficient sun protection practices for a score between 9 and 12.

References

  1. Chen, P.; Hu, P.; Xie, D.; Qin, Y.; Wang, F.; Wang, H. Meta-Analysis of Vitamin D, Calcium and the Prevention of Breast Cancer. Breast Cancer Res. Treat. 2010, 121, 469–477. [Google Scholar] [CrossRef] [PubMed]
  2. Szabó, A. Skeletal and Extra-Skeletal Consequences of Vitamin D Defi Ciency. Orv. Hetil. 2011, 152, 1312–1319. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  3. Holick, M.F.; Chen, T.C. Vitamin D Deficiency: A Worldwide Problem with Health Consequences. Am. J. Clin. Nutr. 2008, 87, 1080–1086. [Google Scholar] [CrossRef] [Green Version]
  4. Hossein-Nezhad, A.; Holick, M.F. Vitamin D for Health: A Global Perspective. Mayo Clin. Proc. 2013, 88, 720–755. [Google Scholar] [CrossRef] [Green Version]
  5. Garland, C.F.; Kim, J.J.; Mohr, S.B.; Gorham, E.D.; Grant, W.B.; Giovannucci, E.L.; Baggerly, L.; Hofflich, H.; Ramsdell, J.W.; Zeng, K.; et al. Meta-Analysis of All-Cause Mortality According to Serum 25-Hydroxyvitamin D. Am. J. Public Health 2014, 104, 43–50. [Google Scholar] [CrossRef]
  6. Grant, W.B. 25-Hydroxyvitamin D and Breast Cancer, Colorectal Cancer, and Colorectal Adenomas: Case-Control versus Nested Case-Control Studies. Anticancer Res. 2015, 35, 1153–1160. [Google Scholar]
  7. Infante, M.; Ricordi, C.; Sanchez, J.; Clare-Salzler, M.J.; Padilla, N.; Fuenmayor, V.; Chavez, C.; Alvarez, A.; Baidal, D.; Alejandro, R.; et al. Influence of Vitamin D on Islet Autoimmunity and Beta-Cell Function in Type 1 Diabetes. Nutrients 2019, 11, 2185. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  8. Manousaki, D.; Harroud, A.; Mitchell, R.E.; Ross, S.; Forgetta, V.; Timpson, N.J.; Smith, G.D.; Polychronakos, C.; Richards, J.B. Vitamin D Levels and Risk of Type 1 Diabetes: A Mendelian Randomization Study. PLoS Med. 2021, 18, 1–16. [Google Scholar] [CrossRef]
  9. McDonnell, S.L.; Baggerly, C.; French, C.B.; Baggerly, L.L.; Garland, C.F.; Gorham, E.D.; Lappe, J.M.; Heaney, R.P. Serum 25-Hydroxyvitamin d Concentrations ≥40 Ng/Ml Are Associated with >65% Lower Cancer Risk: Pooled Analysis of Randomized Trial and Prospective Cohort Study. PLoS ONE 2016, 11, e0152441. [Google Scholar] [CrossRef] [Green Version]
  10. Pludowski, P.; Holick, M.F.; Pilz, S.; Wagner, C.L.; Hollis, B.W.; Grant, W.B.; Shoenfeld, Y.; Lerchbaum, E.; Llewellyn, D.J.; Kienreich, K.; et al. Vitamin D Effects on Musculoskeletal Health, Immunity, Autoimmunity, Cardiovascular Disease, Cancer, Fertility, Pregnancy, Dementia and Mortality-A Review of Recent Evidence. Autoimmun. Rev. 2013, 12, 976–989. [Google Scholar] [CrossRef]
  11. Prietl, B.; Treiber, G.; Pieber, T.R.; Amrein, K. Vitamin D and Immune Function. Nutrients 2013, 5, 2502–2521. [Google Scholar] [CrossRef] [PubMed]
  12. Fernando, M.; Ellery, S.J.; Marquina, C.; Lim, S.; Naderpoor, N.; Mousa, A. Vitamin D-Binding Protein in Pregnancy and Reproductive Health. Nutrients 2020, 12, 1489. [Google Scholar] [CrossRef] [PubMed]
  13. Mousa, A.; Abell, S.; Scragg, R.; Courten, B. Vitamin D in Reproductive Health and Pregnancy. Semin. Reprod. Med. 2016, 34, e1–e13. [Google Scholar] [CrossRef]
  14. Irani, M.; Merhi, Z. Role of Vitamin D in Ovarian Physiology and Its Implication in Reproduction: A Systematic Review. Fertil Steril. 2014, 102, 460–468.e3. [Google Scholar] [CrossRef] [PubMed]
  15. Moridi, I.; Chen, A.; Tal, O.; Tal, R. The Association between Vitamin D and Anti-Müllerian Hormone: A Systematic Review and Meta-Analysis. Nutrients 2020, 12, 1567. [Google Scholar] [CrossRef] [PubMed]
  16. Sodhi, M.; Shah, B.C. Role of Vitamin D Levels on the Ovarian Function and Androgen Profile in Adolescents with Polycystic Ovarian Syndrome. Gynecol. Pelvic Med. 2019, 2, 22. [Google Scholar] [CrossRef]
  17. Simpson, S.; Seifer, D.B.; Shabanova, V.; Lynn, A.Y.; Howe, C.; Rowe, E.; Caprio, S.; Vash-Margita, A. The Association between Anti-Müllerian Hormone and Vitamin 25(OH)D Serum Levels and Polycystic Ovarian Syndrome in Adolescent Females. Reprod. Biol. Endocrinol. 2020, 18, 118. [Google Scholar] [CrossRef] [PubMed]
  18. Muscogiuri, G.; Altieri, B.; de Angelis, C.; Palomba, S.; Pivonello, R.; Colao, A.; Orio, F. Shedding New Light on Female Fertility: The Role of Vitamin D. Rev. Endocr. Metab. Disord. 2017, 18, 273–283. [Google Scholar] [CrossRef]
  19. Voulgaris, N.; Papanastasiou, L.; Piaditis, G.; Angelousi, A.; Kaltsas, G.; Mastorakos, G.; Kassi, E. Vitamin D and Aspects of Female Fertility. Hormones 2017, 16, 5–21. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  20. Almassinokiani, F.; Khodaverdi, S.; Solaymani-dodaran, M.; Akbari, P.; Pazouki, A. Effects of Vitamin D on Endometriosis-Related Pain: A Double-Blind Clinical Trial. Med. Sci. Monit. 2016, 22, 4960–4966. [Google Scholar] [CrossRef] [Green Version]
  21. Zhao, J.; Liu, S.; Wang, Y.; Wang, P.; Qu, D.; Liu, M.; Ma, W.; Li, Y. Vitamin D Improves In-Vitro Fertilization Outcomes in Infertile Women with Polycystic Ovary Syndrome and Insulin Resistance. Minerva. Med. 2019, 110, 199–208. [Google Scholar] [CrossRef] [PubMed]
  22. Mu, Y.; Cheng, D.; Yin, T.; Yang, J. Vitamin D and Polycystic Ovary Syndrome: A Narrative Review. Reprod. Sci. 2021, 28, 2110–2117. [Google Scholar] [CrossRef] [PubMed]
  23. Kasim, S.F. The Relationship between Vitamin D and Spontaneous Abortion among Iraqi Women. J. Med. Life 2022, 15, 757–761. [Google Scholar] [CrossRef] [PubMed]
  24. Azzam, E.Z.; El-Aghoury, A.A.; Abd El-naby, E.S.E.; El-Maadawy, S.A. Studying the Relation between Vitamin D Deficiency and Glycemic State among Pregnant Women with Gestational Diabetes. Diabetes Metab. Syndr. Clin. Res. Rev. 2019, 13, 1505–1509. [Google Scholar] [CrossRef] [PubMed]
  25. Lithy, A.E.; Abdella, R.M.; El-Faissal, Y.M.; Sayed, A.M.; Abdel Samie, R.M. The Relationship between Low Maternal Serum Vitamin D Levels and Glycemic Control in Gestational Diabetes Assessed by HbA1c Levels: An Observational Cross-Sectional Study. BMC Pregnancy Childbirth 2014, 14, 1–6. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  26. Ma, L.; Zhang, Z.; Li, L.; Zhang, L.; Lin, Z.; Qin, H. Vitamin D Deficiency Increases the Risk of Bacterial Vaginosis during Pregnancy: Evidence from a Meta-Analysis Based on Observational Studies. Front. Nutr. 2022, 9, 1016592. [Google Scholar] [CrossRef] [PubMed]
  27. Bakacak, M.; Serin, S.; Ercan, O.; Köstü, B.; Avci, F.; Kılınç, M.; Kıran, H.; Kiran, G. Comparison of Vitamin D Levels in Cases with Preeclampsia, Eclampsia and Healthy Pregnant Women. Int. J. Clin. Exp. Med. 2015, 8, 16280–16286. [Google Scholar] [PubMed]
  28. Benachi, A.; Baptiste, A.; Taieb, J.; Tsatsaris, V.; Guibourdenche, J.; Senat, M.V.; Haidar, H.; Jani, J.; Guizani, M.; Jouannic, J.M.; et al. Relationship between Vitamin D Status in Pregnancy and the Risk for Preeclampsia: A Nested Case-Control Study. Clin. Nutr. 2020, 39, 440–446. [Google Scholar] [CrossRef]
  29. Adán Lanceta, V.; Martín Ruiz, N.; Benito Costey, S.; Alijarde Lorente, R.; Martínez de Zabarte Fernández, J.M. A Neonatal Hypocalcemia Due to Maternal Vitamin D Deficiency. Reviewing Supplementation. Pediatr 2022, 96, 153–154. [Google Scholar] [CrossRef]
  30. Khalessi, N.; Kalani, M.; Araghi, M.; Farahani, Z. The Relationship between Maternal Vitamin D Deficiency and Low Birth Weight Neonates. J. Fam. Reprod. Health 2015, 9, 113–117. [Google Scholar]
  31. Cannell, J. Vitamin D and Autism, What’s New? Rev. Endocr. Metab. Disord. 2017, 18, 183–193. [Google Scholar] [CrossRef] [PubMed]
  32. The World Medical Association Wma Statement on Vitamin D Insufficiency. 2015. Available online: https://www.wma.net/policies-post/wma-statement-on-vitamin-dinsufficiency/ (accessed on 20 May 2019).
  33. Allali, F.; El Aichaoui, S.; Khazani, H.; Benyahia, B.; Saoud, B.; El Kabbaj, S.; Bahiri, R.; Abouqal, R.; Hajjaj-Hassouni, N. High Prevalence of Hypovitaminosis D in Morocco: Relationship to Lifestyle, Physical Performance, Bone Markers, and Bone Mineral Density. Semin. Arthritis Rheum. 2009, 38, 444–451. [Google Scholar] [CrossRef] [PubMed]
  34. Bour, A.; Nejjar, B. Connaissance Sur La Vitamine D: État Des Lieux de La Prévalence de l’Hypovitaminose D Chez La Population Marocaine. Rev. Annales des Sciences de la Santé. 2017, 1, 24–31. [Google Scholar]
  35. El Maataoui, A.; Biaz, A.; El Machtani, S.; Bouhsain, S.; Dami, A.; El Maghraoui, A.; Ouzzif, Z. Vitamin D Status in Healthy Moroccan Men and Women Aged 50 Years and Older: A Cross-Sectional Study. Arch. Osteoporos. 2016, 11, 1–8. [Google Scholar] [CrossRef] [PubMed]
  36. Baki, S.; El Mghari, G.; El Ansari, N.; Harkati, I.; Tali, A.; Chabaa, L. Statut de La Vitamine de La Vitamine D Chez Les Femmes Marocaines Vivant a Marrakech. Ann. Endocrinol. 2015, 76, 490. [Google Scholar] [CrossRef]
  37. Ministère de la Santé. ENQUETE NATIONALE SUR LA NUTRITION (ENN 2019–2020). 2022. pp. 1–144. Available online: https://www.sante.gov.ma/Documents/2022/07/rapport%20ENN%202019-2020%20ajout%20preface%20(1).pdf (accessed on 15 September 2022).
  38. Zouiri, H.; Elmessaoudi, H. Energies Renouvelables et Développment Durable Au Maroc. Rev. Estud. Front. Estrecho Gibraltar. 2018, 6, 1–29. [Google Scholar]
  39. Dadda, S.; Azekour, K.; Sebbari, F.; El Houate, B.; El Bouhali, B. Sun Exposure, Dressing Habits, and Vitamin D Status in Morocco. E3S Web Conf. 2021, 319, 01097. [Google Scholar] [CrossRef]
  40. Barrea, L.; Savastano, S.; Di Somma, C.; Savanelli, M.C.; Nappi, F.; Albanese, L.; Orio, F.; Colao, A. Low Serum Vitamin D-Status, Air Pollution and Obesity: A Dangerous Liaison. Rev. Endocr. Metab. Disord. 2017, 18, 207–214. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  41. Mendes, M.M.; Hart, K.H.; Botelho, P.B.; Lanham-New, S.A. Vitamin D Status in the Tropics: Is Sunlight Exposure the Main Determinant? Nutr. Bull. 2018, 43, 428–434. [Google Scholar] [CrossRef]
  42. Aguilar-Shea, A. Vitamin D, the Natural Way. Clin. Nutr. ESPEN 2021, 41, 10–12. [Google Scholar] [CrossRef]
  43. Schmid, A.; Walther, B. Natural Vitamin D Content in Animal Products. Adv. Nutr. 2013, 4, 453–462. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  44. De Souza de Santana, K.V.; Oliver, S.L.; Mendes, M.M.; Lanham-New, S.; Charlton, K.E.; Ribeiro, H. Association between Vitamin D Status and Lifestyle Factors in Brazilian Women: Implications of Sun Exposure Levels, Diet, and Health. eClinicalMedicine 2022, 47, 101400. [Google Scholar] [CrossRef]
  45. Chen, T.C.; Chimeh, F.; Lu, Z.; Mathieu, J.; Person, K.S.; Zhang, A.; Kohn, N.; Martinello, S.; Berkowitz, R.; Holick, M.F. Factors That Influence the Cutaneous Synthesis and Dietary Sources of Vitamin D. Arch. Biochem. Biophys. 2007, 460, 213–217. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  46. Norval, M.; Björn, L.O.; de Gruijl, F.R. Is the Action Spectrum for the UV-Induced Production of Previtamin D3 in Human Skin Correct? Photochem. Photobiol. Sci. Off. J. Eur. Photochem. Assoc. Eur. Soc. Photobiol. 2010, 9, 11–17. [Google Scholar] [CrossRef]
  47. Holick, M.F. Sunlight and Vitamin D for Bone Health and Prevention of Autoimmune Diseases, Cancers, and Cardiovascular Disease. Am. J. Clin. Nutr. 2004, 80, 1678–1688. [Google Scholar] [CrossRef] [Green Version]
  48. Holick, M.F.; Chen, T.C.; Lu, Z.; Sauter, E. Vitamin D and Skin Physiology: A D-Lightful Story. J. Bone Miner. Res. 2007, 22, 28–33. [Google Scholar] [CrossRef]
  49. Matthias, W.; Michaela, F. Holick Sunlight and Vitamin D—A Global Perspective for Health. Dermato-Endocrinology 2013, 5, 51–108. [Google Scholar] [CrossRef] [Green Version]
  50. Webb, A.R. Who, What, Where and When—Influences on Cutaneous Vitamin D Synthesis. Prog. Biophys. Mol. Biol. 2006, 92, 17–25. [Google Scholar] [CrossRef]
  51. Webb, A.R.; Engelsen, O. Ultraviolet Exposure Scenarios: Risks of Erythema from Recommendations on Cutaneous Vitamin D Synthesis. Adv. Exp. Med. Biol. 2008, 624, 72–85. [Google Scholar] [CrossRef]
  52. Moan, J.; Dahlback, A. PAC At What Time Should One Go Out in the Sun? Adv. Exp. Med. Biol. 2008, 624, 86–88. [Google Scholar] [CrossRef]
  53. Tsiaras, W.G.; Weinstock, M.A. Factors Influencing Vitamin d Status. Acta Derm. Venereol. 2011, 91, 115–124. [Google Scholar] [CrossRef] [PubMed]
  54. Gallagher, J.C. Vitamin D and Aging. Endocrinol. Metab. Clin. N. Am. 2013, 42, 319–332. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  55. Webb, A.R.; Kazantzidis, A.; Kift, R.C.; Farrar, M.D.; Wilkinson, J.; Rhodes, L.E. Meeting Vitamin D Requirements in White Caucasians at UK Latitudes: Providing a Choice. Nutrients 2018, 10, 497. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  56. Webb, A.R.; Kazantzidis, A.; Kift, R.C.; Farrar, M.D.; Wilkinson, J.; Rhodes, L.E. Colour Counts: Sunlight and Skin Type as Drivers of Vitamin D Deficiency at UK Latitudes. Nutrients 2018, 10, 457. [Google Scholar] [CrossRef]
  57. Farrar, M.D.; Webb, A.R.; Kift, R.; Durkin, M.T.; Allan, D.; Herbert, A.; Berry, J.L.; Rhodes, L.E. Efficacy of a dose range of simulated sunlight exposures in raising vitamin D status in South Asian adults: Implications for targeted guidance on sun exposure. Am. J. Clin. Nutr. 2013, 97, 1210–1216. [Google Scholar] [CrossRef] [Green Version]
  58. Fernandes, M.R.; Barreto, W.D.R., Jr. Association between Physical Activity and Vitamin D: A Narrative Literature Review. Rev. Assoc. Médica Bras. 2017, 63, 550–556. [Google Scholar] [CrossRef] [Green Version]
  59. Sarkar, A.K. An Evaluation of UV Protection Imparted by Cotton Fabrics Dyed with Natural Colorants. BMC Dermatol. 2004, 4, 1–8. [Google Scholar] [CrossRef] [PubMed]
  60. Kocić, A.; Bizjak, M.; Popović, D.; Poparić, G.B.; Stanković, S.B. UV Protection Afforded by Textile Fabrics Made of Natural and Regenerated Cellulose Fibres. J. Clean. Prod. 2019, 228, 1229–1237. [Google Scholar] [CrossRef]
  61. Gies, P. Photoprotection by Clothing. Photodermatol. Photoimmunol. Photomed. 2007, 23, 264–274. [Google Scholar] [CrossRef]
  62. Aguilera, J.; De Gálvez, M.V.; Sánchez-Roldán, C.; Herrera-Ceballos, E. New Advances in Protection against Solar Ultraviolet Radiation in Textiles for Summer Clothing. Photochem. Photobiol. 2014, 90, 1199–1206. [Google Scholar] [CrossRef]
  63. Humayun, Q.; Iqbal, R.; Azam, I.; Khan, A.H.; Siddiqui, A.R.; Baig-Ansari, N. Development and Validation of Sunlight Exposure Measurement Questionnaire (SEM-Q) for Use in Adult Population Residing in Pakistan. BMC Public Health 2012, 12, 1–8. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  64. Reid, I.R.; Gallagher, D.J.A.; Bosworth, J. Prophylaxis Against Vitamin D Deficiency in The Elderly by Regular Sunlight Exposure. Age Ageing 1986, 15, 35–40. [Google Scholar] [CrossRef] [PubMed]
  65. Okan, F.; Zincir, H.; Deveci, K. The Effect of Sun Light Exposure to the Level of Vitamin D in Elderly People Living in Nursing Home. J. Clin. Densitom. 2022, 25, 261–271. [Google Scholar] [CrossRef] [PubMed]
  66. Fédération des Agences Urbaines du Maroc (MAJAL). Sur Les Traces Des Pratiques et de Savoir-Faire éco-Responsables Architecture et Urbanisme Traditionnels Au Maroc. 2016. pp. 1–126. Available online: https://www.federation-majal.ma/fr/Actualite/sur-les-traces-des-pratiques-et-de-savoir-faire-éco-responsables-architecture-et-urbanisme (accessed on 24 May 2022).
  67. Brunzell, T.; Duric, S. Moroccan Architecture, Traditional and Modern. Ph.D. Thesis, LTH School of Engineering at Campus Helsingborg Housing Development & Management, Lund University, Lund, Sweden, 2012. [Google Scholar]
  68. Daemei, A.B.; Eghbali, S.R.; Khotbehsara, E.M. Bioclimatic Design Strategies: A Guideline to Enhance Human Thermal Comfort in Cfa Climate Zones. J. Build. Eng. 2019, 25, 100758. [Google Scholar] [CrossRef]
  69. Ministère de l’Habitat et de la Politique de la Ville; Direction de la Qualité et des Affaires Techniques. Guide Des Bonnes Pratiques Pour La Maîtrise de l’énergie à l’échelle de La Ville et de l’habitat. 2014. pp. 1–124. Available online: https://www.mhpv.gov.ma/wp-content/uploads/2021/11/Guide-de-bonnes-pratiques-pour-la-maitrise-de-l-energie.pdf (accessed on 24 May 2022).
  70. Cargill, J.; Lucas, R.M.; Gies, P.; King, K.; Swaminathan, A.; Allen, M.W.; Banks, E. Validation of Brief Questionnaire Measures of Sun Exposure and Skin Pigmentation against Detailed and Objective Measures Including Vitamin D Status. Photochem. Photobiol. 2013, 89, 219–226. [Google Scholar] [CrossRef] [PubMed]
  71. Detert, H.; Hedlund, S.; Anderson, C.D.; Rodvall, Y.; Festin, K.; Whiteman, D.C.; Falk, M. Validation of Sun Exposure and Protection Index (SEPI) for Estimation of Sun Habits. Cancer Epidemiol. 2015, 39, 986–993. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  72. Hanwell, H.E.C.; Vieth, R.; Cole, D.E.C.; Scillitani, A.; Modoni, S.; Frusciante, V.; Ritrovato, G.; Chiodini, I.; Minisola, S.; Carnevale, V. Sun Exposure Questionnaire Predicts Circulating 25-Hydroxyvitamin D Concentrations in Caucasian Hospital Workers in Southern Italy. J. Steroid Biochem. Mol. Biol. 2010, 121, 334–337. [Google Scholar] [CrossRef]
  73. Køster, B.; Søndergaard, J.; Nielsen, J.B.; Allen, M.; Olsen, A.; Bentzen, J. The Validated Sun Exposure Questionnaire: Association of Objective and Subjective Measures of Sun Exposure in a Danish Population-Based Sample. Br. J. Dermatol. 2017, 176, 446–456. [Google Scholar] [CrossRef]
  74. Køster, B.; Søndergaard, J.; Nielsen, J.B.; Olsen, A.; Bentzen, J. Reliability and Consistency of a Validated Sun Exposure Questionnaire in a Population-Based Danish Sample. Prev. Med. Rep. 2018, 10, 43–48. [Google Scholar] [CrossRef]
  75. Vignali, E.; Macchia, E.; Cetani, F.; Reggiardo, G.; Cianferotti, L.; Saponaro, F.; Marcocci, C. Development of an Algorithm to Predict Serum Vitamin D Levels Using a Simple Questionnaire Based on Sunlight Exposure. Endocrine 2017, 55, 85–92. [Google Scholar] [CrossRef] [Green Version]
  76. Wu, S.; Ho, S.C.; Lam, T.P.; Woo, J.; Yuen, P.Y.; Qin, L.; Ku, S. Development and Validation of a Lifetime Exposure Questionnaire for Use among Chinese Populations. Sci. Rep. 2013, 3, 1–6. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  77. Yu, M.G.; Castillo-Carandang, N.; Sison, M.E.G.; Uy, A.B.; Villarante, K.L.; Maningat, P.; Paz-Pacheco, E.; Abesamis-Cubillan, E. Development and Validation of a Sunlight Exposure Questionnaire for Urban Adult Filipinos. Epidemiol. Health 2018, 40, e2018050. [Google Scholar] [CrossRef] [PubMed]
  78. Fitzpatrick, T.B. The Validity and Practicality of Sun-Reactive Skin Types I Through VI. Arch. Dermatol. 1988, 124, 869–871. [Google Scholar] [CrossRef] [PubMed]
  79. Glenn, D. Israel. Determining Sample Size 1. University of Florida IFAS Extension. 2012. pp. 1–5. Available online: Http://Edis.Ifas.Ufl.Edu (accessed on 10 February 2019).
  80. Benhamou, C.; Souberbielle, J.; Cortet, B. La Vitamine D Chez l’adulte: Recommandations Du GRIO. Presse Med. 2011, 40, 673–682. [Google Scholar] [CrossRef]
  81. Abourazzak, F.E.; Khazzani, H.; Mansouri, S.; Ali, S.; Alla, O.; Allali, F.; Maghraoui, A.E.; Larhrissi, S.; Rachidi, W.; Ichchou, L. Recommandations de la Société Marocaine de Rhumatologie sur la vitamine D chez l’Adulte. Rev. Mar. Rhum. 2016, 35, 3–15. [Google Scholar] [CrossRef]
  82. Wadkar, S.K.; Singh, K.; Chakravarty, R.T.; Argade, S.D. Assessing the Reliability of Attitude Scale by Cronbach’s Alpha. J. Glob. Commun. 2016, 9, 113–117. [Google Scholar] [CrossRef]
  83. George, D.; Mallery, P. SPSS for Windows Step by Step: A Simple Guide and Reference, 11.0 Update; Allyn and Bacon: Boston, MA, USA, 2003; ISBN 978-0-205-37552-3. [Google Scholar]
  84. Kaiser, H.F. An Index of Factorial Simplicity. Psychometrika 1974, 39, 31–36. [Google Scholar] [CrossRef]
  85. Liau, A.; Tan, T.K.; Angeline, K. Scale Measurement: Comparing Factor Analysis and Variable Clustering. SAS Glob. Forum 2011, 1–19. Available online: https://support.sas.com/resources/papers/proceedings11/352-2011.pdf (accessed on 5 December 2021).
  86. Serrano, M.A.; Cañada, J.; Moreno, J.C.; Gurrea, G. Solar Ultraviolet Doses and Vitamin D in a Northern Mid-Latitude. Sci. Total Environ. 2017, 574, 744–750. [Google Scholar] [CrossRef]
  87. Blarduni Cardón, E.; Cardón, B.E.; Ugarte, A.H.; Etxebarria, U.I.; González, C.L.; Goivide, G. La Dieta Como Factor de Riesgo de Hipovitaminosis D En La Población Pediátrica Española. Rev. Osteoporos. Metab. Min. 2021, 13, 122–129. [Google Scholar] [CrossRef]
  88. Castano, L.; Madariaga, L.; Grau, G.; García-Castaño, A. 25(OH)Vitamin D Deficiency and Calcifediol Treatment in Pediatrics. Nutrients 2022, 14, 1854. [Google Scholar] [CrossRef]
  89. van der Mei, I.A.F.; Blizzard, L.; Ponsonby, A.-L.; Dwyer, T. Validity and Reliability of Adult Recall of Past Sun Exposure in a Case-Control Study of Multiple Sclerosis. Cancer Epidemiol. Biomarkers Prev. 2006, 15, 1538–1544. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  90. Stewart, A.E.; Kimlin, M.G. The Dislike of Hot Thermal Conditions and Its Relationship with Sun (Ultraviolet Radiation) Exposure in the Southeastern United States. Int. J. Environ. Res. Public. Health 2018, 15, 2161. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  91. Diffey, B.L. Time and Place as Modifiers of Personal UV Exposure. Int. J. Environ. Res. Public. Health 2018, 15, 1112. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  92. Tavakol, M.; Dennick, R. Making Sense of Cronbach’s Alpha. Int. J. Med. Educ. 2011, 2, 53–55. [Google Scholar] [CrossRef] [PubMed]
  93. Blázquez-Sánchez, N.; Rivas-Ruiz, F.; Bueno-Fernández, S.; Arias-Santiago, S.; Fernández-Morano, M.T.; deTroya-Martín, M. Validation of a Questionnaire Designed to Study Knowledge, Attitudes, and Habits Related to Sun Exposure Among Young Adults: The CHACES Questionnaire. Actas Dermo-Sifiliográficas Engl. Ed. 2020, 111, 579–589. [Google Scholar] [CrossRef]
  94. Mansibang, N.M.M.; Yu, M.G.Y.; Jimeno, C.A.; Lantion-Ang, F.L. Association of Sunlight Exposure with 25-Hydroxyvitamin D Levels among Working Urban Adult Filipinos. Osteoporos. Sarcopenia 2020, 6, 133–138. [Google Scholar] [CrossRef] [PubMed]
  95. Abda, N.; El Rhazi, K.; Obtel, M.; Bendahhou, K.; Zidouh, A.; Bennani, M.; Bekkali, R.; Nejjari, C. Determinants of Self-Reported Sun Protection Practices among Moroccan Population. Prev. Med. 2012, 54, 422–424. [Google Scholar] [CrossRef] [PubMed]
  96. Sham, L.; Yeh, E.A.; Magalhaes, S.; Parra, E.J.; Gozdzik, A.; Banwell, B.; Hanwell, H.E. Evaluation of Fall Sun Exposure Score in Predicting Vitamin D Status in Young Canadian Adults, and the Influence of Ancestry. J. Photochem. Photobiol. B 2015, 145, 25–29. [Google Scholar] [CrossRef]
Figure 1. Steps in developing and validating sun exposure score.
Figure 1. Steps in developing and validating sun exposure score.
Nutrients 15 00688 g001
Figure 2. Scree plot by principal component analysis of the sun exposure score (SES).
Figure 2. Scree plot by principal component analysis of the sun exposure score (SES).
Nutrients 15 00688 g002
Figure 3. Sun exposure score classification of women of childbearing age.
Figure 3. Sun exposure score classification of women of childbearing age.
Nutrients 15 00688 g003
Table 1. Results of Kaiser–Meyer–Olkin (KMO) and Bartlett’s test.
Table 1. Results of Kaiser–Meyer–Olkin (KMO) and Bartlett’s test.
KMO Measure of Sampling Adequacy0.755
Bartlett’s Test of SphericityApprox. Chi-Square1882.232
Df105
Sig.0.000
Table 2. Results of principal component analysis of the SES (varimax-rotated with Kaiser Normalization).
Table 2. Results of principal component analysis of the SES (varimax-rotated with Kaiser Normalization).
Item CodeItem DescriptionComponentCommunalities
1234
Indoor sun exposure
1Frequency of indoor sun exposure (in terrace, balcony, courtyard)0.1110.842−0.1460.1410.763
2Indoor exposed body part0.0120.936−0.102−0.0110.887
3Indoor duration sun exposure0.0040.9130.0170.0210.834
4Indoor sun exposure time slot−0.0500.907−0.0340.0740.832
Outdoor professional or routine activities
5Frequency of professional or routine outdoor activities,−0.059−0.2480.7460.0020.622
6A time slot for professional or routine outdoor activities−0.002−0.0440.8560.0390.736
7Duration of professional or routine outdoor activities−0.0130.0680.8950.1310.824
8Outdoor exposed body part−0.166−0.0460.873−0.0090.792
Outdoor recreational activities
9Practice outdoor activities (sports, hiking, walking, camping, swimming, etc.)0.8960.0120.0240.0080.803
10Duration outdoor activities0.9220.0250.0200.0870.858
11Time slot for sun exposure in the open air0.8380.008−0.3060.0790.802
12Part of the body exposed in the open air0.9480.026−0.0570.0410.904
Sun protection practices
13Type of clothing usually used−0.176−0.0410.0040.6990.522
14Type of sunscreen used0.2110.1260.0410.9110.892
15Staying out of the sun0.2210.1380.1120.8680.834
Initial Eigenvalues4.0813.1702.9141.741
Explained variance %.27.20721.13619.42711.604
Cumulative variance %.27.20748.34367.77079.374
Cronbach’s alpha coefficient0.9090.9230.8350.787
Table 3. Correlation of socio-demographic characteristics with sun exposure score classes.
Table 3. Correlation of socio-demographic characteristics with sun exposure score classes.
Socio-Demographic CharacteristicsTotal
(N = 160)
Sun Exposure ScoreSun Exposure Classes
(N = 160)p-ValueInsufficient
(N = 11)
Moderately Sufficient
(N = 58)
Sufficient e
(N = 91)
p-Value
Mean ± SD Frequency (%)
Age (yr)
(Median [IQR])
25 [11]15.82 ± 5.640.211 a 0.858 b
18–2586 (53.7)15.23 ± 5.70 6 (54.5)34 (58.6)46 (50.5)
26–3554 (33.8)17.05 ± 5.62 3 (27.3)18 (31)33 (36.3)
36–4520 (12.5)14.97 ± 5.09 2 (18.2)6 (10.4)12 (13.2)
BMI (kg/m2)
(Median [IQR])
25.70 [8.65] 0.018a 0.02 b
Normal weight
(<25 kg/m2)
68 (42.5)16.31 ± 5.61 3 (27.3)24 (41.4)41 (45.1)
Overweight
(25.0 to <30 kg/m2
44 (27.5)16.93 ± 6.07 4 (36.4)9 (15.5)31 (34.1)
Obese (>30 kg/m2)48 (30)14.09 ± 4.94 4 (36.4)25 (43.1)19 (20.9)
Location living % 0.001C
Urban102 (63.7)14.73 ± 5.47 9 (81.8)42 (72.4)51 (56)0.056 d
Rural58 (36.3)17.72 ± 5.38 2 (18.2)16 (27.6)40 (44)
Housing % 0.001C 0.003d
House93 (58.1)17.03 ± 5.65 6 (54.5)24 (41.4)63 (69.2)
Apartment67 (41.9)14.13 ± 5.21 5 (45.5)34 (58.6)28 (30.8)
Marital status % <0.0001C 0.002d
Married84 (52.5)14.73 ± 5.47 4 (36.4)21 (36.2)59 (64.8)
Single76 (47.5)14.73 ± 5.47 7 (63.6)37 (63.8)76 (47.5)
Parity % <0.0001C 0.006d
Nulliparous76 (47.5)14.05 ± 5.68 7 (36.6)37 (63.8)32 (35.2)
Primiparous18 (11.3)19.46 ± 5.78 1 (9.1)2 (3.4)15 (16.5)
Multiparous66 (41.2)16.84 ± 4.85 3 (27.3)19 (32.8)44 (48.4)
Profession % <0.0001C 0.033d
Housewife80 (50)16.73 ± 5.58 6 (54.5)22 (37.9)52(57.1)
Students56 (35)13.56 ± 5.04 5 (45.5)28 (48.3)23 (25.3)
Official/salaried24 (15)18.02 ± 5.67 08 (13.8)16 (17.6)
a Spearman test. b Kruskal –Wallis test. C Univariate ANOVA test. d Pearson’s chi-squared test. e Due to the small sample size of the high score (n = 2), they were merged with the sufficient score.
Table 4. Correlation of socio-demographic characteristics with sun exposure score domains.
Table 4. Correlation of socio-demographic characteristics with sun exposure score domains.
Socio-Demographic CharacteristicsIndoor Sun ExposureOutdoor Sun ExposureSun Protection Practices
Median [IQR]p-ValueMedian [IQR]p-ValueMedian [IQR]p-Value
Age (yr) 0.16 a 0.633 a 0.266 a
18–254.50 [4.5] 7.31 [6.19] 3.38 [3.52]
26–355.06 [2.81] 9.56 [6.75] 3.38 [2.95]
36–454.5 [4.22] 7.31 [6.47] 3.38 [1.64]
BMI (Kg/m2) 0.152 a <0.0001a 0.673 a
Normal weight
(<25 kg/m2)
4.50 [5.06] 10.13 [6.19] 3.38 [3.94]
Overweight
(25.0 to <30 kg/m2)
5.16 [2.16] 8.34 [5.91] 3.38 [2.06]
Obese(>30 kg/m2)4.78 [3.33] 6.28 [3.38] 3.38 [2.67]
Location living <0.0001b 0.907 b 0.001b
Urban3.75 [5.06] 7.41 [5.63] 3.56 [2.95]
Rural5.63 [1.69] 8.91 [6.75] 3.38 [2.06]
Housing <0.0001b 0.356 b 0.007b
House5.06 [1.41] 7.88 [6.75] 3.38 [3.38]
Apartment1.5 [4.5] 7.88 [5.63] 3.38 [2.06]
Marital status <0.0001b 0.309 b <0.0001b
Married5.06 [1.13] 9.56 [6.19] 3.38 [3.38]
Single3.38 [5.06] 7.31 [5.90] 3.38 [1.69]
Parity <0.0001b 0.14 b 0.001b
Nulliparous3.38 [5.06] 7.31 [5.90] 3.38 [1.68]
Primiparous5.63 [1.26] 10.97 [5.06] 3.38 [2.25]
Multiparous5.06 [1.73] 7.59 [6.75] 3.38 [3.38]
Profession <0.0001b 0.007b 0.003b
Housewife5.06 [1.5] 7.41 [6.61] 3.38 [3.38]
Students3.38 [5.06] 7.31 [5.34] 3.09 [1.69]
Official/salaried4.78 [5.48] 10.69 [5.48] 3.38 [1.36]
a Spearman test. b Univariate ANOVA test.
Table 5. Sun exposure scores by domains.
Table 5. Sun exposure scores by domains.
SES DomainsSun Exposure Classes
Total
Median [IQR]
Spearman’s Rhop-Value aInsufficientModerately SufficientSufficientp-Value b
Median [IQR]
Indoor sun exposure4.78 [3.00]0.65<0.00011.5 [2.06]6.80 [4.84]10.47 [6.66]<0.0001
Outdoor sun exposure7.88 [6.19]0.827<0.00012.48 [1.31]6.09 [2.25]11.25 [4.5]<0.0001
Sun protection practices3.38 [3.18]0.658<0.00011.13 [0.75]2.25 [1.69]3.75 [2.25]<0.0001
Pairwise comparisons of sun exposure classes
Insufficient-moderately sufficient 0.103
Insufficient-sufficient <0.0001
Moderately sufficient-sufficient<0.0001
a Spearman test. b Kruskal–Wallis test.
Table 6. Correlation of sun exposure scores domains with 25-OHD Levels.
Table 6. Correlation of sun exposure scores domains with 25-OHD Levels.
SES DomainsSerum 25-OHD (ng/mL)
Spearman’s Rhop-Value
Sun exposure score0.615<0.0001
Indoor sun exposure0.307<0.0001
Outdoor sun exposure0.605<0.0001
Sun protection practices0.424<0.0001
Table 7. Participants’ vitamin D levels were ranked according to sun exposure score classes.
Table 7. Participants’ vitamin D levels were ranked according to sun exposure score classes.
Sun Exposure ClassesSerum 25-OHD (ng/mL)Vitamin D Status
N = 160
Median [IQR]
p-Value aDeficiencyInsufficiencyp-Value
N = 104N = 56
Frequency (%)
Insufficient4.78 [4.65]<0.000111 (10.6)00.001 b
Moderately sufficient6.80 [4.84]<0.000149 (47.1)9 (16.1)
Sufficient10.47 [6.66]<0.000144 (42.3)47 (83.9)
Sun exposure score (Mean ± SD)8.42 [6.41]<0.000113.62 ± 4.8119.88 ± 4.78<0.0001 c
a Spearman test. b Pearson’s chi-squared test. c Univariate ANOVA test.
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Lhilali, I.; Zouine, N.; Menouni, A.; Godderis, L.; Kestemont, M.-P.; El Midaoui, A.; El Jaafari, S.; Filali-Zegzouti, Y. Sun Exposure Score and Vitamin D Levels in Moroccan Women of Childbearing Age. Nutrients 2023, 15, 688. https://doi.org/10.3390/nu15030688

AMA Style

Lhilali I, Zouine N, Menouni A, Godderis L, Kestemont M-P, El Midaoui A, El Jaafari S, Filali-Zegzouti Y. Sun Exposure Score and Vitamin D Levels in Moroccan Women of Childbearing Age. Nutrients. 2023; 15(3):688. https://doi.org/10.3390/nu15030688

Chicago/Turabian Style

Lhilali, Ilham, Noura Zouine, Aziza Menouni, Lode Godderis, Marie-Paule Kestemont, Adil El Midaoui, Samir El Jaafari, and Younes Filali-Zegzouti. 2023. "Sun Exposure Score and Vitamin D Levels in Moroccan Women of Childbearing Age" Nutrients 15, no. 3: 688. https://doi.org/10.3390/nu15030688

APA Style

Lhilali, I., Zouine, N., Menouni, A., Godderis, L., Kestemont, M. -P., El Midaoui, A., El Jaafari, S., & Filali-Zegzouti, Y. (2023). Sun Exposure Score and Vitamin D Levels in Moroccan Women of Childbearing Age. Nutrients, 15(3), 688. https://doi.org/10.3390/nu15030688

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop