Identification of a novel proinsulin-associated SNP and demonstration that proinsulin is unlikely to be a causal factor in subclinical vascular remodelling using Mendelian randomisation

نویسندگان

  • Rona J. Strawbridge
  • Angela Silveira
  • Marcel den Hoed
  • Stefan Gustafsson
  • Jian'an Luan
  • Denis Rybin
  • Josée Dupuis
  • Ruifang Li-Gao
  • Maryam Kavousi
  • Abbas Dehghan
  • Kadri Haljas
  • Jari Lahti
  • Jesper R. Gådin
  • Alexandra Bäcklund
  • Ulf de Faire
  • Karl Gertow
  • Phillipe Giral
  • Anuj Goel
  • Steve E. Humphries
  • Sudhir Kurl
  • Claudia Langenberg
  • Lars L. Lannfelt
  • Lars Lind
  • Cecilia C.M. Lindgren
  • Elmo Mannarino
  • Dennis O. Mook-Kanamori
  • Andrew P. Morris
  • Renée de Mutsert
  • Rainer Rauramaa
  • Peter Saliba-Gustafsson
  • Bengt Sennblad
  • Andries J. Smit
  • Ann-Christine Syvänen
  • Elena Tremoli
  • Fabrizio Veglia
  • Björn Zethelius
  • Hanna M. Björck
  • Johan G. Eriksson
  • Albert Hofman
  • Oscar H. Franco
  • Hugh Watkins
  • J. Wouter Jukema
  • Jose C. Florez
  • Nicholas J. Wareham
  • James B. Meigs
  • Erik Ingelsson
  • Damiano Baldassarre
  • Anders Hamsten
چکیده

BACKGROUND AND AIMS Increased proinsulin relative to insulin levels have been associated with subclinical atherosclerosis (measured by carotid intima-media thickness (cIMT)) and are predictive of future cardiovascular disease (CVD), independently of established risk factors. The mechanisms linking proinsulin to atherosclerosis and CVD are unclear. A genome-wide meta-analysis has identified nine loci associated with circulating proinsulin levels. Using proinsulin-associated SNPs, we set out to use a Mendelian randomisation approach to test the hypothesis that proinsulin plays a causal role in subclinical vascular remodelling. METHODS We studied the high CVD-risk IMPROVE cohort (n = 3345), which has detailed biochemical phenotyping and repeated, state-of-the-art, high-resolution carotid ultrasound examinations. Genotyping was performed using Illumina Cardio-Metabo and Immuno arrays, which include reported proinsulin-associated loci. Participants with type 2 diabetes (n = 904) were omitted from the analysis. Linear regression was used to identify proinsulin-associated genetic variants. RESULTS We identified a proinsulin locus on chromosome 15 (rs8029765) and replicated it in data from 20,003 additional individuals. An 11-SNP score, including the previously identified and the chromosome 15 proinsulin-associated loci, was significantly and negatively associated with baseline IMTmean and IMTmax (the primary cIMT phenotypes) but not with progression measures. However, MR-Eggers refuted any significant effect of the proinsulin-associated 11-SNP score, and a non-pleiotropic SNP score of three variants (including rs8029765) demonstrated no effect on baseline or progression cIMT measures. CONCLUSIONS We identified a novel proinsulin-associated locus and demonstrated that whilst proinsulin levels are associated with cIMT measures, proinsulin per se is unlikely to have a causative effect on cIMT.

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عنوان ژورنال:

دوره 266  شماره 

صفحات  -

تاریخ انتشار 2017