Application of the genetic risk model for the analysis of predisposition to nonlacunar ischemic stroke

被引:1
|
作者
Korchagin, Vitaly [1 ]
Mironov, Konstantin [1 ]
Platonov, Alexander [1 ]
Dribnokhodova, Olga [1 ]
Akselrod, Elina [1 ]
Dunaeva, Elena [1 ]
Stolyar, Marina [2 ,3 ]
Gorbenko, Aleksey [2 ,3 ]
Gritsan, Galina [4 ]
Olkhovskiy, Igor [2 ,3 ]
Rakova, Natalia [5 ]
Roytman, Alexander [5 ]
Sotnikov, Alexander [5 ]
Raskurazhev, Anton [6 ]
Maksimova, Marina [6 ]
Tanashyan, Marine [6 ]
Illarioshkin, Sergey [6 ]
Shipulin, German [1 ]
机构
[1] Cent Res Inst Epidemiol, Moscow, Russia
[2] Hematol Res Ctr, Dept Hlth, Fed State Budgetary Inst, Krasnoyarsk Branch, Krasnoyarsk, Russia
[3] Russian Acad Sci, Siberian Branch, Krasnoyarsk Sci Ctr, Fed Res Ctr, Krasnoyarsk, Russia
[4] Krasnoyarsk State Med Univ, Krasnoyarsk, Russia
[5] Moscow City Clin Hosp, Moscow, Russia
[6] Res Ctr Neurol, Moscow, Russia
关键词
genetic susceptibility; ischemic stroke; single-nucleotide polymorphism; PREDICTION; DISEASE; LOCI;
D O I
10.2217/pme-2018-0104
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Aim: The purpose of our study was to analyze the predictive ability of the multiplicative model of genetic risk of nonlacunar ischemic stroke (IS) for independent samples from Russia. Patients & methods: A total of 181 patients and 360 healthy controls were included in this study. The discriminative accuracy of model was evaluated by the area under the receiver operating characteristic curve (AUC). Results: Classification model based on 15 single-nucleotide polymorphisms (SNPs), which are associated with a cardioembolic subtype of IS, had an AUC of 0.62 in patients with corresponding subtypes and an AUC of 0.58 for all patients. Conclusion: Risk calculation approach based on IS-associated SNPs had satisfactory performance in predicting the predisposition to the disease.
引用
收藏
页码:369 / 378
页数:10
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