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Decrease of Lipoprotein(a) With Improved Glycemic Control in IDDM Subjects

  1. Steven M Haffner, MD, MPH,
  2. Katherine R Tuttle, MD and
  3. David L Rainwater, PhD
  1. Divisions of Clinical Epidemiology and Nephrology, Department of Medicine, University of Texas Health Science Center at San Antonio, Department of Genetics, Southwest Foundation for Biomedical Research San Antonio, Texas
  1. Address correspondence and reprint requests to Steven M. Haffner, MD, Division of Clinical Epidemiology, Department of Medicine, University of Texas Health Science Center at San Antonio, 7703 Floyd Curl Drive, San Antonio, TX 78284.

Abstract

Objective Recently, lipoprotein(a) [Lp(a)] has been identified as a major risk factor for coronary heart disease. There are few data available on the influence of metabolic control on plasma Lp(a) concentrations in subjects with insulin-dependent diabetes mellitus (IDDM), a group at high risk for coronary heart disease.

Research Design and Methods We examined the effects of improved metabolic control on plasma lipid and lipoproteins and Lp(a) concentrations in 12 subjects before and after 21 days of tight metabolic control.

Results Glycosylated hemoglobin declined from 8.4 to 6.9% (P < 0.001), and Lp(a) declined from 29.7 to 27.1 mg/dl (P = 0.022). There were no significant differences in total, low-density lipoprotein, or highdensity lipoprotein cholesterol, although the decline in triglyceride concentrations were borderline statistically significant. The distribution of apolipoprotein(a) isoforms in IDDM patients was not unusual, and the apolipoprotein(a) isoform phenotypes did not change with improved metabolic control. Lp(a) concentrations were also significantly higher than in a population-based control group of nondiabetic subjects from the San Antonio Heart Study.

Conclusions Although the number of subjects was small and the degree of improvement in metabolic control was modest, the results suggest that improved metabolic control may decrease the risk of coronary heart disease mediated by Lp(a) in IDDM.

  • Received August 6, 1990.
  • Accepted November 7, 1990.
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