Issue: July 2008
July 01, 2008
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Lower HDL not associated with increased risk for ischemic heart disease

Issue: July 2008
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Lower plasma levels of HDL cholesterol due to heterozygosity for loss-of-function mutations in ABCA1 were not associated with an increased risk for ischemic heart disease, according to the findings from a recent study.

The researchers from Denmark and other sites conducted a study to determine if genetically reduced HDL cholesterol due to heterozygosity for four loss-of-function mutations in ABCA1 increased the risk for ischemic heart disease.

They examined data from the Copenhagen City Heart Study (n=9,022; 28 heterozygotes), the Copenhagen General Population Study (n=31,241; 76 heterozygotes) and the Copenhagen Ischemic Heart Disease Study (n=16,623; 44 heterozygotes).

Heterozygotes had HDL levels of 41 mg/dL; with noncarriers had HDL levels of 58 mg/dL). A 17 mg/dL lower HDL level in the Copenhagen City Heart Study was associated with a multifactorially adjusted hazard ratio for ischemic heart disease (1.70; 95% CI, 1.57-1.85), according to the researchers.

In heterozygotes and noncarriers, the hazard ratio was 0.67 (95% CI, 0.28-1.61) in the Copenhagen City Heart Study, 0.82 (95% CI, 0.34-1.96) in the Copenhagen General Population Study and 0.86 (95% CI, 0.32-2.32) in the Copenhagen Ischemic Heart Disease Study. For the studies combined, the hazard ratio was 0.93 (95% CI, 0.53-1.62)

In the Copenhagen City Heart Study, there were 1,741 ischemic heart disease events; in the Copenhagen General Population Study, there were 2,427 ischemic heart disease events, and in the Copenhagen Ischemic Heart Disease Study, there were 2,498 ischemic heart disease events. – by Christen Haigh

JAMA. 2008;299:2524-2532.