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Linkage analysis of chromosome 14 and essential hypertension in Chinese population

机译:中国人14号染色体与原发性高血压的连锁分析

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摘要

Background Hypertension is a complex biological trait that influenced by multiple factors. The encouraging results for hypertension research showed that the linkage analysis can be used to replicate other studies and discover new genetic risk factors. Previous studies linked human chromosome 14 to essential hypertension or blood pressure traits. With a Chinese population, we tried to replicate these findings. Methods A linkage scan was performed on chromosome 14 with 14-microsatellite markers with a density of about 10 centi Morgen (cM) in 147 Chinese hypertensive nuclear families. Multipoint non-parametric linkage analysis and exclusion mapping were performed with the GENEHUNTER software, whereas quantitative analysis was performed with the variance component method integrated in the SOLAR package. Results In the qualitative analysis, the highest non-parametric linkage score is 1. 0 (P =0.14) at D14S261 in the single point analysis, and no loci achieved non-parametric linkage score more than 1. 0 in the multipoint analysis. Maximum-likelihood mapping showed no significant results, either. Subsequently the traditional exclusion criteria of the log-of-the-odds score-2 were adopted, and the chromosome 14 with λs ≥ 2. 4 was excluded. In the quantitative analysis of blood pressure with the SOLAR software, two-point analysis and multipoint analysis suggested no evidence for linkage occurred on chromosome 14 for systolic and diastolic blood pressure. Conclusion There was no substantial evidence to support the linkage of chromosome 14 and essential hypertension or blood pressure trait in Chinese hypertensive subjects in this study.
机译:背景高血压是一种复杂的生物学特征,受多种因素影响。高血压研究的令人鼓舞的结果表明,连锁分析可用于复制其他研究并发现新的遗传危险因素。先前的研究将人类第14号染色体与原发性高血压或血压特征联系在一起。对于中国人,我们试图重复这些发现。方法在147个中国高血压核心家庭中,用14个微卫星标记对14号染色体进行连锁扫描,标记密度约为10厘摩根(cM)。使用GENEHUNTER软件执行多点非参数链接分析和排除映射,而使用集成在SOLAR软件包中的方差分量方法进行定量分析。结果在定性分析中,单点分析中D14S261的最高非参数连锁得分为1. 0(P = 0.14),多点分析中没有基因座的非参数连锁得分超过1. 0。最大似然映射也没有显示出明显的结果。随后,采用对数得分2的传统排除标准,排除了λs≥2。4的14号染色体。在使用SOLAR软件进行的血压定量分析中,两点分析和多点分析表明没有证据表明14号染色体上存在收缩压和舒张压的联系。结论在本研究中,没有实质性证据支持14号染色体与原发性高血压或血压性状的联系。

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