注射吸毒和丙型肝炎的共同出现会增加表观遗传年龄加速,从而导致艾滋病毒感染者的全因死亡率。

IF 2.9 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Xiaoyu Liang, Amy C Justice, Vincent C Marconi, Bradley E Aouizerat, Ke Xu
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引用次数: 0

摘要

注射吸毒(IDU)和丙型肝炎病毒感染(HCV)在HIV感染者中很常见,并导致死亡率显著增加。源自DNA甲基化(DNAm)的表观遗传学时钟与疾病进展和全因死亡率有关。在这项研究中,我们假设表观遗传学年龄介导了IDU和HCV的共现与PLWH死亡率之间的关系。我们在退伍军人老龄化队列研究(n = 927)通过使用DNAm年龄的四个已建立的表观遗传学时钟(即Horvath、Hannum、Pheno、Grim)。与没有IDU和HCV(IDU-HCV-)的个体相比,有IDU和丙型肝炎病毒(IDU+CHCV+)的参与者显示出使用Cox比例风险模型估计的死亡风险高2.23倍(风险比:2.23;95%置信区间:1.62-3.09;p = 1.09E-06)。IDU+HCV+与表观遗传学年龄加速(EAA)显著增加有关,通过4个表观遗传学时钟中的3个来测量,并根据人口统计学和临床变量进行调整(Hannum:p = 8.90E-04,Pheno:p = 2.34E-03,严峻:p = 3.33E-11)。此外,我们发现表观遗传学年龄部分介导IDU+CHCV+与全因死亡率之间的关系,高达13.67%的介导比例。我们的研究结果表明,IDU与HCV共病会增加PLWH中的EAA,这在一定程度上介导了死亡率的增加。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Co-occurrence of injection drug use and hepatitis C increases epigenetic age acceleration that contributes to all-cause mortality among people living with HIV.

Co-occurrence of injection drug use and hepatitis C increases epigenetic age acceleration that contributes to all-cause mortality among people living with HIV.

Co-occurrence of injection drug use and hepatitis C increases epigenetic age acceleration that contributes to all-cause mortality among people living with HIV.

Co-occurrence of injection drug use and hepatitis C increases epigenetic age acceleration that contributes to all-cause mortality among people living with HIV.

Co-occurrence of injection drug use (IDU) and hepatitis C virus infection (HCV) is common in people living with HIV (PLWH) and leads to significantly increased mortality. Epigenetic clocks derived from DNA methylation (DNAm) are associated with disease progression and all-cause mortality. In this study, we hypothesized that epigenetic age mediates the relationships between the co-occurrence of IDU and HCV with mortality risk among PLWH. We tested this hypothesis in the Veterans Aging Cohort Study (n = 927) by using four established epigenetic clocks of DNAm age (i.e., Horvath, Hannum, Pheno, Grim). Compared to individuals without IDU and HCV (IDU-HCV-), participants with IDU and HCV (IDU+HCV+) showed a 2.23-fold greater risk of mortality estimated using a Cox proportional hazards model (hazard ratio: 2.23; 95% confidence interval: 1.62-3.09; p = 1.09E-06). IDU+HCV+ was associated with a significantly increased epigenetic age acceleration (EAA) measured by 3 out of 4 epigenetic clocks, adjusting for demographic and clinical variables (Hannum: p = 8.90E-04, Pheno: p = 2.34E-03, Grim: p = 3.33E-11). Furthermore, we found that epigenetic age partially mediated the relationship between IDU+HCV+ and all-cause mortality, up to a 13.67% mediation proportion. Our results suggest that comorbid IDU with HCV increases EAA in PLWH that partially mediates the increased mortality risk.

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来源期刊
Epigenetics
Epigenetics 生物-生化与分子生物学
CiteScore
6.80
自引率
2.70%
发文量
82
审稿时长
3-8 weeks
期刊介绍: Epigenetics publishes peer-reviewed original research and review articles that provide an unprecedented forum where epigenetic mechanisms and their role in diverse biological processes can be revealed, shared, and discussed. Epigenetics research studies heritable changes in gene expression caused by mechanisms others than the modification of the DNA sequence. Epigenetics therefore plays critical roles in a variety of biological systems, diseases, and disciplines. Topics of interest include (but are not limited to): DNA methylation Nucleosome positioning and modification Gene silencing Imprinting Nuclear reprogramming Chromatin remodeling Non-coding RNA Non-histone chromosomal elements Dosage compensation Nuclear organization Epigenetic therapy and diagnostics Nutrition and environmental epigenetics Cancer epigenetics Neuroepigenetics
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