Santander Nicolás, Figueroa Esteban G, González-Candia Alejandro, Maliqueo Manuel, Echiburú Bárbara, Crisosto Nicolás, Salas-Pérez Francisca
Health Sciences Institute, Universidad de O'Higgins, Rancagua 282000, Chile.
Laboratory of Endocrinology and Metabolism, Department of Internal Medicine, West Division, Faculty of Medicine, Universidad de Chile, Santiago 8350499, Chile.
Antioxidants (Basel). 2024 Sep 26;13(10):1168. doi: 10.3390/antiox13101168.
Polycystic Ovary Syndrome (PCOS) is a complex hormonal disorder that is associated with heightened metabolic risks. While oxidative stress (OS) is known to play a role in PCOS, the precise nature of the relationship between PCOS and increased OS remains not entirely understood. Combined oral contraceptives (COCs) are the first-line treatment to regulate menstrual cycles and androgen levels, but their impact on oxidative stress requires further study. We conducted a transcriptomic analysis using RNAseq and assessed the levels of various oxidative stress (OS) markers in serum samples from women with PCOS and controls and whether they were using combined oral contraceptives (COCs), including enzymatic activities, FRAP, and 8-isoprostane (8-iso). A total of 359 genes were differentially expressed in women with PCOS compared to control women. Genes differentially expressed were enriched in functions related to inflammation and, interestingly, oxidative stress response. In controls, 8-iso levels were increased in women using COCs, whereas in women with PCOS, 8-iso levels were reduced in those using oral contraceptives (191.1 ± 97 vs. 26.4 ± 21 pg/mL, : <0.0001). Correlation analyses showed a trend for a negative correlation between 8-iso and Ferriman score in women with PCOS consuming COCs (r = -0.86, = 0.06) and a negative correlation between GSH and hyperandrogenism in women with PCOS (r = -0.89, = 0.01). These results reveal the presence of lipid peroxidation in women with PCOS, which was modified by the use of COCs, providing new insights into the pathophysiology of PCOS in the Chilean population.
多囊卵巢综合征(PCOS)是一种复杂的激素紊乱疾病,与代谢风险增加有关。虽然已知氧化应激(OS)在PCOS中起作用,但PCOS与氧化应激增加之间关系的确切性质仍不完全清楚。复方口服避孕药(COCs)是调节月经周期和雄激素水平的一线治疗药物,但其对氧化应激的影响需要进一步研究。我们使用RNA测序进行了转录组分析,并评估了PCOS患者和对照组血清样本中各种氧化应激(OS)标志物的水平,以及她们是否正在使用复方口服避孕药(COCs),包括酶活性、铁还原抗氧化能力(FRAP)和8-异前列腺素(8-iso)。与对照女性相比,共有359个基因在PCOS女性中差异表达。差异表达的基因在与炎症相关的功能中富集,有趣的是,还在氧化应激反应相关功能中富集。在对照组中,使用COCs的女性8-iso水平升高,而在PCOS女性中,使用口服避孕药的女性8-iso水平降低(191.1±97 vs. 26.4±21 pg/mL,P<0.0001)。相关性分析显示,在服用COCs的PCOS女性中,8-iso与费里曼评分呈负相关趋势(r = -0.86,P = 0.06),在PCOS女性中,谷胱甘肽(GSH)与高雄激素血症呈负相关(r = -0.89,P = 0.01)。这些结果揭示了PCOS女性中存在脂质过氧化现象,而使用COCs可对其产生影响,这为智利人群中PCOS的病理生理学提供了新的见解。