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Calcium supplementation does not affect CRP levels in postmenopausal women--a randomized controlled trial
1Department of Medicine, University of Auckland, Private Bag 92019, Auckland, New Zealand. a.grey@auckland.ac.nz
Summary
Calcium supplementation did not alter C-reactive protein (CRP) levels in healthy postmenopausal women. CRP levels correlate with insulin resistance markers but do not predict bone mineral density or cardiovascular disease risk factors.
Area of Science:
- Endocrinology
- Cardiovascular Health
- Bone Metabolism
Background:
- Epidemiological studies suggest calcium supplementation may reduce cardiovascular disease (CVD) risk.
- C-reactive protein (CRP) is an inflammatory marker and a CVD risk factor.
- CRP production may be influenced by parathyroid hormone.
Purpose of the Study:
- To investigate the effect of daily calcium supplementation on C-reactive protein (CRP) levels in healthy postmenopausal women.
- To examine the relationship between CRP, bone mineral density (BMD), and markers of metabolic syndrome.
Main Methods:
- A randomized controlled trial involving healthy postmenopausal women.
- Measurement of high-sensitivity CRP at baseline and 12 months.
- Assessment of anthropometric measures, BMD, and metabolic syndrome markers.
Main Results:
- Baseline CRP levels positively correlated with body weight, fat indices, and BMD, but these associations were lost after adjusting for body weight.
- Consistent associations were observed between CRP levels and markers of metabolic syndrome, including fat mass, triglycerides, and fasting glucose.
- No significant difference in CRP levels was found between the calcium supplementation group and the placebo group after 1 year.
Conclusions:
- Calcium supplementation (1 g daily) did not affect CRP levels in healthy postmenopausal women over 1 year.
- CRP levels are associated with insulin resistance features but do not predict BMD or CVD risk in this population.
- The findings suggest calcium's role in CVD prevention may not be mediated through modulation of CRP levels.
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