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Vitamin C treatment reduces elevated C-reactive protein
Gladys Block1, Christopher D Jensen, Tapashi B Dalvi
1University of California, Berkeley, 94720, USA. gblock@berkeley.edu
Insights
Vitamin C significantly reduced C-reactive protein (CRP), a marker of cardiovascular risk, in healthy adults with elevated CRP levels. Vitamin E showed no significant effect, highlighting targeted antioxidant research for specific biomarkers.
Area of Science:
- Biochemistry
- Cardiovascular Medicine
- Nutritional Science
Background:
- Plasma C-reactive protein (CRP) is a key inflammatory biomarker linked to cardiovascular disease (CVD) risk.
- Statins have demonstrated efficacy in reducing CVD incidence by lowering elevated CRP levels.
- The potential of antioxidants like vitamins C and E to modulate CRP requires investigation.
Purpose of the Study:
- To evaluate the efficacy of vitamin C and vitamin E supplementation in reducing CRP levels.
- To determine if baseline CRP concentration influences the effect of vitamin C or E on CRP.
- To explore the potential of vitamin C in managing obesity-related inflammatory conditions.
Main Methods:
- A randomized, placebo-controlled trial involving 396 healthy nonsmokers.
- Participants were assigned to receive 1000 mg/day vitamin C, 800 IU/day vitamin E, or placebo for 2 months.
- Statistical analysis examined treatment effects, including interactions with baseline CRP levels.
Main Results:
- No overall significant reduction in CRP was observed across all participants.
- A significant interaction revealed that vitamin C reduced CRP by 25.3% in participants with baseline CRP ≥ 1.0 mg/L (p=0.02).
- Vitamin E did not produce a significant effect on CRP levels. 75% of obese participants had CRP ≥ 1.0 mg/L.
Conclusions:
- Vitamin C supplementation effectively reduces CRP levels in individuals with elevated CRP (≥ 1.0 mg/L), similar to statin effects.
- Vitamin E supplementation did not demonstrate a significant impact on CRP levels.
- Future research should focus on individuals with elevated biomarkers to assess clinical benefits of antioxidants, particularly for obesity-related diseases.
Abstract:
Plasma C-reactive protein (CRP) is an inflammatory biomarker that predicts cardiovascular disease. Lowering elevated CRP with statins has reduced the incidence of cardiovascular disease. We investigated whether vitamin C or E could reduce CRP. Healthy nonsmokers (N=396) were randomized to three groups, 1000 mg/day vitamin C, 800 IU/day vitamin E, or placebo, for 2 months. Median baseline CRP was low, 0.85 mg/L. No treatment effect was seen when all participants were included. However, a significant interaction was found, indicating that treatment effect depends on baseline CRP concentration. Among participants with CRP indicative of elevated cardiovascular risk (> or =1.0 mg/L), vitamin C reduced the median CRP by 25.3% vs placebo (p=0.02) (median reduction in the vitamin C group, 0.25 mg/L, 16.7%). These effects are similar to those of statins. The vitamin E effect was not significant. In summary, treatment with vitamin C but not vitamin E significantly reduced CRP among individuals with CRP > or =1.0 mg/L. Among the obese, 75% had CRP > or =1.0 mg/L. Research is needed to determine whether reducing this inflammatory biomarker with vitamin C could reduce diseases associated with obesity. But research on clinical benefits of antioxidants should limit participants to persons with elevations in the target biomarkers.
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