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Influence of hormone replacement therapy on C-reactive protein: population-based data
Paola Primatesta1, Emanuela Falaschetti, Neil R Poulter
1Department of Epidemiology and Public Health, Royal Free and University College Medical School, London WC1E 6BT, UK. paolap@public-health.ucl.ac.uk
Journal of Cardiovascular Risk
|February 6, 2003
Summary
Hormone replacement therapy (HRT) use is linked to higher C-reactive protein (CRP) levels, a marker of inflammation. This finding suggests a potential mechanism for adverse cardiovascular effects of HRT.
Area of Science:
- Cardiovascular Health
- Endocrinology
- Public Health
Background:
- Observational studies suggest hormone replacement therapy (HRT) reduces coronary risk, but randomized trials do not.
- A potential explanation for trial findings is that HRT's adverse effects, like elevated C-reactive protein (CRP), may counteract benefits.
Purpose of the Study:
- To investigate the association between current and past HRT use and C-reactive protein (CRP) levels.
- To explore potential mechanisms linking HRT to cardiovascular risk.
Main Methods:
- Analysis of data from the Health Survey for England 1998, a nationally representative study.
- Inclusion of 4,112 women aged 40-74, categorized as current, past, or never HRT users.
- CRP levels measured and analyzed as continuous (logged) and percentile variables, controlling for confounders.
Main Results:
- Current HRT users showed significantly higher median CRP levels (2.5 mg/l) compared to past (1.9 mg/l) and never users (1.4 mg/l).
- After adjusting for age, smoking, and body mass index, CRP remained significantly elevated only in current HRT users.
- Current users exhibited higher physical activity and alcohol consumption than recommended.
Conclusions:
- HRT use is independently associated with elevated CRP levels in a representative English population sample.
- Increased CRP may represent a plausible mechanism for adverse cardiovascular effects of HRT.
- Findings highlight the importance of considering inflammatory markers in HRT risk-benefit assessments.