Next Article in Journal
Insights into Asparaginase from Endophytic Fungus Lasiodiplodia theobromae: Purification, Characterization and Antileukemic Activity
Previous Article in Journal
Hyperthermic Intraperitoneal Chemotherapy in the Management of Gastric Cancer: A Narrative Review
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Consumption of Sugar-Sweetened or Artificially Sweetened Beverages and Semen Quality in Young Men: A Cross-Sectional Study

by
Maiken Meldgaard
1,
Nis Brix
2,3,
Anne Gaml-Sørensen
2,
Andreas Ernst
2,4,
Cecilia Høst Ramlau-Hansen
2,
Sandra Søgaard Tøttenborg
5,
Karin Sørig Hougaard
6,
Jens Peter Ellekilde Bonde
5,7 and
Gunnar Toft
8,*
1
Unit for Applied Public Health, Department of Public Health, Research, Aarhus University, 8000 Aarhus, Denmark
2
Research Unit for Epidemiology, Department of Public Health, Aarhus University, 8000 Aarhus, Denmark
3
Department of Clinical Genetics, Aarhus University Hospital, 8200 Aarhus, Denmark
4
Department of Urology, Aarhus University Hospital, 8200 Aarhus, Denmark
5
Department of Occupational and Environmental Medicine, Bispebjerg and Frederiksberg Hospital, 2400 Copenhagen, Denmark
6
Denmark and National Research Centre for the Working Environment, Department of Public Health, University of Copenhagen, 1353 Copenhagen, Denmark
7
Department of Public Health, University of Copenhagen, 1353 Copenhagen, Denmark
8
Steno Diabetes Center Aarhus, Aarhus University Hospital, 8200 Aarhus, Denmark
*
Author to whom correspondence should be addressed.
Int. J. Environ. Res. Public Health 2022, 19(2), 682; https://doi.org/10.3390/ijerph19020682
Submission received: 1 December 2021 / Revised: 27 December 2021 / Accepted: 30 December 2021 / Published: 7 January 2022
(This article belongs to the Section Reproductive Health)

Abstract

:
Background: Existing literature suggests that frequent consumption of sugar-sweetened drinks may be associated with lower semen quality. Studies performed in mice suggest a dose-response relationship between intake of saccharin or aspartame, two artificial sweeteners, and sperm and testis function. Methods: A cross-sectional study based on data from The Fetal Programming of Semen Quality (FEPOS) Cohort, including 1047 young men (mean age = 19 years) was performed. Each male participant completed an online questionnaire on health, health behavior and diet, and provided a semen sample. The associations between consumption of sugar-sweetened or artificially sweetened beverages (moderate ≥ 3 days/week; infrequent < 3 days/week) and semen quality were analyzed using a multivariable, negative, binomial regression model. Results: Sugar-sweetened or artificially sweetened beverage consumption was not strongly associated with either semen volume, sperm concentration, total sperm count or total motility in young men. The proportion of morphologically normal sperm was 11% lower (0.89 (95% CI 0.76, 1.04)) for moderate (≥3 days/week) consumption of artificially sweetened beverages relative to infrequent (<3 days/week). Conclusion: Consumption of sugar-sweetened or artificially sweetened beverages, at the levels present in this study had limited effect on the measured markers of semen quality in young men.

1. Introduction

Low semen quality is a major cause of poor male fecundity [1], which is a public health burden linked to psycho-social distress, increased mortality, and the development of diseases [2,3,4,5,6,7,8]. Consumption of sugar-sweetened beverages is frequent and increasing among both children and adults [9,10]. In a few studies, frequent consumption of sugar-sweetened beverages has been associated with lower semen quality [11,12,13]. Especially the consumption of cola has been linked to lower semen characteristics, including semen volume, sperm concentration, total sperm count, and total motility [14,15,16,17].
High consumption of sugar-sweetened beverages is associated with weight gain and obesity [18,19,20,21], and several studies find obesity to be associated with poor semen quality in men [22,23,24,25,26,27,28,29]. However, only one study explored the potential mediatory role of obesity, and found that body mass index (BMI) modified the association between sugar-sweetened beverage consumption and progressive sperm motility [11]. It has been proposed that the underlying mechanisms of obesity are linked to insulin resistance and metabolic syndrome with the associated generation of oxidative stress, which might affect spermatogenesis, but could also interfere with production and regulation of sex hormones, including testosterone and sex hormone-binding globulin levels [18,21,30,31,32,33].
Two studies investigated artificially sweetened beverages in relation to fertility in men and found no association [12,34]. Consumption of artificially sweetened beverages is not associated with weight gain and obesity in itself, but it may affect gut microbiome, taste receptors and a learned behavior toward preference for a sweet taste [35,36,37]. This might increase the risk of obesity and metabolic syndrome, due to higher intake of sugary foods and drinks, and potentially impact male reproduction, including semen quality. In addition, mice studies have found that exposure to high levels of artificial sweeteners, such as saccharin and aspartame, affects several sperm and testicular parameters negatively and, furthermore, interfered with hormones of the hypothalamic-pituitary-gonadal axis [38,39,40].
Overall evidence of associations between consumption and semen quality is scarce in studies on humans. We, therefore, aimed to investigate the associations between consumption of sugar or artificially sweetened beverages and semen quality characteristics, using a large cohort of young Danish men. We hypothesized that consumption of sugar-sweetened or artificially sweetened beverages was associated with lower semen quality characteristics in young men, and that the effect is mediated by higher BMI.

2. Materials and Methods

2.1. Study Population

This cross-sectional study was based on data from the Fetal Programming of Semen Quality (FEPOS) cohort, a sub-cohort within the Danish National Birth Cohort [41]. The DNBC recruited more than 92,000 pregnant women during their first trimester, in the years between 1996 and 2002. The women provided information on pregnancy, health behavior, and general health in computer-assisted telephone interviews scheduled around gestational week 12.
Men eligible for participation in the FEPOS cohort were born between 1998 and 2001 to mothers in the DNBC and lived near Aarhus or Copenhagen at the time they turned 18 years and 9 months of age (n = 21,960). Between March 2017–December 2019, a total of 5697 men were selected and invited to participate in the FEPOS cohort [42]. Invited men were encouraged to decline participation if they had a medical history of cryptorchidism, sterilization, or chemotherapy. They filled out a comprehensive online questionnaire to provide in-depth information on diet and health behavior, and information on several anthropometric characteristics, including heigh and weight. In addition, the men delivered a semen sample, a blood sample, and a urine sample. In total, 1047 (19%) participated in both the FEPOS questionnaire and the clinical examination, and had semen characteristics measured, see Figure 1.

2.2. Sugar-Sweetened and Artificially Sweetened Beverage Consumption

Information on consumption of sugar-sweetened and artificially sweetened beverages was obtained from the online FEPOS questionnaire. The participants were asked how many days a week (every day; 5–6 days a week; 3–4 days a week; 1–2 days a week; less than one day a week) they consumed sugar-sweetened drinks and artificially sweetened drinks, respectively. Data on sugar-sweetened and artificially sweetened beverage consumption were each dichotomized into moderate (≥3 days a week) and infrequent (<3 days a week) consumption.

2.3. Semen Quality Measurement

Participants were instructed to provide a semen sample adjacent to or at the clinical examination. The semen sample was placed on a tilt in an incubator at 37 °C. Participants were encouraged not to ejaculate for 2–4 days before sample collection but were included irrespectively of abstinence time.
Semen analyses were performed manually according to the WHO guidelines [1] and in alignment with the checklist for human semen analysis provided in Björndahl et al. [43]. The two trained biomedical laboratory technicians conducting the semen analyses participated in a follow-up quality control with the Reproductive Medicine Centre in Malmö. The validation was satisfactory and met international standards as well as earlier similar comparisons [42,44].
The following semen characteristics were included in the study: sample volume (mL), concentration (mill./mL) total sperm count (mill. [concentration * volume]), total motility (A + B%), and morphology (% normal sperm). The description of semen characteristics, and analyses, are further described in the FEPOS profile paper [42].

2.4. Co-Variates

Prior to analysis, potential confounders were identified using Directed Acyclic Graphs (DAG) [45,46,47] based on existing literature. From the FEPOS questionnaire, we obtained information on the following potential confounders: intake of candy (<3 days a week; ≥3 days a week), intake of cake (<3 days a week; ≥3 days a week), intake of coffee (<3 days a week; ≥3 days a week), intake of energy drink (<3 days a week; ≥3 days a week) and smoking status (yes (yes current, yes occasionally); no (no never, no former)). From the first baseline interview in the DNBC, we obtained information on the following potential confounders: maternal pre-pregnancy BMI (<18.5; 18.5–24.9; ≥25), maternal first trimester smoking status (smoker; non-smoker), and highest parental socioeconomic status (student or unknown; skilled or unskilled worker; low grade professional; high grade professional) based on Danish International Standard Classification of Occupations (DISCO-08), v1:2010 [48].
Other co-variates, including spillage (yes; no), abstinence time (days) and fever within three months prior to sampling (yes; no), were provided by the participants immediately after semen collection, while time to analysis (minutes) was noted by the laboratory technician prior to analysis of the semen sample. The participants’ own BMI was categorized as (<18.5; 18.5–24.9; ≥25 kg/m²) and used in a supplementary analysis. Co-variates were categorized as shown in Table 1. An unhealthy diet variable dichotomized as candy, cake, chocolate, cocoa and chips intake (<5 days a week; ≥5 days a week) was generated and used in a supplementary analysis.

2.5. Statistical Analysis

Statistical analyses were conducted in STATA-16 (StataCorp, College Station, TX, USA). The medians, 5th and 95th pseudo percentiles (average of five observations nearest to the actual percentile) of each semen quality characteristic (volume, sperm concentration, total sperm count, total motility, and morphology) were calculated according to frequency of consumption of sugar-sweetened or artificially sweetened beverages.
We estimated crude and adjusted ratios of semen characteristics according to consumption using negative binomial regression models. This approach was chosen because the conditional distributions were over-dispersed (conditional variance exceeded the conditional mean). The negative binomial regression models were checked by comparing the observed distribution of semen parameters against the model-based distributions from the fitted model using QQ-plots; subsequently, standardized deviance residuals were plotted against model-based predictions. The model check was acceptable (data not shown). The estimates were interpreted as percentage differences between exposure groups. Statistical models were adjusted for the identified potential confounders and the two variables, abstinence time and fever, to increase precision of the estimates. Total motility was additionally adjusted for time from ejaculation to analysis. In the analyses of total sperm count and volume, participants reporting spillage were excluded from the analysis [n = 185].
Selection weights were used in all analyses to account for non-participation [49] and derived by multivariable logistic regression of participation (yes; no) on potential predictors of participation (parental socio-economic status, maternal smoking and maternal BMI) to estimate the probability of participation for each participant. These predictors were chosen a priori based on a DAG. The inverse probabilities were used as selection weights. As information from the FEPOS questionnaire was only available for participants; we considered maternal information as proxies for information on the son’s likelihood of participation.
Supplementary analyses were performed with a finer categorization of exposure data (less than weekly; 1–2 days a week; 3–4 days a week; 5–6 days a week; every day) and, in addition, we introduced this new variable as a continuous variable into the regression model. This was undertaken for both sugar-sweetened and artificially sweetened beverage consumption to capture any potential doses-response associations. Additionally, a supplementary analysis for moderate consumption of sugar-sweetened and artificially sweetened beverages combined was performed. The potential mediatory role of BMI was explored by simple adjustment. A supplementary analysis of associations between consumption of sugar-sweetened beverages and semen quality was performed with additional adjustment for an unhealthy diet variable.

2.6. Ethical Approval

Informed consent was collected from all participants prior to study participation. The establishment of The FEPOS Cohort was approved by the Scientific Research Ethics Committee for Copenhagen and Frederiksberg (No. H-16015857).

3. Results

3.1. Study Participants

The participants who consumed sugar-sweetened beverages infrequently (<3 days a week) had candy intake < 3 days a week (63%), cake intake < 3 days a week (66%), consumed energy drinks < 3 days a week (70%), and were normal weight (54%). Similar characteristics were found for participants who had infrequent (<3 days a week) consumption of artificially sweetened beverages. Mothers of participants with infrequent (<3 days a week) consumption of sugar-sweetened beverages were mainly non-smokers (58%) and normal weight (51%). This was also the case for mothers of participants with infrequent (<3 days a week) consumption of artificially sweetened beverages as well as non-smoking mothers of sons with infrequent (<3 days a week) consumption of artificially sweetened beverages (69%) (Table 1).

3.2. Beverage Consumption and Semen Quality

In total, 28% of participants consumed sugar-sweetened beverages ≥ 3 days a week and 11% of participants consumed artificially sweetened beverages ≥ 3 days a week. A small group of participants had moderate consumption of both sugar-sweetened and artificially sweetened beverages (n = 30). Distributions of semen characteristics according to infrequent or moderate consumption of sugar-sweetened or artificially sweetened beverages are shown in Table 2.

3.3. Associations between Exposure and Outcome

Adjusted ratios for semen volume, sperm concentration, total sperm count and total motility between moderate and infrequent consumption of sugar-sweetened or artificially sweetened beverages were all close to one, after adjustment (Table 3). Adjusted ratios for sperm morphology were 11% lower for moderate consumption of artificially sweetened beverages relative to infrequent consumption, with an adjusted ratio of 0.89 (95% CI 0.76, 1.04).
A supplementary analysis with finer categorization of exposure status and with exposure statuses modeled as continuous variables gave results not substantially different from those obtained in the main analysis (Table 4). Neither did a supplementary analysis with both moderate consumption of sugar-sweetened and artificially sweetened beverages combined (data not shown). In a supplementary analysis, further adjustment for BMI did not give substantially different results (Table S1). Supplementary analyses with inclusion of an unhealthy diet variable (Table S2) or presence of varicocele (no; yes; yes, but treated) (Table S3) in the analyses of sugar-sweetened beverage consumption and semen quality parameters did not change the results.

4. Discussion

4.1. Main Findings

Overall, neither consumption of sugar-sweetened nor artificially sweetened beverages was strongly associated with semen volume, sperm concentration, total motility and total sperm count in this study. The percentage of morphologically normal sperm tended to be lower for moderate than for infrequent consumption of artificially sweetened beverages. However, we did not see any clear dose-response association, and participants with everyday consumption of sugar-sweetened (n = 38) or artificially sweetened (n = 15) beverages constituted a minority in this study.

4.2. Strength and Limitations

The noteworthy strengths of the present study include detailed information on exposures and co-variates collected based on an extensive, online questionnaire that was completed in close proximity to the clinical examination. This allowed for adjustment for potential confounding factors. Further, the study was based on a large population-based sample of young men from the Danish National Birth Cohort [41], which also allowed us to adjust for potential prenatal covariates. Inclusion criteria were limited to ensure a relatively unselected sample of the DNBC participants. However, participants were encouraged to decline participation in case of cryptorchidism, a factor strongly related to semen quality [50].
The cross-sectional study design introduces some limitations. Information on exposure and outcome was collected at one point in time, which prevents the separation of exposure and outcome in time. Participants were instructed to recall consumption of sugar-sweetened and artificially sweetened beverages back in time, which may be imprecise [51,52], potentially leading to measurement error on the exposure. However, this was unlikely to be related to the semen characteristics, as most participants would be unaware of their semen quality due to their young age at recruitment and, hence, low likelihood of participants having tried to reproduce. This reduces the risk of differential measurement error on the exposures and the risk of reverse causation due to the cross-sectional study design. All semen analyses followed WHO guidelines and were performed manually with the technicians blinded to the participants’ exposure, which minimized the risk of measurement error of the outcomes [1]. Internal and external quality control ensured high precision of semen analyses. Biological variation of semen measurement may have caused random measurement error. No physical exam to identify urological diseases was performed, which can be considered a limitation in this study. However, inclusion of varicocele in a supplementary analysis did not impact the findings.
While exposure might be associated with participation, the outcome was likely not due to the young age of participants, limiting the risk of selection bias. However, we cannot rule out that some men opted for participation due to a true suspicion of poor semen quality. Some may be aware of parental fecundability, which might affect the likelihood of participation and potentially introduce selection bias. However, we employed selection weights in all analyses to minimize this potential residual selection problem due to non-participation.
The detailed information on co-variates from the FEPOS questionnaire and the maternal interview during pregnancy in the DNBC [41], allowed us to adjust for potential confounders and strong predictors of the outcome to reduce confounding and improve precision. Although we had solid information on co-variates from both the prenatal and the current period, we did not measure actual, detailed consumption of sugar-sweetened and artificially sweetened beverages from a validated Food Frequency Questionnaire (FFQ).

4.3. Interpretation of Results Compared to Existing Literature

The associations have been studied in previous studies. The young age of participants in our study may be part of the explanation of why our results are inconclusive compared to other similar studies [12]. Additionally, consumption of both sugar-sweetened and artificially sweetened beverages was low compared to the studies that found associations between consumption and semen quality [11,13,39]. A cross-sectional study reported a negative association between sugar-sweetened beverage consumption and total motility among 189 healthy, young men from Rochester University [11]. The major strengths of that study included the use of a validated Food Frequency Questionnaire (FFQ) to collect exposure information as basis for derivation of an overall diet variable. However, the study population was small. Men in the highest quartile of sugar-sweetened beverage consumption had a daily intake of ≥ 1.3 servings. Hence, the exposure contrast was possibly much higher than in our study or might indicate risk of exposure misclassification in our study. This study found no evidence regarding BMI as an intermediate factor of the association. In addition, a recently published study by Nassan et al. found intake of sugar-sweetened beverages to be associated with lower sperm concentration and lower total sperm count [13]. The participants were the same age as in our study, but consumption of sugar-sweetened beverages was much higher compared to our study.
A cross-sectional study also by Nassan et al. investigated associations between dietary patterns and testicular function in 2935 young Danish men (median age 19 years) [53]. They found that higher adherence to a Western diet pattern (high intake of sugar-sweetened beverages, sweets, desserts, french fries, pizza, processed food, energy drink etc.) was associated with lower semen quality. Nassan et al. used a modified version of a previously validated Food Frequency Questionnaire (FFQ). Hence, they were able to determine that the highest quintile of young men, who mainly had a Western diet pattern, had a total sugar intake of 90 g a day. Similar information was not available in our study. The majority of the participants in our study did not have a Western diet pattern. In general, their diet patterns more resembled with what Nassan et al. [53] called the prudent pattern and the open-sandwich pattern (healthier diet patterns). The diet pattern together with the low consumption of sugar-sweetened and artificially sweetened beverages among our study population might explain the differences between the two studies.
A cohort study with prospectively collected exposure data also investigated consumption of sugar-sweetened beverages [12]. However, compared to our study, the outcome measure was fecundability. The target population was pregnancy planners, which were probably aware of their fecundability, hence, introducing risk of selection bias. The study population consisted of both females and their male partners, who were followed from 2013–2017. Consumption of sugar-sweetened beverages 7 days a week by, in the male partner were associated with lower fecundability. As in the cross-sectional study described above, the exposure contrast was much larger compared to our study. In our study, only a minority reported consumption of sugar-sweetened beverages every day, as the majority of participants in our study consumed sugar-sweetened beverages < 3 days a week (72%) and artificially sweetened beverages < 3 days a week (89%). Based on data reported in the FEPOS cohort, we can therefore not exclude that higher consumption might affect semen quality negatively. Hatch et al. found no evidence of association between consumption of artificially sweetened beverages and fecundability. In our study, there were indications of reduced morphology in moderate consumers of artificially sweetened beverages. Morphology, in particular, was not a priori hypothesized to play a significant role. We cannot exclude that the changes found for morphology might be a chance finding. Gong et al. and Anbara et al. found evidence of associations between intake of saccharin and aspartame on testis function in mice, but no particular effect on morphology was found [38,39,40].
Caffeine (especially from cola) was associated with reduced sperm concentration and total sperm count in a Danish study investigating caffeine intake and semen quality in a study population of 2554 young men [14]. In the present study, we did not have an overall caffeine variable. However, our analyses were adjusted for energy drink and coffee consumption. Cola was part of the sugar-sweetened beverage consumption among participants, but we were not able to determine the precise amount.

5. Conclusions

In conclusion, we did not observe marked associations between consumption of sugar-sweetened or artificially sweetened beverages and semen quality in young men, although a slightly lower percentage of morphologically normal sperm was observed among consumers of artificially sweetened beverages ≥ 3 days per week in this study. The study population had only moderate consumption of sugar-sweetened and artificially sweetened beverages compared to similar studies. It is reassuring for young people that moderate consumption of sugar-sweetened or artificially sweetened beverages appears to have limited effects on semen quality, but the finding should be interpreted cautiously and needs confirmation in future studies. Further large-scale studies with higher exposure levels and more precise estimation of consumption of sugar-sweetened and artificially sweetened beverages are warranted.

Supplementary Materials

The following are available online at https://www.mdpi.com/article/10.3390/ijerph19020682/s1, Table S1: Adjusted outcome ratios with and without BMI adjustment according to sugar-sweetened and artificially sweetened beverage consumption among participants, FEPOS 2017–2019, Table S2: Adjusted outcome ratios including unhealthy diet according to sugar-sweetened beverage consumption among participants, FEPOS 2017–2019; Table S3: Adjusted outcome ratios including varicocele according to sugar-sweetened or artificially sweetened beverage consumption among participants, FEPOS 2017–2019.

Author Contributions

M.M. drafted the manuscript, performed statistical analyses, and designed tables and figures. C.H.R.-H., S.S.T., K.S.H., J.P.E.B. and G.T. were involved in the steering committee and project group of FEPOS, study concept and design. S.S.T. and J.P.E.B. were responsible for data collection. N.B. and A.E. supervised analyses. Data management was undertaken by S.S.T., J.P.E.B. and A.G.-S. All authors were involved in the critical revision of the manuscript. All authors have read and agreed to the published version of the manuscript.

Funding

This publication is part of the ReproUnion collaborative study, co-financed by the European Union, Intereg V ÖKS (20200407). The FEPOS project was further funded by the Lundbeck Foundation (R170-2014-855), the Capital Region of Denmark, Medical doctor Sofus Carl Emil Friis and spouse Olga Doris Friis’s Grant, Axel Muusfeldt’s Foundation (2016-491), A.P. Møller Foundation (16–37), the Health Foundation and Dagmar Marshall’s Fond. In addition, this study was supported by Aarhus University.

Institutional Review Board Statement

The study was conducted according to the guidelines of the Declaration of Helsinki and approved by the Scientific Research Ethics Committee for Copenhagen and Frederiksberg (No. H-16015857).

Informed Consent Statement

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

Acknowledgments

We are grateful to all participants and to biomedical laboratory technologists Marianne Lipka Flensborg and Joan Dideriksen for running the clinics and collecting data. We also thank Josefine Rahbæk Larsen for assisting with recruitment and data entry, Katia Keglberg Hærvig for collecting, cleaning and managing data, and Cecilia Tingsmark for doing the morphology analysis. The Danish National Birth Cohort was established with a significant grant from the Danish National Research Foundation. Additional support was obtained from the Danish Regional Committees, the Pharmacy Foundation, the Egmont Foundation, the March of Dimes Birth Defects Foundation, the Health Foundation and other minor grants. The DNBC Biobank has been supported by the Novo Nordisk Foundation and the Lundbeck Foundation. Follow-up of mothers and children has been supported by the Danish Medical Research Council (SSVF 0646, 271-08-0839/06-066023, O602-01042B, 0602-02738B), the Lundbeck Foundation (195/04, R100-A9193), The Innovation Fund Denmark 0603-00294B (09-067124), the Nordea Foundation (02-2013–2014), Aarhus Ideas (AU R9-A959-13-S804), University of Copenhagen Strategic Grant (IFSV 2012), and the Danish Council for Independent Research (DFF—4183-00594 and DFF—4183-00152).

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Cooper, T.G.; Noonan, E.; von Eckardstein, S.; Auger, J.; Baker, H.W.; Behre, H.M.; Haugen, T.B.; Kruger, T.; Wang, C.; Mbizvo, M.T.; et al. World Health Organization reference values for human semen characteristics. Hum. Reprod. Update 2010, 16, 231–245. [Google Scholar] [CrossRef]
  2. Bonde, J.P.; Ernst, E.; Jensen, T.K.; Hjollund, N.H.; Kolstad, H.; Henriksen, T.B.; Scheike, T.; Giwercman, A.; Olsen, J.; Skakkebaek, N.E. Relation between semen quality and fertility: A population-based study of 430 first-pregnancy planners. Lancet 1998, 352, 1172–1177. [Google Scholar] [CrossRef]
  3. Eisenberg, M.L.; Li, S.; Behr, B.; Cullen, M.R.; Galusha, D.; Lamb, D.J.; Lipshultz, L.I. Semen quality, infertility and mortality in the USA. Hum. Reprod. 2014, 29, 1567–1574. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  4. Winters, B.R.; Walsh, T.J. The epidemiology of male infertility. Urol. Clin. N. Am. 2014, 41, 195–204. [Google Scholar] [CrossRef]
  5. Skakkebaek, N.E.; Rajpert-De Meyts, E.; Buck Louis, G.M.; Toppari, J.; Andersson, A.M.; Eisenberg, M.L.; Jensen, T.K.; Jørgensen, N.; Swan, S.H.; Sapra, K.J.; et al. Male Reproductive Disorders and Fertility Trends: Influences of Environment and Genetic Susceptibility. Physiol. Rev. 2016, 96, 55–97. [Google Scholar] [CrossRef] [Green Version]
  6. Elenkov, A.; Giwercman, A.; Søgaard Tøttenborg, S.; Bonde, J.P.E.; Glazer, C.H.; Haervig, K.K.; Bungum, A.B.; Nilsson, P.M. Male childlessness as independent predictor of risk of cardiovascular and all-cause mortality: A population-based cohort study with more than 30 years follow-up. PLoS ONE 2020, 15, e0237422. [Google Scholar] [CrossRef]
  7. Glazer, C.H.; Eisenberg, M.L.; Tøttenborg, S.S.; Giwercman, A.; Flachs, E.M.; Bräuner, E.V.; Vassard, D.; Pinborg, A.; Schmidt, L.; Bonde, J.P. Male factor infertility and risk of death: A nationwide record-linkage study. Hum. Reprod. 2019, 34, 2266–2273. [Google Scholar] [CrossRef]
  8. Bungum, A.B.; Glazer, C.H.; Bonde, J.P.; Nilsson, P.M.; Giwercman, A.; Søgaard Tøttenborg, S. Risk of metabolic disorders in childless men: A population-based cohort study. BMJ Open 2018, 8, e020293. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  9. Rosinger, A.; Herrick, K.; Gahche, J.; Park, S. Sugar-sweetened Beverage Consumption Among U.S. Youth, 2011–2014. NCHS Data Brief. 2017, 1–8. [Google Scholar]
  10. Scharf, R.J.; DeBoer, M.D. Sugar-Sweetened Beverages and Children’s Health. Annu. Rev. Public Health 2016, 37, 273–293. [Google Scholar] [CrossRef] [Green Version]
  11. Chiu, Y.H.; Afeiche, M.C.; Gaskins, A.J.; Williams, P.L.; Mendiola, J.; Jørgensen, N.; Swan, S.H.; Chavarro, J.E. Sugar-sweetened beverage intake in relation to semen quality and reproductive hormone levels in young men. Hum. Reprod. 2014, 29, 1575–1584. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  12. Hatch, E.E.; Wesselink, A.K.; Hahn, K.A.; Michiel, J.J.; Mikkelsen, E.M.; Sorensen, H.T.; Rothman, K.J.; Wise, L.A. Intake of Sugar-sweetened Beverages and Fecundability in a North American Preconception Cohort. Epidemiology 2018, 29, 369–378. [Google Scholar] [CrossRef] [PubMed]
  13. Nassan, F.L.; Priskorn, L.; Salas-Huetos, A.; Halldorsson, T.I.; Jensen, T.K.; Jørgensen, N.; Chavarro, J.E. Association between intake of soft drinks and testicular function in young men. Hum. Reprod. 2021, 36, 3036–3048. [Google Scholar] [CrossRef] [PubMed]
  14. Jensen, T.K.; Swan, S.H.; Skakkebaek, N.E.; Rasmussen, S.; Jørgensen, N. Caffeine intake and semen quality in a population of 2,554 young Danish men. Am. J. Epidemiol. 2010, 171, 883–891. [Google Scholar] [CrossRef] [Green Version]
  15. Hayden, R.P.; Flannigan, R.; Schlegel, P.N. The Role of Lifestyle in Male Infertility: Diet, Physical Activity, and Body Habitus. Curr. Urol. Rrep. 2018, 19, 56. [Google Scholar] [CrossRef]
  16. Yang, H.; Chen, Q.; Zhou, N.; Sun, L.; Bao, H.; Tan, L.; Chen, H.; Zhang, G.; Ling, X.; Huang, L.; et al. Lifestyles Associated With Human Semen Quality: Results From MARHCS Cohort Study in Chongqing, China. Medicine 2015, 94, e1166. [Google Scholar] [CrossRef]
  17. Pokhrel, G.; Yihao, S.; Wangcheng, W.; Khatiwada, S.U.; Zhongyang, S.; Jianqiao, Y.; Yucong, Z.; Xiaming, L.; Dan, Z.; Jihong, L. The impact of sociodemographic characteristics, lifestyle, work exposure and medical history on semen parameters in young Chinese men: A cross-sectional study. Andrologia 2019, 51, e13324. [Google Scholar] [CrossRef]
  18. Malik, V.S.; Schulze, M.B.; Hu, F.B. Intake of sugar-sweetened beverages and weight gain: A systematic review. Am. J. Clin. Nutr. 2006, 84, 274–288. [Google Scholar] [CrossRef]
  19. Hu, F.B. Resolved: There is sufficient scientific evidence that decreasing sugar-sweetened beverage consumption will reduce the prevalence of obesity and obesity-related diseases. Obes. Rev. 2013, 14, 606–619. [Google Scholar] [CrossRef]
  20. Ebbeling, C.B.; Feldman, H.A.; Chomitz, V.R.; Antonelli, T.A.; Gortmaker, S.L.; Osganian, S.K.; Ludwig, D.S. A randomized trial of sugar-sweetened beverages and adolescent body weight. N. Engl. J. Med. 2012, 367, 1407–1416. [Google Scholar] [CrossRef] [Green Version]
  21. Kondaki, K.; Grammatikaki, E.; Jiménez-Pavón, D.; De Henauw, S.; González-Gross, M.; Sjöstrom, M.; Gottrand, F.; Molnar, D.; Moreno, L.A.; Kafatos, A.; et al. Daily sugar-sweetened beverage consumption and insulin resistance in European adolescents: The HELENA (Healthy Lifestyle in Europe by Nutrition in Adolescence) Study. Public Health Nutr. 2013, 16, 479–486. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  22. Ma, J.; Wu, L.; Zhou, Y.; Zhang, H.; Xiong, C.; Peng, Z.; Bao, W.; Meng, T.; Liu, Y. Association between BMI and semen quality: An observational study of 3966 sperm donors. Hum. Reprod. 2019, 34, 155–162. [Google Scholar] [CrossRef]
  23. Tang, W.H.; Zhuang, X.J.; Ma, L.L.; Qiao, J.; Hong, K.; Zhao, L.M.; Liu, D.F.; Mao, J.M.; Zhang, H.L.; Zhou, S.J.; et al. Correlation between body mass index and semen quality in male infertility patients. Turk. J. Med. Sci. 2015, 45, 1300–1305. [Google Scholar] [CrossRef] [PubMed]
  24. Luque, E.M.; Tissera, A.; Gaggino, M.P.; Molina, R.I.; Mangeaud, A.; Vincenti, L.M.; Beltramone, F.; Larcher, J.S.; Estofán, D.; Fiol de Cuneo, M.; et al. Body mass index and human sperm quality: Neither one extreme nor the other. Reprod. Fertil. Dev. 2017, 29, 731–739. [Google Scholar] [CrossRef]
  25. Eisenberg, M.L.; Kim, S.; Chen, Z.; Sundaram, R.; Schisterman, E.F.; Buck Louis, G.M. The relationship between male BMI and waist circumference on semen quality: Data from the LIFE study. Hum. Reprod. 2014, 29, 193–200. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  26. Jensen, T.K.; Andersson, A.M.; Jørgensen, N.; Andersen, A.G.; Carlsen, E.; Petersen, J.H.; Skakkebaek, N.E. Body mass index in relation to semen quality and reproductive hormones among 1558 Danish men. Fertil. Steril. 2004, 82, 863–870. [Google Scholar] [CrossRef]
  27. Sermondade, N.; Faure, C.; Fezeu, L.; Shayeb, A.G.; Bonde, J.P.; Jensen, T.K.; Van Wely, M.; Cao, J.; Martini, A.C.; Eskandar, M.; et al. BMI in relation to sperm count: An updated systematic review and collaborative meta-analysis. Hum. Reprod. Update 2013, 19, 221–231. [Google Scholar] [CrossRef]
  28. Sekhavat, L.; Moein, M.R. The effect of male body mass index on sperm parameters. Aging Male 2010, 13, 155–158. [Google Scholar] [CrossRef]
  29. Sallmén, M.; Sandler, D.P.; Hoppin, J.A.; Blair, A.; Baird, D.D. Reduced fertility among overweight and obese men. Epidemiology 2006, 17, 520–523. [Google Scholar] [CrossRef]
  30. Ehala-Aleksejev, K.; Punab, M. The effect of metabolic syndrome on male reproductive health: A cross-sectional study in a group of fertile men and male partners of infertile couples. PLoS ONE 2018, 13, e0194395. [Google Scholar] [CrossRef] [Green Version]
  31. Leisegang, K.; Bouic, P.J.; Henkel, R.R. Metabolic syndrome is associated with increased seminal inflammatory cytokines and reproductive dysfunction in a case-controlled male cohort. Am. J. Reprod. Immunol. 2016, 76, 155–163. [Google Scholar] [CrossRef] [PubMed]
  32. Stellato, R.K.; Feldman, H.A.; Hamdy, O.; Horton, E.S.; McKinlay, J.B. Testosterone, sex hormone-binding globulin, and the development of type 2 diabetes in middle-aged men: Prospective results from the Massachusetts male aging study. Diabetes Care 2000, 23, 490–494. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  33. Blank, D.M.; Clark, R.V.; Heymsfield, S.B.; Rudman, D.R.; Blank, M.S. Endogenous opioids and hypogonadism in human obesity. Brain Res. Bull. 1994, 34, 571–574. [Google Scholar] [CrossRef]
  34. Serra-Majem, L.; Bassas, L.; García-Glosas, R.; Ribas, L.; Inglés, C.; Casals, I.; Saavedra, P.; Renwick, A.G. Cyclamate intake and cyclohexylamine excretion are not related to male fertility in humans. Food Addit. Contam. 2003, 20, 1097–1104. [Google Scholar] [CrossRef] [PubMed]
  35. Liauchonak, I.; Qorri, B.; Dawoud, F.; Riat, Y.; Szewczuk, M.R. Non-Nutritive Sweeteners and Their Implications on the Development of Metabolic Syndrome. Nutrients 2019, 11, 644. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  36. Rother, K.I.; Conway, E.M.; Sylvetsky, A.C. How Non-nutritive Sweeteners Influence Hormones and Health. Trends Endocrinol. Metab. TEM 2018, 29, 455–467. [Google Scholar] [CrossRef]
  37. Pepino, M.Y. Metabolic effects of non-nutritive sweeteners. Physiol. Behav. 2015, 152 Pt B, 450–455. [Google Scholar] [CrossRef] [Green Version]
  38. Anbara, H.; Sheibani, M.T.; Razi, M.; Kian, M. Insight into the mechanism of aspartame-induced toxicity in male reproductive system following long-term consumption in mice model. Environ. Toxicol. 2020, 36, 223–237. [Google Scholar] [CrossRef]
  39. Anbara, H.; Sheibani, M.T.; Razi, M. Long-Term Effect of Aspartame on Male Reproductive System: Evidence for Testicular Histomorphometrics, Hsp70-2 Protein Expression and Biochemical Status. Int J. Fertil. Steril. 2020, 14, 91–101. [Google Scholar] [CrossRef]
  40. Gong, T.; Wei, Q.W.; Mao, D.G.; Nagaoka, K.; Watanabe, G.; Taya, K.; Shi, F.X. Effects of Daily Exposure to Saccharin and Sucrose on Testicular Biologic Functions in Mice. Biol. Reprod. 2016, 95, 116. [Google Scholar] [CrossRef]
  41. DNBC. Available online: https://www.dnbc.dk/ (accessed on 30 November 2021).
  42. Keglberg Hærvig, K.; Bonde, J.P.; Ramlau-Hansen, C.H.; Toft, G.; Hougaard, K.S.; Specht, I.O.; Giwercman, A.; Nybo Andersen, A.M.; Olsen, J.; Lindh, C.; et al. Fetal Programming of Semen Quality (FEPOS) Cohort—A DNBC Male-Offspring Cohort. Clin. Epidemiol. 2020, 12, 757–770. [Google Scholar] [CrossRef] [PubMed]
  43. Björndahl, L.; Barratt, C.L.; Mortimer, D.; Jouannet, P. ‘How to count sperm properly’: Checklist for acceptability of studies based on human semen analysis. Hum. Reprod. 2016, 31, 227–232. [Google Scholar] [CrossRef] [Green Version]
  44. Palacios, E.R.; Clavero, A.; Gonzalvo, M.C.; Rosales, A.; Mozas, J.; Martínez, L.; Ramírez, J.P.; Björndahl, L.; Morancho-Zaragoza, J.; Fernández-Pardo, E.; et al. Acceptable variability in external quality assessment programmes for basic semen analysis. Hum. Reprod. 2012, 27, 314–322. [Google Scholar] [CrossRef] [Green Version]
  45. Greenland, M.S.; Pearl, M.J.; Robins, M.J. Causal Diagrams for Epidemiologic Research. Epidemiology 1999, 10, 37–48. [Google Scholar] [CrossRef] [PubMed]
  46. Platt Robert, W.; Shrier, I. Reducing bias through directed acyclic graphs. BMC Med. Res. Methodol. 2008, 8, 70. [Google Scholar] [CrossRef] [Green Version]
  47. Robert, H.F.; Suzanne, W.F. Clinical Epidemiology: The Essentials, 4th ed.; Fletcher, R.H., Fletcher, S.W., Eds.; Lippincott Williams & Wilkins: Baltimore, MD, USA, 2005. [Google Scholar]
  48. Statistics Denmark. Statistics Denmark’s Classification of Occupations (DISCO-08), v1:2010. 2010. Available online: https://www.dst.dk/en/Statistik/dokumentation/nomenklaturer/disco-08# (accessed on 30 November 2021).
  49. Hernán, M.A.; Hernández-Díaz, S.; Robins, J.M. A structural approach to selection bias. Epidemiology 2004, 15, 615–625. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  50. Rodprasert, W.; Virtanen, H.E.; Mäkelä, J.A.; Toppari, J. Hypogonadism and Cryptorchidism. Front. Endocrinol. 2019, 10, 906. [Google Scholar] [CrossRef]
  51. Rockett, H.R.; Berkey, C.S.; Colditz, G.A. Evaluation of dietary assessment instruments in adolescents. Curr. Opin. Clin. Nutr. Metab. Care 2003, 6, 557–562. [Google Scholar] [CrossRef]
  52. Schoeller, D.A. Limitations in the assessment of dietary energy intake by self-report. Metabolism 1995, 44, 18–22. [Google Scholar] [CrossRef]
  53. Nassan, F.L.; Jensen, T.K.; Priskorn, L.; Halldorsson, T.I.; Chavarro, J.E.; Jørgensen, N. Association of Dietary Patterns With Testicular Function in Young Danish Men. JAMA Netw. Open 2020, 3, e1921610. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Figure 1. Flowchart of the FEPOS cohort, 2017–2019.
Figure 1. Flowchart of the FEPOS cohort, 2017–2019.
Ijerph 19 00682 g001
Table 1. Characteristics of the 1047 participants sorted by beverage consumption, with available information on sugar-sweetened, artificially sweetened beverage consumption and semen parameters, and maternal characteristics, FEPOS 2017–2019.
Table 1. Characteristics of the 1047 participants sorted by beverage consumption, with available information on sugar-sweetened, artificially sweetened beverage consumption and semen parameters, and maternal characteristics, FEPOS 2017–2019.
Participants’ Characteristics (2017–2019)Sugar-Sweetened
Beverage Consumption a
Artificially Sweetened
Beverage Consumption a
<3 Days a Week≥3 Days a Week<3 Days a Week≥3 Days a Week
Candy intake
<3 days a week658 (63)199 (19)769 (73)88 (8)
≥3 days a week99 (9)91 (9)165 (16)25 (3)
Cake intake
<3 days a week689 (66)246 (24) 841(80)94 (9)
≥3 days a week68 (6)44 (4)93 (9)19 (2)
Cocoa intake
Less than weekly587 (56)203 (19)709 (68)79 (8)
Weekly172 (17)87 (8)225 (21)34 (3)
Energy drink intake
<3 days a week734 (70)234 (22)876 (84)92 (9)
≥3 days a week23 (3)56 (5)58 (5)21 (2)
Coffee intake
<3 days a week303 (35)142 (17)394 (46)51 (6)
≥3 days a week323 (37)94 (11)373 (43)44 (5)
Smoking status
Yes267 (26)146 (14)357 (34)56 (5)
No144 (14)490 (46)577 (56)57 (5)
Body Mass Index
Underweight53 (5)25 (3)72 (7)6 (1)
Normal weight571 (54)203 (19)701 (67)73 (7)
Overweight133 (13)62 (6)161 (15)34 (3)
Spillage
Yes132 (12)50 (5)160 (15)22 (2)
No620 (60)239 (23)770 (74)89 (9)
Abstinence time
<2 h256 (25)107 (10)326 (31)37 (4)
2–4 h388 (37)158 (15)482 (46)64 (6)
>4 h113 (11)25 (2)126 (12)12 (1)
Fever
Yes102 (10)36 (3)121 (12)17 (2)
No570 (54)215 (21)705 (67)80 (7)
Don’t know85 (8)39 (4)108 (10)16 (2)
Time to analysis
<60 min562 (54)216 (21)690 (66)88 (8)
≥60 min188 (18)72 (7)236 (24)24 (2)
Maternal Characteristics (1997–2000)
Maternal smoking status
Yes155 (15)88 (8)214 (20)29 (3)
No602 (58)202 (19)720 (69)84 (8)
Maternal Body Mass Index
Underweight69 (7)28 (3)92 (8)6 (1)
Normal weight525 (51)191 (19)647 (63)69 (7)
Overweight146 (14)63 (6)172 (17)37 (4)
Socio Economic Status (highest of parents)
Student or economically inactive42 (4)7 (1)43 (4)0 (0)
Skilled or unskilled worker193 (18)106 (10)263 (25)36 (3)
Low grade professional242 (23)102 (10)303 (29)41 (4)
High grade professional280 (27)75 (7)320 (32)35 (3)
Displayed as numbers of participants, n (%); a Data on participants appear twice, once for each exposure group.
Table 2. Distribution of semen parameters according to low or high consumption of sugar-sweetened and artificially sweetened beverages, FEPOS 2017–2019.
Table 2. Distribution of semen parameters according to low or high consumption of sugar-sweetened and artificially sweetened beverages, FEPOS 2017–2019.
Semen Parameters
(Medians, 5th, 95th Percentiles) b
Sugar-Sweetened Beverage
Consumption a
Artificially Sweetened Beverage
Consumption a
NInfrequent
(<3 Days a Week)
Moderate
(≥3 Days a Week)
NInfrequent
(<3 Days a Week)
Moderate
(≥3 Days a Week)
Semen volume (mL)10472.7 (1.9, 3.7)2.6 (1.8, 3.6)10472.7 (1.9, 3.7)2.7 (1.8, 3.6)
Sperm concentration (mill./mL)104739.7 (18.7, 73.2)33.7 (18.8, 68.0)104738.9 (19.0, 72.8)34.6 (16.6, 65.3)
Total motility (A + B%)103173.0 (64.0, 80.0)71.4 (63.0, 79.0)1031 72.3 (63.0, 80.0)72.4 (66.8, 80.3)
Sperm morphology (% normal sperm)10266.0 (0.3, 10.0)6.0 (2.9, 10.0)10266.0 (3.0, 10.0)6.0 (3.5, 9.7)
Total sperm count (mill.)1047104.2 (47.9, 203.9)94.3 (39.4, 180.2)1047103.3 (45.8, 202.3)96.9 (39.8, 167.4)
a Data on participants appear twice, once for each exposure group; b Medians and percentiles shown as pseudo-percentiles (an average of 5).
Table 3. Crude and adjusted outcome ratios according to sugar-sweetened and artificially sweetened beverage consumption among participants, FEPOS 2017–2019.
Table 3. Crude and adjusted outcome ratios according to sugar-sweetened and artificially sweetened beverage consumption among participants, FEPOS 2017–2019.
Semen ParametersSugar-Sweetened Beverage
Consumption
Unadjusted
Sugar-Sweetened
Beverage Consumption Adjusted
Artificially Sweetened Beverage Consumption UnadjustedArtificially Sweetened Beverage Consumption Adjusted
Crude Ratio aAdjusted Ratio a,b95% CICrude Ratio aAdjusted Ratio a,b95% CI
Semen volume c0.970.99(0.91, 1.08)1.021.03(0.92, 1.17)
Sperm concentration 0.921.03(0.90, 1.19)0.890.96(0.81, 1.15)
Total motility d0.990.98(0.95, 1.02)1.011.01(0.98, 1.05)
Sperm morphology (% normal sperm)0.990.99(0.87, 1.12)0.900.89(0.76, 1.04)
Total sperm count c0.860.98(0.84, 1.15)0.890.99(0.81, 1.21)
a Ratio between the semen quality characteristics for high consumption relative to low consumption; b Adjusted for candy intake, cake intake, energy drink consumption, coffee consumption, smoking, maternal smoking, maternal BMI, parental socio-economic status, abstinence time and fever; c Participants with recording of spillage excluded from analyses on semen volume and total sperm count (mill.); d Analyses on total motility (A + B%) additionally adjusted for time to analysis.
Table 4. Adjusted outcome ratios according to sugar-sweetened and artificially sweetened beverage consumption among participants, FEPOS 2017–2019.
Table 4. Adjusted outcome ratios according to sugar-sweetened and artificially sweetened beverage consumption among participants, FEPOS 2017–2019.
Semen ParametersSugar-Sweetened Beverage Consumption AdjustedArtificially Sweetened Beverage Consumption Adjusted
Ratio a,b95% CI Ratio a,b95% CI
Semen volume cLess than weekly (n = 362)1 Less than weekly (n = 869)1
1–2 days a week (n = 485) 0.97(0.90, 1.05) 1–2 days a week (n = 171)1.04(0.95, 1.14)
3–4 days a week (n = 208)0.94(0.84, 1.05)3–4 days a week (n = 82)1.05(0.91, 1.22)
5–6 days a week (n = 74)1.05(0.91, 1.22)5–6 days a week (n = 30)1.05(0.87, 1.26)
Every day (n = 38)0.98(0.81, 1.18)Every day (n = 15)0.82(0.56, 1.20)
* Continuous1.00(0.98, 1.02)* Continuous1.01(0.98, 1.04)
Sperm concentrationLess than weekly (n = 362)1 Less than weekly (n = 869)1
1–2 days a week (n = 485)1.02(0.89, 1.17)1–2 days a week (n = 171)1.02(0.86, 1.20)
3–4 days a week (n = 208)1.05(0.87, 1.27)3–4 days a week (n = 82)0.96(0.77, 1.20)
5–6 days a week (n = 74)1.04(0.81, 1.33)5–6 days a week (n = 30)1.03(0.78, 1.36)
Every day (n = 38)0.99(0.69, 1.42)Every day (n = 15)0.81(0.47, 1.41)
* Continuous1.00(0.97, 1.04)* Continuous0.99(0.95, 1.03)
Total motility dLess than weekly (n = 362)1 Less than weekly (n = 869)1
1–2 days a week (n = 485)1.00(0.97, 1.03)1–2 days a week (n = 171)1.00(0.97, 1.04)
3–4 days a week (n = 208)0.98(0.94, 1.02)3–4 days a week (n = 82)1.00(0.96, 1.05)
5–6 days a week (n = 74)0.99(0.94, 1.04)5–6 days a week (n = 30)1.03(0.98, 1.09)
Every day (n = 38)0.95(0.87, 1.03)Every day (n = 15)1.02(0.90, 1.15)
* Continuous0.99(0.99, 1.00)* Continuous1.00(0.99, 1.01)
Sperm morphology (% normal sperm)Less than weekly (n = 362)1 Less than weekly (n = 869)1
1–2 days a week (n = 485)0.92(0.81, 1.05)1–2 days a week (n = 171)0.93(0.81, 1.06)
3–4 days a week (n = 208)0.95(0.80, 1.13)3–4 days a week (n = 82)0.89(0.74, 1.09)
5–6 days a week (n = 74)0.92(0.72, 1.16)5–6 days a week (n = 30)0.86(0.67, 1.11)
Every day (n = 38)0.92(0.68, 1.25)Every day (n = 15)0.86(0.50, 1.49)
* Continuous0.99(0.96, 1.02)* Continuous0.97(0.93, 1.01)
Total sperm count cLess than weekly (n = 362)1 Less than weekly (n = 869)1
1–2 days a week (n = 485)1.08(0.93, 1.24)1–2 days a week (n = 171)0.97(0.83, 1.13)
3–4 days a week (n = 208)1.00(0.81, 1.22)3–4 days a week (n = 82)0.97(0.74, 1.26)
5–6 days a week (n = 74)1.12(0.86, 1.45)5–6 days a week (n = 30)1.08(0.82, 1.41)
Every day (n = 38)0.99(0.67, 1.46)Every day (n = 15)0.66(0.36, 1.23)
* Continuous1.00(0.96, 1.04)* Continuous0.99(0.95, 1.04)
a Reference: Less than weekly b Adjusted for candy intake, cake intake, energy drink consumption, coffee consumption, smoking, maternal smoking, maternal BMI, parental socio-economic status, abstinence time and fever c Participants with recording of spillage excluded from analyses on semen volume and total sperm count (mill.) d Analyses on total motility (A + B%) additionally adjusted for time to analysis * Continuous: Relative change in semen characteristics per 1 category change in weekly consumption.
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Meldgaard, M.; Brix, N.; Gaml-Sørensen, A.; Ernst, A.; Ramlau-Hansen, C.H.; Tøttenborg, S.S.; Hougaard, K.S.; Bonde, J.P.E.; Toft, G. Consumption of Sugar-Sweetened or Artificially Sweetened Beverages and Semen Quality in Young Men: A Cross-Sectional Study. Int. J. Environ. Res. Public Health 2022, 19, 682. https://doi.org/10.3390/ijerph19020682

AMA Style

Meldgaard M, Brix N, Gaml-Sørensen A, Ernst A, Ramlau-Hansen CH, Tøttenborg SS, Hougaard KS, Bonde JPE, Toft G. Consumption of Sugar-Sweetened or Artificially Sweetened Beverages and Semen Quality in Young Men: A Cross-Sectional Study. International Journal of Environmental Research and Public Health. 2022; 19(2):682. https://doi.org/10.3390/ijerph19020682

Chicago/Turabian Style

Meldgaard, Maiken, Nis Brix, Anne Gaml-Sørensen, Andreas Ernst, Cecilia Høst Ramlau-Hansen, Sandra Søgaard Tøttenborg, Karin Sørig Hougaard, Jens Peter Ellekilde Bonde, and Gunnar Toft. 2022. "Consumption of Sugar-Sweetened or Artificially Sweetened Beverages and Semen Quality in Young Men: A Cross-Sectional Study" International Journal of Environmental Research and Public Health 19, no. 2: 682. https://doi.org/10.3390/ijerph19020682

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