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冠心病中的遗传标记物。

Genetic markers in coronary heart disease.

作者信息

Kassem N S, Mokhtar M M, Elbel-Bessy M F

机构信息

Human Genetics Department, Alexandria University, Medical Research Institute, Egypt.

出版信息

J Egypt Public Health Assoc. 1994;69(5-6):359-78.

Abstract

Coronary heart disease (CHD) was found to aggregate in families. So the present study aimed at studying certain genetic markers (lipoproteins, ABO blood groups and dermatoglyphics), in a group of 60 patients with CHD and a control group to detect any significant association between such genetics markers in this disorder. This can throw light on its genetics. The study revealed significant and marked association of CHD with low alpha-lipoprotein, high pre-beta and beta-lipoproteins. No significant association wa detected with ABO phenotypes. Definite significant association was also detected between CHD and certain dermatoglyphics phenotypes including FTP, T-D count and palm patterns. These significant associations of CHD and these genetic markers "which are genetically determined" denoted strongly genetic etiology or at least genetic predisposition of CHD. Detection of such genetic markers may help in determination of risky individuals in population and families of CHD patients. This can help in prevention by proper genetic counseling.

摘要

人们发现冠心病(CHD)在家族中具有聚集性。因此,本研究旨在对60例冠心病患者及一组对照组研究某些遗传标记物(脂蛋白、ABO血型和皮纹),以检测这些遗传标记物与该疾病之间是否存在显著关联。这有助于揭示其遗传特性。研究表明,冠心病与低α脂蛋白、高前β脂蛋白和β脂蛋白之间存在显著且明显的关联。未检测到与ABO血型表型有显著关联。在冠心病与某些皮纹表型(包括指纹总数、总指嵴数和手掌纹路)之间也检测到明确的显著关联。冠心病与这些“由基因决定的”遗传标记物之间的这些显著关联强烈表明冠心病具有遗传病因或至少有遗传易感性。检测这些遗传标记物可能有助于确定人群及冠心病患者家族中的高危个体。这有助于通过适当的遗传咨询进行预防。

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