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中国女性多巴胺能通路相关基因多态性与血压和尿酸水平的关系。

Association of polymorphisms in genes involved in the dopaminergic pathway with blood pressure and uric acid levels in Chinese females.

机构信息

Science Education Center and Graduate Institute of Science Education, National Taiwan Normal University, 88 Sec. 4, Ting-Chou Rd., Taipei 116, Taiwan, ROC.

出版信息

J Neural Transm (Vienna). 2010 Dec;117(12):1371-6. doi: 10.1007/s00702-010-0492-6. Epub 2010 Oct 8.

Abstract

Since the high degree of heritability of physiological traits was demonstrated by twin and adoption studies, contemporary researchers in the fields of clinical medicine, behavioral science, and genetics have acknowledged the crucial role of genetic factors in human physiology. The study described herein explores the association between physiological parameters and the dopaminergic system using molecular genetic techniques. A total of 558 Taiwanese female volunteers, ranging from 16 to 17 years, were recruited. Single nucleotide polymorphisms in genes involved in the dopaminergic pathway were selected for analysis. Systolic blood pressure and diastolic blood pressure were associated significantly with the catechol-O-methyltransferase (COMT) Val158Met polymorphism and the dopamine β-hydroxylase (DBH) C1021T polymorphism. Furthermore, plasma uric acid was associated significantly with the COMT Val158Met polymorphism. Our study suggests the possible involvement of genetic polymorphisms in COMT and DBH in the regulation of blood pressure and plasma uric acid.

摘要

由于双胞胎和收养研究表明生理特征的遗传性很高,临床医学、行为科学和遗传学领域的当代研究人员已经认识到遗传因素在人类生理学中的关键作用。本文所述的研究使用分子遗传技术探讨了生理参数与多巴胺能系统之间的关系。共招募了 558 名年龄在 16 至 17 岁的台湾女性志愿者。选择多巴胺能途径中涉及的基因的单核苷酸多态性进行分析。收缩压和舒张压与儿茶酚-O-甲基转移酶(COMT)Val158Met 多态性和多巴胺β-羟化酶(DBH)C1021T 多态性显著相关。此外,血浆尿酸与 COMT Val158Met 多态性显著相关。我们的研究表明,COMT 和 DBH 中的遗传多态性可能参与了血压和血浆尿酸的调节。

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