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Relation of cholesterol metabolism and non-cholesterol sterols to insulin resistance.

Abstract
Using non-cholesterol sterols investigation several authors postulated a hypothesis that in the metabolic syndrome cholesterol endogenous synthesis is increased and its absorption decreased. Our study is the first attempt to evaluate the direct relation of cholesterol metabolism to the principal pathogenetic phenomenon of the metabolic syndrome--namely to insulin resistance. We have measured insulin sensitivity by two methods--Quicki (Quantitative Sensitivity Check Index) and intravenous insulin tolerance test (Kitt) and 3 indirect markers--fasting insulin level, fasting C-peptide level and SHBG (sex hormone binding globulin). The investigation was performed in three groups of subjects with a different prevalence of insulin resistance: 72 non-diabetics with ischemic heart disease, 117 young blood donors and 63 type 2 diabetics on diet therapy only. Analyzing altogether 60 relationships--between four sterols (lathosterol, squalene, sitosterol and campesterol) and five markers of insulin resistance in three groups of subjects--we have found only six significant relations between cholesterol synthesis and absorption and insulin resistance in all groups of patients. Our results indicate that there exists a significant relationship between insulin sensitivity and indices of either increased cholesterol synthesis or decreased cholesterol absorption. Insulin resistance explains only a part of both abnormalities mentioned above.
AuthorsA Šmahelová, R Hyspler, T Haas
JournalPhysiological research (Physiol Res) Vol. 56 Issue 6 Pg. 749-755 ( 2007) ISSN: 0862-8408 [Print] Czech Republic
PMID17087600 (Publication Type: Journal Article)
Chemical References
  • Biomarkers
  • Cholesterol, Dietary
  • Lipids
  • Sterols
  • Cholesterol
Topics
  • Adult
  • Aged
  • Biomarkers
  • Cholesterol (blood, metabolism)
  • Cholesterol, Dietary (metabolism)
  • Diet
  • Female
  • Glucose Clamp Technique
  • Glucose Tolerance Test
  • Humans
  • Insulin Resistance (physiology)
  • Intestinal Absorption (drug effects)
  • Lipids (blood)
  • Male
  • Middle Aged
  • Regression Analysis
  • Sterols (blood, metabolism)

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