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Estimating narrow-sense heritability using family data from admixed populations.
Athanasiadis, Georgios; Speed, Doug; Andersen, Mette K; Appel, Emil V R; Grarup, Niels; Brandslund, Ivan; Jørgensen, Marit Eika; Larsen, Christina Viskum Lytken; Bjerregaard, Peter; Hansen, Torben; Albrechtsen, Anders.
Afiliación
  • Athanasiadis G; Department of Biology, Section for Computational and RNA Biology, University of Copenhagen, 2200, Copenhagen, Denmark. yorgos.athanasiadis@gmail.com.
  • Speed D; Aarhus Institute of Advanced Studies, Aarhus University, 8000, Aarhus, Denmark.
  • Andersen MK; Bioinformatics Research Centre, Aarhus University, 8000, Aarhus, Denmark.
  • Appel EVR; Novo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, 2200, Copenhagen, Denmark.
  • Grarup N; Novo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, 2200, Copenhagen, Denmark.
  • Brandslund I; Novo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, 2200, Copenhagen, Denmark.
  • Jørgensen ME; Department of Clinical Immunology and Biochemistry, Lillebaelt Hospital, 7100, Vejle, Denmark.
  • Larsen CVL; Steno Diabetes Center Copenhagen, 2820, Gentofte, Denmark.
  • Bjerregaard P; Greenland University, Ilisimatusarfik, 3905, Nuuk, Greenland.
  • Hansen T; National Institute of Public Health, University of Southern Denmark, 1455, Copenhagen, Denmark.
  • Albrechtsen A; National Institute of Public Health, University of Southern Denmark, 1455, Copenhagen, Denmark.
Heredity (Edinb) ; 124(6): 751-762, 2020 06.
Article en En | MEDLINE | ID: mdl-32273574
ABSTRACT
Estimating total narrow-sense heritability in admixed populations remains an open question. In this work, we used extensive simulations to evaluate existing linear mixed-model frameworks for estimating total narrow-sense heritability in two population-based cohorts from Greenland, and compared the results with data from unadmixed individuals from Denmark. When our analysis focused on Greenlandic sib pairs, and under the assumption that shared environment among siblings has a negligible effect, the model with two relationship matrices, one capturing identity by descent and one capturing identity by state, returned heritability estimates close to the true simulated value, while using each of the two matrices alone led to downward biases. When phenotypes correlated with ancestry, heritability estimates were inflated. Based on these observations, we propose a PCA-based adjustment that recovers the true simulated heritability. We use this knowledge to estimate the heritability of ten quantitative traits from the two Greenlandic cohorts, and report differences such as lower heritability for height in Greenlanders compared with Europeans. In conclusion, narrow-sense heritability in admixed populations is best estimated when using a mixture of genetic relationship matrices on individuals with at least one first-degree relative included in the sample.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Población Blanca / Genética de Población / Modelos Genéticos Tipo de estudio: Prognostic_studies Límite: Humans País/Región como asunto: America do norte / Europa Idioma: En Revista: Heredity (Edinb) Año: 2020 Tipo del documento: Article País de afiliación: Dinamarca

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Población Blanca / Genética de Población / Modelos Genéticos Tipo de estudio: Prognostic_studies Límite: Humans País/Región como asunto: America do norte / Europa Idioma: En Revista: Heredity (Edinb) Año: 2020 Tipo del documento: Article País de afiliación: Dinamarca