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Article

Body Composition and Its Impact on the Hormonal Disturbances in Women with Polycystic Ovary Syndrome

by
Anna Bizoń
1,*,
Sylwia Płaczkowska
2,
Justyna Niepsuj
3,
Marta Czwojdzińska
1,
Marcin Leśniewski
4,
Artur Nowak
5,
Dagmara Pluta
6,
Paweł Madej
6,
Agnieszka Piwowar
1 and
Grzegorz Franik
6
1
Department of Toxicology, Faculty of Pharmacy, Wroclaw Medical University, 50-367 Wroclaw, Poland
2
Department of Laboratory Diagnostics, Diagnostics Laboratory for Teaching and Research, Faculty of Pharmacy, Wroclaw Medical University, 50-556 Wroclaw, Poland
3
Students Scientific Society at the Department of Toxicology, Faculty of Pharmacy, Wroclaw Medical University, 50-556 Wroclaw, Poland
4
Department of Gynaecological and Obstetrics, District Hospital, 43-200 Pszczyna, Poland
5
Gynecological and Obstetrician Polyclinic, District Hospital, 15-435 Białystok, Poland
6
Department of Endocrinological Gynecology, Medical University of Silesia, 40-055 Katowice, Poland
*
Author to whom correspondence should be addressed.
Nutrients 2021, 13(12), 4217; https://doi.org/10.3390/nu13124217
Submission received: 7 October 2021 / Revised: 17 November 2021 / Accepted: 22 November 2021 / Published: 24 November 2021
(This article belongs to the Special Issue Interdisciplinary Approach to Nutrition in Cardiometabolic Health and Disease)
Browse Figures
Versions Notes

Abstract

:
We investigated the relationship between selected body composition (BC) parameters and included 55 women diagnosed with PCOS and 29 women in which PCOS was excluded. Hormone concentration and BC parameters were assessed during hospitalization. Women with PCOS had higher concentration of luteinizing hormones, total testosterone, androstenedione, and Anti-Müllerian hormones compared to women that were not diagnosed with PCOS. We did not observe any significant differences in the BC parameters between both groups as well as between four PCOS phenotype subgroups. Only in the group of women with PCOS was the concentration of sex hormone binding globulin and free testosterone correlated with all investigated BC parameters. Correspondence analysis did not confirm unambiguously associations between phenotypes of PCOS and the value of BC parameters, while logistic regression revealed that increased Anti-Müllerian hormone concentration and the value of body mass index could be useful parameters in differentiating women with PCOS and women with other disorders. The ROC analysis performed on the entire group of women also confirmed that the concentration of Anti-Müllerian hormones could be a powerful parameter to categorize women as suffering from PCOS.

1. Introduction

Improper diet, abnormal body weight, and lack of physical activity are some of the crucial factors associated with development of many diseases as well as their exacerbation [1]. Polycystic ovary syndrome (PCOS) is a common reproductive and endocrine disorder in which obesity intensifies metabolic and hormonal disorders [2]. According to studies 30–70% of women with PCOS are obese [3] and many are characterized by abdominal obesity [4], which contributes to the clinical and biochemical expression of PCOS [5,6]. Weight reduction for obese patients with PCOS is beneficial in many ways. It helps decrease the concentration of androgen, luteinizing hormone and insulin as well as regulate ovulation [7], therefore lifestyle improvement is the first line of treatment for women with PCOS [8]. As the primary cause of PCOS is still unknown, the treatment is primarily directed at symptoms [7]. Diagnosis of PCOS is based on meeting at least two out of three Rotterdam criteria: clinical or/and biochemical hyperandrogenism, ovulatory dysfunction, and polycystic ovaries found on an ultrasound [9]. According to these criteria it is possible to identify four PCOS phenotypes: (1) with clinical and/or biochemical hyperandrogenism, oligoovulation or anovulation and polycystic ovaries; (2) with clinical and/or biochemical hyperandrogenism and oligoovulation or anovulation; (3) with clinical and/or biochemical hyperandrogenism and polycystic ovaries; and (4) with oligoovulation or anovulation and polycystic ovaries [10]. However, studies show no significant differences in prevalence of insulin resistance and metabolic syndrome in different PCOS phenotypes [11]. The most widely used parameters which help to diagnose obesity are body mass index (BMI), waist circumference (WC), waist-to-hip ratio (WHR), visceral fat area (VFA), and body fat percentage (BFP) [12]. Considering the presence of sexual dimorphism in fat distribution, we already know that androgens play an important role in distribution of adipose tissue in the human body [13]. Several previous studies showed a correlation between androgen levels and amount of abdominal fat and visceral adipose tissue [14,15]. It was also demonstrated that women with abdominal obesity have lower concentrations of sex hormone bounding globulin (SHBG), which supports the thesis that free androgens are related to increased visceral fat accumulation [14]. Furthermore, earlier studies also pointed out that android type of fat distribution is associated with reduced reproductive capability and infertility [16]. Our study showed that abdominal obesity causes additional disorders in metabolic and hormonal parameters in PCOS women [17], suggesting that further investigation is needed to evaluate the influence of body fat distribution on PCOS to be able to improve the course of future treatment. Our previous study [18] and the results obtained by other authors of [19] indicate that the value of BMI and WC could be insufficient to measure the percentage of body fat. Furthermore, the value of BMI does not capture information on the mass of fat in different body sites and cannot diversify central and peripheral fat [20,21]. Analyzing body composition is much more useful than measuring body weight, since it can distinguish body fat mass from fat free mass [22]. In our previous study we proposed bioelectric impedance as a minimally invasive method that can be recommended for the assessment of body weight, especially in young people [23]. Therefore, in our present study we aimed to investigate the relationships between selected body composition parameters and hormones concentration (follicle-stimulating hormone (FSH), luteinizing hormone (LH), total testosterone (t-test), free testostereone (fTest), androstenedione (AD), dehydroepiandrosterone sulfate (DHEA-S), SHBG, 17α-hydroxyprogesterone (17α-OHP), and Anti-Müllerian hormones (AMH)) in a group of women with and without PCOS. We used bioelectric impedance analysis (Bodystat 1500), which is a non-invasive, reliable, low-cost, easy to use, and clinically validated method.

2. Materials and Methods

The study was conducted on the group of 84 women who were hospitalized in the Gynecological Endocrinology Clinic of the Silesian Medical University in Katowice, Poland, in 2021. On average, 90 ± 10 women suspected of PCOS are hospitalized at the clinic every month. We selected a case-control study of women aged 18–43, who were hospitalized in April 2020. According to Rotterdam criteria, 55 women were diagnosed with PCOS (study group) and 29 women were excluded as not suffering from PCOS (control group). The study was approved by the Bioethical Committee of the Medical University of Silesia (No KNW/0022/KB1/140/II/15/16, 15 November 2016). In addition, in the group of women with PCOS, four different phenotypes of PCOS were recognized based on Rotterdam criteria. In the group of women without PCOS, one woman had polycystic ovaries, six women had oligomenorrhea, and seven women were characterized by high levels of androgens, but none of them were diagnosed with PCOS based on Rotterdam criteria. In both groups, women exposed to tobacco smoke or alcohol abuse were excluded from the study. Other exclusion criteria included previously diagnosed diabetes (type 1 and 2), hypertension, Cushing’s syndrome, and adrenal tumors. Blood samples were collected during the follicular phase (till day eight of the menstrual cycle) in the morning after an overnight fast (>12 h) according to standard procedures. Blood samples were immediately centrifuged and serum and plasma were separated; parameters associated with PCOS were assayed immediately.

2.1. Assessment of Body Composition

During hospitalization in all women body composition parameters were assessed based on bioimpedance methods using Bodystat 1500 (Douglas, Isle of Man) according to the instructions provided by the producer. The participants were asked not to eat for 4–5 h and not to exercise for 12 h before the test. The Bodystat 1500 was calibrated at the beginning of a day of use. We focused on selected body composition parameters including body mass index (BMI) (kg/m2); waist hip ratio (WHR); fat-free mass (FFM); body weight (BW) (kg); skeletal muscle mass (SMM) (kg); fat mass (FAT) (kg); total body water (TBW) (%); percent of body fat (PBF) (%); visceral fat area (VFA) (cm2); and basal metabolic rate (BMR) (kcal).

2.2. Hormone and SHBG Concentrations

FSH, LH, t-test, fTest, AD, DHEA-S and SHBG concentrations were determined by ELISA (DRG Instruments GmbH, Marburg, Germany) with the lower limit of sensitivity at 0.86 IU/L, 1.27 IU/L, 0.083 µg/L, 0.002 ng/L, 0.019 µg/L, 0.044 mg/L and 0.2 nmol/L, respectively; the respective intra- and inter-assay coefficients of variations were 5.5% and 6.1% for FSH, 5.6% and 6.2% for LH, 3.6% and 7.1% for total testosterone, 6.4% and 8.0% for free testosterone, 6.5% and 10.2% for androstenedione, 4.8% and 7.5% for DHEA-S and 5.3% and 9.0% for SHBG. 17α-hydroxyprogesterone (17α-OHP) was assayed by RIA (Diagnostic Products Corporation, Los Angeles, CA, USA) with lower detectable concentrations of 0.2 nmol/L. The respective inter- and intraassay coefficients of variation were 5.6% and 8.0% for 17-OH-P. The concentration of AMH was assayed using commercial ELISA kit (Immunotech a.s., Prague, Czech Republic) with lower detectable concentrations of 0.05 ng/mL, inter- and intra- assay coefficient of variations were 4.6% and 4.6%, respectively.

2.3. Statistical Analysis

Statistical analysis was performed using the Statistica Software Package, version 13.3 (Polish version; StatSoft, Kraków, Poland). Values, except age (presented as mean ± SD) were expressed as median with interquartile range (IQR). Normality of variables was tested using the Shapiro-Wilk test. Homogeneity of variance was assessed using Levene’s test. Significant differences in hormones concentration and body composition parameters between groups of women with and without PCOS were investigated using non-parametric U Mann-Whitney test. Differences between four PCOS phenotype subgroups were analyzed using Kruskal-Wallis one-way analysis of variance by ranks. The correspondence analysis was performed to evaluate the potential association between quartile of body composition parameters and phenotypes of PCOS. Logistic regression was used to indicate which of the analyzed parameters increased the patient’s odds of belonging to the PCOS group. Furthermore, the ROC (receiver operating characteristic) analysis was performed to show which parameter best categorized women as suffering from PCOS. In all instances, p < 0.05 was considered statistically significant.

3. Results

The studied groups were similar in terms of age. Women with PCOS had higher concentration of LH, t-test, AD, and AMH compared to women without PCOS. The median of AMH concentration was two-fold higher in the group of women with PCOS than in the group of women without PCOS. Any other significant differences in hormones concentration and selected values of body composition parameters were not found (Table 1).
Comparison of the value of body composition between four phenotypes of PCOS did not show any statistically significant differences (Table 2).
Separately, in both study and control groups we investigated the relationships between hormones concentrations and selected body composition parameters. In the group of women with PCOS, a negative correlation between the concentration of SHBG and the value of selected body composition parameters was found, while a positive correlation was revealed in case of the concentration of fTest and the value of some body composition parameters (Table 3). In the control group, the concentration of SHBG did not correlate with any parameters of body composition, while the concentration of fTest was only associated with PBF value (r = 0.40; p = 0.035). Only in the control group we found a positive correlation between the concentration of DHEA-S and the value of BMI (r = 0.39; p = 0.038) as well as a negative one between the concentration of 17-OHP and the value of WHR (r = −0.47; p = 0.010) (results not shown in the table).
Correspondence analysis showed that phenotype 2 of PCOS was associated with the highest value (assigned to Q4) of analyzed body composition parameters (FAT, BMI, PBF, VFA, FFM, BMR), while phenotype 4 was related to the lowest value (assigned to Q1 or 2) of body composition parameters (for Q1: VFA, FAT, BMI, WHR, PBF and for Q2: TBW, BMR, FFM). Women with phenotype 1 and 3 presented average values of body composition (Figure 1).
Logistic regression revealed that increased concentration of AMH and selected values of body composition such as BMI, PBF, and VFA analyzed as a separated models could be useful in differentiating women with PCOS and women with other disorders, which are not associated with PCOS (Table 4). Model 4 revealed that among body composition parameters analyzed separately: BMI, PBF and VFA, BMI was the strongest and independent (other than AMH) variable related to increased odds of belonging to the PCOS group.
Both ROC analysis performed in the group of women <30 years old and >30 years old indicated that specific concentrations of AMH could be a powerful parameter to categorize women with PCOS. The cut-off concentration of AMH for women <30 years was estimated as 5.00 ng/mL, while in the group of women >30 years old the threshold value was 4.39 ng/mL (Figure 2).

4. Discussion

The distribution of fat tissue in the visceral area is associated with many metabolic and endocrine disturbances in PCOS [24]. It seems that obesity plays a fundamental role in pathogenesis of PCOS [25]. Furthermore, Della Corte, et al. claimed that the main goal of therapy in PCOS should be the reduction of body mass [26]. Therefore, in our present study we were focused on the potential associations between the value of selected body composition parameters and the magnitude of hormonal disorders in women with PCOS. Firstly, we compared the results of selected body composition parameters between women with and without PCOS. We did not find any significant differences in the value of body composition parameters between those groups, which may be associated with a small number of patients and their similar physical constitution. The same findings were made when we analyzed those differences in four phenotypes of PCOS. Presumably the lack of statistically significant differences between four phenotypes of PCOS was also associated with a small number of cases, especially in phenotype 2 (n = 7) and 4 (n = 6). The correspondence analysis showed that body composition parameters were not directly associated with phenotypes of PCOS. Women with phenotype 2 were mainly associated with quartile 4 of BMI, PBF, and FFM values; regarding body composition parameters, women with phenotype 1 and 3 had average values of body composition parameters (e.g., the value of VFA, FFM and PBF), while women with phenotype 4 had mainly the lowest value of body composition parameters.
Our outcome indicates that the greatest disorders in body composition parameters are present in phenotype 2, which similar to the results obtained by Giampaolino, et al. could suggest that the women with phenotype 2 of PCOS has a different pathophysiologic mechanism of disease [27].
Using logistic regression analysis we showed, especially in Model 4, that among parameters analyzed separately the value of BMI was the strongest (besides AMH) variable related to the increased odds ratio of belonging to PCOS group (Table 4).
When we investigated the coefficient correlation between body composition parameters and hormones concentration in the group of women with PCOS we found a significant negative correlation between the concentration of SHBG and the value of all analyzed body composition parameters. The highest value of coefficient correlations was found between the concentration of SHBG and the value of BMI, WHR, FAT, and VFA, which showed clearly that the concentration of SHBG was associated with the amount and placement of fat tissue in visceral area (WHR and VFA). A study conducted by Azard, et al. [28] demonstrated that in the group of premenopausal women the serum concentration of SHBG was negatively associated with intra-abdominal adipose tissue. Moreover, a fat depot was linked with an abnormal metabolic profile as well as inversely and independently associated with SHBG [28]. Our earlier study showed that women with PCOS who were obese in the visceral area (WHR > 0.8) had lower concentration of SHBG and higher concentration of DHEA-S and value of FAI compared to women with PCOS and a normal value of WHR (<0.8) [17]. Furthermore, our last study revealed that disorders in hormonal status are probably indirectly associated with changes in lipid profile parameters [29]. Higher quartiles of triglycerides concentration increased the odds ratio of lower concentration of SHBG or higher value of free androgen index (FAI), while higher quartiles of HDL-C level decreased concentration of SHBG concentration and FAI value. Moreover, we also discovered that the phenotypes of PCOS, as well as the value of BMI, were significant factors which influenced androgen hormone concentrations [29].
Interestingly, in our present study in the group of women without PCOS the concentration of SHBG was not significantly associated with any parameters associated with body composition analysis. Similar results were previously obtained in the study conducted by Yucel et al. [30], who showed a negative correlation between the concentration of SHBG and the value of total fat mass in PCOS women. At the same time, there was no similar relationship in the group of healthy control. Apart of SHBG, in the women with PCOS fTest concentration was in positive relation to investigated body composition parameters, with the highest value of coefficient correlation with BMI (r = 0.47), WHR (r = 0.45), FAT (r = 0.42) and VFA (r = 0.41), while in the group of women without PCOS the concentration of free testosterone was only positively correlated with the value of PBF. Our study confirmed the results obtained by other authors, with lower concentration of SHBG being associated with an elevation in fTest concentration. Moreover, we confirmed that both of these parameters are closely related to obesity [31], which is in accordance with results obtained by other authors [32].
It was confirmed that SHBG could play an important role in various metabolic disorders in women with PCOS [33]. The meta-analysis conducted by Lim, et al. showed that overweight or obese women with PCOS had decreased concentration of SHBG and increased concentration of t-test and free androgen index [34]. Furthermore, hepatic synthesis of SHBG can be suppressed by insulin, while excess of insulin is common in the group of overweight women. It has been shown that insulin rises free and total testosterone, and this contributes to upper-half type body fat distribution [35]. The results obtained in our study confirmed that a decreased concentration of SHBG is associated with obesity especially distributed in the visceral area.
The second important parameter taken under consideration was the concentration of AMH. We observed a significant difference in AMH concentration between women with and without PCOS, but we did not detect any correlation with body composition parameters. Similar result was obtained by Bialka-Kosiec, et al. [36], who also did not discover any significant correlation between body mass components including body fat, fat-free mass, or water content and the concentration of AMH in women with PCOS. A study conducted by Cassar, et al. also did not reveal any significant correlation between the concentration of AMH and the value of body fat parameters [37]. The newest study conducted in the Chinese population revealed the negative correlation between body fat percentage and the concentration of AMH, and the authors claimed that the study should be continued to explain the association between body fat-related AMH change with pathogenesis of PCOS [38]. In addition, using ROC analysis the authors showed that AMH can be helpful in distinguish between women with and without PCOS (the value of AUC was 88.5%, with a sensitivity of 72.4% and specificity of 87.4%, the positive and negative predictive values were 91.2% and 63.9%, respectively. The same findings were demonstrated in a study conducted by Cassar, et al. [37]. Similarly, in our study we confirmed using the ROC analysis that concentration of AMH is a sensitive and specificity parameter associated with PCOS. We performed the ROC analysis in two groups of women: < and >30 years old, as the concentration of AMH changes with the age [39]. The value of AUC in both groups of women < and >30 years old was 87.6% and 92.5%, which confirmed that concentration of AMH reflects the probability of belonging to the PCOS group. Furthermore, the results obtained by Casarotto, et al. indicated that the concentration of AMH could be a prognostic parameter of PCOS in women with metabolic and hormonal disorders. AMH was associated with the pathophysiology of reproductive dysfunction in PCOS and reflects PCOS status, therefore it may also be useful in PCOS diagnosis [40]. Dadachanji, et al. [41] revealed the importance of clinicians concurrently employing Rotterdam criteria along with obesity status for ascertaining accurate disorders in the course of PCOS status.
Summarizing, in the group of women with PCOS the body composition parameters were mainly associated with the concentration of SHBG and fTest, while the parameters which are most strongly and independently related to belonging to the PCOS group were the concentration of AMH and the value of BMI.
Some limitations should be considered when interpreting these study results. Due to a small number of PCOS phenotype patients as well as of the control group, the obtained results should be treated as a pilot, and should be considered for future studies.

5. Conclusions

  • In the group of women with PCOS, the alteration in the value of body composition parameters were significantly associated with the concentration of SHBG and fTest.
  • The concentration of AMH and the value of BMI were the parameters most strongly and independently related to belonging to the PCOS group.

Author Contributions

Conceptualization, A.B. and G.F.; methodology, A.B., S.P. and G.F.; software, A.B., S.P. and G.F.; validation, S.P. and G.F.; formal analysis, A.B., S.P., A.P. and G.F.; investigation, A.B., S.P., J.N., P.M., M.L., A.N., D.P., A.P. and G.F.; resources, M.L., A.N., D.P., P.M. and G.F.; data curation, G.F.; writing—original draft preparation, A.B.; writing—review and editing, A.B.; S.P., J.N., M.C. and A.P.; visualization, A.B., S.P., M.C. and A.P.; supervision, P.M., A.P. and G.F.; project administration, A.P., P.M. and G.F.; funding acquisition, P.M. and G.F. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

The study was conducted according to the guidelines of the Declaration of Helsinki and approved by the Ethics Committee on Silesian Medical University in Katowice (No KNW/0022/KB1/140/II/15/16, 15 November 2016).

Informed Consent Statement

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

Data Availability Statement

The data presented in this study are available upon request from the corresponding author.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Swinburn, B.A.; Caterson, I.; Seidell, J.C.; James, W.P.T. Diet, nutrition and the prevention of excess weight gain and obesity. Public Health Nutr. 2004, 7, 123–146. [Google Scholar]
  2. Barthelmess, E.K.; Naz, R.K. Polycystic ovary syndrome: Current status and future perspective. Front. Biosci. Elite Ed. 2014, 6, 104–119. [Google Scholar]
  3. Rojas, J.; Chávez, M.; Olivar, L.; Rojas, M.; Morillo, J.; Mejías, J.; Calvo, M.; Bermúdez, V. Polycystic Ovary Syndrome, Insulin Resistance, and Obesity: Navigating the Pathophysiologic Labyrinth. Int. J. Reprod. Med. 2014, 2014, 719050. [Google Scholar] [CrossRef]
  4. Vilmann, L.S.; Thisted, E.; Baker, J.L.; Holm, J.-C. Development of Obesity and Polycystic Ovary Syndrome in Adolescents. Horm. Res. Paediatr. 2012, 78, 269–278. [Google Scholar] [CrossRef]
  5. Barber, T.M.; Hanson, P.; Weickert, M.O.; Franks, S. Obesity and Polycystic Ovary Syndrome: Implications for Pathogenesis and Novel Management Strategies. Clin. Med. Insights Reprod. Health 2019, 13, 1179558119874042. [Google Scholar] [CrossRef] [Green Version]
  6. Yang, H.; Xin, Z.; Feng, J.-P.; Yang, J.-K. Waist-to-height ratio is better than body mass index and waist circumference as a screening criterion for metabolic syndrome in Han Chinese adults. Medicine 2017, 96, e8192. [Google Scholar] [CrossRef] [PubMed]
  7. Ndefo, U.A.; Eaton, A.; Green, M.R. Polycystic ovary syndrome: A review of treatment options with a focus on pharmacological approaches. P T Peer-Rev. J. Formul. Manag. 2013, 38, 336–355. [Google Scholar]
  8. Szczuko, M.; Kikut, J.; Szczuko, U.; Szydłowska, I.; Nawrocka-Rutkowska, J.; Ziętek, M.; Verbanac, D.; Saso, L. Nutrition Strategy and Life Style in Polycystic Ovary Syndrome-Narrative Review. Nutrients 2021, 13, 2452. [Google Scholar] [CrossRef] [PubMed]
  9. Escobar-Morreale, H.F. Polycystic ovary syndrome: Definition, aetiology, diagnosis and treatment. Nat. Rev. Endocrinol. 2018, 14, 270–284. [Google Scholar] [CrossRef] [PubMed]
  10. Rotterdam ESHRE/ASRM-Sponsored PCOS Consensus Workshop Group. Revised 2003 consensus on diagnostic criteria and long-term health risks related to polycystic ovary syndrome (PCOS). Hum. Reprod. Oxf. Engl. 2004, 19, 41–47. [Google Scholar] [CrossRef] [Green Version]
  11. Daan, N.M.P.; Louwers, Y.V.; Koster, M.P.H.; Eijkemans, M.J.C.; de Rijke, Y.B.; Lentjes, E.W.G.; Fauser, B.C.J.M.; Laven, J.S. Cardiovascular and metabolic profiles amongst different polycystic ovary syndrome phenotypes: Who is really at risk? Fertil. Steril. 2014, 102, 1444–1451.e3. [Google Scholar] [CrossRef]
  12. Gažarová, M.; Galšneiderová, M.; Mečiarová, L. Obesity diagnosis and mortality risk based on a body shape index (ABSI) and other indices and anthropometric parameters in university students. Rocz. Panstw. Zakl. Hig. 2019, 70, 267–275. [Google Scholar] [CrossRef] [PubMed]
  13. Tchernof, A.; Brochu, D.; Maltais-Payette, I.; Mansour, M.F.; Marchand, G.B.; Carreau, A.-M.; Kapeluto, J. Androgens and the Regulation of Adiposity and Body Fat Distribution in Humans. Compr. Physiol. 2018, 8, 1253–1290. [Google Scholar] [PubMed]
  14. Blouin, K.; Boivin, A.; Tchernof, A. Androgens and body fat distribution. J. Steroid. Biochem. Mol. Biol. 2008, 108, 272–280. [Google Scholar] [CrossRef]
  15. Polak, A.M.; Adamska, A.; Krentowska, A.; Łebkowska, A.; Hryniewicka, J.; Adamski, M.; Kowalska, I. Body Composition, Serum Concentrations of Androgens and Insulin Resistance in Different Polycystic Ovary Syndrome Phenotypes. J. Clin. Med. 2020, 9, 732. [Google Scholar] [CrossRef] [Green Version]
  16. Kirchengast, S. Body composition characteristics and body fat distribution in lean women with polycystic ovary syndrome. Hum. Reprod. 2001, 16, 1255–1260. [Google Scholar] [CrossRef] [Green Version]
  17. Franik, G.; Bizoń, A.; Włoch, S.; Pluta, D.; Blukacz, Ł.; Milnerowicz, H.; Madej, P. The effect of abdominal obesity in patients with polycystic ovary syndrome on metabolic parameters. Eur. Rev. Med. Pharmacol. Sci. 2017, 21, 4755–4761. [Google Scholar]
  18. Kokot, I.; Lilla Pawlik-Sobecka Płaczkowska, S.; Żółcińska-Wilczyńska, M.; Piwowar, A. The relationship between total body fat and distribution of body fat mass and markers of insulin resistance in young women with normal weight—A pilot study. Clin. Diabetol. 2016, 5, 41–48. [Google Scholar] [CrossRef] [Green Version]
  19. Flegal, K.M.; Shepherd, J.A.; Looker, A.C.; Graubard, B.I.; Borrud, L.G.; Ogden, C.L.; Harris, T.B.; Everhart, J.E.; Schenker, N. Comparisons of percentage body fat, body mass index, waist circumference, and waist-stature ratio in adults. Am. J. Clin. Nutr. 2009, 89, 500–508. [Google Scholar] [CrossRef]
  20. Čuta, M.; Bařicová, K.; Černý, D.; Sochor, O. Normal-weight obesity frequency in the Central European urban adult female population of Brno, Czech Republic. Cent. Eur. J. Public Health 2019, 27, 131–134. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  21. Nuttall, F.Q. Body Mass Index: Obesity, BMI, and Health: A Critical Review. Nutr. Today 2015, 50, 117–128. [Google Scholar] [CrossRef] [Green Version]
  22. Arusoglu, G. The Use of SenseWear Armband for Assessment of Daily Energy Expenditure and the Relation to Body Fat Distribution and Nutritional Intake in Lean Women with Polycystic Ovary Syndrome. J. Nutr. Metab. 2020, 2020, 9191505. [Google Scholar] [CrossRef]
  23. Płaczkowska, S.; Pawlik-Sobecka, L.; Kokot, I.; Żółcińska-Wilczyńska, M.; Piwowar, A. Use of direct and indirect methods for measuring body composition of young people—Preliminary report. Fam. Med. Prim. Care Rev. 2015, 17, 33–38. [Google Scholar]
  24. Després, J.-P. Is visceral obesity the cause of the metabolic syndrome? Ann. Med. 2006, 38, 52–63. [Google Scholar] [CrossRef]
  25. Giampaolino, P.; Foreste, V.; Di Filippo, C.; Gallo, A.; Mercorio, A.; Serafino, P.; Improda, F.P.; Verrazzo, P.; Zara, G.; Buonfantino, C. Microbiome and PCOS: State-of-Art and Future Aspects. Int. J. Mol. Sci. 2021, 22, 2048. [Google Scholar] [CrossRef] [PubMed]
  26. Della Corte, L.; Foreste, V.; Barra, F.; Gustavino, C.; Alessandri, F.; Centurioni, M.G.; Ferrero, S.; Bifulco, G.; Giampaolino, P. Current and experimental drug therapy for the treatment of polycystic ovarian syndrome. Expert Opin. Investig. Drugs 2020, 29, 819–830. [Google Scholar] [CrossRef] [PubMed]
  27. Giampaolino, P.; Della Corte, L.; De Rosa, N.; Mercorio, A.; Bruzzese, D.; Bifulco, G. Ovarian volume and PCOS: A controversial issue. Gynecol. Endocrinol. 2018, 34, 229–232. [Google Scholar] [CrossRef] [PubMed]
  28. Azrad, M.; Gower, B.A.; Hunter, G.R.; Nagy, T.R. Intra-abdominal adipose tissue is independently associated with sex-hormone binding globulin in premenopausal women. Obesity 2012, 20, 1012–1015. [Google Scholar] [CrossRef] [PubMed]
  29. Bizoń, A.; Franik, G.; Niepsuj, J.; Czwojdzińska, M.; Leśniewski, M.; Nowak, A.; Szynkaruk-Matusiak, M.; Madej, P.; Piwowar, A. The Associations between Sex Hormones and Lipid Profiles in Serum of Women with Different Phenotypes of Polycystic Ovary Syndrome. J. Clin. Med. 2021, 10, 3941. [Google Scholar] [CrossRef]
  30. Yucel, A.; Noyan, V.; Sagsoz, N. The association of serum androgens and insulin resistance with fat distribution in polycystic ovary syndrome. Eur. J. Obstet. Gynecol. Reprod. Biol. 2006, 126, 81–86. [Google Scholar] [CrossRef]
  31. Wei, S.; Schmidt, M.D.; Dwyer, T.; Norman, R.J.; Venn, A.J. Obesity and Menstrual Irregularity: Associations With SHBG, Testosterone, and Insulin. Obesity 2009, 17, 1070–1076. [Google Scholar] [CrossRef] [PubMed]
  32. Dumesic, D.A.; Akopians, A.L.; Madrigal, V.K.; Ramirez, E.; Margolis, D.J.; Sarma, M.K.; Thomas, A.M.; Grogan, T.R.; Haykal, R.; Schooler, T.A.; et al. Hyperandrogenism Accompanies Increased Intra-Abdominal Fat Storage in Normal Weight Polycystic Ovary Syndrome Women. J. Clin. Endocrinol. Metab. 2016, 101, 4178–4188. [Google Scholar] [CrossRef] [PubMed]
  33. Deswal, R.; Yadav, A.; Dang, A.S. Sex hormone binding globulin—An important biomarker for predicting PCOS risk: A systematic review and meta-analysis. Syst. Biol. Reprod. Med. 2018, 64, 12–24. [Google Scholar] [CrossRef] [PubMed]
  34. Lim, S.S.; Norman, R.J.; Davies, M.J.; Moran, L.J. The effect of obesity on polycystic ovary syndrome: A systematic review and meta-analysis. Obes. Rev. Off J. Int. Assoc. Study Obes. 2013, 14, 95–109. [Google Scholar] [CrossRef]
  35. Cosar, E.; Uçok, K.; Akgün, L.; Köken, G.; Sahin, F.K.; Arioz, D.T.; Baş, O. Body fat composition and distribution in women with polycystic ovary syndrome. Gynecol. Endocrinol. Off J. Int. Soc. Gynecol. Endocrinol. 2008, 24, 428–432. [Google Scholar] [CrossRef]
  36. Bialka-Kosiec, A.A.; Wilk, K.; Pytel, M.; Skrzypulec-Plinta, V.; Stojko, R.; Drosdzol-Cop, A. Body mass composition and dietary habits in adolescents with polycystic ovary syndrome. Ginekol. Pol. 2019, 90, 589–595. [Google Scholar] [CrossRef] [Green Version]
  37. Cassar, S.; Teede, H.J.; Moran, L.J.; Joham, A.E.; Harrison, C.L.; Strauss, B.J.; Stepto, N.K. Polycystic ovary syndrome and anti-Müllerian hormone: Role of insulin resistance, androgens, obesity and gonadotrophins. Clin. Endocrinol. 2014, 81, 899–906. [Google Scholar] [CrossRef]
  38. Luo, E.; Zhang, J.; Song, J.; Feng, D.; Meng, Y.; Jiang, H.; Li, D.; Fang, Y. Serum Anti-Müllerian Hormone Levels Were Negatively Associated With Body Fat Percentage in PCOS Patients. Front. Endocrinol. 2021, 12, 659717. [Google Scholar] [CrossRef] [PubMed]
  39. Dólleman, M.; Faddy, M.J.; van Disseldorp, J.; van der Schouw, Y.T.; Messow, C.M.; Leader, B.; Peeters, P.H.M.; McConnachie, A.; Nelson, S.M.; Broekmans, F.J.M. The relationship between anti-Müllerian hormone in women receiving fertility assessments and age at menopause in subfertile women: Evidence from large population studies. J. Clin. Endocrinol. Metab. 2013, 98, 1946–1953. [Google Scholar] [CrossRef] [Green Version]
  40. Casarotto, A.A.F.; Galera, B.B.; Sumiyoshi, L.M.; Floôr, T.M. Polymorphism rs7895833 in the SIRT1 gene and its association with dyslipidaemia in the elderly. Rev. Espanola Geriatr. Gerontol. 2019, 54, 214–219. [Google Scholar] [CrossRef]
  41. Dadachanji, R.; Patil, A.; Joshi, B.; Mukherjee, S. Elucidating the impact of obesity on hormonal and metabolic perturbations in polycystic ovary syndrome phenotypes in Indian women. PLoS ONE 2021, 16, e0246862. [Google Scholar] [CrossRef] [PubMed]
Nutrients 13 04217 g001 550
Figure 1. Correspondence analysis showed the potential association between quartiles of body composition parameters and phenotypes of PCOS. Legend: PCOS, polycystic ovary syndrome; BMI, body mass index; WHR, waist hip ratio; FAT, fat mass; TBW, total body water; FFM, fat-free mass; PBF, percent of body fat; VFA, visceral fat area; BMR, basal metabolic rate.
Figure 1. Correspondence analysis showed the potential association between quartiles of body composition parameters and phenotypes of PCOS. Legend: PCOS, polycystic ovary syndrome; BMI, body mass index; WHR, waist hip ratio; FAT, fat mass; TBW, total body water; FFM, fat-free mass; PBF, percent of body fat; VFA, visceral fat area; BMR, basal metabolic rate.
Nutrients 13 04217 g001
Nutrients 13 04217 g002 550
Figure 2. ROC curve of AMH concentration used to distinguish the women with PCOS from the whole group of women younger (a) and older than 30 years old (b). Legend: ROC curve, receiver operating characteristic curve; AMH, Anti-Müllerian hormone; AUC, area under curve; SE, sedimentation equilibrium.
Figure 2. ROC curve of AMH concentration used to distinguish the women with PCOS from the whole group of women younger (a) and older than 30 years old (b). Legend: ROC curve, receiver operating characteristic curve; AMH, Anti-Müllerian hormone; AUC, area under curve; SE, sedimentation equilibrium.
Nutrients 13 04217 g002
Table
Table 1. Characteristics of women with PCOS including selected body composition parameters.
Table 1. Characteristics of women with PCOS including selected body composition parameters.
ParametersWomen
without PCOSwith PCOSp Value
Age (years)28.24 ± 6.2425.91 ± 4.700.058
LH (lU/L)5.08 (4.17–6.55)6.79 (5.23–9.36)0.006
FSH (lU/L)7.09 (5.89–8.21)6.16 (5.27–7.39)0.056
DHEA-S (µg/mL)276.00 (216.00–350.00)284.50 (217.00–384.00)0.566
SHBG (nmol/L)53.2 (37.00–75.10)46.70 (30.70–73.10)0.399
t-test (ng/mL)0.22 (0.13–0.30)0.28 (0.19–0.39)0.025
fTest (pg/mL)1.64 (0.93–3.02)2.26 (1.28–3.39)0.116
AD (ng/mL)1.89 (1.37–2.26)2.36 (1.81–3.13)0.005
17α-OHP (nmol/L)0.67 (0.39–0.92)0.65 (0.46–0.89)0.756
Prolactine (ng/mL)9.81 (6.83–13.30)11.60 (8.80–15.70)0.086
AMH (ng/mL)2.95 (1.58–3.63)6.07 (4.84–8.25)0.000
BMI (kg/m2)20.90 (19.80–23.80)24.00 (20.50–30.30)0.069
WHR0.85 (0.83–0.90)0.87 (0.83–0.96)0.168
SMM (kg)23.40 (21.20–25.10)24.70 (22.20–28.40)0.094
FAT (kg)17.80 (13.50–22.50)21.60 (13.60–31.90)0.157
TBW (%)31.10 (28.50–33.30)32.70 (29.70–37.60)0.081
FFM (%)42.60 (39.00–45.30)44.70 (40.60–51.40)0.082
PBF (%)31.00 (39.00–45.30)32.40 (24.20–39.00)0.271
VFA (cm2)8.00 (5.00–10.00)9.00 (5.00–15.00)0.236
BMR (kcal)1290.0 (1212.0–1349.0)1336.0 (1246.0–1479.0)0.080
Legend: PCOS, polycystic ovary syndrome; LH, luteinizing hormone; FSH, follicle-stimulating hormone; DHEA-S, dehydroepiandrosterone sulfate; SHBG—sex hormone-binding globulin; t-test—total testosterone; fTest, free testosterone; AD, androstenedione; 17α-OHP, 17α-hydroxyprogesterone; AMH, Anti-Müllerian hormone; BMI, body mass index; WHR, waist hip ratio; SMM, skeletal muscle mass; FAT, fat mass; TBW, total body water; FFM, fat-free mass; PBF, percent of body fat; VFA, visceral fat area; BMR, basal metabolic rate.
Table
Table 2. Comparison of the value of body composition parameters dependent on phenotype in the group of women with PCOS.
Table 2. Comparison of the value of body composition parameters dependent on phenotype in the group of women with PCOS.
ParametersPhenotype 1Phenotype 2Phenotype 3Phenotype 4p Value
n = 31n = 7n = 11n = 6
Age (years)26.00 (22.00–29.00)25.000 (19.00–27.00)25.00 (24.00–28.00)27.50 (2500–33.00)0.546
BMI (kg/m2)23.40 (20.50–27.00)30.90 (21.00–35.30)24.80 (23.20–33.00)20.45 (17.30–24.30)0.178
WHR0.87 (0.83–0.93)0.98 (0.84–1.00)0.89 (0.87–0.97)0.81 (0.79–0.90)0.168
SMM (kg)25.90 (23.00–29.00)24.80 (22.30–26.40)22.20 (21.80–27.90)23.05 (20.20–23.40)0.335
FAT (kg)21.60 (12.90–29.40)36.70 (18.80–45.70)21.90 (20.80–41.50)14.00 (11.90–23.40)0.245
TBW (%)34.10 (31.00–38.00)32.70 (29.80–34.60)29.70 (29.10–36.90)30.90 (27.70–31.10)0.311
FFM (%)46.60 (42.30–52.00)44.70 (40.70–47.40)40.70 (39.80–50.50)42.10 (37.90–42.60)0.331
PBF (%)31.70 (23.40–37.80)43.70 (30.10–52.20)36.30 (30.00–42.60)25.90 (22.10–36.70)0.180
VFA (cm2)9.00 (5.00–14.00)19.00 (7.00–22.00)10.00 (8.00–20.00)5.00 (4.00–12.00)0.233
BMR (kcal)1377 (1285–1492)1336 (1249–1393)1249 (1230–1460)1279.5 (1188–1290)0.318
Legend: PCOS, polycystic ovary syndrome; BMI, body mass index; WHR, waist hip ratio; SMM, skeletal muscle mass; FAT, fat mass; TBW, total body water; FFM, fat-free mass; PBF, percent of body fat; VFA, visceral fat area; BMR, basal metabolic rate.
Table
Table 3. Correlation coefficient between SHBG or fTest concentration and selected body composition parameters in the group of women with PCOS.
Table 3. Correlation coefficient between SHBG or fTest concentration and selected body composition parameters in the group of women with PCOS.
ParametersSHBGfTest
BMI (kg/m2)−0.68; 0.0000.47; 0.000
WHR−0.68; 0.0000.45; 0.000
SMM (kg)−0.47; 0.0000.37; 0.004
FAT (kg)−0.63; 0.0000.42; 0.001
TBW (%)−0.47; 0.0000.38; 0.004
FFM (%)−0.47; 0.0000.38; 0.004
PBF (%)−0.57; 0.0000.37; 0.000
VFA (cm2)−0.61; 0.0000.41; 0.001
BMR (kcal)−0.47; 0.0000.38; 0.005
Legend: PCOS, polycystic ovary syndrome; SHBG, sex hormone-binding globulin; fTest, free testosterone; BMI, body mass index; WHR, waist hip ratio; SMM, skeletal muscle mass; FAT, fat mass; TBW, total body water; FFM, fat-free mass; PBF, percent of body fat; VFA, visceral fat area; BMR, basal metabolic rate.
Table
Table 4. Logistic regression of the state variable of study group vs. control group.
Table 4. Logistic regression of the state variable of study group vs. control group.
Model 1Model 2Model 3Model 4
VariablesOR
(95% CI)
p		VariablesOR
(95% CI)
p		VariablesOR
(95% CI)
p		VariablesOR
(95% CI)
p
AMH
(ng/mL)		2.085
(1.451–2.997)
<0.001		AMH
(ng/mL)		2.057
(1.445–2.929)
<0.001		AMH
(ng/mL)		2.064
(1.442–2.952)
<0.001		AMH
(ng/mL)		2.085
(1.451–2.997)
<0.001
BMI
(kg/m2)		1.198
(1.036–1.386)
0.015		PBF
(%)		1.079
(1.002–1.162)
0.043		VFA
(cm2)		1.141
(1.012–1.287)
0.031		BMI
(kg/m2)		1.198
(1.036–1.386)
0.015
Model 1 adjusted to: all hormones under fasting condition and BMI, Model 2 adjusted to all hormones under fasting condition and PBF, Model 3 adjusted to all hormones under fasting condition and VFA, Model 4 adjusted to all hormone under fasting condition and BMI, PBF, VFA. Legend: AMH, Anti-Müllerian hormone; BMI, body mass index; PBF, percent of body fat; VFA, visceral fat area; OR, odds ratio; CI, confidence interval.
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Bizoń, A.; Płaczkowska, S.; Niepsuj, J.; Czwojdzińska, M.; Leśniewski, M.; Nowak, A.; Pluta, D.; Madej, P.; Piwowar, A.; Franik, G. Body Composition and Its Impact on the Hormonal Disturbances in Women with Polycystic Ovary Syndrome. Nutrients 2021, 13, 4217. https://doi.org/10.3390/nu13124217

AMA Style

Bizoń A, Płaczkowska S, Niepsuj J, Czwojdzińska M, Leśniewski M, Nowak A, Pluta D, Madej P, Piwowar A, Franik G. Body Composition and Its Impact on the Hormonal Disturbances in Women with Polycystic Ovary Syndrome. Nutrients. 2021; 13(12):4217. https://doi.org/10.3390/nu13124217

Chicago/Turabian Style

Bizoń, Anna, Sylwia Płaczkowska, Justyna Niepsuj, Marta Czwojdzińska, Marcin Leśniewski, Artur Nowak, Dagmara Pluta, Paweł Madej, Agnieszka Piwowar, and Grzegorz Franik. 2021. "Body Composition and Its Impact on the Hormonal Disturbances in Women with Polycystic Ovary Syndrome" Nutrients 13, no. 12: 4217. https://doi.org/10.3390/nu13124217

APA Style

Bizoń, A., Płaczkowska, S., Niepsuj, J., Czwojdzińska, M., Leśniewski, M., Nowak, A., Pluta, D., Madej, P., Piwowar, A., & Franik, G. (2021). Body Composition and Its Impact on the Hormonal Disturbances in Women with Polycystic Ovary Syndrome. Nutrients, 13(12), 4217. https://doi.org/10.3390/nu13124217

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