4.5 Article

Lipoprotein-associated phospholipase A2 activity, genetics and calcific aortic valve stenosis in humans

Journal

HEART
Volume 106, Issue 18, Pages 1407-1412

Publisher

BMJ PUBLISHING GROUP
DOI: 10.1136/heartjnl-2020-316722

Keywords

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Funding

  1. Fondation de l'IUCPQ
  2. Canadian Institutes of Health Research (CIHR) [FRN149068, FRN155226, MOP102481, MOP137058]
  3. Heart and Stroke Foundation of Canada [PJT153396]
  4. Assistance Publique -Hopitaux de Paris
  5. Fonds de recherche du Quebec: Sante (FRQS)
  6. FRQS Research Chair on the Pathobiology of Calcific Aortic Valve Disease
  7. Canadian Institutes of Health Research [FRN148778, FRN159697]
  8. Canada Research Chair in Valvular Heart Disease
  9. Foundation Scheme Grant from CIHR
  10. Canada Research Chair in Genomics of Heart and Lung Diseases
  11. ANR
  12. FRM grant [13-BSV6-0011, DCV20070409278]
  13. Federation Francaise de Cardiologie
  14. Fondation Coeur et Recherche
  15. Inserm Translational Research grant
  16. 'Connect Talent' research chair from Region Pays de la Loire
  17. Swedish Heart-Lung Foundation [2016-0134, 2016-0315]
  18. Swedish Research Council [2017-02554, 349-2006-237, 2009-1039]
  19. European Research Council [ERC-S TG-2015-679242]
  20. Crafoord Foundation
  21. Skane University Hospital
  22. Scania County
  23. governmental funding of clinical research within the Swedish National Health Service
  24. Swedish Foundation for Strategic Research [IRC15-0067]
  25. NIH/NHLBI [R01 HL128550]
  26. Nantes Metropole
  27. MRC [MC_UU_12015/1] Funding Source: UKRI

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Background Lipoprotein-associated phospholipase A2 (Lp-PLA2) activity has been shown to predict calcific aortic valve stenosis (CAVS) outcomes. Our objective was to test the association between plasma Lp-PLA2 activity and genetically elevated Lp-PLA2 mass/activity with CAVS in humans. Methods and results Lp-PLA2 activity was measured in 890 patients undergoing cardiac surgery, including 476 patients undergoing aortic valve replacement for CAVS and 414 control patients undergoing coronary artery bypass grafting. After multivariable adjustment, Lp-PLA2 activity was positively associated with the presence of CAVS (OR=1.21 (95% CI 1.04 to 1.41) per SD increment). We selected four single nucleotide polymorphisms (SNPs) at the PLA2G7 locus associated with either Lp-PLA2 mass or activity (rs7756935, rs1421368, rs1805017 and rs4498351). Genetic association studies were performed in eight cohorts: Quebec-CA VS (1009 cases/1017 controls), UK Biobank (1350 cases/349 043 controls), European Prospective Investigation into Cancer and Nutrition-N orfolk (504 cases/20 307 controls), Genetic Epidemiology Research on Aging (3469 cases/51 723 controls), Malmo Diet and Cancer Study (682 cases/5963 controls) and three French cohorts (3123 cases/6532 controls), totalling 10 137 CAVS cases and 434 585 controls. A fixed-effect meta-analysis using the inverse-variance weighted method revealed that none of the four SNPs was associated with CAVS (OR=0.99 (95% CI 0.96 to 1.02, p=0.55) for rs7756935, 0.97 (95% CI 0.93 to 1.01, p=0.11) for rs1421368, 1.00 (95% CI 1.00 to 1.01, p=0.29) for rs1805017, and 1.00 (95% CI 0.97 to 1.04, p=0.87) for rs4498351). Conclusions Higher Lp-PLA2 activity is significantly associated with the presence of CAVS and might represent a biomarker of CAVS in patients with heart disease. Results of our genetic association study suggest that Lp-PLA2 is however unlikely to represent a causal risk factor or therapeutic target for CAVS.

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