Correlation between Serum Caspase-1, IL-10, HOMA-IR, FAI, Dyslipidemia, and Oxidative Stress Status in Women with Polycystic Ovary Syndrome
Introduction: Polycystic ovary syndrome (PCOS) is a common endocrinopathy characterized by hyperandrogenism, insulin resistance, and dyslipidemia. Inflammation and oxidative stress play critical roles in its pathogenesis. This observational cross-sectional study evaluated the relationship between se...
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| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
| Published: |
Wolters Kluwer Medknow Publications
2025-05-01
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| Series: | Journal of Pharmacy and Bioallied Sciences |
| Subjects: | |
| Online Access: | https://journals.lww.com/10.4103/jpbs.jpbs_1994_24 |
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| Summary: | Introduction:
Polycystic ovary syndrome (PCOS) is a common endocrinopathy characterized by hyperandrogenism, insulin resistance, and dyslipidemia. Inflammation and oxidative stress play critical roles in its pathogenesis. This observational cross-sectional study evaluated the relationship between serum Caspase-1, interleukin-10 (IL-10), homeostatic model assessment of insulin resistance (HOMA-IR), free androgen index (FAI), lipid profiles, and oxidative stress markers in women with PCOS.
Materials and Methods:
A total of 150 women diagnosed with PCOS participated in this study. Serum levels of Caspase-1, IL-10, HOMA-IR, FAI, lipid profiles (total cholesterol, low-density lipoprotein (LDL), high-density lipoprotein (HDL), triglycerides), malondialdehyde (MDA), and superoxide dismutase (SOD) were measured.
Results:
The results revealed significant elevations in Caspase-1, HOMA-IR, and lipid profiles, while IL-10 levels were lower compared to normal populations. Additionally, oxidative stress markers, including MDA, were significantly increased, while SOD levels showed a decline. Positive correlations were observed between Caspase-1, HOMA-IR, dyslipidemia, and oxidative stress markers.
Conclusion:
These findings suggest a crucial link between inflammation, insulin resistance, and oxidative stress in PCOS, contributing to its complex pathophysiology. |
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| ISSN: | 0976-4879 0975-7406 |