Increased body mass index is negatively associated with ovarian reserve as measured by anti‐Müllerian hormone in patients with polycystic ovarian syndrome

抗苗勒氏激素 医学 体质指数 卵巢储备 置信区间 肥胖 人口 质量指数 内科学 妇科 多囊卵巢 激素 内分泌学 不育 胰岛素抵抗 怀孕 环境卫生 生物 遗传学
作者
Jacqueline Kloos,Jaime Perez,Rachel Weinerman
出处
期刊:Clinical obesity [Wiley]
卷期号:14 (3) 被引量:3
标识
DOI:10.1111/cob.12638
摘要

Summary Anti‐Müllerian hormone (AMH) is commonly used as a marker of ovarian reserve. Although obesity is associated with decreased fertility, the relationship between body mass index (BMI) and AMH remains uncertain, hindering the accurate interpretation of AMH. We sought to assess the relationship between serum AMH and BMI in patients with and without polycystic ovarian syndrome (PCOS). This study analysed 500 patients at a single centre between 2020 and 2021. Patients were divided into cohorts: those with BMI <40 kg/m 2 and those with BMI >40 kg/m 2 . Patients with and without PCOS were included. Chi‐square tests, Fisher's exact tests, multiple linear regression analysis and independent t ‐tests were performed as appropriate. In the general study population, serum AMH was not significantly different in the BMI >40 kg/m 2 group compared to the BMI <40 kg/m 2 group (4.3 ± 5.6 vs. 4.3 ± 5.6, p = .35). Patient ages between these two groups differed, with an average age of 35.4 ± 5.4 years in the BMI <40 kg/m 2 group and 33.7 ± 5.4 years in the BMI <40 kg/m 2 group ( p = .031). Our multivariate regression analysis, which adjusted for age, demonstrated a significant interaction effect between BMI and PCOS diagnosis, indicating that the relationship between BMI and AMH is dependent on PCOS status ( β = −.03, 95% confidence interval [CI]: −0.05, 0.00, p = .044). In patients without PCOS, we found a non‐significant relationship between AMH and BMI ( β = .00, 95% CI −0.01, 0.01, p = .7); however, in patients with PCOS, AMH significantly decreased as BMI increased ( β = −.03, 95% CI −0.06, 0.00, p = .034). BMI has an inverse association with AMH levels in patients with PCOS, indicating a need for future research to determine if that interaction represents a clinically significant negative effect on reproductive function.

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