摘要
目的:探讨环境因素及线粒体基因突变在原发性高血压(EH)发病机制中的协同作用,为临床诊断和治疗EH提供新的思路。方法:在解放军总医院就诊的990例EH患者接受了详细的病史采集、生化检查及线粒体基因测序分析。结果:多元统计分析显示,EH患者收缩压与线粒体A8343G点突变(β=-22.99±9.00,P=0.01),T8603C点突变(β=26.39±10.39,P=0.01)及性别(β=3.52±1.27,P=0.01)相关;动脉舒张压则与的线粒体基因A8343G点突变(β=-16.31±5.44,P=0.01)、性别(β=-0.34±0.03,P<0.01)、心率(β=0.13±0.03,P=0.01)、家族史(β=1.80±0.78,P=0.02)、入选年龄(β=-0.34±0.03,P<0.01)、发病年龄(β=-0.08±0.03,P=0.01)及空腹血糖(β=-1.96±0.80,P=0.01)相关。结论:线粒体多基因突变与环境因素协同作用影响EH患者的血压。
Objective: To investigate the role of environmental factors and mitochondrial mutations in the pathogenesis of Chinese essential hypertensives(EH), to find a new way to diagnose and treat hypertension. Method:The 990 EH patients (18-100 years, average age [66.51± 15.82] years) were recruited. They were outpatients or in - patients at the General Hospital of PLA , China . All patients accepted thorough examinations including medical records review, biochemical assays and mitochondrial genome sequencing. Result: Multivariate analyses showed systolic blood pressure was related to sex (β= 3.52±1.27, P= 0.01), mitochondrial point mutationsA8343G (β=-22. 99±9. 00, P=0.01) and T8603C (β=26.39±10.39, P=0.01). Diastolic blood pressure was associated with sex (β=0.34±0.03, P〈0.01),heart rate (β= 0.13 ± 0. 03 , P=0.01), family history (β=1.80±0.78, P=0.02), age (β=-0.34±0.03, P〈0.01), age-on-set (β= 0.08±0.03, P=0.01), fasting blood glucose (β= -1.96±0.80, P=0.01), mutation A8343G (β=-16.31±5.44, P=0.01). Conclusion: Multigenic changes together with environmental factors may affect blood pressure in EH.
出处
《临床心血管病杂志》
CAS
CSCD
北大核心
2009年第2期109-111,共3页
Journal of Clinical Cardiology
基金
首都发展基金重点项目:老年多病因心力衰竭病因学的基础研究(No:2013-2019)
关键词
高血压
线粒体基因
环境因素
hypertension
mitochondrial genome
environmental factors