Polymorphism of the complement 5 gene is associated with large artery atherosclerosis stroke in Chinese patients

被引:0
作者
Wu, Hui [1 ]
Weng, Yingfeng [1 ]
Zheng, Lan [1 ]
Li, Huanyin [1 ]
Gong, Qi [1 ]
Fu, Yi [2 ]
Zhao, Jing [1 ]
机构
[1] Minhang Dist Cent Hosp, Dept Neurol, Shanghai, Peoples R China
[2] Shanghai Jiao Tong Univ, Sch Med, Shanghai 200030, Peoples R China
基金
中国国家自然科学基金;
关键词
genes; stroke; ACUTE ISCHEMIC-STROKE; DISEASE; RISK; RELIABILITY; ACTIVATION; OUTCOMES; HUMANS; SCALE; MICE;
D O I
10.1590/0004-282X20160139
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The complement system has been confirmed to play an increasingly important role in ischemic stroke (IS). This study aimed to determine whether the single-nucleotide polymorphism of the complement 5 (C5) gene independently influences the occurrence, severity, and long-term outcome of IS in Chinese patients. Methods: C5 rs17611 genetic variants were investigated in 494 IS patients and 330 control individuals. Ischemic stroke was classified into subtypes and patients were assessed 90 days post-stroke with the modified Rankin Scale to determine stroke outcome. Results: The presence of C5 polymorphism was associated with the incidence of large artery atherosclerosis (LAA)-subtype IS (n = 2 00; p = 0.031), which even persisted after adjustment for covariates (OR = 1.518; 95% CI = 1.093-2.018; p = 0.013). However, no association was found between genotypes and the severity and outcome of stroke (p = 0.978; p = 0.296). Conclusions: The C5 polymorphism might contribute to the risk of LAA-subtype IS independently of other known risk predictors.
引用
收藏
页码:881 / 886
页数:6
相关论文
共 23 条
  • [1] Guidelines for the early management of adults with ischemic stroke -: A guideline from the American Heart Association/American Stroke Association Stroke Council, Clinical Cardiology Council, Cardiovascular Radiology and Intervention Council, and the Atherosclerotic Peripheral Vascular Disease and Quality of Care Outcomes in Research Interdisciplinary Working Groups (Reprinted from Stroke, vol 38, pg 1655-1711, 2007)
    Adams, Harold P., Jr.
    del Zoppo, Gregory
    Alberts, Mark J.
    Bhatt, Deepak L.
    Brass, Lawrence
    Furlan, Anthony
    Grubb, Robert L.
    Higashida, Randall T.
    Jauch, Edward C.
    Kidwell, Chelsea
    Lyden, Patrick D.
    Morgenstern, Lewis B.
    Qureshi, Adnan I.
    Rosenwasser, Robert H.
    Scott, Phillip A.
    Wijdicks, Eelco F. M.
    [J]. CIRCULATION, 2007, 115 (20) : E478 - E534
  • [2] CLASSIFICATION OF SUBTYPE OF ACUTE ISCHEMIC STROKE - DEFINITIONS FOR USE IN A MULTICENTER CLINICAL-TRIAL
    ADAMS, HP
    BENDIXEN, BH
    KAPPELLE, LJ
    BILLER, J
    LOVE, BB
    GORDON, DL
    MARSH, EE
    KASE, CS
    WOLF, PA
    BABIKIAN, VL
    LICATAGEHR, EE
    ALLEN, N
    BRASS, LM
    FAYAD, PB
    PAVALKIS, FJ
    WEINBERGER, JM
    TUHRIM, S
    RUDOLPH, SH
    HOROWITZ, DR
    BITTON, A
    MOHR, JP
    SACCO, RL
    CLAVIJO, M
    ROSENBAUM, DM
    SPARR, SA
    KATZ, P
    KLONOWSKI, E
    CULEBRAS, A
    CAREY, G
    MARTIR, NI
    FICARRA, C
    HOGAN, EL
    CARTER, T
    GURECKI, P
    MUNTZ, BK
    RAMIREZLASSEPAS, M
    TULLOCH, JW
    QUINONES, MR
    MENDEZ, M
    ZHANG, SM
    ALA, T
    JOHNSTON, KC
    ANDERSON, DC
    TARREL, RM
    NANCE, MA
    BUDLIE, SR
    DIERICH, M
    HELGASON, CM
    HIER, DB
    SHAPIRO, RA
    [J]. STROKE, 1993, 24 (01) : 35 - 41
  • [3] Complement Factor H Y402H polymorphism is associated with an increased risk of mortality after intracerebral hemorrhage
    Appelboom, Geoffrey
    Piazza, Matthew
    Hwang, Brian Y.
    Bruce, Samuel
    Smith, Steve
    Bratt, Alexander
    Bagiella, Emilia
    Badjatia, Neeraj
    Mayer, Stephan
    Connolly, E. Sander
    [J]. JOURNAL OF CLINICAL NEUROSCIENCE, 2011, 18 (11) : 1439 - 1443
  • [4] The glu298asp polymorphism in the nitric oxide synthase 3 gene is associated with the risk of ischemic stroke in two large independent case-control studies
    Berger, Klaus
    Stoegbauer, Florian
    Stoll, Monika
    Wellmann, Juergen
    Huge, Andreas
    Cheng, Suzanne
    Kessler, Christof
    John, Ulrich
    Assmann, Gerd
    Ringelstein, E. Bernd
    Funke, Harald
    [J]. HUMAN GENETICS, 2007, 121 (02) : 169 - 178
  • [5] Brain-Derived Neurotrophic Factor and the Development of Structural Neuronal Connectivity
    Cohen-Cory, Susana
    Kidane, Adhanet H.
    Shirkey, Nicole J.
    Marshak, Sonya
    [J]. DEVELOPMENTAL NEUROBIOLOGY, 2010, 70 (05) : 271 - 288
  • [6] Functional Analysis of a Complement Polymorphism (rs17611) Associated with Rheumatoid Arthritis
    Giles, Joanna L.
    Choy, Ernest
    van den Berg, Carmen
    Morgan, B. Paul
    Harris, Claire L.
    [J]. JOURNAL OF IMMUNOLOGY, 2015, 194 (07) : 3029 - 3034
  • [7] Atherosclerosis: The road ahead
    Glass, CK
    Witztum, JL
    [J]. CELL, 2001, 104 (04) : 503 - 516
  • [8] Polymorphisms in Inflammatory Genes and the Risk of Ischemic Stroke and Transient Ischemic Attack: Results of a Multilocus Genotyping Assay
    Greisenegger, Stefan
    Zehetmayer, Sonja
    Bauer, Peter
    Endler, Georg
    Ferrari, Julia
    Lang, Wilfried
    Janisiw, Michael
    Steiner, Lori
    Cheng, Suzanne
    Lalouschek, Wolfgang
    Mannhalter, Christine
    [J]. CLINICAL CHEMISTRY, 2009, 55 (01) : 134 - 138
  • [9] Complement factor 5 is a quantitative trait gene that modifies liver fibrogenesis in mice and humans
    Hillebrandt, S
    Wasmuth, HE
    Weiskirchen, R
    Hellerbrand, C
    Keppeler, H
    Werth, A
    Schirin-Sokhan, R
    Wilkens, G
    Geier, A
    Lorenzen, J
    Köhl, J
    Gressner, AM
    Matern, S
    Lammert, F
    [J]. NATURE GENETICS, 2005, 37 (08) : 835 - 843
  • [10] Polymorphism of the complement 5 gene and cardiovascular outcome in patients with atherosclerosis
    Hoke, Matthias
    Speidl, Walter
    Schillinger, Martin
    Minar, Erich
    Zehetmayer, Sonja
    Schoenherr, Michael
    Wagner, Oswald
    Mannhalter, Christine
    [J]. EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 2012, 42 (09) : 921 - 926