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Apolipoprotein A-IV levels and phenotype distribution in NIDDM
B L Vergès1, G Vaillant, A Goux
1Service d'Endocrinologie, Hôpital du Bocage, Dijon, France.
Diabetes Care
|August 1, 1994
Summary
Plasma apolipoprotein A-IV (apoA-IV) levels are elevated in non-insulin-dependent diabetes mellitus (NIDDM) patients, linked to higher triglycerides and lower HDL cholesterol. The apoA-IV phenotype’s protective effects on lipid profiles are lost in NIDDM.
Area of Science:
- Endocrinology and Metabolism
- Lipidology
- Cardiovascular Disease Research
Background:
- Non-insulin-dependent diabetes mellitus (NIDDM) is often associated with dyslipidemia, impacting cardiovascular risk.
- Apolipoprotein A-IV (apoA-IV) plays a role in lipid metabolism, but its association with NIDDM and specific phenotypes requires further elucidation.
Purpose of the Study:
- To determine plasma apoA-IV levels and phenotype distribution in NIDDM patients.
- To analyze the influence of apoA-IV phenotype on lipid profiles within the NIDDM population.
Main Methods:
- Measurement of total cholesterol, triglycerides, HDL cholesterol (HDL2 and HDL3 subfractions), free fatty acids, and apoA-IV levels.
- Analysis conducted on 83 NIDDM patients and 100 normal control subjects.
- Determination of apoA-IV phenotype for all participants.
Main Results:
- NIDDM patients exhibited significantly higher triglyceride and free fatty acid levels, and lower HDL and HDL2 cholesterol levels compared to controls.
- Plasma apoA-IV levels were significantly higher in both male and female NIDDM patients versus controls.
- In controls, the apoA-IV-1-2 phenotype was linked to higher HDL and HDL2 cholesterol, a protective association absent in NIDDM patients.
Conclusions:
- Elevated plasma apoA-IV in NIDDM is primarily associated with hypertriglyceridemia and secondarily with HDL cholesterol levels.
- The apoA-IV phenotype distribution did not differ between NIDDM patients and controls.
- The metabolic dysregulation in NIDDM appears to abolish the potential cardioprotective lipid profile associated with the apoA-IV-1-2 phenotype.