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采用 Cox 回归分析,基于发病年龄和随机选择的短串联重复序列(STR)杂合度之间的关系,筛选与脑梗死相关的遗传标记物。

Screening of cerebral infarction-related genetic markers using a Cox regression analysis between onset age and heterozygosity at randomly selected short tandem repeat loci.

机构信息

College of Medical Laboratory, Dalian Medical University, Dalian, China.

出版信息

J Thromb Thrombolysis. 2012 May;33(4):318-21. doi: 10.1007/s11239-012-0724-8.

Abstract

The aim of this paper is to explore whether the heterozygosity at the 9 CODIS short tandem repeats (STR) loci including D3S1358, vWA, FGA, D8S1179, D21S11, D18S51, D5S818, D13S317 and D7S820 is associated with the risk of atherosclerotic cerebral infarction (CI). The DNA samples were collected from patients with CI (n = 72) and people over the age of 90 years without CI (n = 59). Alleles of the STR loci were determined using the STR Profiler Plus PCR amplification kit. The relationship between the age of onset and heterozygosity was determined with the Cox regression method. A correlation between the age of onset and heterozygosity was observed for the D8S1179 locus (p < 0.05). It implied that regions in the vicinity of locus D8S1179 may harbor susceptibility genes for CI. The analysis of heterozygosity for particular loci as genetic markers using our new study design may be an efficient and reliable approach to estimate genetic predispositions.

摘要

本文旨在探讨 9 个 CODIS 短串联重复(STR)位点(包括 D3S1358、vWA、FGA、D8S1179、D21S11、D18S51、D5S818、D13S317 和 D7S820)杂合性与动脉粥样硬化性脑梗死(CI)风险之间的关系。从 CI 患者(n=72)和 90 岁以上无 CI 的人群(n=59)中采集 DNA 样本。使用 STR Profiler Plus PCR 扩增试剂盒确定 STR 位点的等位基因。采用 Cox 回归方法确定发病年龄与杂合性之间的关系。在 D8S1179 位点观察到发病年龄与杂合性之间存在相关性(p<0.05)。这意味着 D8S1179 附近的区域可能存在 CI 的易感基因。使用我们的新研究设计,将特定基因座的杂合性作为遗传标记进行分析,可能是评估遗传易感性的有效和可靠方法。

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