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
相关论文
共 50 条
  • [1] Detecting Association with Rare Genetic Variants in Common Diseases
    Li, Yali
    Feng, Tao
    Elston, Robert C.
    Zhu, Xiaofeng
    GENETIC EPIDEMIOLOGY, 2009, 33 (08) : 754 - 754
  • [2] Common genetic variants and the heritability of ALS
    Ammar Al-Chalabi
    Peter M. Visscher
    Nature Reviews Neurology, 2014, 10 : 549 - 550
  • [3] Genetic variants and common diseases - Better late than never
    O'Rahilly, Stephen
    Wareham, Nicholas J.
    NEW ENGLAND JOURNAL OF MEDICINE, 2006, 355 (03): : 306 - 308
  • [4] Common genetic epilepsies, pathogenicity of genes/variants, and genetic dependence
    He, Na
    Li, Bin
    Lin, Zhi-Jian
    Zhou, Peng
    Su, Tao
    Liao, Wei-Ping
    SEIZURE-EUROPEAN JOURNAL OF EPILEPSY, 2023, 109 : 38 - 39
  • [5] Common Genetic Variants and Risk of Ischemic Heart Failure: An Evaluation of a Negative Genetic Study
    Jabbari, Reza
    Haunso, Stig
    Tfelt-Hansen, Jacob
    CARDIOLOGY, 2015, 130 (03) : 167 - 168
  • [6] Deciphering the genetic basis of common diseases by integrated functional annotation of common and rare variants
    Harismendy, Olivier
    Bhatia, Gaurav
    Rahim, Nazli G.
    Bansal, Vikas
    Nakano, Masakazu
    Scott, Michael
    Wang, Xiaoyun
    Dib, Colette
    Turlotte, Edouard
    Heintzman, Nathaniel
    Murray, Sarah S.
    Deleuze, Jean-Francois
    Sipe, Jack C.
    Ren, Bing
    Bafna, Vineet
    Topol, Eric J.
    Frazer, Kelly A.
    GENOME BIOLOGY, 2010, 11
  • [7] Deciphering the genetic basis of common diseases by integrated functional annotation of common and rare variants
    Olivier Harismendy
    Gaurav Bhatia
    Nazli G Rahim
    Vikas Bansal
    Masakazu Nakano
    Michael Scott
    Xiaoyun Wang
    Colette Dib
    Edouard Turlotte
    Nathaniel Heintzman
    Sarah S Murray
    Jean-Francois Deleuze
    Jack C Sipe
    Bing Ren
    Vineet Bafna
    Eric J Topol
    Kelly A Frazer
    Genome Biology, 11 (Suppl 1)
  • [8] Genetic approaches to solving common diseases
    Abou-Sleiman, PM
    Healy, DG
    Wood, NW
    JOURNAL OF NEUROLOGY, 2004, 251 (10) : 1169 - 1172
  • [9] Genetic Approaches to Solving Common Diseases
    P. M. Abou-Sleiman
    D. G. Healy
    N. W. Wood
    Journal of Neurology, 2004, 251 : 1169 - 1172
  • [10] Shared genetic variants suggest common pathways in allergy and autoimmune diseases
    Kreiner, Eskil
    Waage, Johannes
    Standl, Marie
    Brix, Susanne
    Pers, Tune H.
    Alves, Alexessander Couto
    Warrington, Nicole M.
    Tiesler, Carla M. T.
    Fuertes, Elaine
    Franke, Lude
    Hirschhorn, Joel N.
    James, Alan
    Simpson, Angela
    Tung, Joyce Y.
    Koppelman, Gerard H.
    Postma, Dirkje S.
    Pennell, Craig E.
    Jarvelin, Marjo-Riitta
    Custovic, Adnan
    Timpson, Nicholas
    Ferreira, Manuel A.
    Strachan, David P.
    Henderson, John
    Hinds, David
    Bisgaard, Hans
    Bonnelykke, Klaus
    JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2017, 140 (03) : 771 - 781