Published online before print October 27, 2003, doi: 10.1161/01.CIR.0000097113.11419.9E
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(Circulation. 2003;108:2312.)
© 2003 American Heart Association, Inc.
Clinical Investigation and Reports |
Comparison of the Associations of Apolipoprotein B and Low-Density Lipoprotein Cholesterol With Other Cardiovascular Risk Factors in the Insulin Resistance Atherosclerosis Study (IRAS)
From the Department of Medicine, University of Texas Health Science Center, San Antonio (K.W., S.M.H.); the Mike Rosenbloom Laboratory for Cardiovascular Research, Royal Victoria Hospital, Montreal, Canada (A.D.S.); the Department of Pathological Biochemistry, North Glasgow Hospitals University NHS Trust, UK (N.S.); and the Department of Public Health Sciences, Wake Forest University School of Medicine, Winston Salem, NC (R.D., L.E.W.).
Correspondence to Steve Haffner, MD, Department of Medicine (#7873), 7703 Floyd Curl Dr, San Antonio, TX 78229-3900. E-mail haffner{at}uthscsa.edu
Received May 23, 2003; de novo received July 7, 2003; revision received August 4, 2003; accepted August 7, 2003.
Background— Risk factors for vascular disease include obesity, dyslipidemia, hypertension, dysglycemia, insulin resistance, inflammation, thrombosis, and subclinical atherosclerosis. This study compares the associations of apolipoprotein B (apoB) and LDL cholesterol (LDLC) with a wide array of measures of these risk factors.
Methods and Results— In 1522 individuals in the Insulin Resistance Atherosclerosis Study, anthropometric measures and measures of lipids, apoB, C-reactive protein, fibrinogen, plasminogen activator inhibitor-1 (PAI-1), fasting and postglucose load glucose and insulin concentrations, and carotid artery intima-media thickness (IMT) were taken and insulin sensitivity was determined by frequently sampled intravenous glucose tolerance test. There were significant differences in measures of abdominal obesity, dyslipidemia, hyperinsulinemia, and thrombosis between subjects with elevated apoB but normal LDLC versus those with elevated LDLC but normal apoB. In each statistically significant comparison, the elevated-apoB group had higher associated risk than the elevated-LDLC group. Moreover, apoB is highly significantly (P<0.0001) correlated with each measure in the direction of higher risk, whereas LDLC was significantly correlated (P<0.05) only with blood pressure, triglyceride, fibrinogen, and C-reactive protein. After further adjustment for LDLC, apoB correlations remained significant, whereas several LDLC correlations adjusted for apoB became significant in the direction of lower risk.
Conclusions— Elevated apoB is more strongly associated than LDLC with other risk factors, including measures in the National Cholesterol Education Program guidelines for lipid treatment and other more recently established risk factors. This may provide new insight into why apoB is a better predictor of vascular risk than LDLC.
Key Words: apolipoproteins • lipoproteins • risk factors • atherosclerosis
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