血液静止的遗传学:一个双胞胎研究
M de Lange1, H Snieder, R A Ariëns
1Twin Research and Genetic Epidemiology Unit, St Thomas' Hospital, London, UK.
Lancet (London, England)
|February 24, 2001
概括
遗传因素显著影响关键血液凝固蛋白的水平,影响心血管疾病的风险. 这凸显了研究血液静止和动脉血性疾病中的遗传调节的重要性.
科学领域:
- 遗传学 遗传学 是一个
- 心血管科学 心血管科学
- 血液学 血液学 血液学
背景情况:
- 纤维素原,第七因子,第八因子,·威尔布兰德因子,等离子素激活剂抑制剂-1 (PAI-1) 和组织等离子素激活剂的血度与冠心病有关.
- 纤维素素,因子VII,PAI-1和因子XIII的基因多态性影响蛋白质水平和心血管疾病风险.
研究的目的:
- 用经典双胞胎研究设计来评估关键血静止因子的遗传性.
- 调查遗传因素对血中血静蛋白度变化的贡献.
主要方法:
- 这是一项经典的双胞胎研究,涉及1002名女性双胞胎 (149名单胞胎和352名双胞胎).
- 在89个单胞胎双胞胎和196个双胞胎双胞胎双胞胎中分析VII因子度.
主要成果:
- 定量基因建模表明,遗传因素占纤维素度变化的41-75%,因子VII,因子VIII,PAI-1,组织等离子素激活剂,因子XIII (A和B子单元) 和·维勒布兰德因子.
- XIII因子活动表现出更高的遗传性 (82%),而XIIa因子表现出更低的遗传性 (38%).
结论:
- 遗传因素在决定血中血静蛋白度方面发挥着重要作用.
- 这些发现强调了研究参与血液静止和心肌梗塞和中风等动脉血病的蛋白质的遗传调节的必要性.
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