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The Relationship Between Menopause and Metabolic Syndrome: Experimental and Bioinformatics Analysis
Abir Jaballah1, Ismael Soltani2, Wael Bahia2
1Research Unit of Clinical and Molecular Biology (UR17ES29), Department of Biochemistry, Faculty of Pharmacy, University of Monastir, 5000, Monastir, Tunisia. abir.jaballah@hotmail.fr.
Menopausal hormonal changes increase metabolic syndrome (MetS) risk, especially after menopause. This study identified 47 common genes and pathways linking menopause, MetS, type 2 diabetes (T2D), and cardiovascular diseases (CVD).
Area of Science:
- Endocrinology and Metabolism
- Genetics and Bioinformatics
- Cardiovascular Research
Background:
- Menopausal hormonal shifts are linked to metabolic syndrome (MetS), type 2 diabetes (T2D), and cardiovascular diseases (CVD).
- A common genetic basis and signaling pathways connecting MetS, T2D, CVD, and menopause status remain understudied.
Purpose of the Study:
- To investigate the association between menopausal status and MetS, T2D, and CVD.
- To identify common gene signatures and signaling pathways related to MetS, T2D, CVD, and menopause.
Main Methods:
- Analysis of 314 women (35-75 years) divided into premenopausal and postmenopausal groups.
- Evaluation of MetS components, T2D, and CVD occurrence.
- Translational bioinformatics approach for gene mining and pathway analysis.
Main Results:
- MetS prevalence was significantly higher in postmenopausal women (67.1%) compared to premenopausal women (27.2%).
- 47 common genes were identified across MetS, T2D, CVD, and menopausal changes.
- Enriched pathways included P53 signaling and regulation of leukocyte cell-cell adhesion; key hub genes like TGFB1, MMP9, and IL6 were identified.
Conclusions:
- Menopause significantly increases the risk of metabolic syndrome.
- Identified gene signatures and pathways offer insights into the molecular mechanisms linking menopause to MetS, T2D, and CVD.
- Hub genes like TGFB1, MMP9, and IL6 may be critical targets for understanding and managing menopausal-related metabolic and cardiovascular risks.
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