cetpinhibition.org

Genetics

Weight gain prevention counteracts the HDL-lowering effect of CETP variant rs3764261 in young adults, randomized trial finds (Nutr Metab Cardiovasc Dis 2018)

Original title: Weight gain prevention buffers the impact of CETP rs3764261 on high density lipoprotein cholesterol in young adulthood: The Study of Novel Approaches to Weight Gain Prevention (SNAP)

Nutr Metab Cardiovasc Dis · · 6

McCaffery JM, Ordovas JM, Huggins GS, Lai CQ, Espeland MA, Tate DF, Wing RR

This study examined whether two randomized weight gain prevention strategies, one targeting small changes and one large changes to diet and physical activity, blunt genetic risk for HDL-cholesterol (HDL-C) lowering over two years, in 524 young adults (mean age 28.2, mean BMI 25.5) from the Study of Novel Approaches to Weight Gain Prevention (SNAP) trial. Each copy of the HDL-C risk C allele at CETP rs3764261 was associated with lower baseline HDL-C, consistent with prior literature. A significant interaction was found between rs3764261 and treatment arm for change in HDL-C (p=0.02): in the control group, HDL-C declined continuously in C allele carriers (p=0.004), while in the two intervention groups, HDL-C increased on average regardless of rs3764261 genotype (p greater than 0.24). Even among CC genotype carriers, the intervention arms showed increased HDL-C while the control arm showed a reduction (p=0.013).

Read the paper (DOI)PubMed

Original abstract

Background And Aims: Two weight gain prevention strategies, one targeting small changes to diet and physical activity and a second targeting large changes, significantly reduced weight gain in young adulthood. We examined whether weight gain prevention blunts genetic risk for body weight increase and/or high density lipoprotein cholesterol (HDL-C) lowering over two years.

Methods And Results: Participants were 524 male and female young adults (mean age = 28.2, SD = 4.3; mean BMI = 25.5, SD = 2.6). Obesity-related SNPs accounting for ≥ 0.04% of the variance were genotyped and combined into a genetic risk score. For HDL-C, SNPs within CETP, LIPC and FADS2 were genotyped. The obesity-related genetic risk score did not predict change in BMI independently or in interaction with treatment arm. However, consistent with the prior literature, each copy of the HDL-C risk, C, allele at CETP rs3764261 was associated with lower HDL-C at baseline. Moreover, significant interaction between SNP and treatment arm for change in HDL-C was observed (p = 0.02). In the control group, HDL-C change was dependent upon rs3764261 (p = 0.004) with C allele carriers showing a continued reduction in HDL-C. In contrast, within the two intervention groups, HDL-C increased on average with no differential effect of rs3764261 (p > 0.24). Notably, even among carriers of the CC genotype, small and large change arms were associated with increased HDL-C and the control arm a reduction (p = 0.013).

Conclusions: The C allele at CETP rs3764261 is a strong risk factor for low HDL-C in young adulthood but weight gain prevention may mitigate this risk. CLINICAL TRIAL REGISTRY NUMBER AND WEBSITE: clinicaltrials.gov Identifier: NCT01183689, https://clinicaltrials.gov/.

geneticsHDL biology

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