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Modelling biological age based on plasma peptides in Han Chinese adults

机译:基于血浆多肽的汉族成年人生物年龄建模

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摘要

Age-related disease burdens increased over time, and whether plasma peptides can be used to accurately predict age in order to explain the variation in biological indicators remains inadequately understood. Here we first developed a biological age model based on plasma peptides in 1890 Chinese Han adults. Based on mass spectrometry, 84 peptides were detected with masses in the range of 0.6-10.0 kDa, and 13 of these peptides were identified as known amino acid sequences. Five of these thirteen plasma peptides, including fragments of apolipoprotein A-I (m/z 2883.99), fibrinogen alpha chain (m/z 3060.13), complement C3 (m/z 2190.59), complement C4-A (m/z 1898.21), and breast cancer type 2 susceptibility protein (m/z 1607.84) were finally included in the final model by performing a multivariate linear regression with stepwise selection. This biological age model accounted for 72.3% of the variation in chronological age. Furthermore, the linear correlation between the actual age and biological age was 0.851 (95% confidence interval: 0.836-0.864) and 0.842 (95% confidence interval: 0.810-0.869) in the training and validation sets, respectively. The biological age based on plasma peptides has potential positive effects on primary prevention, and its biological meaning warrants further investigation.
机译:与年龄有关的疾病负担随着时间的推移而增加,并且血浆肽是否可用于准确预测年龄以解释生物学指标的变化仍未得到足够的了解。在这里,我们首先在1890年的中国汉族成年人中建立了基于血浆多肽的生物年龄模型。基于质谱法,检测到质量在0.6-10.0 kDa范围内的84种肽,其中13种被鉴定为已知氨基酸序列。这13种血浆肽中有5种包括载脂蛋白AI(m / z 2883.99),纤维蛋白原α链(m / z 3060.13),补体C3(m / z 2190.59),补体C4-A(m / z 1898.21)和通过逐步选择进行多元线性回归,最终将乳腺癌2型易感性蛋白(m / z 1607.84)纳入最终模型。这种生物年龄模型占年代年龄变化的72.3%。此外,在训练和验证集中,实际年龄和生物学年龄之间的线性相关性分别为0.851(95%置信区间:0.836-0.864)和0.842(95%置信区间:0.810-0.869)。基于血浆肽的生物学年龄对一级预防具有潜在的积极影响,其生物学意义值得进一步研究。

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