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A Meta-Analysis and Genome-Wide Association Study of Platelet Count and Mean Platelet Volume in African Americans
Several genetic variants associated with platelet count and mean platelet volume (MPV) were recently reported in people of European ancestry. In this meta-analysis of 7 genome-wide association studies (GWAS) enrolling African Americans, our aim was to identify novel genetic variants associated with platelet count and MPV. For all cohorts, GWAS analysis was performed using additive models after adjusting for age, sex, and population stratification. For both platelet phenotypes, meta-analyses were conducted using inverse-variance weighted fixed-effect models. Platelet aggregation assays in whole blood were performed in the participants of the GeneSTAR cohort. Genetic variants in ten independent regions were associated with platelet count (N = 16,388) with p<5×10−8 of which 5 have not been associated with platelet count in previous GWAS. The novel genetic variants associated with platelet count were in the following regions (the most significant SNP, closest gene, and p-value): 6p22 (rs12526480, LRRC16A, p = 9.1×10−9), 7q11 (rs13236689, CD36, p = 2.8×10−9), 10q21 (rs7896518, JMJD1C, p = 2.3×10−12), 11q13 (rs477895, BAD, p = 4.9×10−8), and 20q13 (rs151361, SLMO2, p = 9.4×10−9). Three of these loci (10q21, 11q13, and 20q13) were replicated in European Americans (N = 14,909) and one (11q13) in Hispanic Americans (N = 3,462). For MPV (N = 4,531), genetic variants in 3 regions were significant at p<5×10−8, two of which were also associated with platelet count. Previously reported regions that were also significant in this study were 6p21, 6q23, 7q22, 12q24, and 19p13 for platelet count and 7q22, 17q11, and 19p13 for MPV. The most significant SNP in 1 region was also associated with ADP-induced maximal platelet aggregation in whole blood (12q24). Thus through a meta-analysis of GWAS enrolling African Americans, we have identified 5 novel regions associated with platelet count of which 3 were replicated in other ethnic groups. In addition, we also found one region associated with platelet aggregation that may play a potential role in atherothrombosis.
Vyšlo v časopise: A Meta-Analysis and Genome-Wide Association Study of Platelet Count and Mean Platelet Volume in African Americans. PLoS Genet 8(3): e32767. doi:10.1371/journal.pgen.1002491
Kategorie: Research Article
prolekare.web.journal.doi_sk: https://doi.org/10.1371/journal.pgen.1002491Souhrn
Several genetic variants associated with platelet count and mean platelet volume (MPV) were recently reported in people of European ancestry. In this meta-analysis of 7 genome-wide association studies (GWAS) enrolling African Americans, our aim was to identify novel genetic variants associated with platelet count and MPV. For all cohorts, GWAS analysis was performed using additive models after adjusting for age, sex, and population stratification. For both platelet phenotypes, meta-analyses were conducted using inverse-variance weighted fixed-effect models. Platelet aggregation assays in whole blood were performed in the participants of the GeneSTAR cohort. Genetic variants in ten independent regions were associated with platelet count (N = 16,388) with p<5×10−8 of which 5 have not been associated with platelet count in previous GWAS. The novel genetic variants associated with platelet count were in the following regions (the most significant SNP, closest gene, and p-value): 6p22 (rs12526480, LRRC16A, p = 9.1×10−9), 7q11 (rs13236689, CD36, p = 2.8×10−9), 10q21 (rs7896518, JMJD1C, p = 2.3×10−12), 11q13 (rs477895, BAD, p = 4.9×10−8), and 20q13 (rs151361, SLMO2, p = 9.4×10−9). Three of these loci (10q21, 11q13, and 20q13) were replicated in European Americans (N = 14,909) and one (11q13) in Hispanic Americans (N = 3,462). For MPV (N = 4,531), genetic variants in 3 regions were significant at p<5×10−8, two of which were also associated with platelet count. Previously reported regions that were also significant in this study were 6p21, 6q23, 7q22, 12q24, and 19p13 for platelet count and 7q22, 17q11, and 19p13 for MPV. The most significant SNP in 1 region was also associated with ADP-induced maximal platelet aggregation in whole blood (12q24). Thus through a meta-analysis of GWAS enrolling African Americans, we have identified 5 novel regions associated with platelet count of which 3 were replicated in other ethnic groups. In addition, we also found one region associated with platelet aggregation that may play a potential role in atherothrombosis.
Zdroje
1. DaviGPatronoC 2007 Platelet activation and atherothrombosis. N Engl J Med 357 2482 2494
2. NikolskyEGrinesCLCoxDAGarciaETchengJE 2007 Impact of baseline platelet count in patients undergoing primary percutaneous coronary intervention in acute myocardial infarction (from the CADILLAC trial). Am J Cardiol 99 1055 1061
3. TurakhiaMPMurphySAPintoTLAntmanEMGiuglianoRP 2004 Association of platelet count with residual thrombus in the myocardial infarct-related coronary artery among patients treated with fibrinolytic therapy for ST-segment elevation acute myocardial infarction. Am J Cardiol 94 1406 1410
4. TuckerEIMarzecUMBernyMAHurstSBuntingS 2010 Safety and antithrombotic efficacy of moderate platelet count reduction by thrombopoietin inhibition in primates. Sci Transl Med 2 37ra45
5. BiinoGBalduiniCLCasulaLCavalloPVaccargiuS 2011 Analysis of 12,517 inhabitants of a Sardinian geographic isolate reveals that predispositions to thrombocytopenia and thrombocytosis are inherited traits. Haematologica 96 96 101
6. BuckleyMFJamesJWBrownDEWhyteGSDeanMG 2000 A novel approach to the assessment of variations in the human platelet count. Thromb Haemost 83 480 484
7. EvansDMFrazerIHMartinNG 1999 Genetic and environmental causes of variation in basal levels of blood cells. Twin Res 2 250 257
8. TragliaMSalaCMasciulloCCverhovaVLoriF 2009 Heritability and demographic analyses in the large isolated population of Val Borbera suggest advantages in mapping complex traits genes. PLoS One 4 e7554
9. BrayPFMathiasRAFaradayNYanekLRFallinMD 2007 Heritability of platelet function in families with premature coronary artery disease. J Thromb Haemost 5 1617 1623
10. ChuSGBeckerRCBergerPBBhattDLEikelboomJW 2010 Mean platelet volume as a predictor of cardiovascular risk: a systematic review and meta-analysis. J Thromb Haemost 8 148 156
11. GoncalvesSCLabinazMLe MayMGloverCFroeschlM 2011 Usefulness of mean platelet volume as a biomarker for long-term outcomes after percutaneous coronary intervention. Am J Cardiol 107 204 209
12. KlovaiteJBennMYazdanyarSNordestgaardBG 2011 High platelet volume and increased risk of myocardial infarction: 39 531 participants from the general population. J Thromb Haemost 9 49 56
13. KamataniYMatsudaKOkadaYKuboMHosonoN 2010 Genome-wide association study of hematological and biochemical traits in a Japanese population. Nat Genet 42 210 215
14. MeisingerCProkischHGiegerCSoranzoNMehtaD 2009 A genome-wide association study identifies three loci associated with mean platelet volume. Am J Hum Genet 84 66 71
15. SoranzoNSpectorTDManginoMKuhnelBRendonA 2009 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. Nat Genet 41 1182 1190
16. LoKSWilsonJGLangeLAFolsomARGalarneauG 2011 Genetic association analysis highlights new loci that modulate hematological trait variation in Caucasians and African Americans. Hum Genet 129 307 317
17. SegalJBMoliternoAR 2006 Platelet counts differ by sex, ethnicity, and age in the United States. Ann Epidemiol 16 123 130
18. CastoAMFeldmanMW 2011 Genome-wide association study SNPs in the human genome diversity project populations: does selection affect unlinked SNPs with shared trait associations? PLoS Genet 7 e1001266
19. LettreGPalmerCDYoungTEjebeKGAllayeeH 2011 Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project. PLoS Genet 7 e1001300
20. KolzMJohnsonTSannaSTeumerAVitartV 2009 Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations. PLoS Genet 5 e1000504
21. ToreSCasulaSCasuGConcasMPPistiddaP 2011 Application of a new method for GWAS in a related case/control sample with known pedigree structure: identification of new loci for nephrolithiasis. PLoS Genet 7 e1001281
22. BenyaminBMcRaeAFZhuGGordonSHendersAK 2009 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. Am J Hum Genet 84 60 65
23. SilversteinRLFebbraioM 2009 CD36, a scavenger receptor involved in immunity, metabolism, angiogenesis, and behavior. Sci Signal 2 re3
24. GhoshAMurugesanGChenKZhangLWangQ 2011 Platelet CD36 surface expression levels affect functional responses to oxidized LDL and are associated with inheritance of specific genetic polymorphisms. Blood 117 6355 6366
25. JonesCIBraySGarnerSFStephensJde BonoB 2009 A functional genomics approach reveals novel quantitative trait loci associated with platelet signaling pathways. Blood 114 1405 1416
26. JohnsonADYanekLRChenMHFaradayNLarsonMG 2010 Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists. Nat Genet 42 608 613
27. DanialNN 2008 BAD: undertaker by night, candyman by day. Oncogene 27 Suppl 1 S53 70
28. LianLWangYDrazninJEslinDBennettJS 2005 The relative role of PLCbeta and PI3Kgamma in platelet activation. Blood 106 110 117
29. BugertPKluterH 2006 Profiling of gene transcripts in human platelets: an update of the platelet transcriptome. Platelets 17 503 504
30. ItalianoJEBergmeierWTiwariSFaletHHartwigJH 2003 Mechanisms and implications of platelet discoid shape. Blood 101 4789 4796
31. O'NeillEEBrockCJvon KriegsheimAFPearceACDwekRA 2002 Towards complete analysis of the platelet proteome. Proteomics 2 288 305
32. SoranzoNRendonAGiegerCJonesCIWatkinsNA 2009 A novel variant on chromosome 7q22.3 associated with mean platelet volume, counts, and function. Blood 113 3831 3837
33. ItalianoJEHartwigJH 2007 Megakaryocyte Development and Platelet Formation. MichelsonAD Boston Elsevier 27 34
34. YangCPringMWearMAHuangMCooperJA 2005 Mammalian CARMIL inhibits actin filament capping by capping protein. Dev Cell 9 209 221
35. WatkinsNAGusnantoAde BonoBDeSMiranda-SaavedraD 2009 A HaemAtlas: characterizing gene expression in differentiated human blood cells. Blood 113 e1 9
36. RaslovaHKauffmannASekkaiDRipocheHLarbretF 2007 Interrelation between polyploidization and megakaryocyte differentiation: a gene profiling approach. Blood 109 3225 3234
37. UrunoTRemmertKHammerJA3rd 2006 CARMIL is a potent capping protein antagonist: identification of a conserved CARMIL domain that inhibits the activity of capping protein and uncaps capped actin filaments. J Biol Chem 281 10635 10650
38. LimCKHwangWYAwSESunL 2008 Study of gene expression profile during cord blood-associated megakaryopoiesis. Eur J Haematol 81 196 208
39. De BottonSSabriSDaugasEZermatiYGuidottiJE 2002 Platelet formation is the consequence of caspase activation within megakaryocytes. Blood 100 1310 1317
40. MasonKDCarpinelliMRFletcherJICollingeJEHiltonAA 2007 Programmed anuclear cell death delimits platelet life span. Cell 128 1173 1186
41. KimSMKimJYChoeNWChoIHKimJR 2010 Regulation of mouse steroidogenesis by WHISTLE and JMJD1C through histone methylation balance. Nucleic Acids Res 38 6389 6403
42. ChasmanDIPareGMoraSHopewellJCPelosoG 2009 Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis. PLoS Genet 5 e1000730
43. WolfSSPatchevVKObendorfM 2007 A novel variant of the putative demethylase gene, s-JMJD1C, is a coactivator of the AR. Arch Biochem Biophys 460 56 66
44. YuanXWaterworthDPerryJRLimNSongK 2008 Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes. Am J Hum Genet 83 520 528
45. KomorMGullerSBaldusCDde VosSHoelzerD 2005 Transcriptional profiling of human hematopoiesis during in vitro lineage-specific differentiation. Stem Cells 23 1154 1169
46. GunningPO'NeillGHardemanE 2008 Tropomyosin-based regulation of the actin cytoskeleton in time and space. Physiol Rev 88 1 35
47. KunishimaSKobayashiRItohTJHamaguchiMSaitoH 2009 Mutation of the beta1-tubulin gene associated with congenital macrothrombocytopenia affecting microtubule assembly. Blood 113 458 461
48. Navarro-NunezLLozanoMLRiveraJCorralJRoldanV 2007 The association of the beta1-tubulin Q43P polymorphism with intracerebral hemorrhage in men. Haematologica 92 513 518
49. FerreiraMAHottengaJJWarringtonNMMedlandSEWillemsenG 2009 Sequence variants in three loci influence monocyte counts and erythrocyte volume. American Journal of Human Genetics 85 745 749
50. BisJCKavousiMFranceschiniNIsaacsAAbecasisGR 2011 Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque. Nat Genet 43 940 947
51. WainLVVerwoertGCO'ReillyPFShiGJohnsonT 2011 Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure. Nat Genet 43 1005 1011
52. DraviamVMStegmeierFNalepaGSowaMEChenJ 2007 A functional genomic screen identifies a role for TAO1 kinase in spindle-checkpoint signalling. Nat Cell Biol 9 556 564
53. WuMFWangSG 2008 Human TAO kinase 1 induces apoptosis in SH-SY5Y cells. Cell Biol Int 32 151 156
54. FolsomARRosamondWDShaharECooperLSAleksicN 1999 Prospective study of markers of hemostatic function with risk of ischemic stroke. The Atherosclerosis Risk in Communities (ARIC) Study Investigators. Circulation 100 736 742
55. MargolisKLMansonJEGreenlandPRodaboughRJBrayPF 2005 Leukocyte count as a predictor of cardiovascular events and mortality in postmenopausal women: the Women's Health Initiative Observational Study. Arch Intern Med 165 500 508
56. NallsMAWilsonJGPattersonNJTandonAZmudaJM 2008 Admixture mapping of white cell count: genetic locus responsible for lower white blood cell count in the Health ABC and Jackson Heart studies. Am J Hum Genet 82 81 87
57. QayyumRBeckerDMYanekLRMoyTFBeckerLC 2008 Platelet inhibition by aspirin 81 and 325 mg/day in men versus women without clinically apparent cardiovascular disease. Am J Cardiol 101 1359 1363
58. ShimakawaTBildDE 1993 Relationship between hemoglobin and cardiovascular risk factors in young adults. J Clin Epidemiol 46 1257 1266
59. JenningsLKWhiteMM 2007 Platelet Aggregation. MichelsonAD Platelets. 2nd ed Boston Elsevier 495 507
60. HarkerLASlichterSJ 1972 The bleeding time as a screening test for evaluation of platelet function. N Engl J Med 287 155 159
61. LiYWillerCJDingJScheetPAbecasisGR 2010 MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes. Genet Epidemiol 34 816 834
62. PurcellSNealeBTodd-BrownKThomasLFerreiraMA 2007 PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet 81 559 575
63. ChenMHYangQ 2010 GWAF: an R package for genome-wide association analyses with family data. Bioinformatics 26 580 581
64. WillerCJLiYAbecasisGR 2010 METAL: fast and efficient meta-analysis of genomewide association scans. Bioinformatics 26 2190 2191
65. MagiRLindgrenCMMorrisAP 2010 Meta-analysis of sex-specific genome-wide association studies. Genet Epidemiol 34 846 853
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