Human Genomics Laboratory, Pennington Biomedical Research Center, Baton Rouge, LA 70808, USA.
J Appl Physiol (1985). 2011 May;110(5):1160-70. doi: 10.1152/japplphysiol.00973.2010. Epub 2010 Dec 23.
Low cardiorespiratory fitness is a powerful predictor of morbidity and cardiovascular mortality. In 473 sedentary adults, all whites, from 99 families of the Health, Risk Factors, Exercise Training, and Genetics (HERITAGE) Family Study, the heritability of gains in maximal O(2) uptake (VO(2max)) after exposure to a standardized 20-wk exercise program was estimated at 47%. A genome-wide association study based on 324,611 single-nucleotide polymorphisms (SNPs) was undertaken to identify SNPs associated with improvements in VO(2max) Based on single-SNP analysis, 39 SNPs were associated with the gains with P < 1.5 × 10(-4). Stepwise multiple regression analysis of the 39 SNPs identified a panel of 21 SNPs that accounted for 49% of the variance in VO(2max) trainability. Subjects who carried ≤9 favorable alleles at these 21 SNPs improved their VO(2max) by 221 ml/min, whereas those who carried ≥19 of these alleles gained, on average, 604 ml/min. The strongest association was with rs6552828, located in the acyl-CoA synthase long-chain member 1 (ACSL1) gene, which accounted by itself for ~6% of the training response of VO(2max). The genes nearest to the SNPs that were the strongest predictors were PR domain-containing 1 with ZNF domain (PRDM1); glutamate receptor, ionotropic, N-methyl-D-aspartate 3A (GRIN3A); K(+) channel, voltage gated, subfamily H, member 8 (KCNH8); and zinc finger protein of the cerebellum 4 (ZIC4). The association with the SNP nearest to ZIC4 was replicated in 40- to 65-yr-old, sedentary, overweight, and dyslipidemic subjects trained in Studies of a Targeted Risk Reduction Intervention Through Defined Exercise (STRRIDE; n = 183). Two SNPs were replicated in sedentary obese white women exercise trained in the Dose Response to Exercise (DREW) study (n = 112): rs1956197 near dishevelled associated activator of morphogenesis 1 (DAAM1) and rs17117533 in the vicinity of necdin (NDN). The association of SNPs rs884736 in the calmodulin-binding transcription activator 1 (CAMTA1) locus and rs17581162 ~68 kb upstream from regulator of G protein signaling 18 (RGS18) with the gains in VO(2max) in HERITAGE whites were replicated in HERITAGE blacks (n = 247). These genomic predictors of the response of Vo(2max) to regular exercise provide new targets for the study of the biology of fitness and its adaptation to regular exercise. Large-scale replication studies are warranted.
低心肺功能适应性是发病率和心血管死亡率的有力预测因子。在来自健康、风险因素、运动训练和遗传学(HERITAGE)家族研究的 99 个家族的 473 名久坐成年人中,暴露于标准化 20 周运动计划后最大 O(2)摄取量(VO(2max))增加的遗传性估计为 47%。基于 324611 个单核苷酸多态性(SNP)进行了全基因组关联研究,以确定与 VO(2max)改善相关的 SNP。基于单 SNP 分析,有 39 个 SNP 与增益相关,P < 1.5 × 10(-4)。对 39 个 SNP 的逐步多元回归分析确定了一组 21 个 SNP,这些 SNP 解释了 VO(2max)可训练性变化的 49%。携带这些 21 个 SNP 的≤9 个有利等位基因的受试者 VO(2max)增加了 221ml/min,而携带这些等位基因≥19 个的受试者 VO(2max)平均增加了 604ml/min。最强的关联是与 rs6552828 相关,该 SNP 位于酰基辅酶 A 合成酶长链成员 1(ACSL1)基因中,其本身占 VO(2max)训练反应的6%。与最强预测 SNP 最接近的基因是富含 PR 结构域的 1 型锌指蛋白(PRDM1);谷氨酸受体,离子型,N-甲基-D-天冬氨酸 3A(GRIN3A);K(+)通道,电压门控,亚家族 H,成员 8(KCNH8);和小脑 4 型锌指蛋白(ZIC4)。与 ZIC4 附近 SNP 的关联在通过定义运动进行靶向风险降低干预的研究(STRRIDE;n = 183)中得到了 40-65 岁、久坐、超重和血脂异常的受试者的复制。在运动训练的剂量反应研究(DREW)中(n = 112),两个 SNP 在久坐肥胖的白人女性中得到了复制:rs1956197 附近的畸形相关形态发生激活物 1(DAAM1)和 rs17117533 附近的神经纤维瘤蛋白(NDN)。在 HERITAGE 白人和 HERITAGE 黑人中,钙调蛋白结合转录激活因子 1(CAMTA1)基因座上的 rs884736 与 rs17581162(RGS18)上游68kb 处的调节 G 蛋白信号 18(RGS18)的 SNP 与 VO(2max)的增加之间的关联得到了复制(n = 247)。这些 VO(2max)对常规运动反应的基因组预测因子为研究健身的生物学及其对常规运动的适应提供了新的靶点。需要进行大规模的复制研究。