학술논문

Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals
Document Type
article
Author
Eicher, John DChami, NathalieKacprowski, TimNomura, AkihiroChen, Ming-HueiYanek, Lisa RTajuddin, Salman MSchick, Ursula MSlater, Andrew JPankratz, NathanPolfus, LindaSchurmann, ClaudiaGiri, AyushBrody, Jennifer ALange, Leslie AManichaikul, AniHill, W DavidPazoki, RahaElliot, PaulEvangelou, EvangelosTzoulaki, IoannaGao, HeVergnaud, Anne-ClaireMathias, Rasika ABecker, Diane MBecker, Lewis CBurt, AmberCrosslin, David RLyytikäinen, Leo-PekkaNikus, KjellHernesniemi, JussiKähönen, MikaRaitoharju, EmmaMononen, NinaRaitakari, Olli TLehtimäki, TerhoCushman, MaryZakai, Neil ANickerson, Deborah ARaffield, Laura MQuarells, RakaleWiller, Cristen JPeloso, Gina MAbecasis, Goncalo RLiu, Dajiang JConsortium, Global Lipids GeneticsDeloukas, PanosSamani, Nilesh JSchunkert, HeribertErdmann, JeanetteConsortium, CARDIoGRAM ExomeConsortium, Myocardial Infarction GeneticsFornage, MyriamRichard, MelissaTardif, Jean-ClaudeRioux, John DDube, Marie-Pierrede Denus, SimonLu, YingchangBottinger, Erwin PLoos, Ruth JFSmith, Albert VernonHarris, Tamara BLauner, Lenore JGudnason, VilmundurEdwards, Digna R VelezTorstenson, Eric SLiu, YongmeiTracy, Russell PRotter, Jerome IRich, Stephen SHighland, Heather MBoerwinkle, EricLi, JinLange, EthanWilson, James GMihailov, EvelinMägi, ReedikHirschhorn, JoelMetspalu, AndresEsko, TõnuVacchi-Suzzi, CaterinaNalls, Mike AZonderman, Alan BEvans, Michele KEngström, GunnarOrho-Melander, MarjuMelander, OlleO’Donoghue, Michelle LWaterworth, Dawn MWallentin, LarsWhite, Harvey DFloyd, James SBartz, Traci MRice, Kenneth MPsaty, Bruce MStarr, JMLiewald, David CMHayward, CarolineDeary, Ian J
Source
American Journal of Human Genetics. 99(1)
Subject
Genetics
Cardiovascular
Hematology
1.1 Normal biological development and functioning
Underpinning research
Blood
Blood Platelets
Exome
Female
Genetic Variation
Genome-Wide Association Study
Humans
Male
Mean Platelet Volume
Platelet Count
Global Lipids Genetics Consortium
CARDIoGRAM Exome Consortium
Myocardial Infarction Genetics Consortium
Biological Sciences
Medical and Health Sciences
Genetics & Heredity
Language
Abstract
Platelet production, maintenance, and clearance are tightly controlled processes indicative of platelets' important roles in hemostasis and thrombosis. Platelets are common targets for primary and secondary prevention of several conditions. They are monitored clinically by complete blood counts, specifically with measurements of platelet count (PLT) and mean platelet volume (MPV). Identifying genetic effects on PLT and MPV can provide mechanistic insights into platelet biology and their role in disease. Therefore, we formed the Blood Cell Consortium (BCX) to perform a large-scale meta-analysis of Exomechip association results for PLT and MPV in 157,293 and 57,617 individuals, respectively. Using the low-frequency/rare coding variant-enriched Exomechip genotyping array, we sought to identify genetic variants associated with PLT and MPV. In addition to confirming 47 known PLT and 20 known MPV associations, we identified 32 PLT and 18 MPV associations not previously observed in the literature across the allele frequency spectrum, including rare large effect (FCER1A), low-frequency (IQGAP2, MAP1A, LY75), and common (ZMIZ2, SMG6, PEAR1, ARFGAP3/PACSIN2) variants. Several variants associated with PLT/MPV (PEAR1, MRVI1, PTGES3) were also associated with platelet reactivity. In concurrent BCX analyses, there was overlap of platelet-associated variants with red (MAP1A, TMPRSS6, ZMIZ2) and white (PEAR1, ZMIZ2, LY75) blood cell traits, suggesting common regulatory pathways with shared genetic architecture among these hematopoietic lineages. Our large-scale Exomechip analyses identified previously undocumented associations with platelet traits and further indicate that several complex quantitative hematological, lipid, and cardiovascular traits share genetic factors.