吸烟微滴数字PCR检测预测全因死亡率。

Q3 Medicine Journal of insurance medicine (New York, N.Y.) Pub Date : 2018-01-01 Epub Date: 2019-01-31 DOI:10.17849/insm-47-4-1-10.1
Allan M Andersen, Philip T Ryan, Fredrick X Gibbons, Ronald L Simons, Jeffrey D Long, Robert A Philibert
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引用次数: 0

摘要

目的:确定参与爱荷华州被收养者纵向研究的成年人吸烟的表观遗传分析是否能预测全因死亡率。背景:考虑到吸烟对公共卫生的巨大影响,以及自我报告和现有生物标志物(如可替宁)在检测吸烟方面的显著局限性,需要改进吸烟的生物标志物。在过去的5年中,多项吸烟表观基因组关联研究已经确定了适合翻译为吸烟表观遗传生物标志物的位点,特别是CpG cg05575921。数字聚合酶链反应方法为这种和其他表观遗传生物标志物的开发带来了希望。方法:对爱荷华州收养研究的参与者进行了关于吸烟习惯的访谈。从全血中制备DNA,亚硫酸氢盐转化用于甲基化分析,并对cg05575921进行甲基化的数字液滴聚合酶链反应。584名研究参与者获得了国家死亡指数记录,得到24个完全匹配记录,210个部分匹配记录和350个不匹配记录。完全匹配的被编码为死亡,而其余的被编码为活着(即被审查)。总共有N = 193名受试者的甲基化数据和重要状态信息,包括15名死者和178名非死者。采用Cox回归来检验cg05575921甲基化作为一个连续值预测死亡率时间的能力,无论是否将年龄、性别、种族、BMI、婚姻状况、教育状况、社会经济状况、心血管危险因素和癌症史作为协变量。结果:在考虑了主要的人口统计学和临床危险因素后,cg05575921位点的甲基化作为唯一的预测因素预测了死亡的危险。拟合模型显示,甲基化每降低1%,风险比增加3.5%。结论:在一项成人纵向研究中,考虑到主要人口统计学和临床风险因素对全因死亡率的影响后,c05575921甲基化降低与早期死亡率相关,这是一种新兴的吸烟表观遗传生物标志物。这种方法可用于临床研究或精算评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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A Droplet Digital PCR Assay for Smoking Predicts All-Cause Mortality.

Objectives: -Determine whether an epigenetic assay for smoking predicts all-cause mortality in adults participating in a longitudinal study of Iowa adoptees.

Background: -Improved biomarkers for smoking are needed given its large public health impact and significant limitations of both self-report and current biomarkers, such as cotinine in detecting smoking. In the past 5 years, multiple epigenome-wide association studies of smoking have identified loci suitable for translation as epigenetic biomarkers for smoking, in particular the CpG cg05575921. Digital polymerase chain reaction methods hold promise for the development of this and other epigenetic biomarkers.

Methods: -Participants in the Iowa Adoption Studies were interviewed regarding their smoking habits. DNA was prepared from whole blood and bisulfite-converted for methylation analysis and digital droplet polymerase chain reaction assay of methylation at cg05575921 was performed. National Death Index records were requested for 584 study participants, resulting in 24 complete matches, 210 partial matches and 350 non-matching records. Complete matches were coded as deceased while the remainder were coded as alive (ie, censored). In total, methylation data and vital status information were available for a total of N = 193 subjects, including 15 deceased and 178 non-deceased. Cox regression was used to examine the ability of cg05575921 methylation as a continuous value to predict the timing of mortality with and without the inclusion of age, sex, race, BMI, marital status, educational status, socioeconomic status, cardiovascular risk factors, and a history of cancer as covariates.

Results: -Methylation at cg05575921 predicted the hazard of mortality as the sole predictor and after accounting for major demographic and clinical risk factors. The fitted model showed the hazard ratio increased by 3.5% for every 1% decrease in methylation.

Conclusions: -Decreased methylation at cg05575921, an emerging epigenetic biomarker for smoking, was associated with early mortality in a longitudinal study of adults after accounting for the impact of major demographic and clinical risk factors for all-cause mortality. This approach may be useful in clinical research or actuarial assessments.

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期刊介绍: The Journal of Insurance Medicine is a peer reviewed scientific journal sponsored by the American Academy of Insurance Medicine, and is published quarterly. Subscriptions to the Journal of Insurance Medicine are included in your AAIM membership.
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