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360His polymorphism of the apolipoproteinA-IV gene and plasma lipid response to energy restricted diets in overweight subjects.
- Source :
-
Atherosclerosis [Atherosclerosis] 2000 May; Vol. 150 (1), pp. 187-92. - Publication Year :
- 2000
-
Abstract
- Obesity is commonly associated with high rates of cardiovascular disease (CVD). Weight loss in obese subjects reduces risk factors for CVD but this response is not uniform. Genetic factors could be involved in this variability. The 360His polymorphism of apolipoproteinA-IV (apoA-IV) influences the lipid response to fat intake, but it is unclear whether this polymorphism could contribute to lipid variability during weight loss. Therefore, we assessed the effects of an energy restricted diet (6.3 MJ) for 12 weeks on weight loss and plasma lipids according to apoA-IV genotype in 186 overweight/obese subjects (BMI mean 33+/-4.3, range 25.0-48.0 kg/m(2)). The frequency of the 360His allele was 0.083. Energy restriction for 12 weeks resulted in an average weight loss of 8. 25+/-0.28 kg. HDL-C increased 5.4% in subjects with the apoA-IV-1/1 genotype with weight loss compared to a 2.6% decrease in apoA-IV-1/2 subjects (P=0.035). This was more apparent when only the subjects with type 2 diabetes (n=57) were analyzed (P=0.003). ApoA-IV genotype was not related to change in total cholesterol, LDL-C or triglyceride concentrations. Therefore, weight loss as a treatment to reduce CVD risk factors may be more effective in subjects with the apoA-IV-1/1 variant as compared to those with the apoA-IV-1/2 variant, especially in subjects with type 2 diabetes.
- Subjects :
- Alleles
Apolipoproteins A blood
Cholesterol blood
Cholesterol, HDL blood
Cholesterol, LDL blood
Diabetes Mellitus blood
Diabetes Mellitus diet therapy
Diabetes Mellitus genetics
Female
Humans
Male
Middle Aged
Obesity blood
Obesity diet therapy
Triglycerides blood
Weight Loss
Apolipoproteins A genetics
Diet, Reducing
Energy Intake
Lipids blood
Obesity genetics
Polymorphism, Genetic
Subjects
Details
- Language :
- English
- ISSN :
- 0021-9150
- Volume :
- 150
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Atherosclerosis
- Publication Type :
- Academic Journal
- Accession number :
- 10781650
- Full Text :
- https://doi.org/10.1016/s0021-9150(99)00367-6