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首页> 外文期刊>Clinical and experimental pharmacology & physiology >Increased carotid plaque burden in men with the fibrillin-1 2/3 genotype
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Increased carotid plaque burden in men with the fibrillin-1 2/3 genotype

机译:纤维蛋白-1 2/3基因型男性的颈动脉斑块负担增加

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Fibrillin-1 (FBN1) is an important constituent of the vascular wall and earlier studies have indicated an effect of the FBN1 2/3 genotype on blood pressure as well as aortic stiffness in men. The aim of the present study was to determine whether the FBN1 2/3 genotype was associated with the presence of carotid plaque and incident cardiovascular morbidity and mortality in middle-aged subjects. The FBN1 genotype was characterized in 5765 subjects (2424 men, 3341 women; age 45-69 years) recruited from the Malm? Diet and Cancer Study Cardiovascular Cohort, Sweden. Plaque occurrence and intima-media thickness (IMT) of the carotid artery were assessed by ultrasound. The incidence of first cardiovascular events (myocardial infarction and stroke) and cause-specific mortality were monitored over a mean follow-up period of 13.2 years. The most common FBN1 genotypes were 2/2, 2/3 and 2/4, which accounted for 92.2% (n = 5317) of subjects. There were no differences between the three genotypes regarding age, blood pressure, glucose, lipids, smoking habits, common carotid artery diameter and intima-media thickness in men and women. The presence of plaque in the carotid artery was higher in men with the 2/3 genotype compared with the 2/2 and 2/4 genotypes (55% vs 46% and 50%, respectively; P = 0.007). No similar differences were observed in women. No significant relationship was observed between FBN1 genotypes and the incidence of cardiovascular disease or all-cause mortality. The increased prevalence of plaque in the carotid artery of middle-aged men with the FBN1 2/3 genotype indicates pathological arterial wall remodelling with a more pronounced atherosclerotic burden.
机译:Fibrillin-1(FBN1)是血管壁的重要组成部分,早期的研究表明FBN1 2/3基因型对男性的血压以及主动脉僵硬都有影响。本研究的目的是确定FBN1 / 2/3基因型是否与颈动脉斑块的存在以及中年受试者的心血管发病率和死亡率有关。 FBN1基因型的特征是从马尔姆(Malm)招募的5765名受试者中(2424名男性,3341名女性;年龄45-69岁)。瑞典饮食与癌症研究心血管研究队列。通过超声评估颈动脉斑块的发生和内膜中层厚度(IMT)。在平均13.2年的随访期内,监测了首次心血管事件(心肌梗塞和中风)的发生率和特定原因的死亡率。最常见的FBN1基因型为2 / 2、2 / 3和2/4,占受试者的92.2%(n = 5317)。男女之间在年龄,血压,葡萄糖,脂质,吸烟习惯,颈总动脉直径和内膜中层厚度这三种基因型之间没有差异。具有2/3基因型的男性与2/2和2/4基因型的男性相比,颈动脉斑块的存在更高(分别为55%,46%和50%; P = 0.007)。在女性中没有观察到类似的差异。 FBN1基因型与心血管疾病或全因死亡率之间没有显着相关性。 FBN1 2/3基因型的中年男性颈动脉斑块患病率增加表明病理性动脉壁重塑,动脉粥样硬化负担更明显。

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