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CETP variant rs1800777 is linked to greater fat mass, central obesity, and lower HDL cholesterol in obese adults (Endocrinol Diabetes Nutr 2018)

Original title: Association of a cholesteryl ester transfer protein variant (rs1800777) with fat mass, HDL cholesterol levels, and metabolic syndrome

Endocrinol Diabetes Nutr (Engl Ed) · · 5

de Luis D, Izaola O, Primo D, Gomez E, Lopez JJ, Ortola A, Aller R

This study analyzed the association of the CETP rs1800777 polymorphism with anthropometric parameters, lipid profile, metabolic syndrome and its components, and adipokine levels in 1005 obese subjects without type 2 diabetes or hypertension, using electrical bioimpedance and biochemical testing. Genotype distribution was 96.3% GG and 3.7% GA, with no AA genotype detected. Fat mass, waist circumference, and waist-to-hip ratio were all significantly higher in A allele carriers than non-carriers (p=0.04, p=0.02, p=0.01 respectively), while HDL-cholesterol was lower in A allele carriers (p=0.04). In logistic regression, the GA genotype was associated with increased risk of central obesity (OR 7.55, 95% CI 1.10-55.70, p=0.02) and low HDL-cholesterol (OR 2.46, 95% CI 1.23-4.91, p=0.014). The authors conclude the CETP variant is associated with lower HDL-cholesterol, increased fat mass, and central obesity, suggesting a role in adipose tissue pathophysiology.

Read the paper (DOI)PubMed

Original abstract

Background: There is little evidence of the association between CETP SNPs and obesity and/or related metabolic parameters.

Objective: To analyze the association of the polymorphism rs1800777 of the CETP gene with anthropometric parameters, lipid profile, metabolic syndrome and its components, and adipokine levels in obese subjects without type 2 diabetes mellitus or hypertension.

Design: A population of 1005 obese subjects was analyzed. Electrical bioimpedance was performed, and blood pressure, presence of metabolic syndrome, dietary intake, physical activity, and biochemical tests were recorded.

Results: Nine hundred and sixty eight patients (96.3%) had the GG genotype, 37 patients the GA genotype (3.7%) (no AA genotype was detected). Fat mass (delta: 4.4±1.1kg; p=0.04), waist circumference (delta: 5.6±2.1cm; p=0.02), and waist to hip ratio (delta: 0.04±0.01cm; p=0.01) were higher in A allele carriers than in non-A allele carriers. HDL cholesterol levels were lower in A allele carriers than in non-A allele carriers (delta: 4.2±1.0mg/dL; p=0.04). In the logistic regression analysis, the GA genotype was associated to an increased risk of central obesity (OR 7.55, 95% CI 1.10-55.70, p=0.02) and low HDL cholesterol levels (OR 2.46, 95% CI 1.23-4.91, p=0.014).

Conclusion: The CETP variant at position +82 is associated to lower HDL cholesterol levels, increased fat mass, and central obesity in obese subjects. These results may suggest a potential role of this variant gene in pathophysiology of adipose tissue.

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Summary written by cetpinhibition.org from the published abstract; figures as published. Page updated 19 August 2026. Methods.