Rare Protein-truncating Variants in APOB, Lower LDL-C, and Protection Against Coronary Heart Disease.

BACKGROUND: Familial hypobetalipoproteinemia is a genetic disorder caused by rare protein-truncating variants (PTV) in the gene encoding APOB (apolipoprotein B), the major protein component of LDL (low-density lipoprotein) and triglyceride-rich lipoprotein particles. Whether heterozygous APOB deficiency is associated with decreased risk for coronary heart disease (CHD) is uncertain. We combined family-based and large scale gene-sequencing to characterize the association of rare PTVs in APOB with circulating LDL-C (LDL cholesterol), triglycerides, and risk for CHD. METHODS: We sequenced the APOB gene in 29 Japanese hypobetalipoproteinemia families, as well as 57 973 individuals derived from 12 CHD case-control studies-18 442 with early-onset CHD and 39 531 controls. We defined PTVs as variants that lead to a premature stop, disrupt canonical splice-sites, or lead to insertions/deletions that shift reading frame. We tested the association of rare APOB PTV carrier status with blood lipid levels and CHD. RESULTS: Among 29 familial hypobetalipoproteinemia families, 8 families harbored APOB PTVs. Carrying 1 APOB PTV was associated with 55 mg/ dL lower LDL-C (P= 3x10(-5)) and 53% lower triglyceride level (P= 2x10(-4)). Among 12 case-control studies, an APOB PTV was present in 0.038% of CHD cases as compared to 0.092% of controls. APOB PTV carrier status was associated with a 43 mg/dL lower LDL-C (P= 2x10(-7)), a 30% decrease in triglycerides (P= 5x10(-4)), and a 72% lower risk for CHD (odds ratio, 0.28; 95% CI, 0.12-0.64; P= 0.002). CONCLUSIONS: Rare PTV mutations in APOB which are associated with lower LDL-C and reduced triglycerides also confer protection against CHD.