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Influence of Age on Clock Gene Expression in Peripheral Blood Cells of Healthy Women

机译:年龄对健康女性外周血细胞时钟基因表达的影响

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Recent studies have demonstrated a close relationship between circadian clock function and the development of obesity and various age-related diseases. In this study, we investigated whether messenger RNA (mRNA) levels of clock genes are associated with age, body mass index, blood pressures, fasting plasma glucose, or shift work. Peripheral blood cells were obtained from 70 healthy women, including 25 shift workers, at approximately 9:00 am. Transcript levels of clock genes (CLOCK, BMAL1, PERI, and PER3) were determined by real-time quantitative polymerase chain reaction. Step-wise multiple regression analysis demonstrated that BMAL1 mRNA levels were correlated only with age (p = -.50, p < .001). In contrast, PER3 levels were correlated with fasting plasma glucose (P = -.29, p < .05) and shift work (p = .31, p < .05): These results suggest that increased age, glucose intolerance, and irregular hours independently affect the intracellular clock in humans.
机译:最近的研究表明,昼夜节律功能与肥胖和各种与年龄有关的疾病的发展之间有着密切的关系。在这项研究中,我们调查了时钟基因的信使RNA(mRNA)水平是否与年龄,体重指数,血压,空腹血糖或轮班工作有关。大约上午9:00从70名健康女性(包括25名轮班工人)获得了外周血细胞。通过实时定量聚合酶链反应确定时钟基因(CLOCK,BMAL1,PERI和PER3)的转录水平。逐步多元回归分析表明,BMAL1 mRNA水平仅与年龄相关(p = -.50,p <.001)。相比之下,PER3水平与空腹血糖(P = -.29,p <.05)和轮班工作(p = .31,p <.05)相关:这些结果表明年龄增加,葡萄糖耐受不良和不规则小时独立地影响人类的细胞内时钟。

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