儿童原发性高血压的遗传易感性:17个单核苷酸多态性分析。

S. Goncharov, V. Gurianova, D. Stroy, T. Drevytska, S. P. Kaplinskii, E. A. Nastenko, M. Litvinenko, R. V. Terletskiy, M. Khaitovych, O. Moibenko, V. Dosenko
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引用次数: 3

摘要

对17个单核苷酸多态性进行了研究,以确定原发性高血压的遗传易感性因素。采用聚合酶链反应(PCR)、限制性内切片段长度分析、等位基因特异性PCR或实时荧光定量PCR对145例原发性高血压患儿和144例健康人的14个基因的17个单核苷酸多态性进行基因分型,并进行复杂的多因素统计分析。两个单核苷酸多态性——MMP9 (C(-1562)—> T)和NOS3 (Glu298—> Asp)—rs3918242和rs1799983——被证明是具有最高预测潜力的主要独立效应(二元逻辑回归显示77.1%,多因子降维显示74.6%的测试准确性)。MMP9 (C(-1562 -> T)和NOS3 (Glu298 -> Asp)可能被用于建立预测算法,以确定儿童动脉高血压易感。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genetic predisposition to essential hypertension in children: analysis of 17 single nucleotide polymorphisms.
Study of 17 single nucleotide polymorphisms has been performed to determine the factors of genetic predisposition to essential hypertension. Polymerase chain reaction (PCR) with subsequent analysis of restriction fragment length, allele specific PCR or real-time PCR was used for genotyping of 17 single nucleotide polymorphisms in 14 genes in 145 children with essential hypertension and 144 healthy persons with following complex multivariate statistical analysis. Two single nucleotide polymorphisms--MMP9 (C(-1562) --> T) and NOS3 (Glu298 --> Asp)--rs3918242 and rs1799983--were shown to represent the main independent effects with the highest predictive potential (77.1% as indicated by binary logistic regression and 74.6% testing accuracy shown by Multifactorial Dimensionality Reduction). MMP9 (C(-1562 --> T) and NOS3 (Glu298 --> Asp) potentially may be used to create predictive algorithm for determination of predisposition to arterial hypertension in children.
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