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      Dataset of allele and genotype frequencies of the three functionally significant polymorphisms of the MMP genes in Russian patients with primary open-angle glaucoma, essential hypertension and peptic ulcer

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          Abstract

          Data on the allele and genotype frequencies of the three functionally significant single nucleotide polymorphisms (SNPs) of the matrix metalloproteinases ( MMP) genes (rs1799750 MMP1, rs3918242 and rs17576 MMP9) in Russian patients with primary open-angle glaucoma (POAG), essential hypertension (EH) and peptic ulcer (PU) are presented. Association studies identified these SNPs as possible significant markers associated with many multifactorial disorders, including POAG, EH, and PU. The frequencies of alleles and genotypes of the three SNPs in Russian patients with POAG, EH, and PU were presented separately for the entire study sample, females, and males, respectively. The data can be used as a reference for the Russian population.

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          Association between matrix metalloproteinase family gene polymorphisms and risk of ischemic stroke: A systematic review and meta-analysis of 29 studies

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            Matrix Metalloproteinase-9 (MMP-9) Gene Polymorphism in Stroke Patients

            Matrix metalloproteinases (MMPs), endopeptidases degrading extracellular matrix, play an important role in the pathogenesis of atherosclerosis and vascular disease. The aim of this study was to evaluate the association between the C(-1562)T functional polymorphism in the MMP-9 gene and risk of stroke. We examined 322 patients with stroke and 410 controls. In the patient group, 52 % had type 2 diabetes. All subjects were genotyped for the C(-1562)T polymorphism by polymerase chain reaction and restriction analysis. A significant increase in T allele and CT + TT genotype frequencies was observed in patients compared with controls (OR 1.73, 95 % CI 1.34–2.23 and 1.89, 95 % CI 1.39–2.56, respectively). The T allele carriers were younger at the onset of stroke (63.5 ± 11.7 years) than patients with CC genotype (71 ± 14.1 years) (p = 0.0002). The comparison between patients with T2DM and without it showed that the T allele and CT + TT genotype were more frequent in T2DM patients (OR 1.48, 95 % CI 1.03–2.12 for T allele and 1.44, 95 % CI 1.93–2.24 for CT + TT genotype). In conclusion, our findings suggest that MMP-9 C(-1562)T polymorphism is significantly associated with risk of stroke in patients with and without T2DM.
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              Association of genetic polymorphisms with age at menarche in Russian women

              Examine the association of genetic polymorphisms with age at menarche (AAM) in Russian women.
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                Author and article information

                Contributors
                Journal
                Data Brief
                Data Brief
                Data in Brief
                Elsevier
                2352-3409
                08 July 2020
                August 2020
                08 July 2020
                : 31
                : 106004
                Affiliations
                [a ]Department of Medical Biological Disciplines, Belgorod State University, Belgorod 308015, Russia
                [b ]Department of Life Sciences, College of Science and General Studies, Alfaisal University, Riyadh 11533, Saudi Arabia
                Author notes
                [* ]Corresponding author. reshetnikov@ 123456bsu.edu.ru
                Article
                S2352-3409(20)30898-2 106004
                10.1016/j.dib.2020.106004
                7365972
                c24c7495-74a2-4c98-9f0f-40a72f160617
                © 2020 The Author(s)

                This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).

                History
                : 7 June 2020
                : 1 July 2020
                : 3 July 2020
                Categories
                Biochemistry, Genetics and Molecular Biology

                single nucleotide polymorphism,primary open-angle glaucoma,essential hypertension,peptic ulcer,mmp

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