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Interaction of the common apolipoprotein C-III (APOC3 -482C > T) and hepatic lipase (LIPC -514C > T) promoter variants affects glucose tolerance in young adults: European Atherosclerosis Research Study II (EARS-II)

  • on behalf of the EARS-II Study Group
  • , Hans M. Jansen*
  • , Dawn M. Waterworth
  • , Viviane Nicaud
  • , Christian P. Ehnholm
  • , Philippa J. Talmud
  • *Corresponding author for this work
  • Royal Free and University College London School of Medicine
  • Hôpital La Pitié-Salpêtrière
  • National Public Health Institute - Finland

Research output: Contribution to journalArticleAcademicpeer-review

29 Citations (Scopus)

Abstract

Both hepatic lipase (HL) and apolipoprotein C-III (apoC-III) influence lipid metabolism. Common variation in promoters of both genes, LIPC -514C > T and APOC3 -482C > T, respectively, have been shown to affect plasma lipids and lipoproteins and glucose tolerance. We studied the interaction between both variants on parameters of glucose tolerance and lipid metabolism in 714 healthy young males participating in the second European Atherosclerosis Research Study (EARS-II). Approximately 18% of the subjects were carriers of at least one rare LIPC and APOC3 allele. These subjects exhibited, after fasting and oral fat loading, the highest values of triglyceride-rich lipoproteins, but there was no significant interactive effect on any lipid variable. However, interaction occurred on basal diastolic blood pressure (p = 0.036) and, during oral glucose tolerance testing, on peak (p = 0.0065) and area under the curve for glucose (p = 0.049), and insulin (p = 0.035). This resulted in the highest diastolic blood pressure and lowest glucose tolerance in carriers of at least one rare allele of both genes. Thus gene:gene interaction between LIPC and APOC3, even in these healthy young males, leads to changes in parameters that are typically characteristic of Syndrome-X.

Original languageEnglish
Pages (from-to)237-243
Number of pages7
JournalAnnals of Human Genetics
Volume65
Issue number3
DOIs
Publication statusPublished - May 2001

Research programs

  • EMC 05-03-21-01-00
  • EMC 05-03-38-04-00

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