2002
DOI: 10.1016/s0009-8981(01)00746-x
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A family-based study of hyperinsulinemia and hypertriglyceridemia in heterozygous lipoprotein lipase deficiency

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Cited by 2 publications
(1 citation statement)
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“…Previous evidences showed that carriers with LPL heterozygous had a trend to hyperinsulinemia which indicated the presence of insulin resistance [8,9]. Our study suggests that with aging, systemic LPL deficiency causes increased lipid accumulation in tissues (liver, skeletal muscle, pancreas), which results in tissue-specific and whole-body insulin resistance, b-cell dysfunction and even impaired glucose tolerance ultimately.…”
Section: Discussionmentioning
confidence: 50%
“…Previous evidences showed that carriers with LPL heterozygous had a trend to hyperinsulinemia which indicated the presence of insulin resistance [8,9]. Our study suggests that with aging, systemic LPL deficiency causes increased lipid accumulation in tissues (liver, skeletal muscle, pancreas), which results in tissue-specific and whole-body insulin resistance, b-cell dysfunction and even impaired glucose tolerance ultimately.…”
Section: Discussionmentioning
confidence: 50%