4.6 Article

Intracranial Aneurysm Risk Locus 5q23.2 Is Associated with Elevated Systolic Blood Pressure

Journal

PLOS GENETICS
Volume 8, Issue 3, Pages -

Publisher

PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pgen.1002563

Keywords

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Funding

  1. Orion-Farmos Research Foundation
  2. Academy of Finland [250207, 129494, 129322, 129287, 134839, 120315, 129255, 129907, 135072, 114382, 126775, 127437, 129306, 130326, 209072, 210595, 213225, 216374, 126925, 121584, 124282, 129378, 117797, 41071, 104781, 1114194]
  3. Finnish Foundation for Cardiovascular Research
  4. Sigrid Juselius Foundation
  5. Finnish Diabetes Research Society
  6. Samfundet Folkhalsan
  7. Juho Vainio Foundation
  8. Novo Nordisk Foundation
  9. Finska Lakaresallskapet
  10. Paivikki and Sakari Sohlberg Foundation
  11. Signe and Ane Gyllenberg Foundation
  12. Yrjo Jahnsson Foundation
  13. Social Insurance Institution of Finland
  14. Kuopio, Tampere, and Turku University
  15. Paavo Nurmi Foundation
  16. Finnish Foundation of Cardiovascular Research and Finnish Cultural Foundation
  17. Tampere Tuberculosis Foundation
  18. Emil Aaltonen Foundation
  19. University Hospital Oulu, Biocenter [5R01HL087679-02]
  20. University of Oulu, Finland, NHLBI [HEALTH-F4-2007-201413]
  21. Medical Research Council [G0500539, G0600705]
  22. Wellcome Trust, UK [GR069224]
  23. MRC [G0600705] Funding Source: UKRI
  24. Medical Research Council [G0600705, G0801056B] Funding Source: researchfish
  25. Academy of Finland (AKA) [213225, 134839, 210595, 114382, 129287, 216374, 129322, 209072, 213225, 134839, 129287, 216374, 129322, 210595, 114382, 209072] Funding Source: Academy of Finland (AKA)

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Although genome-wide association studies (GWAS) have identified hundreds of complex trait loci, the pathomechanisms of most remain elusive. Studying the genetics of risk factors predisposing to disease is an attractive approach to identify targets for functional studies. Intracranial aneurysms (IA) are rupture-prone pouches at cerebral artery branching sites. IA is a complex disease for which GWAS have identified five loci with strong association and a further 14 loci with suggestive association. To decipher potential underlying disease mechanisms, we tested whether there are IA loci that convey their effect through elevating blood pressure (BP), a strong risk factor of IA. We performed a meta-analysis of four population-based Finnish cohorts (n(FIN) = 11 266) not selected for IA, to assess the association of previously identified IA candidate loci (n = 19) with BP. We defined systolic BP (SBP), diastolic BP, mean arterial pressure, and pulse pressure as quantitative outcome variables. The most significant result was further tested for association in the ICBP-GWAS cohort of 200 000 individuals. We found that the suggestive IA locus at 5q23.2 in PRDM6 was significantly associated with SBP in individuals of European descent (p(FIN) = 3.01E-05, p(ICBP-GWAS) = 0.0007, p(ALL) = 8.13E-07). The risk allele of IA was associated with higher SBP. PRDM6 encodes a protein predominantly expressed in vascular smooth muscle cells. Our study connects a complex disease (IA) locus with a common risk factor for the disease (SBP). We hypothesize that common variants in PRDM6 can contribute to altered vascular wall structure, hence increasing SBP and predisposing to IA. True positive associations often fail to reach genome-wide significance in GWAS. Our findings show that analysis of traditional risk factors as intermediate phenotypes is an effective tool for deciphering hidden heritability. Further, we demonstrate that common disease loci identified in a population isolate may bear wider significance.

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