Sr. No |
Author/ Year [Reference] |
Type of Study |
Conclusion |
1 |
Kandelouei et al (2022) [41] |
Systematic review and meta-analysis |
This systematic review and meta-analysis showed that the statins are efficacious in reducing the concentrations of CRP and Hs-CRP in patients with different types of cardiovascular diseases and coronary artery diseases like acute coronary syndrome, myocardial infarction, stable atherosclerotic plaques, and unstable angina. |
2 |
Gholoobi et al (2021) [42] |
Randomized, placebo-controlled, double-blind clinical trial. |
Hs-CRP is an important inflammatory marker for non-ST-segment elevation myocardial infarction and is related to cardiovascular events. |
3 |
Carrero et al (2019) [34] |
Randomized controlled trial |
Most patients with myocardial infarction exhibit elevated Hs-CRP levels and Hs-CRP ≥2 mg/L levels were associated with a higher risk of major adverse cardiovascular events (adjusted hazard ratio, 1.28) and death (adjusted hazard ratio, 1.42). Increased Hs-CRP levels have prognostic validity as biomarkers beyond the trial evidence; in real‐world healthcare-based settings. |
4 |
Tayefi et al (2017) [43] |
Decision tree algorithm |
This study indicated that serum Hs-CRP levels are the most important variable associated with coronary artery diseases and this biomarker has a stronger association with coronary heart disease in comparison to traditional biomarkers such as fasting blood glucose and low-density lipoproteins. |
5 |
Li et al (2017) [44] |
Meta-analysis |
The risk of cardiovascular mortality increased by 2.03 times among study subjects with the highest Hs-CRP levels. Hs-CRP can stratify all-cause and cardiovascular mortality risks in the general population. |
6 |
Wang et al (2017) [45] |
Cross-sectional |
This study concluded that cumulative exposure to Hs‐CRP was associated with a subsequent increased risk of CVD and myocardial infarction in a dose-dependent manner. Cumulative measurements of Hs-CRP are better than single measurement of risk prediction of disease development of CVD and myocardial infarction. |