Sabatti Chiara, Service Susan K, Hartikainen Anna-Liisa, Pouta Anneli, Ripatti Samuli, Brodsky Jae, Jones Chris G, Zaitlen Noah A, Varilo Teppo, Kaakinen Marika, Sovio Ulla, Ruokonen Aimo, Laitinen Jaana, Jakkula Eveliina, Coin Lachlan, Hoggart Clive, Collins Andrew, Turunen Hannu, Gabriel Stacey, Elliot Paul, McCarthy Mark I, Daly Mark J, Järvelin Marjo-Riitta, Freimer Nelson B, Peltonen Leena
Department of Human Genetics and Los Angeles, Los Angeles, California 90095, USA.
Nat Genet. 2009 Jan;41(1):35-46. doi: 10.1038/ng.271. Epub 2008 Dec 7.
Genome-wide association studies (GWAS) of longitudinal birth cohorts enable joint investigation of environmental and genetic influences on complex traits. We report GWAS results for nine quantitative metabolic traits (triglycerides, high-density lipoprotein, low-density lipoprotein, glucose, insulin, C-reactive protein, body mass index, and systolic and diastolic blood pressure) in the Northern Finland Birth Cohort 1966 (NFBC1966), drawn from the most genetically isolated Finnish regions. We replicate most previously reported associations for these traits and identify nine new associations, several of which highlight genes with metabolic functions: high-density lipoprotein with NR1H3 (LXRA), low-density lipoprotein with AR and FADS1-FADS2, glucose with MTNR1B, and insulin with PANK1. Two of these new associations emerged after adjustment of results for body mass index. Gene-environment interaction analyses suggested additional associations, which will require validation in larger samples. The currently identified loci, together with quantified environmental exposures, explain little of the trait variation in NFBC1966. The association observed between low-density lipoprotein and an infrequent variant in AR suggests the potential of such a cohort for identifying associations with both common, low-impact and rarer, high-impact quantitative trait loci.
对纵向出生队列进行全基因组关联研究(GWAS)能够联合调查环境和基因对复杂性状的影响。我们报告了1966年芬兰北部出生队列(NFBC1966)中9种定量代谢性状(甘油三酯、高密度脂蛋白、低密度脂蛋白、葡萄糖、胰岛素、C反应蛋白、体重指数以及收缩压和舒张压)的GWAS结果,该队列来自芬兰基因隔离程度最高的地区。我们重复了之前报道的这些性状的大多数关联,并确定了9个新的关联,其中几个关联突出了具有代谢功能的基因:高密度脂蛋白与NR1H3(LXRA)、低密度脂蛋白与AR和FADS1 - FADS2、葡萄糖与MTNR1B以及胰岛素与PANK1。其中两个新关联是在对体重指数结果进行调整后出现的。基因 - 环境相互作用分析表明还有其他关联,这需要在更大样本中进行验证。目前确定的基因座,连同量化的环境暴露,在NFBC1966中对性状变异的解释很少。在低密度脂蛋白与AR中一个罕见变异之间观察到的关联表明,这样的队列有潜力识别与常见的、低影响以及罕见的、高影响定量性状基因座的关联。