Association between genetic variant on chromosome 12p13 and stroke survival and recurrence: A one year prospective study in Taiwan

Journal of Biomedical Science

Volumn 19, Issue 1, 2012, Pages

  Hsieh, Yi Chen ^a   Seshadri, Sudha ^b,c   Chung, Wen Ting ^a,d   Hsieh, Fang I ^a   Hsu, Yi Hsiang ^e,f   Lin, Huey Juan ^g   Tseng, Hung Pin ^h   Lien, Li Ming ⁱ   Bai, Chyi Huey ^a,i   Hu, Chaur Jong ^j   Jeng, Jiann Shing ^k   Tang, Sung Chun ^k   Chen, Chin I ^d   Yu, Chia Chen ^a   Chiou, Hung Yi ^a  

^a TAIPEI MEDICAL UNIVERSITY   (Taiwan)

^b BOSTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c FRAMINGHAM HEART STUDY   (United States)

^d TAIPEI MEDICAL UNIVERSITY   (Taiwan)

^e HARVARD MEDICAL SCHOOL   (United States)

^f HARVARD SCHOOL OF PUBLIC HEALTH   (United States)

^g CHI MEI MEDICAL CENTER   (Taiwan)

^h LOTUNG POH AI HOSPITAL   (Taiwan)

ⁱ SHIN KONG WU HO SU MEMORIAL HOSPITAL   (Taiwan)

^j TAIPEI MEDICAL UNIVERSITY HOSPITAL   (Taiwan)

^k NATIONAL TAIWAN UNIVERSITY HOSPITAL   (Taiwan)

more..

Author keywords

single nucleotide polymorphisms; stroke; survival

Indexed keywords

ADULT; AGE; ALLELE; ARTICLE; BRAIN ATHEROSCLEROSIS; BRAIN ISCHEMIA; CARDIOVASCULAR RISK; CHROMOSOME 12P; CONTROLLED STUDY; DISEASE SEVERITY; FEMALE; FLUORESCENCE ANALYSIS; GENE LOCUS; GENETIC ASSOCIATION; GENETIC VARIABILITY; GENOTYPE; HOMOZYGOSITY; HUMAN; MAJOR CLINICAL STUDY; MALE; MOLECULAR DYNAMICS; MORTALITY; PRIORITY JOURNAL; RECURRENT DISEASE; RISK FACTOR; SEX; SINGLE NUCLEOTIDE POLYMORPHISM; SURVIVAL; TAIWAN; AGED; CASE CONTROL STUDY; CHROMOSOME 12; CLINICAL TRIAL; GENETICS; MIDDLE AGED; MULTICENTER STUDY; PROPORTIONAL HAZARDS MODEL; PROSPECTIVE STUDY; RISK;

AGED; BRAIN ISCHEMIA; CASE-CONTROL STUDIES; CHROMOSOMES, HUMAN, PAIR 12; FEMALE; GENOTYPE; HUMANS; MALE; MIDDLE AGED; ODDS RATIO; POLYMORPHISM, SINGLE NUCLEOTIDE; PROPORTIONAL HAZARDS MODELS; PROSPECTIVE STUDIES; RECURRENCE; RISK FACTORS; TAIWAN;

EID: 84855218762     PISSN: 10217770     EISSN: 14230127     Source Type: Journal    
DOI: 10.1186/1423-0127-19-1     Document Type: Article

References (17)

1. Genomewide association studies of stroke. Ikram MA, Seshadri S, Bis JC, Fornage M, DeStefano AL, Aulchenko YS, Debette S, Lumley T, Folsom AR, van den Herik EG, Bos MJ, Beiser A, Cushman M, Launer LJ, Shahar E, Struchalin M, Du Y, Glazer NL, Rosamond WD, Rivadeneira F, Kelly-Hayes M, Lopez OL, Coresh J, Hofman A, DeCarli C, Heckbert SR, Koudstaal PJ, Yang Q, Smith NL, Kase CS, Rice K, Haritunians T, Roks G, de Kort PLM, Taylor KD, de Lau LM, Oostra BA, Uitterlinden AG, Rotter JI, Boerwinkle E, Psaty BM, Mosley TH, van Duijn CM, Breteler MMB, Longstreth WT Jr, Wolf PA, N Engl J Med 2009 360 1718 1728 10.1056/NEJMoa0900094 19369658
2. Failure to validate association between 12p13 variants and ischemic stroke. International Stroke Genetics Consortium; Wellcome Trust Case-Control Consortium 2, N Engl J Med 2010 362 1547 1550 20410525
3. No association between chromosome 12p13 single nucleotide polymorphisms and early-onset ischemic stroke. Lotta LA, Giusti B, Saracini C, Vestrini A, Volpe M, Rubattu S, Peyvandi F, J Thromb Haemost 2010 8 1858 1860 10.1111/j.1538-7836.2010.03912.x 20497308
4. Genetic variant on chromosome 12p13 does not show association to ischemic stroke in 3 Swedish case-control studies. Olsson S, Melander O, Jood K, Smith JG, Lövkvist H, Sjögren M, Engström G, Norrving B, Lindgren A, Jern C, International Stroke Genetics Consortium (ISGC), Stroke 2010 42 214 216 21148441
5. Association study of the polymorphisms on chromosome 12p13 with atherothrombotic stroke in the Japanese population. Matsushita T, Umeno J, Hirakawa Y, Yonemoto K, Ashikawa K, Amitani H, Ninomiya T, Hata J, Doi Y, Kitazono T, Iida M, Nakamura Y, Kiyohara Y, Kubo M, J Hum Genet 2010 55 473 476 10.1038/jhg.2010.45 20448654
6. Ninjurin, a novel adhesion molecule, is induced by nerve injury and promotes axonal growth. Araki T, Milbrandt J, Neuron 1996 17 353 361 10.1016/S0896-6273(00)80166-X 8780658 (Pubitemid 26296161)
7. AHA/ASA Get With The Guidelines-Stroke Performance Indicators: Surveillance of Stroke Care in the Taiwan Stroke Registry. Hsieh FI, Lien LM, Chen ST, Bai CH, Sun MC, Tseng HP, Chen YW, Chen CH, Jeng JS, Tsai SY, Lin HJ, Liu CH, Lo YK, Chen HJ, Chiu HC, Lai ML, Lin RT, Sun MH, Yip BS, Chiou HY, Hsu CY, Circulation 2010 122 1116 1123 10.1161/CIRCULATIONAHA.110.936526 20805428
8. Classification of subtype of acute ischemic stroke. Definitions for use in a multicenter clinical trial. TOAST. Trial of Org 10172 in Acute Stroke Treatment. Adams HP Jr, Bendixen BH, Kappelle LJ, Biller J, Love BB, Gordon DL, Marsh EE III, Stroke 1993 24 35 41 10.1161/01.STR.24.1.35 7678184 (Pubitemid 23014379)
9. A significant decrease in blood pressure through a family-based nutrition health education programme among community residents in Taiwan. Hsieh YC, Hung CT, Lein LM, Bai CH, Chen WH, Yeh CY, Chen YH, Hsieh FI, Chiu HC, Chiou HY, Hsu CY, Public Health Nutr 2009 12 570 577 10.1017/S1368980008002875 18561875
10. STATA 11.0 Statistics/Data Analysis. Stata Corporation, College Station, Texas, Stata corporation 2009 http://www.stata.com
11. Controlling the false discovery rate: a practical and powerful approach to multiple testing. Benjamini Y, Hochberg Y, JR Stat Soc Ser B 1995 57 289 300
12. Ninjurin2, a novel homophilic adhesion molecule, is expressed in mature sensory and enteric neurons and promotes neurite outgrowth. Araki T, Milbrandt J, J Neurosci 2002 20 187 195
13. Analysis of genes induced in peripheral nerve after axotomy using cDNA microarrays. Kubo T, Yamashita T, Yamaguchi A, Hosokawa K, Tohyama M, J Neurochem 2002 82 1129 1136 12358760 (Pubitemid 34966625)
14. Genetic association studies in ischaemic stroke: replication failure and prospects. Pruissen DM, Kappelle LJ, Rosendaal FR, Algra A, Cerebrovasc Dis 2009 27 290 294 10.1159/000199467 19202334
15. Association of a Genetic Variant in the ALOX5AP with Higher Risk of Ischemic Stroke: A Case-Control, Meta-Analysis and Functional Study. Domingues-Montanari S, Fernández-Cadenas I, del Rio-Espinola A, Corbeto N, Krug T, Manso H, Gouveia L, Sobral J, Mendioroz M, Fernández-Morales J, Alvarez-Sabin J, Ribá M, Rubiera M, Obach V, Martí-Fbregas J, Freijo M, Serena J, Ferro JM, Vicente AM, Oliveira SA, Montaner J, Cerebrovasc Dis 2010 29 528 537 10.1159/000302738 20357438
16. Population stratification and spurious allelic association. Cardon LR, Palmer LJ, Lancet 2003 361 598 604 10.1016/S0140-6736(03)12520-2 12598158 (Pubitemid 36207482)
17. Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease. Lohmueller KE, Pearce CL, Pike M, Lander ES, Hirschhorn JN, Nat Genet 2003 33 177 182 10.1038/ng1071 12524541 (Pubitemid 36177070)