Epigenetic age acceleration mediates the association between smoking and diabetes-related outcomes.

IF 5.7 2区 医学 Q1 Medicine
Xue-Yong Chang, Wan-Yu Lin
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引用次数: 0

Abstract

Background: Smoking can lead to the deterioration of lung function and susceptibility to diabetes. Recently, smoking was found to induce DNA methylation (DNAm) changes in some cytosine-phosphate-guanine sites (CpGs). As linear combinations of DNAm levels of aging-related CpGs, five measures of epigenetic age acceleration (EAA) have received extensive attention: HannumEAA, IEAA, PhenoEAA, GrimEAA, and DunedinPACE. It is of interest to explore whether some measures of EAA can mediate the associations of smoking with diabetes-related outcomes and indices of ventilatory lung function.

Methods and results: In this study, we included self-reported smoking variables (smoking status, the number of pack-years, and years since smoking cessation), seven DNAm markers (HannumEAA, IEAA, PhenoEAA, GrimEAA, DNAm-based smoking pack-years, DNAm plasminogen activator inhibitor 1 [PAI-1] levels, and DunedinPACE), and four health outcomes (fasting glucose, hemoglobin A1C, forced expiratory volume in 1.0 s [FEV1], and forced vital capacity [FVC]) from 2474 Taiwan Biobank participants. Mediation analyses were conducted while adjusting for chronological age, sex, body mass index, drinking status, regular exercise status, educational attainment, and five cell-type proportions. We demonstrated that GrimEAA, DNAm-based smoking pack-years, DNAm PAI-1 levels, DunedinPACE, and PhenoEAA mediated smoking associations with diabetes-related outcomes. Moreover, current and former smoking both had an adverse indirect effect on FVC through DNAm PAI-1 levels. For former smokers, a long time since smoking cessation had a positive indirect impact on FVC through GrimEAA and on FEV1 through PhenoEAA.

Conclusions: This is one of the first studies to comprehensively investigate the role of five measures of EAA in mediating the associations of smoking with the health outcomes of an Asian population. The results showed that the second-generation epigenetic clocks (GrimEAA, DunedinPACE, and PhenoEAA) significantly mediated the associations between smoking and diabetes-related outcomes. In contrast, the first-generation epigenetic clocks (HannumEAA and IEAA) did not significantly mediate any associations of smoking variables with the four health outcomes. Cigarette smoking can, directly and indirectly, deteriorate human health through DNAm changes in aging-related CpG sites.

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表观遗传年龄加速介导吸烟与糖尿病相关结果之间的关联。
背景:吸烟可导致肺功能恶化,易患糖尿病。近年来,研究人员发现吸烟可诱导部分胞嘧啶-磷酸-鸟嘌呤位点(CpGs)的DNA甲基化(DNAm)变化。作为DNAm水平与衰老相关的CpGs的线性组合,五种表观遗传年龄加速(EAA)指标受到了广泛关注:HannumEAA、IEAA、PhenoEAA、GrimEAA和DunedinPACE。我们有兴趣探讨EAA的一些测量是否可以介导吸烟与糖尿病相关结局和通气肺功能指标的关联。方法和结果:在本研究中,我们纳入了来自2474名台湾生物银行参与者的自我报告吸烟变量(吸烟状况、包年数和戒烟年限)、7种DNAm标记物(HannumEAA、IEAA、PhenoEAA、GrimEAA、基于DNAm的吸烟包年、DNAm纤溶酶原激活物抑制剂1 [PAI-1]水平和DunedinPACE)和4种健康指标(空腹血糖、血红蛋白A1C、1.0 s用力呼气量[FEV1]和用力肺活量[FVC])。在调整了年龄、性别、体重指数、饮酒状况、定期运动状况、受教育程度和五种细胞类型比例后,进行了中介分析。我们证明了GrimEAA、基于DNAm的吸烟包年、DNAm PAI-1水平、DunedinPACE和PhenoEAA介导吸烟与糖尿病相关结局的关联。此外,目前和以前吸烟均通过DNAm PAI-1水平对FVC产生不利的间接影响。对于已戒烟者,戒烟时间较长通过GrimEAA对FVC有间接正向影响,通过PhenoEAA对FEV1有间接正向影响。结论:本研究首次全面探讨了五项EAA指标在亚洲人群吸烟与健康结果之间的中介作用。结果表明,第二代表观遗传时钟(GrimEAA、DunedinPACE和PhenoEAA)显著介导了吸烟与糖尿病相关结局之间的关联。相比之下,第一代表观遗传时钟(HannumEAA和IEAA)没有显著调节吸烟变量与四种健康结果的任何关联。吸烟可通过与衰老相关的CpG位点的DNAm变化直接或间接地恶化人体健康。
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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来源期刊
Clinical Epigenetics
Clinical Epigenetics Biochemistry, Genetics and Molecular Biology-Developmental Biology
CiteScore
8.90
自引率
5.30%
发文量
150
审稿时长
12 weeks
期刊介绍: Clinical Epigenetics, the official journal of the Clinical Epigenetics Society, is an open access, peer-reviewed journal that encompasses all aspects of epigenetic principles and mechanisms in relation to human disease, diagnosis and therapy. Clinical trials and research in disease model organisms are particularly welcome.
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