V.I. Kulakov National Medical Research Center for Obstetrics, Gynecology and Perinatology, Ministry of Healthcare of Russian Federation, 117997 Moscow, Russia.
V.L. Talrose Institute for Energy Problems of Chemical Physics, N.N. Semenov Federal Research Center of Chemical Physics, Russian Academy of Sciences, 119334 Moscow, Russia.
Int J Mol Sci. 2024 Oct 2;25(19):10636. doi: 10.3390/ijms251910636.
Polycystic ovary syndrome (PCOS) is a complex disorder that impacts both the endocrine and metabolic systems, often resulting in infertility, obesity, insulin resistance, and cardiovascular complications. The aim of this study is to investigate the role of intestinal flora and its metabolites, particularly short-chain fatty acids (SCFAs), in the development of PCOS, and to assess the effects of metformin therapy on these components. SCFA levels in fecal and blood samples from women with PCOS (n=69) and healthy controls (n=18) were analyzed using Gas Chromatography-Mass Spectrometry (GC/MS) for precise measurement. Fecal microbiota were quantitatively detected by real-time polymerase chain reaction (PCR). To assess the efficacy of six months of metformin treatment, changes in the microbiota and SCFAs in the PCOS group (n=69) were also evaluated. The results revealed that women with PCOS exhibited a significant reduction in beneficial bacteria (namely, the group and spp.) alongside a notable overgrowth of opportunistic microorganisms (, , spp., and spp.). An overproduction of acetic acid (AA, FC=0.47, p<0.05) and valeric acid (VA, FC=0.54, p<0.05) suggests a link between elevated SCFAs and the development of obesity and PCOS. Interestingly, AA in the bloodstream might offer a protective effect against PCOS by ameliorating key symptoms such as high body mass index (r=-0.33, p=0.02), insulin resistance (r=-0.39, p=0.02), and chronic inflammation. Although serum SCFA levels showed non-significant changes following metformin treatment (p>0.05), the normalization of AA in the gut underscores that metformin exerts a more pronounced effect locally within the gastrointestinal tract. Furthermore, the study identified the most effective model for predicting the success of metformin therapy, based on serum concentrations of butyric acid (BA) and VA, achieving a 91% accuracy rate, 100% sensitivity, and 80% specificity. These promising findings highlight the potential for developing targeted interventions and personalized treatments, ultimately improving clinical outcomes for women with PCOS.
多囊卵巢综合征(PCOS)是一种影响内分泌和代谢系统的复杂疾病,常导致不孕、肥胖、胰岛素抵抗和心血管并发症。本研究旨在探讨肠道菌群及其代谢产物,特别是短链脂肪酸(SCFAs)在 PCOS 发病机制中的作用,并评估二甲双胍治疗对这些成分的影响。采用气相色谱-质谱联用技术(GC/MS)对 69 例 PCOS 患者和 18 例健康对照者的粪便和血液样本中的 SCFA 水平进行精确测量。采用实时聚合酶链反应(PCR)定量检测粪便微生物群。为评估二甲双胍治疗 6 个月的疗效,还评估了 PCOS 组(n=69)的微生物群和 SCFAs 的变化。结果显示,PCOS 患者有益菌(即 组和 spp.)显著减少,机会致病菌( 、 、 spp.和 spp.)明显过度生长。乙酸(AA,FC=0.47,p<0.05)和戊酸(VA,FC=0.54,p<0.05)产量增加提示 SCFAs 升高与肥胖和 PCOS 的发生有关。有趣的是,血液中的 AA 可能通过改善关键症状(如高体重指数(r=-0.33,p=0.02)、胰岛素抵抗(r=-0.39,p=0.02)和慢性炎症)提供对 PCOS 的保护作用。尽管二甲双胍治疗后血清 SCFA 水平无显著变化(p>0.05),但肠道中 AA 的正常化表明二甲双胍在胃肠道内局部发挥更显著的作用。此外,该研究基于血清中丁酸(BA)和 VA 浓度确定了预测二甲双胍治疗成功的最有效模型,准确率为 91%,灵敏度为 100%,特异性为 80%。这些有希望的发现强调了开发靶向干预和个体化治疗的潜力,最终改善 PCOS 女性的临床结局。