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http://elar.urfu.ru/handle/10995/117975
Название: | Anamnestic, clinical and laboratory features of the acute period of ischemic stroke in young patients |
Авторы: | Gusev, V. V. Kovtun, O. P. Lvova, O. A. Partylova, E. A. Sergeev, A. P. Sergeeva, M. V. Yanchuk, I. T. Dobrazova, D. A. Suvorkov, P. A. Shamalov, N. A. |
Дата публикации: | 2022 |
Издатель: | Ima-Press Publishing House |
Библиографическое описание: | Anamnestic, clinical and laboratory features of the acute period of ischemic stroke in young patients / V. V. Gusev, O. P. Kovtun, O. A. Lvova et al. // Nevrologiya, Neiropsikhiatriya, Psikhosomatika. — 2022. — Vol. 14. — Iss. 3. — P. 12-18. |
Аннотация: | Objective: to study the anamnestic, clinical and laboratory features of the acute period of ischemic stroke (IS) and to determine the risk factors for its development in young patients. Patients and methods. Clinical and statistical processing of data of 256 patients aged 18 to 44 years included, who had IS, confirmed by computed and/or magnetic resonance imaging of the brain in the acute period, was carried out. Furthermore, in 154 patients and in 117 healthy participants, who made up the control group, eight polymorphisms of the thrombophilic spectrum genes were determined – FGB: -455G>A, F2: 20210G>A, F5: 1691G>A, F7: 10976G>A, F13: 103 G>T, ITGA2: 807C>T, ITGB3: 1565 T>C, PAI-1: -675 5G>4G. Results and discussion. 154 (60.15%) patients demonstrated good recovery (achievement of a level of ≤2 points on the Rankin scale by the patient). None of the patients died during their hospitalization. In the evaluated group of patients, we identified allelic variants of the thrombophilic spectrum genes and gene-gene combinations, the carriage of which increased the likelihood of IS development at the young age by 1.74 and 2.19 times, respectively. Taking into consideration additional examination methods, the pathogenetic variant of IS according to the TOAST classification was verified in 226 (88%) patients. Conclusion. In IS at a young age a detailed assessment of risk factors is required, including an analysis of carrier variants and combinations of procoagulant and prothrombotic spectrum gene polymorphisms. © 2022 Ima-Press Publishing House. All rights reserved. |
Ключевые слова: | ISCHEMIC STROKE RISK FACTORS SINGLE NUCLEOTIDE SUBSTITUTIONS THROMBOPHILIA YOUNG AGE ALPHA2 INTEGRIN BETA3 INTEGRIN BLOOD CLOTTING FACTOR 5 BLOOD CLOTTING FACTOR 7 FIBRINOGEN FIBRINOGEN BETA PLASMINOGEN ACTIVATOR INHIBITOR 1 UNCLASSIFIED DRUG ADULT ANAMNESIS ARTICLE ATHEROSCLEROTIC PLAQUE ATRIAL FIBRILLATION BRACHIOCEPHALIC ARTERY STENOSIS BRAIN INFARCTION BRAIN VASCULITIS CEREBROVASCULAR MALFORMATION CLINICAL FEATURE COHORT ANALYSIS COMPUTER ASSISTED TOMOGRAPHY CONTROLLED STUDY DNA POLYMORPHISM DYSLIPOPROTEINEMIA ERYTHROCYTE SEDIMENTATION RATE FEMALE GENETIC PREDISPOSITION GENETIC VARIABILITY HEART LEFT VENTRICLE HYPERTROPHY HETEROZYGOTE HOSPITAL ADMISSION HOSPITALIZATION HUMAN HYPERLIPIDEMIA INTENSIVE CARE ISCHEMIC STROKE MAJOR CLINICAL STUDY MALE METABOLIC DISORDER MIGRAINE MITRAL VALVE PROLAPSE NUCLEAR MAGNETIC RESONANCE IMAGING NUCLEIC ACID BASE SUBSTITUTION OCCLUSIVE CEREBROVASCULAR DISEASE PARALYSIS PARESIS RANKIN SCALE RISK FACTOR SELF CARE SPEECH DISORDER THROMBOPHILIA |
URI: | http://elar.urfu.ru/handle/10995/117975 |
Условия доступа: | info:eu-repo/semantics/openAccess |
Идентификатор SCOPUS: | 85133840987 |
Идентификатор PURE: | 30625889 |
ISSN: | 20742711 |
DOI: | 10.14412/2074-2711-2022-3-12-18 |
Располагается в коллекциях: | Научные публикации ученых УрФУ, проиндексированные в SCOPUS и WoS CC |
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2-s2.0-85133840987.pdf | 122,56 kB | Adobe PDF | Просмотреть/Открыть |
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