Evidence map›Paper›PMID 37034760›Full record

ArticlebioRxiv : the preprint server for biology2023

Genetic and environmental contributions to ancestry differences in gene expression in the human brain.

Kynon J M Benjamin, Qiang Chen, Nicholas J Eagles, Louise A Huuki-Myers, Leonardo Collado-Torres, Joshua M Stolz, Geo Pertea, Joo Heon Shin, Apuã C M Paquola, Thomas M Hyde and 4 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2023. 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

14 authors.

Kynon J M BenjaminLieber Institute for Brain Development, Baltimore, MD, USA.
Qiang ChenLieber Institute for Brain Development, Baltimore, MD, USA.
Nicholas J EaglesLieber Institute for Brain Development, Baltimore, MD, USA.
Louise A Huuki-MyersLieber Institute for Brain Development, Baltimore, MD, USA.
Leonardo Collado-TorresLieber Institute for Brain Development, Baltimore, MD, USA.
Joshua M StolzLieber Institute for Brain Development, Baltimore, MD, USA.
Geo PerteaLieber Institute for Brain Development, Baltimore, MD, USA.
Joo Heon ShinLieber Institute for Brain Development, Baltimore, MD, USA.
Apuã C M PaquolaLieber Institute for Brain Development, Baltimore, MD, USA.
Thomas M HydeLieber Institute for Brain Development, Baltimore, MD, USA.
Joel E KleinmanLieber Institute for Brain Development, Baltimore, MD, USA.
Andrew E JaffeDepartment of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Shizhong HanLieber Institute for Brain Development, Baltimore, MD, USA.
Daniel R WeinbergerLieber Institute for Brain Development, Baltimore, MD, USA.

Funding

Integrative cellular deconvolution of human brain RNA sequencing dataR01MH123183 · NIMH · LIEBER INSTITUTE, INC. · PI HICKS, STEPHANIE CARINNE, MAYNARD, KRISTEN ROSE · 2020 to 2023
$2.3M
Comprehensive computational analysis of genetic and regulatory differences between individuals with African and European ancestries across four brain regionsK99MD016964 · NIMHD · LIEBER INSTITUTE, INC. · PI BENJAMIN, KYNON JADE M · 2022 to 2023
$197k
NIMHD NIH HHS K99 MD016964NIMH NIH HHS R01 MH123183
6 · The paper itself

Abstract

Ancestral differences in genomic variation are determining factors in gene regulation; however, most gene expression studies have been limited to European ancestry samples or adjusted for ancestry to identify ancestry-independent associations. We instead examined the impact of genetic ancestry on gene expression and DNA methylation (DNAm) in admixed African/Black American neurotypical individuals to untangle effects of genetic and environmental factors. Ancestry-associated differentially expressed genes (DEGs), transcripts, and gene networks, while notably not implicating neurons, are enriched for genes related to immune response and vascular tissue and explain up to 26% of heritability for ischemic stroke, 27% of heritability for Parkinson's disease, and 30% of heritability for Alzhemier's disease. Ancestry-associated DEGs also show general enrichment for heritability of diverse immune-related traits but depletion for psychiatric-related traits. The cell-type enrichments and direction of effects vary by brain region. These DEGs are less evolutionarily constrained and are largely explained by genetic variations; roughly 15% are predicted by DNAm variation implicating environmental exposures. We also compared Black and White Americans, confirming most of these ancestry-associated DEGs. Our results highlight how environment and genetic background affect genetic ancestry differences in gene expression in the human brain and affect risk for brain illness.

Identifiers

PMID37034760
PMCPMC10081196

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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.