Letters to the Editor |
Department of Internal Medicine, University of Turin, Turin, Italy
To the Editor:
Human apolipoprotein CII (apo CII) consists of 79 amino acid residues and is required as a cofactor in the hydrolysis of triacylglycerides of chylomicrons and VLDL by lipoprotein lipase.1 2 Familial apo CII deficiency is an autosomal recessive genetic disorder characterized by fasting hypertriglyceridemia and an accumulation of chylomicrons in the plasma.3 Shachter et al4 generated transgenic mice overexpressing human apo CII, and these authors reported the unexpected observation of marked hypertriglyceridemia with an accumulation of triglyceride-enriched VLDL in the plasma. We are the first to report a case of resistant hypertriglyceridemia in a young man with high plasma levels of apo CII (turbidimetric method by Alpha-Biotech, Milan, Italy).
A 42-year-old white man was referred to our lipid clinic for diet- and
drug-resistant
hypertriglyceridemia. His familial history
was positive for cardiovascular diseases (father with
hypercholesterolemia and myocardial
infarction). He had stopped smoking 9 years ago. He presented a
history of chest pain, but the baseline ECG and a strength test
were normal. He also underwent an ultrasound scan of the abdomen, which
showed normal morphology of the liver and gallbladder. His blood
pressure was normal (120/80 mm Hg), and he usually performed
adequate physical activity. The Table
shows the lipid profile of the
patient at the first visit, after 1 month of diet therapy (1800 kcal/d
and total abstention from alcohol consumption), and after 1 month of
diet plus 400 mg of fenofibrate. We also treated the patient with 1200
mgx3/d of gemfibrozil without changes in
This article has been cited by other articles:
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L. K. Pulawa, D. R. Jensen, A. Coates, and R. H. Eckel Reduction of plasma triglycerides in apolipoprotein C-II transgenic mice overexpressing lipoprotein lipase in muscle J. Lipid Res., January 1, 2007; 48(1): 145 - 151. [Abstract] [Full Text] [PDF] |
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