Department of Endocrinology and Metabolism, Ren Ji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Sci Rep. 2024 Oct 31;14(1):26215. doi: 10.1038/s41598-024-77645-7.
The levels of fasting-state serum bile acids (BAs) in individuals with polycystic ovary syndrome (PCOS) differ from those of control subjects. However, there is a lack of research on the BAs profile in lean women with PCOS and whether these changes are linked to the host metabolism. Therefore, our objective was to investigate the synthesis and metabolism of serum BAs in lean women with PCOS and assess the correlation between BAs and clinical characteristics. This study employed a cross-sectional design of lean women with PCOS (n = 240) in comparison to a control group (n = 80) consisting of healthy lean women. The findings revealed significant increases in the levels of non-12-OH BAs and chenodeoxycholic acid (CDCA)% (both P < 0.05) in lean women with PCOS. Additionally, a positive correlation was observed between CDCA% and total testosterone (T) (r = 0.130, P = 0.044) and free androgen index (FAI) (r = 0.153, P = 0.019). Furthermore, a decreased ratio of cholic acid/chenodeoxycholic acid (CA/CDCA) (P < 0.001) was observed in lean women with PCOS, suggesting the depletion or downregulation of CYP8B1. Receiver operating characteristic curve analysis indicated that the combination of CDCA/CA and DHEAS could potentially be used as a characteristic factor for PCOS in lean women. It is possible that enzymatic modifications in the liver could play a role in regulating hyperandrogenism in this specific subgroup of lean women with PCOS.
多囊卵巢综合征(PCOS)患者的空腹血清胆汁酸(BAs)水平与对照组不同。然而,关于 PCOS 瘦型女性的 BAs 谱及其变化是否与宿主代谢有关的研究较少。因此,我们的目的是研究瘦型 PCOS 女性的血清 BAs 合成和代谢,并评估 BAs 与临床特征之间的相关性。本研究采用横断面设计,比较了 240 例瘦型 PCOS 患者(病例组)和 80 例健康瘦型女性(对照组)。结果显示,瘦型 PCOS 患者的非 12-OH BAs 和鹅脱氧胆酸(CDCA)%水平显著升高(均 P<0.05)。此外,CDCA%与总睾酮(T)(r=0.130,P=0.044)和游离雄激素指数(FAI)(r=0.153,P=0.019)呈正相关。此外,PCOS 瘦型患者的胆酸/鹅脱氧胆酸(CA/CDCA)比值降低(P<0.001),提示 CYP8B1 耗竭或下调。受试者工作特征曲线分析表明,CDCA/CA 和 DHEAS 的组合可能可作为瘦型 PCOS 女性的特征因子。肝脏中的酶修饰可能在调节该特定瘦型 PCOS 女性亚群的高雄激素血症中发挥作用。