Evidence for causal effects of polycystic ovary syndrome on oxidative stress: a two-sample mendelian randomisation study

• Published in: BMC medical genomics 2023-06, Vol.16 (1), p.141-141, Article 141
• Main Author: Yifu, Pu
• Format: Article
• Language: English
• Subjects: Acids; Analysis; Androgens; Ascorbic acid; Bilirubin; Biomarkers; Body mass index; Causality; Causes of; Confounding (Statistics); Enzymes; Female; Genetic aspects; Genome-wide association studies; Genome-Wide Association Study; Genomes; Genomics; Globulins; Glutathione peroxidase; Glutathione transferase; Health aspects; High density lipoprotein; Humans; Lipoproteins; Lipoproteins, HDL; Low density lipoproteins; Medical research; Medicine, Experimental; Menarche; Mendelian randomisation study; Observational studies; Operating systems; Organic acids; Ovaries; Oxidative Stress; Peroxidase; Pleiotropy; Polycystic ovary syndrome; Polycystic Ovary Syndrome - genetics; Retinoids; Sensitivity analysis; Sex Hormone-Binding Globulin; Sex hormones; Statistical analysis; Stein-Leventhal syndrome; Superoxide; Testosterone; Tocopherols; Triglycerides; Uric acid; Vitamin A
• ISSN: 1755-8794; 1755-8794
• DOI: 10.1186/s12920-023-01581-0

Polycystic ovary syndrome (PCOS) is often accompanied by increased oxidative stress levels; however, it is still unclear whether PCOS itself is causally related to oxidative stress (OS), whether OS can increase the occurrence of PCOS, and which characteristics of PCOS increase OS levels. Therefore, this study explored the causal relationship between PCOS, its characteristics, and OS. Two-sample bidirectional and two-sample Mendelian randomisation studies were performed based on publicly available statistics from genome-wide association studies. PCOS; its characteristics, such as testosterone, low-density lipoprotein, high-density lipoprotein; and 11 major OS markers (superoxide dismutase, glutathione S-transferase, glutathione peroxidase, catalase, uric acid, zinc, tocopherol, ascorbic acid, retinol, albumin, and total bilirubin), were studied. The main analytical method used was inverse variance weighting (IVW). Pleiotropy was evaluated using the Mendelian randomisation-Egger intercept. Q and P values were used to assess heterogeneity. There was no causal relationship between PCOS and the OS indices (all P > 0.05). There was a causal relationship between the OS index, ascorbate level, and PCOS (IVW, odds ratio: 2.112, 95% confidence interval: 1.257-3.549, P = 0.005). In addition, there was a causal relationship between testosterone, low-density lipoprotein, high-density lipoprotein, sex hormone-binding globulin, body mass index, triacylglycerol, age at menarche, and most OS indices according to the IVW method. The F statistics showed that there was no weak instrumental variable. A sensitivity analysis was performed using the leave-one-out method. No pleiotropy was observed. The results were robust, and the conclusions were reliable. This study showed for the first time that there was no causal relationship between PCOS and OS. However, there was a causal relationship between the OS index, ascorbate level, and PCOS. It revealed that PCOS itself could not increase OS, and the increase in OS in PCOS was related to other potential factors, such as testosterone, low-density lipoprotein, high-density lipoprotein, sex hormone-binding globulin, body mass index, triacylglycerol, and age at menarche.