California Pacific Medical Center Research Institute, San Francisco, CA 94107-1728, USA.
Sleep. 2013 Mar 1;36(3):431-46. doi: 10.5665/sleep.2466.
To determine the association between common genetic variation in the clock gene pathway and objectively measured acti-graphic sleep and activity rhythm traits.
Genetic association study in two population-based cohorts of elderly participants: the Study of Osteoporotic Fractures (SOF) and the Osteoporotic Fractures in Men (MrOS) study.
Population-based.
SOF participants (n = 1,407, 100% female, mean age 84 years) and MrOS participants (n = 2,527, 100% male, mean age 77 years) with actigraphy and genotype data.
N/A.
Common genetic variation in 30 candidate genes was captured using 529 single nucleotide polymorphisms (SNPs). Sleep and activity rhythm traits were objectively measured using wrist actigraphy. In a region of high linkage disequilibrium on chromosome 12p13 containing the candidate gene GNB3, the rs1047776 A allele and the rs2238114 C allele were significantly associated with higher wake after sleep onset (meta-analysis: rs1047776 PADD = 2 × 10(-5), rs2238114 PADD = 5 × 10(-5)) and lower LRRC23 gene expression (rs1047776: ρ = -0.22, P = 0.02; rs2238114: ρ = -0.50, P = 5 × 10(-8)). In MrOS participants, SNPs in ARNTL and NPAS2, genes coding for binding partners, were associated with later sleep and wake onset time (sleep onset time: ARNTL rs3816358 P2DF = 1 × 10(-4), NPAS2 rs3768984 P2DF = 5 × 10(-5); wake onset time: rs3816358 P2DF = 3 × 10(-3), rs3768984 P2DF = 2 × 10(-4)) and the SNP interaction was significant (sleep onset time PINT = 0.003, wake onset time PINT = 0.001). A SNP association in the CLOCK gene replicated in the MrOS cohort, and rs3768984 was associated with sleep duration in a previously reported study. Cluster analysis identified four clusters of genetic associations.
These findings support a role for common genetic variation in clock genes in the regulation of inter-related sleep traits in the elderly.
Evans DS; Parimi N; Nievergelt CM; Blackwell T; Redline S; Ancoli-Israel S; Orwoll ES; Cummings SR; Stone KL; Tranah GJ. Common genetic variants in ARNTL and NPAS2 and at chromosome 12p13 are associated with objectively measured sleep traits in the elderly. SLEEP 2013;36(3):431-446.
确定时钟基因通路中的常见遗传变异与客观测量的活动图睡眠和活动节律特征之间的关联。
基于两个老年参与者人群队列的遗传关联研究:骨质疏松性骨折研究(SOF)和男性骨质疏松性骨折研究(MrOS)。
基于人群。
SOF 参与者(n=1407,100%女性,平均年龄 84 岁)和 MrOS 参与者(n=2527,100%男性,平均年龄 77 岁),具有活动计和基因型数据。
无。
使用 529 个单核苷酸多态性(SNP)捕获 30 个候选基因中的常见遗传变异。使用腕部活动计客观测量睡眠和活动节律特征。在包含候选基因 GNB3 的 12p13 染色体高连锁不平衡区域中,rs1047776A 等位基因和 rs2238114C 等位基因与睡眠后觉醒时间较高(荟萃分析:rs1047776PADD=2×10(-5),rs2238114PADD=5×10(-5))和较低的 LRRC23 基因表达(rs1047776:ρ=-0.22,P=0.02;rs2238114:ρ=-0.50,P=5×10(-8))相关。在 MrOS 参与者中,编码结合伴侣的 ARNTL 和 NPAS2 基因中的 SNP 与睡眠和觉醒时间较晚相关(睡眠起始时间:ARNTLrs3816358P2DF=1×10(-4),NPAS2rs3768984P2DF=5×10(-5);觉醒起始时间:rs3816358P2DF=3×10(-3),rs3768984P2DF=2×10(-4)),并且 SNP 相互作用具有显著性(睡眠起始时间 PINT=0.003,觉醒起始时间 PINT=0.001)。CLOCK 基因中的 SNP 关联在 MrOS 队列中得到复制,rs3768984 与先前报道的研究中的睡眠持续时间相关。聚类分析确定了四个遗传关联群。
这些发现支持时钟基因中的常见遗传变异在调节老年人相互关联的睡眠特征中的作用。
Evans DS;Parimi N;Nievergelt CM;Blackwell T;Redline S;Ancoli-Israel S;Orwoll ES;Cummings SR;Stone KL;Tranah GJ。ARNTL 和 NPAS2 中的常见遗传变异与老年人中客观测量的睡眠特征相关。睡眠 2013;36(3):431-446。