دورية أكاديمية

The fine art of vascular wall maintenance. Carriership of XPC, TP53 and APOE polymorphisms may be a risk factor for cerebral vascular accidents in the Bulgarian population

التفاصيل البيبلوغرافية
العنوان: The fine art of vascular wall maintenance. Carriership of XPC, TP53 and APOE polymorphisms may be a risk factor for cerebral vascular accidents in the Bulgarian population
المؤلفون: Pavlina Chelenkova, Rumena Petkova, Teodora Chamova, Sashka Zhelyazkova, Ivaylo Tournev, Stoyan Chakarov
المصدر: Biotechnology & Biotechnological Equipment, Vol 32, Iss 6, Pp 1558-1566 (2018)
بيانات النشر: Taylor & Francis Group, 2018.
سنة النشر: 2018
المجموعة: LCC:Biotechnology
مصطلحات موضوعية: Oxidative damage, individual repair capacity, cerebral vascular accident, endothelial integrity, risk of stroke, Biotechnology, TP248.13-248.65
الوصف: Efficient maintenance of the integrity of the endothelium of cerebral blood vessels is crucially important, especially when the vessel walls are subjected to greater-than-normal levels of stress. Persistently high levels of genotoxic stress may result from lower capacity to detect and repair DNA damage conferred by carriership of variants of key genes of DNA repair/maintenance of genomic integrity. Adult Bulgarian patients with a history of cerebral vascular accidents (CVAs) and age-matched healthy controls were analyzed for 11 markers, including 7 DNA polymorphisms in genes coding for proteins of DNA repair and maintenance of genomic integrity, 3 hypercoagulability markers and 1 marker for susceptibility for cerebral amyloidosis. Homozygous carriership of the del allele of the polymorphism XPCins83 was associated with decreased risk of CVAs (RR = 0.446, 95% CI:0.225–0.886, p = 0.021). In individuals carrying the 'protective' del/del XPCins83 genotype, carriership of the 'pro-apoptotic' genotype Arg/Arg in the TP53 locus was associated with increased risk of CVAs (RR = 1.845, 95% CI:1.049–3.244, p = 0.034). Carriers of the Lys751Gln genotype at the ERCC2 locus were at increased risk of CVAs (RR = 2.055, 95% CI:1.09–3.876, p = 0.025). Carriership of the E2/E3 genotype at the APOE locus decreased the risk of CVAs in Bulgarian males (RR = 0.279, 95% CI:0.090–0.873, p = 0.028). Male Bulgarian carriers of the APOE4 allele were at increased risk of CVAs. Carriership of the common prothrombotic mutations Factor V Leiden, PT G20210A, MTHFR C677T and PAI1 4G/5G had no significant effect on the risk of CVAs in Bulgarian adults.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1310-2818
1314-3530
13102818
العلاقة: https://doaj.org/toc/1310-2818Test; https://doaj.org/toc/1314-3530Test
DOI: 10.1080/13102818.2018.1529542
الوصول الحر: https://doaj.org/article/fb4d6f66bcea44b3b65fd6af54e72aa5Test
رقم الانضمام: edsdoj.fb4d6f66bcea44b3b65fd6af54e72aa5
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:13102818
13143530
DOI:10.1080/13102818.2018.1529542