Evidence map›Paper›PMID 39237910›Full record

ArticleBMC genomics2024

Novel insights into the pleiotropic health effects of growth differentiation factor 11 gained from genome-wide association studies in population biobanks.

Jessica Strosahl, Kaixiong Ye, Robert Pazdro

Abstract read
In one paragraph

Article in BMC genomics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Jessica StrosahlDepartment of Nutritional Sciences, University of Georgia, 305 Sanford Drive, Athens, GA, 30602, USA.
Kaixiong YeDepartment of Genetics, University of Georgia, Athens, GA, 30602, USA.
Robert PazdroDepartment of Nutritional Sciences, University of Georgia, 305 Sanford Drive, Athens, GA, 30602, USA. rpazdro@uga.edu.ORCID http://orcid.org/0000-0001-9976-4817

Funding

Defining the Genetic Architecture of the Glutathione Redox SystemR01GM121551 · NIGMS · UNIVERSITY OF GEORGIA · PI PAZDRO, ROBERT · 2017 to 2021
$1.4M
NIGMS NIH HHS R01 GM121551
6 · The paper itself

Abstract

backgroundGrowth differentiation factor 11 (GDF11) is a member of the transforming growth factor-β (TGF-β) superfamily that has gained considerable attention over the last decade for its observed ability to reverse age-related deterioration of multiple tissues, including the heart. Yet as many researchers have struggled to confirm the cardioprotective and anti-aging effects of GDF11, the topic has grown increasingly controversial, and the field has reached an impasse. We postulated that a clearer understanding of GDF11 could be gained by investigating its health effects at the population level. METHODS AND

resultsWe employed a comprehensive strategy to interrogate results from genome-wide association studies in population Biobanks. Interestingly, phenome-wide association studies (PheWAS) of GDF11 tissue-specific cis-eQTLs revealed associations with asthma, immune function, lung function, and thyroid phenotypes. Furthermore, PheWAS of GDF11 genetic variants confirmed these results, revealing similar associations with asthma, immune function, lung function, and thyroid health. To complement these findings, we mined results from transcriptome-wide association studies, which uncovered associations between predicted tissue-specific GDF11 expression and the same health effects identified from PheWAS analyses.

conclusionsIn this study, we report novel relationships between GDF11 and disease, namely asthma and hypothyroidism, in contrast to its formerly assumed role as a rejuvenating factor in basic aging and cardiovascular health. We propose that these associations are mediated through the involvement of GDF11 in inflammatory signaling pathways. Taken together, these findings provide new insights into the health effects of GDF11 at the population level and warrant future studies investigating the role of GDF11 in these specific health conditions.

Indexed as

Biological Specimen BanksBone Morphogenetic ProteinsGenome-Wide Association StudyGrowth Differentiation FactorsGenetic PleiotropyHumansPhenotypePolymorphism, Single NucleotideQuantitative Trait LociBone Morphogenetic ProteinsGDF11 protein, humanGrowth Differentiation FactorsAsthmaGrowth differentiation factor 11PheWAS

Identifiers

PMID39237910
PMCPMC11378601

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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 Socratic graph.