Stroke, Vol 19, 1097-1100, Copyright © 1988 by American Heart Association
M Kaste and P Koivisto
We followed 54 subjects with heterozygous familial hypercholesterolemia for
an average of 10 (range 3-14) years. Half were treated surgically with
partial ileal bypass and the other half (matched for age, sex, coronary
heart disease, blood pressure, diabetes mellitus, smoking, obesity, and
serum cholesterol concentration) were treated conservatively with diet and
hypolipidemic drugs. The mean decrease in serum cholesterol concentration
from the average value of 522 mg/dl on entry into the study was 32% in the
surgically treated group and 10% in the conservatively treated group. One
quarter of the subjects (14 of 54) had symptomatic cerebrovascular
disorders and one tenth (six of 54) suffered a brain infarction at a mean
age of 43 (range 30-57) years. Two thirds of the brain infarctions occurred
during follow-up. The method of treatment of familial hypercholesterolemia
did not affect the number of new cerebrovascular events. The incidence of
brain infarction was 7.4/1000/yr. The risk of brain infarction in these
subjects with familial hypercholesterolemia was at least 20 times higher
than in the general population. We conclude that symptomatic subjects with
familial hypercholesterolemia have not only a high risk of coronary heart
disease but also a high risk of cerebrovascular disorders.
ARTICLES
Risk of brain infarction in familial hypercholesterolemia
Department of Neurology, University of Helsinki, Finland.
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