Past Issue

Volume 11, Number 2, Jul-Sep 2017 Pages: 105-111

Original Article(s)

Evaluation of Relationship between Body Mass Index with Vitamin D Receptor Gene Expression and Vitamin D Levels of Follicular Fluid in Overweight Patients with Polycystic Ovary Syndrome

Esmat Aghadavod, Ph.D, 1Hakimeh Mollaei, M.Sc, 2,3Mohammad Nouri, Ph.D, 4Hamed Hamishehkar, Ph.D, 5,*
Gametogenesis Research Center, Kashan University of Medical Sciences, Kashan, Iran
Research Center for Pharmaceutical Nanotechnology, Tabriz University of Medical Sciences, Tabriz, Iran
Department of Biology, Science and Research Branch of Islamic Azad University, Tehran, Iran
Women Reproductive Health Research Center, Tabriz University of Medical Sciences, Tabriz, Iran
Drug Applied Research Center, Tabriz University of Medical Sciences, Tabriz, Iran
*Corresponding Address: P.O.Box: 51656-65811 Drug Applied Research Center Tabriz University of Medical Sciences Tabriz Iran



Polycystic ovary syndrome (PCOS) is the most common endocrine disorder associated with reproductive disorders and metabolic dysfunctions including insulin resistance. The roles of vitamin D in the regulation of metabolic modulations specifically involving insulin and reproduction processing are introduced. In addition, obesity appears to be closely associated with severity of PCOS. The present study is to evaluate the effect of body mass index (BMI) on vitamin D levels in follicular fluid and vitamin D receptor (VDR) expression levels in granulos cells.

Materials and Methods

A comparative study was conducted on 80 women with average age of 20-35 years referred for in vitro fertilization (IVF). Patients were divided into four groups, and serum levels of testosterone and insulin resistance (IR) were evaluated at the puncture time. Also, vitamin D levels of follicular fluid were evaluated. VDR gene expression was assayed by quantified-polymerase chain reaction (PCR) technique. Correlations were evaluated with calculation of the Spearman coefficient, and also independent relationships were assessed by means of multiple regression analysis.


Vitamin D levels of follicular fluid decreased in PCOS patients compared with non-PCOS. Also, over-weight individuals had lower vitamin D levels compared with normal-weight patients. Vitamin D levels of follicular fluid were highly correlated with BMI (r=-0.51, P<0.01). Homeostatic model assessment-IR (HOMA-IR) values were significantly higher in women of PCOS/overweight and PCOS/normal weight in comparison with women of non-PCOS/normal weight (P<0.01). The gene expression data of VDR in granulosa cells were significantly lower in the PCOS/overweight group compared with the non-PCOS/normal weight (P<0.01).


The findings indicated significant differences in VDR gene expression in granulosa cells and vitamin D of follicular fluid in PCOS/overweight patients.


Polycystic ovary syndrome (PCOS) is the most common endocrine disorder that can affect 8% to 10% of women in their reproductive age (1, 2). PCOS is associated not only with reproductive disorders, but also with significantly increased risks of metabolic dysfunctions, including insulin resistance (IR) (3), dyslipidemia (4), systemic inflammation (5), increased oxidative stress (6), and endothelial dysfunction (7). It can be noticed that PCOS, as a heterogeneous androgen excess disorder with varying degrees of reproductive and metabolic abnormalities, is determined by the interaction of multiple genetic and environmental factors (8).

Several studies have revealed that certain metabolic disturbances such as IR and hyperinsulinemia are majour defects in the majority of PCOS patients (9, 10). Emerging data characterize serious roles for vitamin D in biological processes, including regulation of cellular growth (11), differentiation, and metabolic modulations specifically involving insulin action (12, 13). Among the many physiologic processes influenced by vitamin D, serious roles in reproductive physiology are submitted (14). Biological actions of vitamin D are intermediated through vitamin D receptor (VDR) gene expression which is a member of the steroid/thyroid nuclear hormone receptor superfamily, displayed in calcium-regulating tissues, intestines (12), the skeleton (15), parathyroid glands (16), and reproductive tissues including ovary, uterus, placenta (17), testis (18), and granulosa cells (19, 20).

Additionally, investigations of animals have confirmed the role of calcium in oocyte maturation and its impact on the resumption and progression of follicular development. Furthermore, disturbances in calcium regulation can be responsible for follicular arrest (21). Previous study have suggested the functions of vitamin D in reproduction (22). They have also indicated that VDR regulates more than 3% of the human genome, including genes that are crucial for glucose metabolism. VDR is a transcription factor regulating the transcription of other downstream genes in many tissues that are crucial for glucose metabolism (23, 24). On the other hand, calcium fluxes and regulation of intracellular calcium stores are essential in the regulation of insulin secretion by b-cells. Therefore, vitamin D and VDR gene are important factors in calcium regulation and control of bcell functions, respectively. This is further supported by the fact that low vitamin D levels are associated with IR and that they can induce type-2 diabetes in PCOS patients (25). However, the exact mechanisms underlying the association of vitamin D and IR are not fully understood. One complication of PCOS is obesity which appears to be closely associated with severity of the disease phenotype (26).

In Iran, more than half of the patients with PCOS are either overweight or obese (27). It is well known that obesity influences the phenotypic expression of PCOS and might play a significant role in the pathophysiology of hyperandrogenism, severity of insulin resistance, and also chronic anovulation (28). Increased adiposity is associated with several abnormalities of sex steroid metabolism and results in increased androgen production and suppression of sex hormone binding globulin (SHBG) (29). Thus, obesity may affect vitamin D levels in healthy women and PCOS patients. The present study aimed to evaluate the effect of obesity on vitamin D levels in follicular fluid and VDR expression levels in granulosa cells. The results of this research may contribute to the diagnosis and treatment of overweight PCOS patients.

Materials and Methods

The current comparative study was carried out on 80 women of 20 to 35 years old and who referred to Alzahra-Hospital of Tabriz, Iran for in vitro fertilization (IVF). Before entering the study, all the patients provided written consent forms. This study was approved by the Ethics Committee of Tabriz University of Medical Sciences (code: 5/4/2781). Weight and height of all the patients were measured, and then the body mass index (BMI, Kg/m2) was calculated by dividing weight by height square. The patients were divided into two groups based on BMI categories, using the specified criteria by the World Health Organization (WHO): the normal weight and overweight groups with the BMI of 18.5-24.9 and 25-29.9, respectively. The control group consisted of 40 non-PCOS patients (20 normal weights and 20 over-weights) who had referred for IVF due to tubal and/or male infertility or even ovulatory volunteers with normal ovaries. The PCOS group included 40 patients (20 normal weights and 20 over-weights) who had referred for IVF. These patients were recognized based on Rotterdam Consensus criteria and had at least two of the three following criteria: ovulatory disturbance, hyerandrogenism, and more than twelve 2 to 9 mm follicles in each ovary. The exclusion criteria were as follows: history of menstrual disorders such as cycle length either less than 25 days or more than 35 days, patients with other endocrine disorders or neoplastic causes of hyperandrogenemia such as androgen-secreting tumors (serum testosterone levels above 0.6 ng/mL), congenital adrenal hyperplasia, and Cushingʼs syndrome.

Ovarian stimulation

For pituitary down-regulation, the patients were treated with 0.5-1 mg subcutaneous (SC) injection of gonadotropin releasing hormone (GnRH) agonist (Lucrin, Abbott Pharmaceuticals, Kurnell, Australia), depending on the age of every woman. When at least three follicles reached a diameter of almost 17 mm and the levels of peripheral plasma estradiol concentrations were ≥3 nmol/l, 5000-IU of human chorionic gonadotropin (hCG, Profasi, Serono, Aubonne, Switzerland) was given as a single IM injection. Thirty six hours after hCG administration, the oocytes were retrieved and collected with sterile Pasteur pipettes, and then the remainder of the follicular fluid was poured into 50 ml sterile falcon tubes for subsequent isolation of granulosa cells. The follicular fluid was centrifuged, and vitamin D levels were measured in the supernatant. 25-OH vitamin D was estimated by chemiluminescence enzyme immunoassay (IDS, Boldon, UK). The blood samples were obtained before the operation for subsequent biochemical analyses. These samples were analyzed for follicle-stimulating hormone (FSH), luteinizing hormone (LH), testosterone, prolactin, insulin, and glucose levels.

Granulosa cells collection

The freshly collected follicular fluid samples were then centrifuged at 3000 rpm for 1 minute at 4°C; afterwards, 4 ml of phosphate buffer saline (PBS) was added to the pallet. After mixing, the solution was placed on 50% Percoll gradient (Amersham Pharmacia Biotech, Uppsala, Sweden). The sample was centrifuged at 700 rpm for 30 minutes to remove red blood cells. After the centrifugation, the granulosa cells were placed between PBS and Percoll solutions. The cells were harvested by gentle pipetting, and also washed several times with PBS, and used for RNA extraction and cDNA synthesis. The total RNA of the collected samples was the recommended protocol of manufacture. In brief, 1 ml of RNX plus was added to the sample in a clean RNase-free tube. The sample was homogenated via gentle up and downing and then was incubated for 5 minutes at room temperature. After adding chloroform (200 μl), the mixture was incubated at room temperature for 5 minutes and was centrifuged at 12,000 rpm for 15 minutes at 4°C. The aqueous phase containing RNA was transferred to a clean RNase-free tube. This solution was put on ice, and 500 μl of ice isopropanol was added to it; the sample was then incubated for 30 minutes at -80°C. Afterwards, the tube was centrifuged at 12,000 rpm for 15 minutes at 4°C, and the supernatant was discarded. The pellet, including the total RNA, was washed using 75% ethanol and was centrifuged at 7,500 rpm for 8 minutes. After drying ethanol, the RNA pellet was re-suspended in 50 μl or less of DEPC-treatment water. The concentration of total RNA was calculated based on OD 260/280 ratio measurements as a means to address the purity of RNA.

To confirm the integrity of the extracted RNA, it was electrophoresed. The genomic DNA was removed from the extracted RNA by adding RNase free DNase I (Thermo, Fermentase). The cDNA was synthesized with Moloney murine leukemia virus reverse-transcriptase (MMLV-RT, 200 U/μl, Sigma-Aldrich Co., UK) according to the manufacture’s protocol. As soon as the RNA was isolated from the granulosa cells, the reverse transcriptase reactions were performed on all the samples to generate cDNA.

To quantify the mRNA expression levels of VDR gene in the granulosa cells, real-time polymerase chain reaction (RT-PCR) was performed on a Bio-Rad iQ5 system (Bio-Rad Laboratories, Hercules, USA), using EVA-Green quantitative PCR mix kit (Sinaclon, Tehran-Iran). GAPDH gene was used as reference standard gene for all analyses to control the amount of the synthesized cDNA. PCR reactions were carried out in triplicate for each sample, and then the mean of the three readings was taken as fold-induction value. Fold change (X) values were calculated, using X=2-ΔΔCt equation, in which ΔCt represents the difference between the Ct values of the target genes and the Ct values of the reference standard genes, and ΔΔCt describes the difference between ΔCt value of each sample for each target gene and the average ΔCt of the reference standard gene. The sequence of PCR primers for amplifying VDR and GAPDH genes is provided in Table 1. IR was estimated, using the homeostatic model assessment-IR (HOMA-IR) method. In addition, HOMA-IR was calculated as the product of the fasting plasma insulin value (mU/mL) and the fasting plasma glucose value (mg/dL). Insulin levels were also estimated by ELISA kit (Siemens, Erlangen, Germany) according to the manufacture’s recommendations.

Statistical analysis

All statistical procedures were run, using SPSS-16 software (SPSS Inc., Chicago, IL), and P<0.05 was considered statistically significant. Normal distribution of data was evaluated through the one-sample Kolmogorov-Smirnoff test. The comparisons of the means were performed by one-way ANOVA and the general linear model multi-variance by post-hoc analysis for pairwise comparisons. Correlations were evaluated by calculating the Spearman coefficient, and independent relationships were assessed via multiple regression analysis.


Table 1 shows the variables measured in PCOS patients. The statistical Kolmogorov-Smirnoff test proved a normal distribution for the measured parameters. The multiple regression analysis was applied to examine the relationship between obesity and testosterone, HOMA-IR levels, vitamin D levels of follicular fluid, and VDR gene expression on gramulosa cells. The results demonstrated that vitamin D levels of follicular fluid decreased in PCOS patients and over-weight individuals compared with non-PCOS and normal-weight patients. The results also revealed that 25 OH-D levels of follicular fluid were highly correlated with BMI (r=-0.51, P<0.01). In addition, HOMA-IR values were significantly higher in the women in PCOS/overweight and PCOS/normal weight than group those in non-PCOS/normal weight group (P<0.01). However, the difference in HOMA-IR values between the women in non-PCOS/overweight and non-PCOS/normal weight group was not significant (P=0.1, Table 1,).

Table 1-Applied primer sequences for quantitative polymerase chain reaction (PCR)
Table 2-Clinical and biochemical characteristics of studied women

Table 2 represents the correlation between age, BMI, and HOMA-IR and the number of follicles, serum testosterone levels, follicular fluid vitamin D levels, and VDR expression levels of granulosa cells. Furthermore, there was a considerable positive correlation between HOMA-IR and BMI (r=0.43, P<0.05). The results indicated that testosterone levels in PCOS/overweight patients were not substantially higher than those in non-PCOS/overweight patients (P=0.2). Similarly, there was not a significant correlation between BMI and testosterone (r=0.09, P>0.05, Table 3,).

Table 3-Relationship between age‚ body mass index (BMI) and homeostatic model assessment-insulin resistance (HOMA-IR) with the studied variables

Quantitative RT-PCR results exhibited a lower VDR gene expression in PCOS patients compared to the control group (Fig .1,).

- The fold change in gene expression patterns of VDR in polycystic ovary syndrome (PCOS)/overweight, PCOS/normal weight, non-PCOS/overweight, compared with non-PCOS/normal weight individuals. Expression levels are given as fold change compared with non-PCOS/normal weight samples. The error bars represent the 95% confidence intervals.

The fold change in the expression of the target gene, VDR, was normalized to GAPDH in the PCOS/overweight, PCOS/normal weight, and non-PCOS/overweight groups. Afterwards, its expression in the control group, non-PCOS/normal weight, was analyzed. Melting curve analysis confirmed the specificity of the PCR (data not shown). A negative strong correlation was found between VDR expression levels and BMI (r=-0.43, P<0.05), using Spearman statistical test (Table 3,). The gene expression data of VDR in granulosa cells were significantly lower (three times) in PCOS/overweight group in comparison with non-PCOS/normal weight (P<0.01). The level of VDR expression in PCOS/overweight group was similar to that of VDR expression in PCOS/normal weight group.


Two PCOS related complications are obesity and IR. Studies which show low vitamin D levels are associated with IR, and administration of vitamin D may ameliorate insulin sensitivity; however, the mechanisms of this effect are not clear (30). Moreover, studies demonstrate that insulin plays a significant role in the regulation of renal 1-a-hydroxylase activity and serum 1,25(OH) 2D3 levels in response to parathyroid hormone (PTH), while 1,25(OH) 2D3 is observed to act like a genomic stimulator of the insulin response in the control of glucose transport (31). Therefore, vitamin D may exert a positive effect on insulin action by stimulating the expression of insulin receptor, thus stimulating insulin responsiveness for glucose transport. Additionally, vitamin D responsive element is present in the promoter of the human insulin gene, and the transcription of insulin gene is activated by 1,25(OH) 2D3 (32). In accordance with the previous study, the current results confirmed that the majority of PCOS patients had vitamin D deficiency. There was a significant negative correlation between BMI increase and vitamin D levels of follicular fluid. It should be noted that the overweight PCOS individuals had lower vitamin D levels in their follicular fluid in comparison with other patients. Recent reports have indicated possible mechanisms for lower serum 25-OH-D3 associated with obesity. IR and obesity are also related to a reduction in growth hormone (GH) secretion in PCOS patients. This could be accounted for decreased levels of 1,25(OH) 2D3 because GH significantly increases renal 1-a-hydroxylase expression and, consequently, serum 1,25(OH) 2D3 concentrations (33). The findings revealed a negative correlation between vitamin D levels of follicular fluid and IR. Although this negative correlation was not substantial, its value level was imperative. Studies have also shown that obesity has been consistently associated with vitamin D deficiency, and this fact is supported in the present study by the negative correlation of weight and BMI with vitamin D level in follicular fluid (34). Hence, obesity can affect the decline of vitamin D concentrations in PCOS patients. On the other hand, vitamin D receptors are present in the majority of body cells, such as granulosa cells, and can influence the inhibition of cell proliferation and the induction of cell differentiation. Hence, vitamin D levels of follicular fluid and vitamin D receptors in granulosa cells may play an important role in proliferation and differentiation of granulosa and theca cells (35).

The relationship between allelic variation of VDR in pancreatic island and insulin secretion and glucose tolerance indicates a role for vitamin D in the pathogenesis of IR (36). Furthermore, vitamin D administration can improve insulin sensitivity and decrease insulin level (37). Accordingly, it is logical to state that in PCOS patients with increased BMI, vitamin D levels and VDR gene expression decrease, but IR increases (19). The findings indicated a significant negative correlation between VDR gene expression and HOMA-IR, which is in agreement with previous reports (38).

Based on the recent research, 25(OH) D levels are correlated with androgen levels in men, and one might speculate on an association of vitamin D with androgen. The underlying mechanisms, however, remain to be explored. The current study showed a negative correlation between vitamin D levels of follicular fluid and serum testosterone levels. Although this negative correlation is not significant, it is imperative. Vitamin D levels and intracellular calcium stores may regulate serum androgen levels of PCOS patients. As a result, vitamin D has a biologically plausible role in female reproduction, including the regulation of insulin secretion (39), androgen synthesis (40), proliferation of granulosa cells, and oocyte differentiation (41). In the previous studies, reduced vitamin D levels of serum in PCOS individuals were introduced as a possible factor affecting the reproductive disorders and metabolic disturbances of these patients (39). Overweight or obesity is one of the most important characteristics of PCOS individuals that may be employed as a powerful predictor of decreasing vitamin D levels. Previous studies have revealed the association of vitamin D status which improved IVF outcome. Women with higher levels of 25(OH) D in serum and follicular fluid were significantly more likely to achieve clinical pregnancy following IVF. On the other hand, high vitamin D levels were significantly associated with improved parameters of controlled ovarian hyper-stimulation (42). The present study revealed that the incidence of PCOS was associated with lower vitamin D levels of follicular fluid and decreased level of VDR gene expression in granulosa cells, which was more dominant in the PCOS patients with obesity.


There are fundamental and significant differences in VDR gene expression in granulosa cells and vitamin D of follicular fluid in PCOS/overweight patients. Further investigations on larger sample populations are required to confirm that changes in the expression of VDR and vitamin D level of follicular fluid influence the development of different appearances of PCOS.


The study was financially supported by Drug Applied Research Center of Tabriz University of Medical Sciences (grant # 92/34). Authors would like to thank Research Center for Pharmaceutical Nanotechnology (RCPN) for supporting this project. There is no conflict of interest in this study.


Alnakash AH. Polycystic ovarian syndrome: the correlation between the LH/FSH ratio and disease manifestations. Middle East Fertil Soc J. 2007; 12(1): 35-40.
Farzadi L, Nouri M, Ghojazadeh M, Mohiti M, Aghadavod E. Evaluation of ovarian reserve after laparoscopic surgery in patients with polycystic ovary syndrome. Bioimpacts. 2012; 2(3): 167-170.
Cappelli V, Di Sabatino A, Musacchio M, De Leo V. Evaluation of a new association between insulin-sensitizers and α-lipoic acid in obese women affected by pcos. Minerva Ginecol. 2013; 65(4): 425-433.
Kim JJ, Choi YM. Dyslipidemia in women with polycystic ovary syndrome. Obstet Gynecol Sci. 2013; 56(3): 137-142.
Aziz M, Wissing ML, Naver KV, Faber J, Skouby SO. Polycystic ovary syndrome and low-grade inflammation with special reference to YKL-40. Gynecol Endocrinol. 2014; 30(4): 311-315.
Zhang R, Liu H, Bai H, Zhang Y, Liu Q, Guan L. Oxidative stress status in Chinese women with different clinical phenotypes of polycystic ovary syndrome. Clin Endocrinol (Oxf). 2017; 86(1): 88-96.
Kucur C, Kucur SK, Gozukara I, Seven A, Yuksel KB, Keskin N. Extended high frequency audiometry in polycystic ovary syndrome. ScientificWorldJournal. 2013; 2013: 482689-482689.
Celik C, Tasdemir N, Abali R, Bastu E, Yilmaz M. Progression to impaired glucose tolerance or type 2 diabetes mellitus in polycystic ovary syndrome: a controlled follow-up study. Fertil Steril. 2014; 101(4): 1123-1128.
Dasgupta A, Khan A, Banerjee U, Ghosh M, Pal M, Chowdhury KM. Predictors of Insulin resistance and metabolic complications in polycystic ovarian syndrome in an eastern Indian population. Indian J Clin Biochem. 2013; 28(2): 169-176.
Ghaffari T, Nouri M, Irannejad E, Rashidi MR. Effect of vitamin E and selenium supplement on paraoxonase-1 activity, oxidized low density lipoprotein and antioxidant defense in diabetic rats. Bioimpacts. 2011; 1(2): 121-128.
Nociti FH Jr, Foster B, Tran AB, Dunn D, Presland RB, Wang L. Vitamin D represses dentin matrix protein 1 in cementoblasts and osteocytes. J Dent Res. 2014; 93(2): 148-154.
Liu W, Chen Y, Golan MA, Annunziata ML, Du J, Dougherty U. Intestinal epithelial vitamin D receptor signaling inhibits experimental colitis. J Clin Invest. 2013; 123(9): 3983-3996.
Ostadrahimi A, Mahboob S, Abbasalizad Farhangi M, Vahed Jabbari M. The effect of cholecalciferol injection on serum 25 hydroxy vitamin D and parathyroid hormone in obese and none obese reproductive age women. Pharmaceutical Sciences. 2009; 15(1): 9-16.
Blomberg Jensen M. Vitamin D and male reproduction. Nat Rev Endocrinol. 2014; 10(3): 175-186.
Bouillon R, Suda T. Vitamin D: calcium and bone homeostasis during evolution. Bonekey Rep. 2014; 3: 480-480.
Pi M, Quarles LD. Novel bone endocrine networks integrating mineral and energy metabolism. Curr Osteoporos Rep. 2013; 11(4): 391-399.
Stein SH, Livada R, Tipton DA. Re-evaluating the role of vitamin D in the periodontium. J Periodontal Res. 2014; 49: 545-553.
Blomberg Jensen M, Nielsen JE, Jørgensen A, Rajpert-De Meyts E, Kristensen DM, Jørgensen N. Vitamin D receptor and vitamin D metabolizing enzymes are expressed in the human male reproductive tract. Hum Reprod. 2010; 25(5): 1303-1311.
Smolikova K, Mlynarcikova A, Scsukova S. Effect of 1α, 25-dihydroxyvitamin D3 on progesterone secretion by porcine ovarian granulosa cells. Endocr Regul. 2013; 47(3): 123-131.
Rashedi J, Asgharzadeh M, Moaddab SR, Sahebi L, Khalili M, Mazani M. Vitamin D receptor gene polymorphism and vitamin D plasma concentration: Correlation with susceptibility to tuberculosis. Adv Pharm Bull. 2014; 4: 607-611.
Nikiforaki D, Meerschaut FV, Qian C, De Croo I, Lu Y, Deroo T. Oocyte cryopreservation and in vitro culture affect calcium signalling during human fertilization. Hum Reprod. 2014; 29(1): 29-40.
Kottke TE, Courneya PT. Optimizing the health of mothers, Infants, and communities through research. Mayo Clin Proc. 2013; 88(12): 1350-1352.
Tamilselvan B, Seshadri KG, Venkatraman G. Role of vitamin D on the expression of glucose transporters in L6 myotubes. Indian J Endocrinol Metab. 2013; 17: S326-S326.
Khan KH. Gene expression in mammalian cells and its applications. Adv Pharm Bull. 2013; 3(2): 257-263.
Zhang Y, Oguzhan B, Louchami K, Chardigny JM, Portois L, Carpentier YA. Pancreatic islet function in omega-3 fatty acid-depleted rats: alteration of calcium fluxes and calcium-dependent insulin release. Am J Physiol Endocrinol Metab. 2006; 291(3): E441-E448.
Brewer CJ, Balen AH. The adverse effects of obesity on conception and implantation. Reproduction. 2010; 140(3): 347-364.
Hosseinpanah F, Barzin M, Keihani S, Ramezani Tehrani F, Azizi F. Metabolic aspects of different phenotypes of polycystic ovary syndrome: Iranian PCOS Prevalence Study. Clin Endocrinol (Oxf). 2014; 81(1): 93-99.
Alebić MŠ, Bulum T, Stojanović N, Duvnjak L. Definition of insulin resistance using the homeostasis model assessment (HOMA-IR) in IVF patients diagnosed with polycystic ovary syndrome (PCOS) according to the Rotterdam criteria. Endocrine. 2014; 47(2): 625-630.
Hong Y, Chen D, Li Y, Li C, Liu Y, Xie M. Serum sex hormone binding globulin profile and its association with insulin resistance in Chinese peri-menopausal women. Endokrynol Pol. 2013; 64(3): 197-202.
Mirzaei K, Hossein-Nezhad A, Keshavarz S, Eshaghi S, Koohdani F, Saboor-Yaraghi A. Insulin resistance via modification of PGC1α function identifying a possible preventive role of vitamin D analogues in chronic inflammatory state of obesity.A double blind clinical trial study. Minerva Med. 2014; 105(1): 63-78.
Danziger J, Biggs ML, Niemi M, Ix JH, Kizer JR, Djoussé L. Circulating 25-hydroxyvitamin D is associated with insulin resistance cross-sectionally but not longitudinally in older adults: the cardiovascular health study. Metabolism. 2013; 62(12): 1788-1794.
Salles J, Chanet A, Giraudet C, Patrac V, Pierre P, Jourdan M. 1, 25 (OH) 2-vitamin D3 enhances the stimulating effect of leucine and insulin on protein synthesis rate through Akt/PKB and mTOR mediated pathways in murine C2C12 skeletal myotubes. Mol Nutr Food Res. 2013; 57(12): 2137-2146.
Kim JJ, Choi YM, Chae SJ, Hwang KR, Yoon SH, Kim MJ. Vitamin D deficiency in women with polycystic ovary syndrome. Clin Exp Reprod Med. 2014; 41(2): 80-85.
Grant WB. Overweight/obesity and vitamin D deficiency contribute to the global burden of low back pain. Ann Rheum Dis. 2014; 73(8): e48-e48.
Wojtusik J, Johnson PA. Vitamin D regulates anti-Mullerian hormone expression in granulosa cells of the hen. Biol Reprod. 2012; 86(3): 91-91.
Schuch NJ, Garcia VC, Vívolo SR, Martini LA. Relationship between Vitamin D Receptor gene polymorphisms and the components of metabolic syndrome. Nutr J. 2013; 12: 96-96.
Burris HH, Camargo CA Jr. Vitamin D and gestational diabetes mellitus. Curr Diab Rep. 2014; 14(1): 451-451.
Marcotorchino J, Tourniaire F, Astier J, Karkeni E, Canault M, Amiot MJ. Vitamin D protects against diet-induced obesity by enhancing fatty acid oxidation. J Nutr Biochem. 2014; 25(10): 1077-1083.
Lerchbaum E, Obermayer-Pietsch B. Vitamin D and fertility: a systematic review. Eur J Endocrinol. 2012; 166(5): 765-778.
Pilz S, Frisch S, Koertke H, Kuhn J, Dreier J, Obermayer-Pietsch B. Effect of vitamin D supplementation on testosterone levels in men. Horm Metab Res. 2011; 43(03): 223-225.
Corduk N, Abban G, Yildirim B, Sarioglu-Buke A. The effect of vitamin D on expression of TGF β1 in ovary. Exp Clin Endocrinol Diabetes. 2012; 120(8): 494-493.
Velija-Ašimi Z. Evaluation of the association of vitamin D deficiency with gona-dotropins and sex hormone in obese and non-obese women with polycystic ovary syndrome. Med Glas (Zenica). 2014; 11(1): 170-176.