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January 28, 2022Mediators of Inflammation135 citationsOpen Access

Effect of Statins on Serum level of hs-CRP and CRP in Patients with Cardiovascular Diseases: A Systematic Review and Meta-Analysis of Randomized Controlled Trials

TKTahmineh KandeloueiMAMitra AbbasifardDIDanyal Imani

Key Result

Statins significantly reduced serum levels of hs-CRP (WMD -0.97 mg/L; 95% CI -1.26 to -0.68; P<0.001) and CRP (WMD -3.05 mg/L; 95% CI -4.86 to -1.25; P<0.001) in patients with cardiovascular diseases.

Key Points

  • This research aims to systematically review and analyze the effects of statins on CRP and hs-CRP levels in patients with cardiovascular diseases.
  • Conducted a literature search for eligible randomized controlled trials assessing statins' effects on CRP and hs-CRP.
  • Analyzed 26 studies for hs-CRP and 20 studies for CRP, involving over 3000 patients and controls.
  • Used weighted mean difference and 95% confidence intervals to determine effect sizes.
  • Statins reduced hs-CRP levels by WMD = -0.97 mg/L (95% CI: -1.26 to -0.68 mg/L, P<0.001).
  • Statins reduced CRP levels by WMD = -3.05 mg/L (95% CI: -4.86 to -1.25 mg/L, P<0.001).
  • Treatments longer than 10 weeks effectively decreased hs-CRP levels.

Study Design

Type

Meta-Analysis (n=5,978)

Structured PICO

Do statins reduce serum levels of hs-CRP and CRP in patients with cardiovascular diseases?

P
Population
Patients with cardiovascular diseases (CVDs). Meta-analysis of 26 RCTs (n=5,978) for hs-CRP and 20 RCTs (n=5,994) for CRP.
I
Intervention
Statins (including high-intensity and moderate/low-intensity treatments)
C
Comparator
Control (not further specified)
O
Outcome
Serum levels of high-sensitivity C-reactive protein (hs-CRP) and C-reactive protein (CRP)surrogate

Statins significantly reduce inflammatory biomarkers (hs-CRP and CRP) in patients with cardiovascular diseases, supporting their pleiotropic anti-inflammatory effects.

Main Result

Effect estimate: WMD -0.97 mg/L (95% CI -1.26 to -0.68)

p-value: p=<0.001

Abstract

Background. Several studies have reported that statins have anti-inflammatory effects. Nevertheless, results of clinical trials concerning the effect of statins on the levels of C-reactive protein (CRP) and high-sensitivity CRP (hs-CRP) have been inconsistent. Therefore, we performed a systematic review and meta-analysis of randomized clinical trials (RCTs) evaluating the effect of statins on CRP and hs-CRP levels in patients with cardiovascular diseases (CVDs). Methods. Literature search of the major databases was performed to find eligible RCTs assessing the effect of statins on serum levels of CRP and hs-CRP from the inception until the last week of April 2021. The effect sizes were determined for weighted mean difference (WMD) and 95% confidence intervals (CI). Results. 26 studies were identified (3010 patients and 2968 controls) for hs-CRP and 20 studies (3026 patients and 2968 controls) for CRP. Statins reduced the serum levels of hs-CRP ( WMD = − 0.97 mg / L ; 95% CI: -1.26 to -0.68 mg/L; P 0.001 ) and CRP ( WMD = − 3.05 mg / L ; 95% CI: -4.86 to -1.25 mg/L; P 0.001 ) in patients with CVDs. Statins decreased the serum levels of hs-CRP in patients receiving both high-intensity and moderate/low-intensity treatments with these drugs. In addition, the duration of treatment longer than 10 weeks decreased hs-CRP levels. Only high-intensity statin treatment could marginally decrease serum levels of CRP in CVDs patients. Conclusions. This meta-analysis showed the efficacy of statins to reduce the concentrations of CRP and hs-CRP in patients with different types of CVDs.

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Cite This Study

Kandelouei et al. (2022) conducted a meta-analysis in Cardiovascular diseases (n=5,978). Statins vs. Control was evaluated on Serum levels of hs-CRP (WMD -0.97 mg/L, 95% CI -1.26 to -0.68, p=<0.001). Statins significantly reduced serum levels of hs-CRP (WMD -0.97 mg/L; 95% CI -1.26 to -0.68; P<0.001) and CRP (WMD -3.05 mg/L; 95% CI -4.86 to -1.25; P<0.001) in patients with cardiovascular diseases.

synapsesocial.com/papers/6a0e9bb0a03ab94435046760https://doi.org/10.1155/2022/8732360
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