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Journal of Lipid Research, Vol. 41, 1231-1236, August 2000
Copyright © 2000 by Lipid Research, Inc.
Plasma apolipoprotein L concentrations correlate with plasma triglycerides and cholesterol levels in normolipidemic, hyperlipidemic, and diabetic subjects
Philippe N. Duchateaua,
Irina Movsesyana,
Shizuya Yamashitab,
Naohiko Sakaib,
Ken-Ichi Hiranob,
Samantha A. Schoenhausa,
Patricia M. O'Connor-Kearnsa,
Susan J. Spencerc,
Robert B. Jaffec,
Rita F. Redberga,d,
Brian Y. Ishidaa,
Yugi Matsuzawab,
John P. Kanea, and
Mary J. Malloya
a Cardiovascular Research Institute, University of California, San Francisco, CA 94143
b Second Department of Internal Medicine, Osaka University Medical School, Osaka 565, Japan
c Reproductive Endocrinology Center, University of California, San Francisco, CA 94143
d Division of Cardiology, University of California, San Francisco, CA 94143
Correspondence to:
Philippe N. Duchateau
Apolipoprotein L is a newly recognized component of human plasma lipoproteins. Mainly associated with apoA-I-containing lipoproteins, it is a marker of distinct HDL subpopulations. In an effort to gain inference as to its as yet unknown function, we studied biological determinants of apoL levels in human plasma. The distribution of apoL in normal subjects is asymmetric, with marked skewing toward higher values. No difference was found in apoL concentrations between males and females, but we observed an elevation of apoL in primary hypercholesterolemia (10.1 vs. 8.5 µg/mL in control), in endogenous hypertriglyceridemia (13.8 µg/mL, P < 0.001), combined hyperlipidemia phenotype (18.7 g/mL, P < 0.0001), and in patients with type II diabetes (16.2 µg/mL, P < 0.02) who were hyperlipidemic.
Significant positive correlations were observed between apoL and the log of plasma triglycerides in normolipidemia (0.446, P < 0.0001), endogenous hypertriglyceridemia (0.435, P < 0.01), primary hypercholesterolemia (0.66, P < 0.02), combined hyperlipidemia (0.396, P < 0.04), hypo-alphalipoproteinemia (0.701, P < 0.005), and type II diabetes with hyperlipidemia (0.602, P < 0.01). Apolipoprotein L levels were also correlated with total cholesterol in normolipidemia (0.257, P < 0.004), endogenous hypertriglyceridemia (0.446, P = 0.001), and non-insulin-dependent diabetes mellitus (NIDDM) (0.548, P < 0.02). No significant correlation was found between apoL and body mass index, age, sex, HDL-cholesterol or fasting glucose and glycohemoglobin levels. ApoL levels in plasma of patients with primary cholesteryl ester transfer protein deficiency significantly increased (7.1 ± 0.5 vs. 5.47 ± 0.27, P < 0.006).Duchateau, P. N., I. Movsesyan, S. Yamashita, N. Sakai, K-I. Hirano, S. A. Schoenhaus, P. M. O'Connor-Kearns, S. J. Spencer, R. B. Jaffe, R. F. Redberg, B. Y. Ishida, Y. Matsuzawa, J. P. Kane, and M. J. Malloy. Plasma apolipoprotein L concentrations correlate with plasma triglycerides and cholesterol levels in normolipidemic, hyperlipidemic, and diabetic subjects. J. Lipid Res. 2000. 41: 1231;1236.
Supplementary key words:
apolipoprotein L, triglycerides, hypercholesterolemia, hypertriglyceridemia, combined hyperlipidemia, diabetes, CETP deficiency

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Copyright © 2000 by the American Society for Biochemistry and Molecular Biology.
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