Genome-wide association studies and fine-mapping identify genomic loci for n-3 and n-6 polyunsaturated fatty acids in Hispanic American and African American cohorts
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Author
Yang, C.Veenstra, J.
Bartz, T.M.
Pahl, M.C.
Hallmark, B.
Chen, Y.-D.I.
Westra, J.
Steffen, L.M.
Brown, C.D.
Siscovick, D.
Tsai, M.Y.
Wood, A.C.
Rich, S.S.
Smith, C.E.
O’Connor, T.D.
Mozaffarian, D.
Grant, S.F.A.
Chilton, F.H.
Tintle, N.L.
Lemaitre, R.N.
Manichaikul, A.
Affiliation
Center for Biomedical Informatics and Biostatistics, University of ArizonaIssue Date
2023-08-16
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Nature ResearchCitation
Yang, C., Veenstra, J., Bartz, T.M. et al. Genome-wide association studies and fine-mapping identify genomic loci for n-3 and n-6 polyunsaturated fatty acids in Hispanic American and African American cohorts. Commun Biol 6, 852 (2023). https://doi.org/10.1038/s42003-023-05219-wJournal
Communications BiologyRights
© The Author(s) 2023. This article is licensed under a Creative Commons Attribution 4.0 International License.Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
Omega-3 (n-3) and omega-6 (n-6) polyunsaturated fatty acids (PUFAs) play critical roles in human health. Prior genome-wide association studies (GWAS) of n-3 and n-6 PUFAs in European Americans from the CHARGE Consortium have documented strong genetic signals in/near the FADS locus on chromosome 11. We performed a GWAS of four n-3 and four n-6 PUFAs in Hispanic American (n = 1454) and African American (n = 2278) participants from three CHARGE cohorts. Applying a genome-wide significance threshold of P < 5 × 10−8, we confirmed association of the FADS signal and found evidence of two additional signals (in DAGLA and BEST1) within 200 kb of the originally reported FADS signal. Outside of the FADS region, we identified novel signals for arachidonic acid (AA) in Hispanic Americans located in/near genes including TMX2, SLC29A2, ANKRD13D and POLD4, and spanning a > 9 Mb region on chromosome 11 (57.5 Mb ~ 67.1 Mb). Among these novel signals, we found associations unique to Hispanic Americans, including rs28364240, a POLD4 missense variant for AA that is common in CHARGE Hispanic Americans but absent in other race/ancestry groups. Our study sheds light on the genetics of PUFAs and the value of investigating complex trait genetics across diverse ancestry populations. © 2023, Springer Nature Limited.Note
Open access journalISSN
2399-3642PubMed ID
37587153Version
Final Published Versionae974a485f413a2113503eed53cd6c53
10.1038/s42003-023-05219-w
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Except where otherwise noted, this item's license is described as © The Author(s) 2023. This article is licensed under a Creative Commons Attribution 4.0 International License.

