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Associations of HDL subclasses and lipid content with complement proteins over the menopause transition: The SWAN HDL
Samar R El Khoudary1, Xirun Chen1, Dan McConnell2
1University of Pittsburgh School of Public Health, Public Health Building, 130 De Soto St, Pittsburgh, PA 15261, USA (Drs Khoudary, Chen, Brooks, and Orchard).
Insights
Complement proteins C3 and C4 increase around menopause, impacting high-density lipoprotein (HDL) subclasses and lipid content. These changes may influence inflammation and atherosclerosis risk in midlife women.
Area of Science:
- Cardiovascular Science
- Immunology
- Endocrinology
Background:
- Menopause transition (MT) is linked to chronic inflammation, potentially altering high-density lipoproteins (HDL) and promoting atherosclerosis.
- Understanding inflammatory changes during MT is crucial for cardiovascular disease (CVD) prevention.
Purpose of the Study:
- To investigate if complement proteins C3 and C4 increase around the final menstrual period (FMP).
- To determine if changes in HDL subclasses and lipid content correlate with C3 and C4 levels during MT in midlife women.
Main Methods:
- Longitudinal study of 471 women during MT.
- Measurements included nuclear magnetic resonance spectroscopy for HDL subclasses and lipid content, alongside C3 and C4 levels, assessed up to five times.
Main Results:
- Complement proteins C3 and C4 significantly increased around FMP, with C3 showing a steeper rise, particularly between 1 year before and 2 years after FMP.
- Decreases in large HDL particles, HDL size, and HDL-phospholipids, along with increases in small HDL particles and HDL-triglycerides, were associated with higher C3 and C4 levels.
- Associations were stronger with C3 than with C4.
Conclusions:
- Complement proteins C3 and C4 rise significantly around menopause, influencing HDL characteristics.
- These HDL modifications during MT may modulate inflammation, contributing to atherosclerosis development.
- Targeting HDL-focused therapies could offer novel strategies for CVD protection by modulating inflammation.
Background:
The menopause transition (MT) could trigger low-grade chronic inflammation which may modify high-density lipoproteins (HDL) and lead to additional inflammatory responses contributing to atherosclerosis development.
Objective:
To test whether complement proteins C3 and C4 increase around the final menstrual period (FMP), and whether changes in HDL subclasses and lipid content associate with C3 and C4 levels over time in midlife women.
Methods:
The study included 471 women (at baseline: age 50.2(2.7) years; 87.3% pre or peri-menopausal) who had nuclear magnetic resonance spectroscopy HDL subclasses, lipid content, and C3 and C4 measured up to 5 times over the MT.
Results:
Adjusted annual changes in C3 and C4 varied by time segments relative to FMP with significant increases, steeper for C3, only observed within 1 year before to 2 years after the FMP. Greater decreases in large HDL particles (HDL-P), HDL size, and HDL-phospholipids, and greater increases in small HDL-P and HDL-Triglycerides were associated with higher C3 and C4 over time, although associations with C4 were weaker than those with C3.
Conclusion:
Complement proteins C3 and C4 significantly rise around menopause with C3 showing the steepest rise. Changes in HDL subclasses, overall size, and lipid content, over the MT may play a role in modulating inflammation responses known to be related to atherosclerosis. These results raise the possibility that novel therapeutic agents focusing on HDL might contribute to CVD protection by modulating inflammation.
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