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)

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 lip...

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Veröffentlicht in:Nutrition, metabolism, and cardiovascular diseases metabolism, and cardiovascular diseases, 2018-08, Vol.28 (8), p.816-821
Hauptverfasser: McCaffery, J.M., Ordovas, J.M., Huggins, G.S., Lai, C.-Q., Espeland, M.A., Tate, D.F., Wing, R.R.
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container_issue 8
container_start_page 816
container_title Nutrition, metabolism, and cardiovascular diseases
container_volume 28
creator McCaffery, J.M.
Ordovas, J.M.
Huggins, G.S.
Lai, C.-Q.
Espeland, M.A.
Tate, D.F.
Wing, R.R.
description 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. 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). 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. clinicaltrials.gov Identifier: NCT01183689, https://clinicaltrials.gov/ •Randomized weight gain prevention strategies blunted the impact of CETP rs3764261, representing the region mostly strongly associated with high density lipoprotein cholesterol (HDL-C) in genome-wide association studies, on lowering of HDL-C over two years in young adulthood.•Even among those with the highest risk genotype for low HDL-C, the CC genotype, randomized weight gain prevention produced an increase in HDL-C whereas lowering was observed in the control group.•Obesity-related genetic variants, either independently or interaction with treatment arm, did not predict weight change.
doi_str_mv 10.1016/j.numecd.2018.02.018
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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. 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 &gt; 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). 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. clinicaltrials.gov Identifier: NCT01183689, https://clinicaltrials.gov/ •Randomized weight gain prevention strategies blunted the impact of CETP rs3764261, representing the region mostly strongly associated with high density lipoprotein cholesterol (HDL-C) in genome-wide association studies, on lowering of HDL-C over two years in young adulthood.•Even among those with the highest risk genotype for low HDL-C, the CC genotype, randomized weight gain prevention produced an increase in HDL-C whereas lowering was observed in the control group.•Obesity-related genetic variants, either independently or interaction with treatment arm, did not predict weight change.</description><identifier>ISSN: 0939-4753</identifier><identifier>EISSN: 1590-3729</identifier><identifier>DOI: 10.1016/j.numecd.2018.02.018</identifier><identifier>PMID: 29699816</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>alleles ; Body mass index ; body weight ; cardiovascular diseases ; diet ; females ; Genetics ; genotype ; genotyping ; High-density lipoprotein cholesterol ; males ; metabolism ; physical activity ; Prevention ; risk factors ; single nucleotide polymorphism ; variance ; weight gain ; Young adulthood ; young adults</subject><ispartof>Nutrition, metabolism, and cardiovascular diseases, 2018-08, Vol.28 (8), p.816-821</ispartof><rights>2018 The Italian Society of Diabetology, the Italian Society for the Study of Atherosclerosis, the Italian Society of Human Nutrition, and the Department of Clinical Medicine and Surgery, Federico II University</rights><rights>Copyright © 2018 The Italian Society of Diabetology, the Italian Society for the Study of Atherosclerosis, the Italian Society of Human Nutrition, and the Department of Clinical Medicine and Surgery, Federico II University. 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In contrast, within the two intervention groups, HDL-C increased on average with no differential effect of rs3764261 (p &gt; 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). 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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. 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 &gt; 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). 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. clinicaltrials.gov Identifier: NCT01183689, https://clinicaltrials.gov/ •Randomized weight gain prevention strategies blunted the impact of CETP rs3764261, representing the region mostly strongly associated with high density lipoprotein cholesterol (HDL-C) in genome-wide association studies, on lowering of HDL-C over two years in young adulthood.•Even among those with the highest risk genotype for low HDL-C, the CC genotype, randomized weight gain prevention produced an increase in HDL-C whereas lowering was observed in the control group.•Obesity-related genetic variants, either independently or interaction with treatment arm, did not predict weight change.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>29699816</pmid><doi>10.1016/j.numecd.2018.02.018</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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source Elsevier ScienceDirect Journals
subjects alleles
Body mass index
body weight
cardiovascular diseases
diet
females
Genetics
genotype
genotyping
High-density lipoprotein cholesterol
males
metabolism
physical activity
Prevention
risk factors
single nucleotide polymorphism
variance
weight gain
Young adulthood
young adults
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)
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