HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Interactions of obesity and glucose-stimulated insulin secretion in familial hypertriglyceridemia.

Abstract
Plasma lipids and lipoproteins, glucose tolerance, plasma insulin response to glucose load, and liver function were examined in 81 relatives of 12 index cases with primary endogenous hypertriglyceridemia, hyperinsulinemia, and hepatic steatosis, as well as in 90 nonrelatives, including the spouses, as controls. Insulin hypersecretion (with or without glucose intolerance), endogenous hypertriglyceridemia, and abnormal liver function suggesting hepatic steatosis were shown to exist in the relatives mostly in combined fashion. Correlation analysis and stepwise multiple regression analysis revealed that the combined disorder developed on the basis of obesity. The incidence of diabetes mellitus was significantly high in the relatives (14.8 per cent) as compared with the normal Japanese population (3.5 per cent). Although the vertical transmission of the combined disorder was noted in almost all pedigrees, the frequency distribution analysis of insulin response, glucose tolerance, and plasma triglyceride showed the histograms of these variables similarly skewed to the right as compared with those of the controls, with no apparent bimodality. In view of the hitherto suggested role of insulin in triglyceride metabolism, it is concluded that hyperinsulinemia coupled with obesity seems to be the basic trait of this form of familial hypertriglyceridemia and hepatic steatosis, though the mode of transmission remains to be elucidated.
AuthorsY Maruhama, R Abe, F Okuguchi, S Oikawa, A Ohneda, Y Goto
JournalDiabetes (Diabetes) Vol. 27 Issue 6 Pg. 682-93 (Jun 1978) ISSN: 0012-1797 [Print] United States
PMID658614 (Publication Type: Comparative Study, Journal Article)
Chemical References
  • Insulin
  • Triglycerides
  • Glucose
Topics
  • Adolescent
  • Adult
  • Aged
  • Child
  • Fatty Liver (complications, metabolism)
  • Female
  • Glucose (pharmacology)
  • Humans
  • Hyperinsulinism (complications, metabolism)
  • Hyperlipidemias (complications, genetics, metabolism)
  • Insulin (metabolism)
  • Insulin Secretion
  • Japan
  • Male
  • Middle Aged
  • Obesity (complications, metabolism)
  • Triglycerides (blood)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: