Evidence map›Paper›PMID 32273574›Full record

ArticleHeredity2020

Estimating narrow-sense heritability using family data from admixed populations.

Georgios Athanasiadis, Doug Speed, Mette K Andersen, Emil V R Appel, Niels Grarup, Ivan Brandslund, Marit Eika Jørgensen, Christina Viskum Lytken Larsen, Peter Bjerregaard, Torben Hansen and 1 more

Abstract read
In one paragraph

Article in Heredity, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
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  5. Article
  6. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Georgios AthanasiadisDepartment of Biology, Section for Computational and RNA Biology, University of Copenhagen, 2200, Copenhagen, Denmark. yorgos.athanasiadis@gmail.com.ORCID 0000-0002-2927-4035
Doug SpeedAarhus Institute of Advanced Studies, Aarhus University, 8000, Aarhus, Denmark.ORCID 0000-0002-0096-9765
Mette K AndersenNovo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, 2200, Copenhagen, Denmark.
Emil V R AppelNovo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, 2200, Copenhagen, Denmark.
Niels GrarupNovo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, 2200, Copenhagen, Denmark.
Ivan BrandslundDepartment of Clinical Immunology and Biochemistry, Lillebaelt Hospital, 7100, Vejle, Denmark.
Marit Eika JørgensenSteno Diabetes Center Copenhagen, 2820, Gentofte, Denmark.
Christina Viskum Lytken LarsenNational Institute of Public Health, University of Southern Denmark, 1455, Copenhagen, Denmark.
Peter BjerregaardNational Institute of Public Health, University of Southern Denmark, 1455, Copenhagen, Denmark.
Torben HansenNovo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, 2200, Copenhagen, Denmark.
Anders AlbrechtsenDepartment of Biology, Section for Computational and RNA Biology, University of Copenhagen, 2200, Copenhagen, Denmark. albrecht@binf.ku.dk.ORCID 0000-0001-7306-031X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

Genetics, PopulationModels, GeneticWhite PeopleDenmarkGreenlandHumansLinear ModelsPhenotypeQuantitative Trait, Heritable

Identifiers

PMID32273574
PMCPMC7239878

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.