Absence of Association between TNF-α Polymorphism and Cerebral Large-Vessel Abnormalities in Adults with Sickle Cell Anemia

被引:8
|
作者
Vicari, Perla [1 ]
Silva, Gisele Sampaio [2 ]
Elko Nogutti, Maria Aparecida [1 ]
Moreira Neto, Faustino [1 ]
dos Santos, Normelia Jesus [1 ]
Massaro, Ayrton Roberto [2 ]
Figueiredo, Maria Stella [1 ]
机构
[1] Univ Fed Sao Paulo, EPM, Disciplina Hematol & Hemoterapia, BR-04023000 Sao Paulo, Brazil
[2] Univ Fed Sao Paulo, EPM, Disciplina Neurol, BR-04023000 Sao Paulo, Brazil
基金
巴西圣保罗研究基金会;
关键词
Sickle cell disease; Stroke; Genetic polymorphism; Interleukins; TRANSCRANIAL DOPPLER; GENE POLYMORPHISM; IMAGING FINDINGS; ISCHEMIC-STROKE; DISEASE; RISK; CHILDREN; INFARCTION; MRA;
D O I
10.1159/000321935
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Stroke is a serious complication of sickle cell anemia (SCA) affecting children and adults. Recent reports suggested that tumor necrosis factor-alpha (TNF-alpha) (-308) polymorphism is an important risk factor for stroke in children with SCA. The role of TNF-alpha polymorphism in the frequency of brain magnetic resonance imaging (MRI) and magnetic resonance angiography (MRA) abnormalities in adults with SCA is still uncertain. Our objective was to evaluate the frequency of INF-alpha polymorphism in adults with SCA and to correlate it to brain MRI and MRA findings. TNF-alpha (-308) polymorphism was determined in 49 adults with SCA. All subjects were evaluated with brain MRI/MRA to establish the presence of intracranial abnormalities. Thirty-three (67.3%) had abnormal brain MRA scans, 8 (16.3%) had intracranial stenosis and 29 (59.2%) showed arterial tortuosity. Forty-one (83.7%) had the GG genotype and 8 had the GA genotype. There was no correlation between homozygosity for G allele and MRA or MRI abnormalities. Although INF-alpha (-308) polymorphism is a potential predictor of the genetic risk for stroke in children, we found no association between the polymorphism and large vessel abnormalities in adults with SCA. Copyright (C)2010 S. Karger AG, Basel
引用
收藏
页码:141 / 144
页数:4
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