4.6 Article

Four Novel Loci (19q13, 6q24, 12q24, and 5q14) Influence the Microcirculation In Vivo

Journal

PLOS GENETICS
Volume 6, Issue 10, Pages -

Publisher

PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pgen.1001184

Keywords

-

Funding

  1. National Institute on Aging [Z01AG007380]
  2. NIH [N01-AG-12100, Z01EY000426]
  3. National Eye Institute [Z01EY000401]
  4. Althingi (the Icelandic Parliament)
  5. National Heart, Lung, and Blood Institute [N01-HC-55015, N01-HC-55016, N01-HC-55018, N01-HC-55019, N01-HC-55020, N01-HC-55021, N01-HC-55022, R01HL087641, N01-HC-85079, N01-HC-85086, N01-HC-35129, N01 HC-15103, N01 HC-55222, N01-HC-75150, N01-HC-45133, U01 HL080295, R01 HL087652, T32HL007902]
  6. National Human Genome Research Institute [U01HG004402]
  7. National Institutes of Health [HHSN268200625226C, UL1RR025005]
  8. National Center for Research Resources [M01RR00069]
  9. National Institute of Diabetes and Digestive and Kidney Diseases [DK063491]
  10. Netherlands Genomics Initiative (NGI)/Netherlands Organisation for Scientific Research (NWO) [050-060-810]
  11. Erasmus Medical Center
  12. Erasmus University, Rotterdam
  13. Netherlands Organization for scientific research (NWO)
  14. Netherlands Organization for the Health Research and Development (ZonMw)
  15. Research Institute for Diseases in the Elderly (RIDE)
  16. Ministry of Education, Culture, and Science
  17. Ministry for Health, Welfare, and Sports
  18. European commission
  19. Municipality of Rotterdam
  20. Australian National Health and Medical Research Council (NHMRC)
  21. MRC [G0801056, MC_UP_A100_1003, G0701863, MC_U105630924] Funding Source: UKRI
  22. Medical Research Council [MC_UP_A100_1003, G0801056, MC_U105630924, G0701863, G0801056B, G0401527] Funding Source: researchfish

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There is increasing evidence that the microcirculation plays an important role in the pathogenesis of cardiovascular diseases. Changes in retinal vascular caliber reflect early microvascular disease and predict incident cardiovascular events. We performed a genome-wide association study to identify genetic variants associated with retinal vascular caliber. We analyzed data from four population-based discovery cohorts with 15,358 unrelated Caucasian individuals, who are members of the Cohort for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium, and replicated findings in four independent Caucasian cohorts (n = 6,652). All participants had retinal photography and retinal arteriolar and venular caliber measured from computer software. In the discovery cohorts, 179 single nucleotide polymorphisms (SNP) spread across five loci were significantly associated (p<5.0x10(-8)) with retinal venular caliber, but none showed association with arteriolar caliber. Collectively, these five loci explain 1.0%-3.2% of the variation in retinal venular caliber. Four out of these five loci were confirmed in independent replication samples. In the combined analyses, the top SNPs at each locus were: rs2287921 (19q13; p = 1.61x10(-25), within the RASIP1 locus), rs225717 (6q24; p = 1.25x10(-16), adjacent to the VTA1 and NMBR loci), rs10774625 (12q24; p = 2.15x10(-13), in the region of ATXN2, SH2B3 and PTPN11 loci), and rs17421627 (5q14; p = 7.32x10(-16), adjacent to the MEF2C locus). In two independent samples, locus 12q24 was also associated with coronary heart disease and hypertension. Our population-based genome-wide association study demonstrates four novel loci associated with retinal venular caliber, an endophenotype of the microcirculation associated with clinical cardiovascular disease. These data provide further insights into the contribution and biological mechanisms of microcirculatory changes that underlie cardiovascular disease.

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