#PAGE_PARAMS# #ADS_HEAD_SCRIPTS# #MICRODATA#

Large-Scale Gene-Centric Analysis Identifies Novel Variants for Coronary Artery Disease


Coronary artery disease (CAD) has a significant genetic contribution that is incompletely characterized. To complement genome-wide association (GWA) studies, we conducted a large and systematic candidate gene study of CAD susceptibility, including analysis of many uncommon and functional variants. We examined 49,094 genetic variants in ∼2,100 genes of cardiovascular relevance, using a customised gene array in 15,596 CAD cases and 34,992 controls (11,202 cases and 30,733 controls of European descent; 4,394 cases and 4,259 controls of South Asian origin). We attempted to replicate putative novel associations in an additional 17,121 CAD cases and 40,473 controls. Potential mechanisms through which the novel variants could affect CAD risk were explored through association tests with vascular risk factors and gene expression. We confirmed associations of several previously known CAD susceptibility loci (eg, 9p21.3:p<10−33; LPA:p<10−19; 1p13.3:p<10−17) as well as three recently discovered loci (COL4A1/COL4A2, ZC3HC1, CYP17A1:p<5×10−7). However, we found essentially null results for most previously suggested CAD candidate genes. In our replication study of 24 promising common variants, we identified novel associations of variants in or near LIPA, IL5, TRIB1, and ABCG5/ABCG8, with per-allele odds ratios for CAD risk with each of the novel variants ranging from 1.06–1.09. Associations with variants at LIPA, TRIB1, and ABCG5/ABCG8 were supported by gene expression data or effects on lipid levels. Apart from the previously reported variants in LPA, none of the other ∼4,500 low frequency and functional variants showed a strong effect. Associations in South Asians did not differ appreciably from those in Europeans, except for 9p21.3 (per-allele odds ratio: 1.14 versus 1.27 respectively; P for heterogeneity = 0.003). This large-scale gene-centric analysis has identified several novel genes for CAD that relate to diverse biochemical and cellular functions and clarified the literature with regard to many previously suggested genes.


Vyšlo v časopise: Large-Scale Gene-Centric Analysis Identifies Novel Variants for Coronary Artery Disease. PLoS Genet 7(9): e32767. doi:10.1371/journal.pgen.1002260
Kategorie: Research Article
prolekare.web.journal.doi_sk: https://doi.org/10.1371/journal.pgen.1002260

Souhrn

Coronary artery disease (CAD) has a significant genetic contribution that is incompletely characterized. To complement genome-wide association (GWA) studies, we conducted a large and systematic candidate gene study of CAD susceptibility, including analysis of many uncommon and functional variants. We examined 49,094 genetic variants in ∼2,100 genes of cardiovascular relevance, using a customised gene array in 15,596 CAD cases and 34,992 controls (11,202 cases and 30,733 controls of European descent; 4,394 cases and 4,259 controls of South Asian origin). We attempted to replicate putative novel associations in an additional 17,121 CAD cases and 40,473 controls. Potential mechanisms through which the novel variants could affect CAD risk were explored through association tests with vascular risk factors and gene expression. We confirmed associations of several previously known CAD susceptibility loci (eg, 9p21.3:p<10−33; LPA:p<10−19; 1p13.3:p<10−17) as well as three recently discovered loci (COL4A1/COL4A2, ZC3HC1, CYP17A1:p<5×10−7). However, we found essentially null results for most previously suggested CAD candidate genes. In our replication study of 24 promising common variants, we identified novel associations of variants in or near LIPA, IL5, TRIB1, and ABCG5/ABCG8, with per-allele odds ratios for CAD risk with each of the novel variants ranging from 1.06–1.09. Associations with variants at LIPA, TRIB1, and ABCG5/ABCG8 were supported by gene expression data or effects on lipid levels. Apart from the previously reported variants in LPA, none of the other ∼4,500 low frequency and functional variants showed a strong effect. Associations in South Asians did not differ appreciably from those in Europeans, except for 9p21.3 (per-allele odds ratio: 1.14 versus 1.27 respectively; P for heterogeneity = 0.003). This large-scale gene-centric analysis has identified several novel genes for CAD that relate to diverse biochemical and cellular functions and clarified the literature with regard to many previously suggested genes.


Zdroje

1. Wellcome Trust Case Control Consortium 2007 Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature 447 661 678

2. SamaniNJErdmannJHallASHengstenbergCManginoM 2007 Genomewide association analysis of coronary artery disease. N Engl J Med 357 443 453

3. HelgadottirAThorleifssonGManolescuAGretarsdottirSBlondalT 2007 A common variant on chromosome 9p21 affects the risk of myocardial infarction. Science 316 1491 1493

4. McPhersonRPertsemlidisAKavaslarNStewartARobertsR 2007 A common allele on chromosome 9 associated with coronary heart disease. Science 316 1488 1491

5. KathiresanSVoightBFPurcellSMusunuruKArdissinoD 2009 Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. Nat Genet 41 334 341

6. ErdmannJGrosshennigABraundPSKönigIRHengstenbergC 2009 New susceptibility locus for coronary artery disease on chromosome 3q22.3. Nat Genet 41 280 282

7. TregouetDAKönigIRErdmannJMunteanuABraundPS 2009 Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease. Nat Genet 41 283 285

8. ErdmannJWillenborgCNahrstaedtJPreussMKönigIR 2011 Genome-wide association study identifies a new locus for coronary artery disease on chromosome 10p11.23. Eur Heart J 32 158 168

9. ReillyMPLiMHeJFergusonJFStylianouIM 2011 Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies. Lancet 377 383 392

10. KeatingBJTischfieldSMurraySSBhangaleTPriceTS 2008 Concept, design and implementation of a cardiovascular gene-centric 50 k SNP array for large-scale genomic association studies. PLoS ONE 3 e3583 doi:10.1371/journal.pone.0003583

11. ClarkeRPedenJFHopewellJCKyriakouTGoelA 2009 Genetic variants associated with Lp(a) lipoprotein level and coronary disease. N Engl J Med 361 2518 2528

12. SchunkertHKönigIRKathiresanSReillyMPAssimesTL 2011 Large-scale association analyses identifies 13 new susceptibility loci for coronary artery disease. Nat Genet 43 333 338

13. ZegginiEScottLJSaxenaRVoightBFMarchiniJL 2008 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. Nat Genet 40 638 645

14. Newton-ChehCJohnsonTGatevaVTobinMDBochudM 2009 Genome-wide association study identifies eight loci associated with blood pressure. Nat Genet 41 666 676

15. TeslovichTMMusunuruKSmithAVEdmondsonACStylianouIM 2010 Biological, clinical and population relevance of 95 loci for blood lipids. Nature 466 707 713

16. PisciottaLFresaRBellocchioAPinoEGuidoV 2009 Cholesteryl Ester Storage Disease (CESD) due to novel mutations in the LIPA gene. Mol Genet Metab 97 143 148

17. The Coronary Artery Disease (C4D) Genetics Consortium 2011 A genome-wide association study in Europeans and South Asians reveals five novel loci for coronary disease. Nat Genet 43 339 344

18. WildPSZellerTSchillertASzymczakSSinningCR 2011 A genome-wide association study identifies LIPA as a susceptibility gene for coronary artery disease. Circ Cardiovasc Genet Epub ahead of print

19. HanssonGK 2005 Inflammation, atherosclerosis, and coronary artery disease. N Engl J Med 352 1685 1695

20. BinderCJHartvigsenKChangMKMillerMBroideD 2004 IL-5 links adaptive and natural immunity specific for epitopes of oxidized LDL and protects from atherosclerosis. J Clin Invest 114 427 437

21. SampiMUkkolaOPaivansaloMKesaniemiYABinderCJHorkkoS 2008 Plasma interleukin-5 levels are related to antibodies binding to oxidized low-density lipoprotein and to decreased subclinical atherosclerosis. J Am Coll Cardiol 52 1370 1378

22. TalebSTedguiAMallatZ 2010 Adaptive T cell immune responses and atherogenesis. Curr Opin Pharmacol 10 197 202

23. BergeKETianHGrafGAYuLGrishinNV 2000 Accumulation of dietary cholesterol in sitosterolemia caused by mutations in adjacent ABC transporters. Science 290 1771 1775

24. TeupserDBaberRCeglarekUScholzMIlligT 2010 Genetic regulation of serum phytosterol levels and risk of coronary artery disease. Circ Cardiovasc Genet 3 331 339

25. HegedusZCzibulaAKiss-TothE 2007 Tribbles: a family of kinase-like proteins with potent signalling regulatory function. Cell Signal 19 238 250

26. WaterworthDMRickettsSLSongKChenLZhaoJH 2010 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. Arterioscler Thromb Vasc Biol 30 2264 2276

27. BurkhardtRTohS-ALagorWRBirkelandALevinM 2010 Trib1 is a lipid- and myocardial infarction-associated gene that regulates hepatic lipogenesis and VLDL production in mice. J Clin Invest 120 4410 4414

28. BhopalR 2000 What is the risk of coronary heart disease in South Asians? A review of UK research. J Public Health Med 22 375 385

29. SaleheenDAlexanderMRasheedAWormserDSoranzoN 2010 Association of the 9p21.3 locus with risk of first-ever myocardial infarction in Pakistanis: case-control study in South Asia and updated meta-analysis of Europeans. Arterioscler Thromb Vasc Biol 30 1467 1473

30. PurcellSNealeBTodd-BrownKThomasLFerreiraMA 2007 PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet 81 559 575

31. BeulensJWMonninkhofEMVerschurenWMvan der SchouwYTSmitJ 2010 Cohort Profile: The EPIC-NL study. Int J Epidemiol 39 1170 1178

32. HindorffLASethupathyPJunkinsHARamosEMMehtaJP 2009 Potential etiologic and functional implications of genome-wide association loci for human diseases and traits. Proc Natl Acad Sci U S A 106 9362 9367

Štítky
Genetika Reprodukčná medicína

Článok vyšiel v časopise

PLOS Genetics


2011 Číslo 9
Najčítanejšie tento týždeň
Najčítanejšie v tomto čísle
Kurzy

Zvýšte si kvalifikáciu online z pohodlia domova

Aktuální možnosti diagnostiky a léčby litiáz
nový kurz
Autori: MUDr. Tomáš Ürge, PhD.

Všetky kurzy
Prihlásenie
Zabudnuté heslo

Zadajte e-mailovú adresu, s ktorou ste vytvárali účet. Budú Vám na ňu zasielané informácie k nastaveniu nového hesla.

Prihlásenie

Nemáte účet?  Registrujte sa

#ADS_BOTTOM_SCRIPTS#