Evidence map›Paper›PMID 40654817›Full record

ArticlebioRxiv : the preprint server for biology2025

No evidence for disassortative mating based on HLA in a small-scale, endogamous population.

Gillian L Meeks, Brooke Scelza, Katherine M Kichula, Catrinel Berevoescu, Kristin Hardy, Ticiana D J Farias, Genelle F Harrison, Nicholas R Pollock, Neus Font-Porterias, Sean Prall and 2 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Gillian L MeeksGraduate Program in Integrative Genetics and Genomics, University of California Davis, Davis, 95616, CA, USA.ORCID 0000-0002-8436-6514
Brooke ScelzaDepartment of Anthropology, University of California Los Angeles, Los Angeles, 90095, CA, USA.ORCID 0000-0001-5875-8875
Katherine M KichulaDepartment of Biomedical Informatics, University of Colorado School of Medicine, Aurora, 80045, CO, USA.ORCID 0000-0002-9817-3043
Catrinel BerevoescuUndergraduate Program in Genetics and Genomics, University of California Davis, Davis, 95616, CA, USA.
Kristin HardyCenter for Population Biology, University of California Davis, Davis, CA, USA.
Ticiana D J FariasDepartment of Biomedical Informatics, University of Colorado School of Medicine, Aurora, 80045, CO, USA.ORCID 0000-0002-3606-2428
Genelle F HarrisonDepartment of Biomedical Informatics, University of Colorado School of Medicine, Aurora, 80045, CO, USA.ORCID 0000-0003-3386-8159
Nicholas R PollockDepartment of Biomedical Informatics, University of Colorado School of Medicine, Aurora, 80045, CO, USA.ORCID 0000-0003-0114-528X
Neus Font-PorteriasDepartment of Biomedical Informatics, University of Colorado School of Medicine, Aurora, 80045, CO, USA.ORCID 0000-0002-1357-9096
Sean PrallDepartment of Anthropology, University of California Los Angeles, Los Angeles, 90095, CA, USA.ORCID 0000-0001-5719-6460
Paul J NormanDepartment of Biomedical Informatics, University of Colorado School of Medicine, Aurora, 80045, CO, USA.ORCID 0000-0001-8370-7703
Brenna M HennCenter for Population Biology, University of California Davis, Davis, CA, USA.ORCID 0000-0003-4998-287X

Funding

Evolution and Function of Immunogenetic Diversity across the Eastern HemisphereR01AI151549 · NIAID · UNIVERSITY OF COLORADO DENVER · PI Paul John Norman · 2022 to 2026
$3.9M
Supplement: Improving Inference of Genetic Architecture and Selection with African GenomesR35GM133531 · NIGMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI HENN, BRENNA M · 2019 to 2023
$2.3M
NIAID NIH HHS R01 AI151549NIGMS NIH HHS R35 GM133531
6 · The paper itself

Abstract

Studies dating back several decades have suggested that humans prefer potential mates with dissimilar HLA genotypes. Evidence for actualized disassortative mating based on the human-specific MHC remains inconclusive. For instance, cosmopolitan populations have often exhibited the opposite trend whereby assortative mating at the MHC is observed, indicating that social stratification may overwhelm potential biological mate preferences. However, small-scale, endogamous populations-whose social structures more closely resemble those throughout most of human evolution-have been largely overlooked. Here, we assess HLA dissimilarity among Himba pastoralists from Namibia, where socially accepted concurrency allows individuals to maintain both arranged marital and self-selected ("love match") partnerships. This provides a rare opportunity to directly test HLA similarity across contrasting partnership types (arranged vs chosen) within the same social system (n = 249 observed partnerships). We find no difference in HLA dissimilarity (neither at the genotype nor protein divergence level) between partnership types, nor in their fitness benefits to potential offspring as assessed via computationally predicted pathogen binding affinities. The effects of the partnership types likewise do not differ from a random, background distribution of 18,487 possible unrelated pairings. Finally, we detect extensive haplotype sharing across the HLA region, suggesting that episodes of fluctuating positive selection may be a stronger force maintaining HLA polymorphism than disassortative mating, even in an evolutionarily relevant social context.

Indexed as

disassortative matingheterozygote advantageHLAMHCSexual selection

Identifiers

PMID40654817
PMCPMC12247893

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.