Serum testosterone levels are positively associated with serum anti-mullerian hormone levels in infertile women.

This was a retrospective cross-sectional study. Infertile women were first identified based on the International Classification of Diseases, Ninth Revision, Clinical Modification (ICD-9-CM), code 628, from the clinical database in Kaohsiung Veterans General Hospital. To avoid any potential misclassifications, among the infertile women identified by the ICD-9-CM code, only subjects who received a complete infertility survey in the reproductive center of Kaohsiung Veterans General Hospital were selected. A total of 2476 infertile women were identified from May 2013 through March 2020. Then, we performed the chart review of these 2476 infertile women and selected the women who truly met the definition of infertility among them. Infertility was defined by the failure to achieve a successful pregnancy after 12 months or more of regular, unprotected sexual intercourse 52 . Moreover, we excluded the following subjects based on chart review: (1) subjected who experienced repeated surveys; (2) subjects who had extreme age ( 46 years) (3) subjected who was diagnosed as primary ovarian insufficiency; (4) subjects who ever underwent ovarian surgery; (5) subjected who had a history of exposure to cytotoxic agents or pelvic irradiation for malignancy; (6) subjected who had androgen-secreting tumors; (7) subjected who was diagnosed as congenital adrenal hyperplasia (8) subjects who had androgen supplementation or hormonal therapy during the previous 3 months. A total of 1935 infertile women were finally included in the study. The study protocol was approved by the institutional review board in Kaohsiung Veterans General Hospital, with the identifier KSVGH20-CT11-03, and conformed to the “Declaration of Helsinki for Medical Research involving Human Subjects.” Need of informed consent was waived by the institutional review board in Kaohsiung Veterans General Hospital due to the retrospective design. For the infertility survey, we checked blood examinations including AMH, T, DHEA-S, FSH, luteinizing hormone (LH), estradiol, thyroid-stimulating hormone (TSH), prolactin and 25-OH-vitamin D levels. Serum AMH levels were measured by chemiluminescent immunoassay using the Access Immunoassay Systems, the Beckman Coulter enzyme-linked immunoassay (Beckman Coulter, Marseille, France). The analytical range of the lower limit of detection was 0.02 ng/mL. The intra-assay coefficient of variation (CV) was 3.0%, and the interassay CV was 7.0%. DOR was defined as serum AMH levels < 1.2 ng/mL based on the POSEIDON criteria 53 ; serum AMH levels ≥ 5.0 ng/mL, modified from the revised Rotterdam criteria 54 , were considered EOR in this study. Serum T was measured by chemiluminescent microparticle immunoassay using the ARCHITECT 2nd Generation Testosterone assay (Abbott GmbH, Max-Planck-Ring 2, Wiesbaden, Germany). The range was 0.04 ng/mL to 18.62 ng/mL. The assay had a limit of quantitation of ≤ 0.04 ng/mL and had a within-laboratory imprecision of ≤ 10% CV. Potential interference in the ARCHITECT 2nd Generation Testosterone assay from hemoglobin, bilirubin, triglycerides, protein and biotin was evaluated to be ≤ 10%. This assay had a correlation coefficient ( r ) of ≥ 0.95 for samples with testosterone concentrations ranging from 0.04 ng/mL to 10.09 ng/mL when compared to Liquid Chromatography-Tandem Mass Spectrometry (LCMS). Serum DHEA-S, FSH, LH, estradiol, TSH, prolactin and 25-OH-vitamin D concentrations were measured by a chemiluminescent microparticle immunoassay on the ARCHITECT iSystem (Abbott, Longford, Ireland or Abbott, Wiesbaden, Germany). The total CV of these analyses were consistently < 3–10%. The specificity of these assays was determined by studying the cross-reactivity of structurally similar compounds. The cross-reactivity was calculated as a percent cross-reactivity. DHEA-S assay was shown to be 0% for testosterone, 0.003% for androstenedione, 0.025% for 19-hydroxyandrostenedione, 0.006% for DHEA glucuronide and 0.001% for estradiol. FSH assay was shown to be 0.002% for LH, 0.043% for TSH and 0.001% for hCG. LH assay was shown to be 0.01% for FSH, 0% for TSH and 0.01% for hCG. Estradiol assay was shown to be 0.1% for 17β-estradiol 3-sulfate and 0.7% for estrone. Prolactin assay was shown to be 0% for FSH, hCG, TSH and 0.001% for LH. TSH assay had an analytical specificity of < 10% cross reactivity with FSH, LH and hCG. 25-OH Vitamin D assay was shown to be 0.8% for vitamin D3 (Cholecalciferol), 0.4% for vitamin D2 (Ergocalciferol), 0.1% for 1,25-(OH)2-vitamin D3 and 0% for 1,25-(OH)2-vitamin D2. Blood samples were collected on the 2nd or 3rd day of the menstrual cycle. The reference intervals in the follicular phase were as follows: T, 0.14–0.53 ng/mL; DHEA-S, 35.0–430.0 µg/dL; FSH, 4–13 mIU/mL; LH, 1–18 mIU/mL; estradiol, 39–189 pg/mL; TSH, 0.35–4.94 μIU/mL; prolactin, 1.39–24.20 ng/mL; and 25-OH-vitamin D, 30 ~ 100 ng/mL. The normality of the distribution was tested using the Kolmogorov–Smirnov test. Continuous variables were presented as the mean ± standard deviation. The subjects were categorized into four quartile groups (Q1 to Q4) based on serum T concentrations. Quantitative variables were evaluated using the analysis of variance (ANOVA) and linear regression analysis among T quartile categories. Bonferroni’s method was used for post hoc pairwise comparison in the ANOVA test. Generalized linear model was performed to examine the correlation between serum AMH levels and T quartile categories after adjusting for potential confounders including age, weight, BMI and FSH. Odds ratios (ORs) and 95% confidence intervals (CIs) for DOR and EOR among T quartile categories were assessed using binary logistic regression after adjustment for potential confounders (age, weight, BMI and FSH). All analyses were conducted using statistical software, Statistical Package for Social Sciences (SPSS) version 20.0 (Chicago, IL, USA). All statistical tests used a two-tailed α of 0.05, and statistical significance was defined as p  < 0.05. The study conformed to the ‘‘Declaration of Helsinki for Medical Research involving Human Subjects’’. Additionally, approval was obtained from the institutional review board at Kaohsiung Veterans General Hospital, with the identifier KSVGH20-CT11-03. The study was performed in accordance with approved guidelines. Need of informed consent was waived by the institutional review board in Kaohsiung Veterans General Hospital.

The characteristics of the 1935 infertile women included in the study are shown in Table 1 . The average age was 35.1 ± 4.7 years (range 21–46 years); the average body mass index (BMI) was 22.4 ± 3.8 kg/m 2 (range 14.7–40.8 kg/m 2 ). The mean serum T level was 0.33 ± 0.35 ng/mL (range 0.05–4.81 ng/mL) and the mean serum AMH level was 3.6 ± 2.8 ng/mL (range 0.03–22.08 ng/mL). Infertility causes included tubal factor (12.1%), male factor (11.6%), diminished ovarian reserve (13.0%), PCOS (9.6%), endometriosis (13.8%), uterine factor (8.0%), multiple factors (21.7%) and unexplained infertility (10.1%). In the group of women < 35 years (n = 887), the mean serum T level was 0.35 ± 0.31 ng/mL and the mean serum AMH level was 4.7 ± 3.1 ng/mL. In women ≥ 35 years (n = 1048), the average serum T level was 0.31 ± 0.38 ng/mL, and the average serum AMH level was 2.6 ± 2.0 ng/mL. Table 1 The characteristics of the study population. Variables All population (n = 1935) Age < 35 years (n = 887) Age ≥ 35 years (n = 1048) Age (years) 35.1 ± 4.7 30.9 ± 2.7 38.6 ± 2.8 Body height (cm) 160.5 ± 5.8 160.8 ± 5.8 160.3 ± 5.7 Body weight (kg) 57.7 ± 10.5 56.8 ± 10.6 58.5 ± 10.3 BMI (kg/m 2 ) 22.4 ± 3.8 22.0 ± 3.9 22.7 ± 3.8 TSH (μIU/mL) 1.7 ± 1.4 1.7 ± 1.8 1.7 ± 1.1 Prolactin (ng/mL) 15.6 ± 15.3 15.4 ± 12.0 15.7 ± 17.7 25-OH-vitamin D (ng/mL) 21.8 ± 6.8 21.1 ± 6.2 22.2 ± 7.2 FSH (mIU/mL) 5.2 ± 3.3 4.8 ± 2.5 5.6 ± 3.8 Testosterone (ng/mL) 0.33 ± 0.35 0.35 ± 0.31 0.31 ± 0.38 DHEA-S (μg/dL) 239.5 ± 114.2 262.0 ± 107.7 220.1 ± 116.1 AMH (ng/mL) 3.6 ± 2.8 4.7 ± 3.1 2.6 ± 2.0 Causes of infertility Tubal factor 12.1%(235/1,935) 15.1%(134/887) 9.6%(101/1,048) Male factor 11.6%(225/1,935) 11.2%(99/887) 12.0%(126/1,048) DOR* 13.0%(252/1,935) 4.5%(40/887) 20.2%(212/1,048) PCOS* 9.6%(186/1,935) 12.1%(107/887) 7.5%(79/1,048) Endometriosis 13.8%(267/1,935) 15.3%(136/887) 12.5%(131/1,048) Uterine factor 8.0%(155/1,935) 9.9%(88/887) 6.4%(67/1,048) Multiple factors 21.7%(420/1,935) 16.5%(146/887) 26.1%(274/1,048) Unexplained infertility 10.1%(195/1,935) 15.4%(137/887) 5.5%(58/1,048) Data are presented as the mean ± standard deviation. BMI body mass index, TSH thyroid-stimulating hormone, FSH follicle stimulation hormone, DHEA-S dehydroepiandrosterone sulfate, AMH anti-Müllerian hormone. *DOR, diminished ovarian reserve, was defined as AMH < 1.2 ng/mL based on POSEIDON criteria. *PCOS, polycystic ovarian syndrome, was determined by Rotterdam criteria. The characteristics of the study population. Data are presented as the mean ± standard deviation. BMI body mass index, TSH thyroid-stimulating hormone, FSH follicle stimulation hormone, DHEA-S dehydroepiandrosterone sulfate, AMH anti-Müllerian hormone. *DOR, diminished ovarian reserve, was defined as AMH < 1.2 ng/mL based on POSEIDON criteria. *PCOS, polycystic ovarian syndrome, was determined by Rotterdam criteria. The subjects were then categorized into four quartile groups (Q1 to Q4) based on serum T concentrations (Table 2 ). AMH, DHEA-S, body weight and BMI were positively associated with the T quartile category, whereas age linearly decreased as the T quartile category rose from Q1 to Q4 (all p for tend < 0.001). Body height, TSH, prolactin, 25-OH-vitamin D and FSH were not significantly different among the T quartile categories. Furthermore, compared to the AMH levels in the subjects in the highest T quartile (Q4), those in the lower T quartile (Q1, Q2 and Q3) demonstrated significantly lower AMH levels ( p  < 0.05). Table 2 Clinical characteristics according to serum testosterone quartile categories. Variables Quartile of serum testosterone Q1 (n = 481) Q2 (n = 491) Q3 (n = 478) Q4 (n = 435) p for tend Testosterone (ng/mL)  ≤ 0.21 0.22 ~ 0.27 0.28 ~ 0.35  ≥ 0.36 Age (years) 36.9 ± 4.5* 35.4 ± 4.6* 34.6 ± 4.5* 33.3 ± 4.5  < 0.001 Body height (cm) 160.5 ± 5.7 160.4 ± 5.6 160.4 ± 5.7 160.7 ± 6.0 0.723 Body weight (kg) 56.9 ± 9.2* 56.4 ± 9.5* 57.2 ± 10.2* 60.9 ± 12.5  < 0.001 BMI (kg/m 2 ) 22.1 ± 3.3* 21.9 ± 3.4* 22.2 ± 3.9* 23.6 ± 4.6  < 0.001 TSH (μIU/mL) 1.7 ± 1.0 1.7 ± 1.9 1.6 ± 1.0 1.7 ± 1.6 0.743 Prolactin (ng/mL) 14.4 ± 11.1 16.5 ± 21.8 15.3 ± 10.2 16.0 ± 15.2 0.248 Vitamin D (ng/mL) 21.5 ± 7.5 21.5 ± 6.8 21.7 ± 6.2 22.4 ± 6.5 0.141 FSH (mIU/mL) 5.4 ± 3.6 5.1 ± 3.1 5.1 ± 3.1 5.2 ± 3.3 0.344 DHEA-S (μg/dL) 170.3 ± 70.1* 221.4 ± 76.0* 260.3 ± 96.9* 319.1 ± 151.0  < 0.001 AMH (ng/mL) 2.1 ± 1.5* 3.3 ± 2.1* 3.9 ± 2.7* 5.6 ± 3.7  < 0.001 Data are presented as the mean ± standard deviation. p values for trends were generated by linear regression analysis. *Statistically significantly different from the highest quartile category (Q4) using Bonferroni’s method in an analysis of variance (ANOVA) test. BMI body mass index, TSH thyroid-stimulating hormone, Vitamin D 25-OH-vitamin D, FSH follicle stimulation hormone, DHEA-S dehydroepiandrosterone sulfate, AMH anti-Müllerian hormone. Clinical characteristics according to serum testosterone quartile categories. Data are presented as the mean ± standard deviation. p values for trends were generated by linear regression analysis. *Statistically significantly different from the highest quartile category (Q4) using Bonferroni’s method in an analysis of variance (ANOVA) test. BMI body mass index, TSH thyroid-stimulating hormone, Vitamin D 25-OH-vitamin D, FSH follicle stimulation hormone, DHEA-S dehydroepiandrosterone sulfate, AMH anti-Müllerian hormone. Generalized linear models were used to assess the independent association of serum T quartile categories with AMH levels after adjusting for potential confounding factors, including age, body weight, BMI and FSH. Regardless of all women or different age groups (< 35 or ≥ 35 years) or different AMH groups (< 1.2, 1.2–5.0, or ≥ 5.0 ng/mL), AMH levels significantly increased in a dose-dependent fashion across increasing T quartile categories in the multivariate adjustment model as shown in Fig.  1 . Figure 1 Serum AMH levels according to serum testosterone quartile categories in different groups. ( a ) all women, ( b ) age < 35 years, ( c ) age ≥ 35 years, ( d ) AMH < 1.2 ng/mL, ( e ) 1.2 ≤ AMH < 5.0 ng/mL and ( f ) AMH ≥ 5.0 ng/mL. The p values for the trends were generated using generalized linear models after adjustment for multivariate confounders. Multivariable confounders included age, weight, body mass index, and FSH. Error bar represented 95% confidence interval of AMH. AMH anti-Mullerian hormone, Q quartile. Serum AMH levels according to serum testosterone quartile categories in different groups. ( a ) all women, ( b ) age < 35 years, ( c ) age ≥ 35 years, ( d ) AMH < 1.2 ng/mL, ( e ) 1.2 ≤ AMH < 5.0 ng/mL and ( f ) AMH ≥ 5.0 ng/mL. The p values for the trends were generated using generalized linear models after adjustment for multivariate confounders. Multivariable confounders included age, weight, body mass index, and FSH. Error bar represented 95% confidence interval of AMH. AMH anti-Mullerian hormone, Q quartile. The overall proportions of subjects who met the criteria for diminished ovarian reserve (DOR, AMH < 1.2 ng/mL) and excess ovarian reserve (EOR, AMH ≥ 5.0 ng/mL) were 16.3% (242/1485) and 24.2% (359/1485), respectively. The prevalence of DOR among subjects in Q1, Q2, Q3 and Q4 was 33.9% (128/378), 16.3% (65/398), 10.5% (41/392) and 2.5% (8/317), respectively (Fig.  2 a). Multiple logistic regression analyses revealed that the ORs for the risk of DOR dose-dependently increased across decreasing T quartile categories, and the odds for the risk of DOR were 11.44-fold higher in subjects in Q1 than in those in Q4 after adjustment for potential confounders (Table 3 ). The prevalence of EOR among subjects in Q1, Q2, Q3 and Q4 was 5.6% (21/378), 19.6% (78/398), 30.1% (118/392) and 44.8% (142/317), respectively (Fig.  2 b). Multiple logistic regression analyses revealed that the ORs for the risk of EOR dose-dependently increased across increasing T quartile categories, and the odds for the risk of EOR were 10.41-fold higher in subjects in Q4 than in those in Q1 after adjustment for potential confounders (Table 3 ). Figure 2 Prevalence of ( a ) diminished ovarian reserve (DOR) and ( b ) excess ovarian reserve (EOR) according to serum T quartile categories. DOR was defined as serum AMH levels < 1.2 ng/mL; serum AMH levels ≥ 5.0 ng/mL were defined as EOR. Q quartile. Table 3 Risk for diminished ovarian reserve (DOR) or excess ovarian reserve (EOR) according to serum testosterone quartile categories. Variables Risk for DOR (AMH < 1.2 ng/mL) Risk for EOR (AMH ≥ 5.0 ng/mL) Adjusted OR (95% CI) p value Adjusted OR (95% CI) p value T quartile categories Q1 (0.05 ~ 0.21 ng/mL) 11.44 (4.75–27.53)  < 0.001 1.00 (Ref.) Q2 (0.22 ~ 0.27 ng/mL) 5.45 (2.23–13.33)  < 0.001 3.74 (2.09–6.71)  < 0.001 Q3 (0.28 ~ 0.35 ng/mL) 3.12 (1.23–7.88) 0.016 6.54 (3.70–11.54)  < 0.001 Q4 (0.36 ~ 4.81 ng/mL) 1.00 (Ref.) 10.41 (5.84–18.55)  < 0.001 ORs (95% CI) for DOR or EOR according to serum testosterone quartile categories after adjustment for multivariate confounders in infertile women (n = 1,935). Binary logistic regression analysis was performed. Multivariate confounders included age, weight, body mass index, and FSH. T testosterone, AMH anti-Müllerian hormone, OR odds ratio, CI confidence interval, Q quartile, Ref. reference. Prevalence of ( a ) diminished ovarian reserve (DOR) and ( b ) excess ovarian reserve (EOR) according to serum T quartile categories. DOR was defined as serum AMH levels < 1.2 ng/mL; serum AMH levels ≥ 5.0 ng/mL were defined as EOR. Q quartile. Risk for diminished ovarian reserve (DOR) or excess ovarian reserve (EOR) according to serum testosterone quartile categories. ORs (95% CI) for DOR or EOR according to serum testosterone quartile categories after adjustment for multivariate confounders in infertile women (n = 1,935). Binary logistic regression analysis was performed. Multivariate confounders included age, weight, body mass index, and FSH. T testosterone, AMH anti-Müllerian hormone, OR odds ratio, CI confidence interval, Q quartile, Ref. reference. The age-dependent distribution of serum T levels in all patients (n = 1885) is shown in Table 4 . The median serum T level in all patients was 0.27 ng/mL; the median serum T levels in the 20–25, 26–30, 31–35, 36–40 and 41–46 age groups were 0.36, 0.32, 0.28, 0.26 and 0.23 ng/mL, respectively. Table 4 Serum testosterone level distribution (ng/mL) based on age. Age (years) Mean Percentile n 5 th 10 th Median 90 th 95 th 20 ~ 25 0.38 0.20 0.21 0.36 0.63 0.76 35 26 ~ 30 0.40 0.17 0.21 0.32 0.56 0.89 288 31 ~ 35 0.34 0.16 0.18 0.28 0.47 0.54 688 36 ~ 40 0.32 0.15 0.17 0.26 0.42 0.51 627 41 ~ 46 0.27 0.13 0.15 0.23 0.37 0.45 247 All 0.33 0.15 0.17 0.27 0.46 0.55 1,885 Serum testosterone level distribution (ng/mL) based on age.

To the best of our knowledge, the present study is the largest clinical study to investigate the association between serum T and AMH levels in infertile women. In this large retrospective cross-sectional study of 1935 infertile women, higher serum T concentrations were associated with higher serum AMH levels after adjustment for potential confounders. Consistently, infertile women in the lowest T quartile had a 11.44-fold higher odds for the risk of DOR than those in the highest T quartile. The odds for the risk of EOR were 10.41-fold higher in infertile women in the highest T quartile than in those in in the lowest T quartile. Androgens play important roles in the regulation of ovarian function. AR, expressed in oocytes, GCs and theca cells, is pivotal for normal follicular development 10 , 11 . AR is most highly expressed in the GCs of preantral and early antral follicles, and its expression decreases as the follicles grow 13 . Via the AR, androgens increase the FSH receptor and synergize with FSH to enhance follicle growth 19 – 21 . Moreover, androgens support follicle health by decreasing follicle atresia and GC apoptosis, and stimulating the proliferation and differentiation of GC 20 , 22 , 23 . Although AR is not expressed in primordial follicles, androgens promote primordial follicle initiation 24 , 25 via indirect mechanisms, such as upregulation of insulin-like growth factor 1 expression 25 . The above information supports our results that lower T levels were associated with a higher risk of DOR. Studies have shown that women with DOR or POI demonstrated significantly lower serum T levels than controls 26 , 27 . On the other hand, androgen excess may lead to impaired ovarian function and dysregulated follicle development, displaying irregular cycles, oligo-ovulation and polycystic ovaries 28 , 29 . These findings agree with our results that infertile women with higher T levels had a higher risk of EOR. Thus, an optimal balance in androgenic actions is necessary for maintaining normal ovarian function. Serum T concentrations decline with age 14 . Thus, our study demonstrated an age-specific normal reference range for serum T levels to aid in identifying women who suffer from androgen insufficiency or excess (Table 4 ). As mentioned above, androgens enhance FSH activity through increased FSH receptor expression 20 , 21 . FSH stimulates AMH expression 30 , 31 , which could inhibit the sensitivity of preantral follicles to FSH to avoid premature selection by FSH in the gonadotrophin-independent stage 32 , 33 . Therefore, Dewailly et al. proposed that androgens may promote AMH generation via enhancement of FSH-stimulated AMH expression 34 . Elevated AMH could attenuate FSH-induced aromatase activity, leading to an increase in androgen levels 33 . Moreover, via AMH receptor type 2 on the hypothalamus and pituitary, elevated AMH may boost GnRH-dependent LH pulsatility and secretion which stimulates androgen production in theca cells 35 , 36 . Taken together, it seems that androgens and AMH mutually stimulate each other. These results support our results that serum T concentrations positively correlated with serum AMH levels. Some studies also showed a positive correlation between serum androgens and AMH 37 – 39 . However, some studies revealed contradictory results, which indicated that androgens or FSH may have an inhibitory effect on AMH expression 40 – 42 . Thus, the accurate relationship between androgens and AMH remains unclear. Further studies with ideal experimental models are needed to clarify the relationship. Serum T levels have been suggested to be positively associated with ovarian response 43 , 44 and even pregnancy outcomes 44 , 45 in women undergoing IVF cycles. Although some conflicting studies have shown that serum T levels do not predict IVF outcomes 43 , 46 , available data have indicated that T supplementation may improve ovarian response and IVF outcomes in PORs 47 , 48 . In a randomized controlled trial of 110 PORs undergoing IVF cycles, Kim et al. reported that pretreatment with transdermal T gel significantly increased AFC and reduced the day of stimulation and total dosage of gonadotropins. In addition, the numbers of oocytes retrieved, mature oocytes, fertilized oocytes, and good-quality embryos were significantly higher in the T pretreatment group than in the control group 16 . A meta-analysis of 7 randomized controlled trials conducted by Noventa and colleagues revealed that PORs receiving T therapy demonstrated higher numbers of total oocytes, MII oocytes and total embryos, as well as a higher clinical pregnancy rate and live birth rate than controls 47 . On the other hand, the addition of insulin sensitizing agents to suppress insulin resistance and excess androgen may ameliorate the results of ovulation induction in PCOS patients 49 , 50 . In the present study, we provided an age-specific normal reference range for serum T levels to help determine whether infertile women require agents for androgen enhancement or suppression (Table 4 ). Further large-scale, well-defined randomized controlled trials are still mandatory to confirm the effectiveness of androgen supplementation and androgen suppression by agents. Several potential limitations should be taken into consideration when interpreting the data. First, the retrospective design of this study presented the major limitation. Second, since this is a cross-sectional study, a causal relationship could not be determined between serum T and AMH levels. Third, our study population only consisted of infertile women. We cannot be sure that our results would be applicable to the general population. Fourth, direct testosterone immunoassays have limitations for clinical use, particularly for low concentrations found in women and children 51 . This would be a relevant source of bias. Although high correlation ( r  ≥ 0.95) of serum T levels was observed between the ARCHITECT 2nd Generation Testosterone assay and the LCMS, the bias could not be totally excluded. Fifth, serum concentrations of free T, androstenedione, and sex hormone-binding globulin (SHBG) were not measured in our routine infertility evaluation. Thus, accurate androgen status would be uncertain in this study. In conclusion, our data reveal an obvious positive association between serum T and AMH levels in infertile women. Additionally, the risk of DOR was significantly increased in a dose-dependent manner across decreasing T quartile categories; the risk of EOR dose-dependently increased across increasing T quartile categories. Long-term longitudinal studies are required to confirm our results.

Anti-Mullerian hormone (AMH), a glycoprotein belonging to the transforming growth factor β superfamily, is generated by granulosa cells (GCs) of growing follicles from the primary to the small antral follicles in the ovary 1 . The expression of AMH increases prior to follicle-stimulating hormone (FSH)-dependent selection (follicles up to 8 mm) and rapidly decreases after FSH-dependent selection (follicles > 8 mm) 2 . Serum AMH levels reflect the pool of growing follicles and thus are currently well known as a reliable biomarker for functional ovarian reserve 3 . Serum AMH levels gradually decline with age from the age of 25 years onward 4 , 5 . Serum AMH levels aid in the prediction of ovarian responses to controlled ovarian hyperstimulation 6 , 7 and may be used in the individualization of starting doses of gonadotropin 8 , 9 . However, little is known about possible factors that affect serum AMH concentrations. Androgens have been described to be involved in follicle recruitment and promotion of follicle growth 10 , 11 . The major circulating androgens in women include dehydroepiandrosterone sulfate (DHEA-S), dehydroepiandrosterone (DHEA), androstenedione, testosterone (T) and dihydrotestosterone (DHT). T and DHT, which are generated equally from the ovary and adrenals, are the only bioactive androgens that directly bind to the androgen receptor (AR) 12 . Similar to AMH, the action of T primarily occurs during the early stages of folliculogenesis because AR is the most abundant in the GCs of small follicles 13 . Peak serum T levels are achieved in early adulthood and show a decline with age as AMH 14 . Furthermore, studies have revealed that T supplementation may have a positive effect on antral follicle count (AFC) in poor ovarian responders (PORs) 15 , 16 and T suppression by oral contraceptives might decrease the number of antral follicles and even serum AMH levels in polycystic ovary syndrome (PCOS) patients 17 , 18 . Based on the abovementioned findings, we hypothesized that serum levels of T had a positive association with serum AMH levels. However, few large-scale studies have examined the relationship between serum T and AMH levels. Therefore, we conducted a large cross-sectional study in infertile women to clarify the association between serum T and AMH concentrations.