Authors

Peter K. Joshi, Edinburgh Medical School
Tonu Esko, Tartu Ülikooli Genoomika Instituut
Hannele Mattsson, Terveyden ja Hyvinvoinnin Laitos
Niina Eklund, Terveyden ja Hyvinvoinnin Laitos
Ilaria Gandin, Ospedale di Cattinara
Teresa Nutile, Institute of Genetics and Biophysics Adriano Buzzati Traverso
Anne U. Jackson, University of Michigan, Ann Arbor
Claudia Schurmann, Icahn School of Medicine at Mount Sinai
Albert V. Smith, Icelandic Heart Association
Weihua Zhang, Imperial College London
Yukinori Okada, Tokyo Medical and Dental University
Alena Stančáková, Itä-Suomen yliopisto
Jessica D. Faul, University of Michigan, Ann Arbor
Wei Zhao, University of Michigan, Ann Arbor
Traci M. Bartz, University of Washington School of Medicine
Maria Pina Concas, Consiglio Nazionale delle Ricerche
Nora Franceschini, UNC Gillings School of Global Public Health
Stefan Enroth, Biomedicinskt centrum
Veronique Vitart, MRC Human Genetics Unit
Stella Trompet, Leids Universitair Medisch Centrum
Xiuqing Guo, The Lundquist Institute
Daniel I. Chasman, Harvard Medical School
Jeffrey R. O'Connel, University of Maryland School of Medicine
Tanguy Corre, Université de Lausanne (UNIL)
Suraj S. Nongmaithem, Centre for Cellular and Molecular Biology india
Yuning Chen, Boston University
Massimo Mangino, King's College London
Daniela Ruggiero, Institute of Genetics and Biophysics Adriano Buzzati Traverso
Michela Traglia, IRCCS Ospedale San Raffaele
Aliki Eleni Farmaki, Harokopio University of Athens
Tim Kacprowski, Universitätsmedizin Greifswald
Andrew Bjonnes, Massachusetts General Hospital
Ashley Van Der Spek, Erasmus MC

Document Type

Article

Publication Date

7-23-2015

Abstract

Homozygosity has long been associated with rare, often devastating, Mendelian disorders, and Darwin was one of the first to recognize that inbreeding reduces evolutionary fitness. However, the effect of the more distant parental relatedness that is common in modern human populations is less well understood. Genomic data now allow us to investigate the effects of homozygosity on traits of public health importance by observing contiguous homozygous segments (runs of homozygosity), which are inferred to be homozygous along their complete length. Given the low levels of genome-wide homozygosity prevalent in most human populations, information is required on very large numbers of people to provide sufficient power. Here we use runs of homozygosity to study 16 health-related quantitative traits in 354,224 individuals from 102 cohorts, and find statistically significant associations between summed runs of homozygosity and four complex traits: height, forced expiratory lung volume in one second, general cognitive ability and educational attainment (P < 1 × 10-300, 2.1 × 10-6, 2.5 × 10-10 and 1.8 × 10-10, respectively). In each case, increased homozygosity was associated with decreased trait value, equivalent to the offspring of first cousins being 1.2 cm shorter and having 10 months' less education. Similar effect sizes were found across four continental groups and populations with different degrees of genome-wide homozygosity, providing evidence that homozygosity, rather than confounding, directly contributes to phenotypic variance. Contrary to earlier reports in substantially smaller samples, no evidence was seen of an influence of genome-wide homozygosity on blood pressure and low density lipoprotein cholesterol, or ten other cardio-metabolic traits. Since directional dominance is predicted for traits under directional evolutionary selection, this study provides evidence that increased stature and cognitive function have been positively selected in human evolution, whereas many important risk factors for late-onset complex diseases may not have been.

Publication Source (Journal or Book title)

Nature

First Page

459

Last Page

462

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