Evaluation of Common Unfavourable Genetic Variants in Cerebrovascular Diseases: Recommendation for Supportive Genetic Examinations and Methodological Approaches for Common Genetic Variants

被引:4
|
作者
Szolnoki, Zoltan [1 ]
机构
[1] Kalman Pandy Cty Hosp, Dept Cerebrovasc Dis, H-5600 Gyula, Bekescsaba, Hungary
关键词
NITRIC-OXIDE SYNTHASE; RENIN-ANGIOTENSIN SYSTEM; WHITE-MATTER LESIONS; SMALL VESSEL DISEASE; ISCHEMIC-STROKE; ENDOTHELIAL DYSFUNCTION; RISK-FACTORS; PLASMA HOMOCYSTEINE; OXIDATIVE STRESS; MTHFR; 677T;
D O I
10.2174/092986709788803006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The present paper summarizes the possible roles of frequent and unfavourable genetic variants in cerebrovascular disorders, such as stroke and leukoaraiosis. It also approaches the topic theoretically from functional and mathematical points of view, which can help make the accumulating data on genetic variants more understandable. The interplay of an unfavourable genetic polymorphism and environmental clinical factors can result in a cerebrovascular disease or a state of vascular dementia. These constantly changing functional interactions need a highly specialised approach. There is, therefore, a great need to summarise the results on genetic polymorphisms concisely, and to discuss their special but shared features, which make their evaluation difficult with the methods used for the well-known Mendelian factors. The development of a correct approach to genetic polymorphisms may have a great impact on the understanding and prevention of cerebrovascular diseases.
引用
收藏
页码:3168 / 3173
页数:6
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