Genome-Wide Association Studies and fine-mapping of genomic loci for n-3 and n-6 Polyunsaturated Fatty Acids in Hispanic American and African American Cohorts

Author:

Yang Chaojie1ORCID,Veenstra Jenna2,Bartz Traci3,Pahl Matthew4,Hallmark Brian5ORCID,Chen Yii-Der Ida6,Westra Jason2,Steffen Lyn7,Brown Christopher8,Siscovick David9,Tsai Michael10,Wood Alexis11,Rich Stephen1ORCID,Smith Caren12,O'Connor Timothy13ORCID,Mozaffarian Dariush12ORCID,Grant Struan14ORCID,Chilton Floyd5,Tintle Nathan15ORCID,Lemaitre Rozenn16ORCID,Manichaikul Ani17ORCID

Affiliation:

1. University of Virginia

2. Dordt University

3. University of Washington

4. Children's Hospital of Philadelphia

5. University of Arizona

6. Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center

7. University of Mineesota

8. Perelman School of Medicine, University of Pennsylvania

9. 42. The New York Academy of Medicine, New York, NY

10. University of Minneosta

11. Baylor College of Medicine

12. Tufts University

13. University of Maryland, Baltimore

14. Children's Hospital of Philadelphia Research Institute

15. Fatty Acid Research Institute

16. Cardiovascular Health Research Unit, University of Washington

17. University of Virginia School of Medicine

Abstract

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 x 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 (57.5Mb ~ 67.1Mb). 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.

Publisher

Research Square Platform LLC

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