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Obesity, cigarette smoking, and telomere length in women.

机译:女性肥胖,吸烟和端粒长度。

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Obesity and smoking are important risk factors for many age-related diseases. Both are states of heightened oxidative stress, which increases the rate of telomere erosion per replication, and inflammation, which enhances white blood cell turnover. Together, these processes might accelerate telomere erosion with age. We therefore tested the hypothesis that increased body mass and smoking are associated with shortened telomere length in white blood cells. We investigated 1122 white women aged 18-76 years and found that telomere length decreased steadily with age at a mean rate of 27 bp per year. Telomeres of obese women were 240 bp shorter than those of lean women (p=0.026). A dose-dependent relation with smoking was recorded (p=0.017), and each pack-year smoked was equivalent to an additional 5 bp of telomere length lost (18%) compared with the rate in the overall cohort. Our results emphasise the pro-ageing effects of obesity and cigarette smoking.
机译:肥胖和吸烟是许多与年龄有关的疾病的重要危险因素。两种状态都具有较高的氧化应激状态,这会增加每次复制时端粒的腐蚀速率,并具有发炎的状态,从而会增加白细胞的更新。这些过程在一起可能会随着年龄的增长而加速端粒侵蚀。因此,我们检验了以下假设:体重增加和吸烟与白细胞端粒长度缩短有关。我们调查了1122名18-76岁的白人妇女,发现端粒长度随着年龄的增长而稳定下降,平均每年27 bp。肥胖妇女的端粒比肥胖妇女的端粒短240 bp(p = 0.026)。记录了与吸烟的剂量依赖性关系(p = 0.017),与整个队列的发生率相比,每包年吸烟量相当于损失了另外5 bp的端粒长度(18%)。我们的结果强调了肥胖和吸烟的衰老效应。

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