Population
38 men with primary hypertriglyceridemia, comprising 17 with familial combined hyperlipidemia, 7 with…
Design
Cross-sectional
Authors
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These apolipoprotein shifts may identify higher-risk FCH phenotypes; leaves open causal links to outcomes in longitudinal cohorts.
Familial combined hyperlipidemia and familial hypertriglyceridemia share increased triglyceride overproduction and decreased HDL, but FCH is distinguished by higher LDL cholesterol and LDL/HDL ratio, potentially explaining higher cardiovascular risk.
Stalenhoef et al. (1986) studied this question.
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