학술논문

Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects
Document Type
article
Author
Howe, Laurence JNivard, Michel GMorris, Tim THansen, Ailin FRasheed, HumairaCho, YoonsuChittoor, GeethaAhlskog, RafaelLind, Penelope APalviainen, Teemuvan der Zee, Matthijs DCheesman, RosaMangino, MassimoWang, YunzhangLi, ShuaiKlaric, LucijaRatliff, Scott MBielak, Lawrence FNygaard, MarianneGiannelis, AlexandrosWilloughby, Emily AReynolds, Chandra ABalbona, Jared VAndreassen, Ole AAsk, HelgaBaras, ArisBauer, Christopher RBoomsma, Dorret ICampbell, ArchieCampbell, HarryChen, ZhengmingChristofidou, ParaskeviCorfield, ElizabethDahm, Christina CDokuru, Deepika REvans, Luke Mde Geus, Eco JCGiddaluru, SudheerGordon, Scott DHarden, K PaigeHill, W DavidHughes, AmandaKerr, Shona MKim, YongkangKweon, HyeokmoonLatvala, AnttiLawlor, Deborah ALi, LimingLin, KuangMagnus, PerMagnusson, Patrik KEMallard, Travis TMartikainen, PekkaMills, Melinda CNjølstad, Pål RasmusOverton, John DPedersen, Nancy LPorteous, David JReid, JeffreySilventoinen, KarriSouthey, Melissa CStoltenberg, CamillaTucker-Drob, Elliot MWright, Margaret JHewitt, John KKeller, Matthew CStallings, Michael CLee, James JChristensen, KaareKardia, Sharon LRPeyser, Patricia ASmith, Jennifer AWilson, James FHopper, John LHägg, SaraSpector, Tim DPingault, Jean-BaptistePlomin, RobertHavdahl, AlexandraBartels, MeikeMartin, Nicholas GOskarsson, SvenJustice, Anne EMillwood, Iona YHveem, KristianNaess, ØyvindWiller, Cristen JÅsvold, Bjørn OlavKoellinger, Philipp DKaprio, JaakkoMedland, Sarah EWalters, Robin GBenjamin, Daniel JTurley, PatrickEvans, David MDavey Smith, GeorgeHayward, CarolineBrumpton, BenHemani, GibranDavies, Neil M
Source
Nature Genetics. 54(5)
Subject
Human Genome
Genetics
Pediatric
2.1 Biological and endogenous factors
Aetiology
Mental health
Generic health relevance
Genome-Wide Association Study
Humans
Mendelian Randomization Analysis
Multifactorial Inheritance
Phenotype
Polymorphism
Single Nucleotide
Social Science Genetic Association Consortium
Within Family Consortium
Biological Sciences
Medical and Health Sciences
Developmental Biology
Language
Abstract
Estimates from genome-wide association studies (GWAS) of unrelated individuals capture effects of inherited variation (direct effects), demography (population stratification, assortative mating) and relatives (indirect genetic effects). Family-based GWAS designs can control for demographic and indirect genetic effects, but large-scale family datasets have been lacking. We combined data from 178,086 siblings from 19 cohorts to generate population (between-family) and within-sibship (within-family) GWAS estimates for 25 phenotypes. Within-sibship GWAS estimates were smaller than population estimates for height, educational attainment, age at first birth, number of children, cognitive ability, depressive symptoms and smoking. Some differences were observed in downstream SNP heritability, genetic correlations and Mendelian randomization analyses. For example, the within-sibship genetic correlation between educational attainment and body mass index attenuated towards zero. In contrast, analyses of most molecular phenotypes (for example, low-density lipoprotein-cholesterol) were generally consistent. We also found within-sibship evidence of polygenic adaptation on taller height. Here, we illustrate the importance of family-based GWAS data for phenotypes influenced by demographic and indirect genetic effects.