Literature DB >> 17016617

Genetic risk for atherothrombotic cerebral infarction in individuals stratified by sex or conventional risk factors for atherosclerosis.

Sachiyo Yamaguchi1, Yoshiji Yamada, Norifumi Metoki, Hidemi Yoshida, Kei Satoh, Sahoko Ichihara, Kimihiko Kato, Takashi Kameyama, Kiyoshi Yokoi, Hitoshi Matsuo, Tomonori Segawa, Sachiro Watanabe, Yoshinori Nozawa.   

Abstract

The aim of the present study was to assess the genetic risk for atherothrombotic cerebral infarction (ACI) in men and women separately as well as in individuals with or without conventional risk factors for atherosclerosis and thereby to contribute to the personalized prevention of ACI. The study population comprised 2705 unrelated Japanese individuals (1244 men, 1461 women), including 636 subjects (372 men, 264 women) with ACI. Subjects with ACI and controls either had or did not have conventional risk factors for atherosclerosis, including hypertension, hypercholesterolemia, and diabetes mellitus. The genotypes for 202 polymorphisms of 152 candidate genes were determined by a method that combines polymerase chain reaction and sequence-specific oligonucleotide probes with suspension array technology. Multivariable logistic regression analysis and a stepwise forward selection procedure revealed that 11 different polymorphisms were significantly (P < 0.005) associated with ACI in women or men or in individuals with or without hyper-tension, hypercholesterolemia, or diabetes mellitus: the 584C-->T polymorphism of LIPG, 5665G-->T of EDN1, and G-->A of CCL11 in women; 677C-->T of MTHFR, 1323C-->T of ITGB2, 3932T-->C of APOE, and -231A-->G of EDNRA in men; -572 G -->C of IL6 in hypertensive individuals; -403G-->A of CCL5 and G-->A of COMT in individuals with hypercholesterolemia; and 3932T--> C of APOE and A-->G of TNFSF4 in diabetic individuals. Polymorphisms associated with ACI may thus differ between women and men as well as among individuals with different risk factors. Stratification of subjects on the basis of sex or conventional risk factors for atherosclerosis may therefore be important in order to achieve the personalized prevention of ACI with the use of genetic information.

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Year:  2006        PMID: 17016617

Source DB:  PubMed          Journal:  Int J Mol Med        ISSN: 1107-3756            Impact factor:   4.101


  12 in total

1.  EDNRA variants associate with smooth muscle mRNA levels, cell proliferation rates, and cystic fibrosis pulmonary disease severity.

Authors:  Rebecca Darrah; Edward McKone; Clare O'Connor; Christine Rodgers; Alan Genatossio; Sharon McNamara; Ronald Gibson; J Stuart Elborn; Madeleine Ennis; Charles G Gallagher; Noor Kalsheker; Moira Aitken; Dawn Wiese; John Dunn; Paul Smith; Rhonda Pace; Douglas Londono; Katrina A B Goddard; Michael R Knowles; Mitchell L Drumm
Journal:  Physiol Genomics       Date:  2009-12-22       Impact factor: 3.107

2.  Genetic variants of TNFSF4 and risk for carotid artery disease and stroke.

Authors:  P S Olofsson; L A Söderström; C Jern; A Sirsjö; M Ria; E Sundler; U de Faire; P G Wiklund; J Ohrvik; U Hedin; G Paulsson-Berne; A Hamsten; P Eriksson; G K Hansson
Journal:  J Mol Med (Berl)       Date:  2008-11-08       Impact factor: 4.599

Review 3.  Nature, nurture and epigenetics.

Authors:  David Crews; Ross Gillette; Isaac Miller-Crews; Andrea C Gore; Michael K Skinner
Journal:  Mol Cell Endocrinol       Date:  2014-08-04       Impact factor: 4.102

4.  TNFSF4 gene polymorphism rs3861950 but not rs3850641 is associated with the risk of cerebral infarction in a Chinese population.

Authors:  Jie Feng; Yun-Hai Liu; Qi-Dong Yang; Zan-Hua Zhu; Kun Xia; Xing-Lin Tan; Jian Xia; Wen-Ping Gu; Lin Zhou; Bo Xiao; Bei-Sha Tang; Qing Huang
Journal:  J Thromb Thrombolysis       Date:  2013-10       Impact factor: 2.300

Review 5.  The chemokine network. II. On how polymorphisms and alternative splicing increase the number of molecular species and configure intricate patterns of disease susceptibility.

Authors:  R Colobran; R Pujol-Borrell; M P Armengol; M Juan
Journal:  Clin Exp Immunol       Date:  2007-10       Impact factor: 4.330

6.  Association of OX40L polymorphisms with sporadic breast cancer in northeast Chinese Han population.

Authors:  Yuan Weiguang; Li Dalin; Xu Lidan; Cai Yonggang; Chen Shuang; Liu Yanhong; Xu Fengyan; Fu Zhenkun; Pang Da; Li Dianjun
Journal:  PLoS One       Date:  2012-08-03       Impact factor: 3.240

7.  Positive Association between EDN1 rs5370 (Lys198Asn) Polymorphism and Large Artery Stroke in a Ukrainian Population.

Authors:  Yevhen I Dubovyk; Tetyana B Oleshko; Viktoriia Yu Harbuzova; Alexander V Ataman
Journal:  Dis Markers       Date:  2018-04-03       Impact factor: 3.434

8.  Association between Lys198Asn polymorphism of endothelin-1 gene and ischemic stroke: A meta-analysis.

Authors:  Gaurav Nepal; Rajeev Ojha; Hari Prasad Dulal; Binod Kumar Yadav
Journal:  Brain Behav       Date:  2019-09-30       Impact factor: 2.708

9.  Association of nNOS gene polymorphism with ischemic stroke in Han Chinese of North China.

Authors:  Yingjie Dai; Zhiyi He; Rubo Sui; Zhilin Jiang; Shanshan Ma
Journal:  ScientificWorldJournal       Date:  2013-09-03

10.  The SNPs rs429358 and rs7412 of APOE gene are association with cerebral infarction but not SNPs rs2306283 and rs4149056 of SLCO1B1 gene in southern Chinese Hakka population.

Authors:  Heming Wu; Qingyan Huang; Zhikang Yu; Hailing Wu; Zhixiong Zhong
Journal:  Lipids Health Dis       Date:  2020-09-05       Impact factor: 3.876

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