4.3 Article

Soluble Urokinase Plasminogen Activator Receptor: Genetic Variation and Cardiovascular Disease Risk in Black Adults

期刊

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1161/CIRCGEN.121.003421

关键词

biomarkers; cardiovascular diseases; epidemiologic studies; genome-wide association study; receptors; urokinase plasminogen activator

资金

  1. National Heart, Lung, and Blood Institute (NHLBI) [R01HL132947]
  2. National Center for Advancing Translational Sciences (NCATS) [KL2TR002490]
  3. Jackson State University [HHSN268201800013I]
  4. Tougaloo College [HHSN268201800014I]
  5. Mississippi State Department of Health [HHSN268201800015I]
  6. University of Mississippi Medical Center from the NHLBI [HHSN268201800010I, HHSN268201800011I, HHSN268201800012I]
  7. National Institute for Minority Health and Health Disparities (NIMHD)
  8. Northwest Genomics Center [HHSN268201100037C]
  9. TOPMed Informatics Research Center [3R01HL-117626-02S1, HHSN268201800002I]
  10. TOPMed Data Coordinating Center [R01HL-120393, U01HL-120393, HHSN268201800001I]
  11. NIH [S10OD017985, S10RR025141]
  12. CTSA grants from National Center for Advancing Translational Sciences [UL1TR002243, UL1TR000445, UL1RR024975]
  13. NHLBI
  14. [T32 HL129982]
  15. [R00HL129045]
  16. [R01DK072193]
  17. [T32 HG008341]
  18. [R01-MD012765]
  19. [R01 DK117445-01A1]
  20. [R01-HL132947]
  21. [U01HG004798]
  22. [R01NS032830]
  23. [RC2GM092618]
  24. [P50GM115305]
  25. [U01HG006378]
  26. [U19HL065962]
  27. [R01HD074711]

向作者/读者索取更多资源

The study found that suPAR levels are associated with cardiovascular disease risk in Black adults, and certain genetic variants can influence suPAR levels. Genetic factors play an important role in determining suPAR levels.
Background: suPAR (Soluble urokinase plasminogen activator receptor) has emerged as an important biomarker of coagulation, inflammation, and cardiovascular disease (CVD) risk. The contribution of suPAR to CVD risk and its genetic influence in Black populations have not been evaluated. Methods: We measured suPAR in 3492 Black adults from the prospective, community-based JHS (Jackson Heart Study). Cross-sectional associations of suPAR with lifestyle and CVD risk factors were assessed, whole-genome sequence data were used to evaluate genetic associations of suPAR, and relationships of suPAR with incident CVD outcomes and overall mortality were estimated over follow-up. Results: In Cox models adjusted for traditional CVD risk factors, estimated glomerular filtration rate, and CRP (C-reactive protein), each 1-SD higher suPAR was associated with a 21% to 31% increased risk of incident coronary heart disease, heart failure, stroke, and mortality. In the genome-wide association study, 2 missense (rs399145 encoding p.Thr86Ala, rs4760 encoding p.Phe272Leu) and 2 noncoding regulatory variants (rs73935023 within an enhancer element and rs4251805 within the promoter) of PLAUR on chromosome 19 were each independently associated with suPAR and together explained 14% of suPAR phenotypic variation. The allele frequencies of each of the four suPAR-associated genetic variants differ considerably across African and European populations. We further show that PLAUR rs73935023 can alter transcriptional activity in vitro. We did not find any association between genetically determined suPAR and CVD in JHS or a larger electronic medical record-based analyses of Blacks or Whites. Conclusions: Our results demonstrate the importance of ancestry-differentiated genetic variation on suPAR levels and indicate suPAR is a CVD biomarker in Black adults.

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