Why the study?
Are circulating amyloid and misfolded biomarkers associated with early myocardial injury and adverse cardiovascular events?
Population
30 studies investigating misfolded protein oligomers in early myocardial injury
Comparison
Circulating amyloid and misfolded biomarkers vs Controls
Design
Meta-analysis
Key result
Higher serum amyloid A concentration acted as an independent predictor of mortality in reperfused acute myocardial infarction (RR 5.8; 95% CI 1.3-27.7) and cardiac rupture.
Authors
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Elevated SAA may flag higher-risk reperfused AMI patients for closer surveillance; leaves open its role as a routine biomarker pending prospective validation.
Meta-Analysis (n=30)
Are circulating amyloid and misfolded biomarkers associated with early myocardial injury and adverse cardiovascular events?
Relative Risk: 5.8 (95% CI 1.3–27.7)
Circulating misfolded protein oligomers are elevated in cardiovascular and metabolic diseases and may serve as novel biomarkers for early myocardial injury and adverse outcomes.
Chable-Guerrero et al. (2026) conducted a meta-analysis in Early myocardial injury (n=30). Misfolded protein oligomers (including serum amyloid A) vs. Controls was evaluated on Mortality in reperfused AMI (RR 5.8, 95% CI 1.3-27.7). Higher serum amyloid A concentration acted as an independent predictor of mortality in reperfused acute myocardial infarction (RR 5.8; 95% CI 1.3-27.7) and cardiac rupture.
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