Suppr超能文献

在瑞士,接受抗逆转录病毒疗法之前,表观遗传衰老会加速,而在病毒抑制之后,其衰老速度会减缓:一项长达 17 年的纵向研究。

Epigenetic ageing accelerates before antiretroviral therapy and decelerates after viral suppression in people with HIV in Switzerland: a longitudinal study over 17 years.

机构信息

Department of Infectious Diseases, Bern University Hospital, University of Bern, Bern, Switzerland; University Department of Medicine and Infectious Diseases Service, Kantonsspital Baselland, University of Basel, Bruderholz, Switzerland.

HIV/AIDS and Infectious Diseases Research Group, Hospital La Paz Institute for Health Research, Madrid, Spain; CIBER of Infectious Diseases, Madrid, Spain.

出版信息

Lancet Healthy Longev. 2023 May;4(5):e211-e218. doi: 10.1016/S2666-7568(23)00037-5.

Abstract

BACKGROUND

Accelerated epigenetic ageing can occur in untreated HIV infection and is partially reversible with effective antiretroviral therapy (ART). We aimed to make a long-term comparison of epigenetic ageing dynamics in people with HIV during untreated HIV infection and during suppressive ART.

METHODS

In this longitudinal study, conducted over 17 years in HIV outpatient clinics in Switzerland, we applied 5 established epigenetic age estimators (epigenetic clocks) in peripheral blood mononuclear cells (PBMCs) in Swiss HIV Cohort Study participants before or during suppressive ART. All participants had a longitudinal set of PBMC samples available at four timepoints (T1-T4). T1 and T2 had to be 3 years or longer apart, as did T3 and T4. We assessed epigenetic age acceleration (EAA) and a novel rate of epigenetic ageing.

FINDINGS

Between March 13, 1990, and Jan 18, 2018, we recruited 81 people with HIV from the Swiss HIV Cohort Study. We excluded one participant because a sample did not meet quality checks (transmission error). 52 (65%) of 80 patients were men, 76 (95%) were white, and the median patient age was 43 (IQR 37·5-47) years. Per year of untreated HIV infection (median observation 8·08 years, IQR 4·83-11·09), mean EAA was 0·47 years (95% CI 0·37 to 0·57) for Horvath's clock, 0·43 years (0·3 to 0·57) for Hannum's clock, 0·36 years (0·27 to 0·44) for SkinBlood clock, and 0·69 years (0·51 to 0·86) for PhenoAge. Per year of suppressive ART (median observation 9·8 years, IQR 7·2-11), mean EAA was -0·35 years (95% CI -0·44 to -0·27) for Horvath's clock, -0·39 years (-0·50 to -0·27) for Hannum's clock, -0·26 years (-0·33 to -0·18) for SkinBlood clock, and -0·49 years (-0·64 to -0·35) for PhenoAge. Our findings indicate that people with HIV epigenetically aged by a mean of 1·47 years for Horvath's clock, 1·43 years for Hannum's clock, 1·36 years for SkinBlood clock, and 1·69 years for PhenoAge per year of untreated HIV infection; and 0·65 years for Horvath's clock, 0·61 years for Hannum's clock, 0·74 years for SkinBlood clock, and 0·51 years for PhenoAge, per year of suppressive ART. GrimAge showed some change in the mean EAA during untreated HIV infection (0·10 years, 0·02 to 0·19) and suppressive ART (-0·05 years, -0·12 to 0·02). We obtained very similar results using the rate of epigenetic ageing. Contribution of multiple HIV-related, antiretroviral, and immunological variables, and of a DNA methylation-associated polygenic risk score to EAA was small.

INTERPRETATION

In a longitudinal study over more than 17 years, epigenetic ageing accelerated during untreated HIV infection and decelerated during suppressive ART, highlighting the importance of limiting the duration of untreated HIV infection.

FUNDING

Swiss HIV Cohort Study, Swiss National Science Foundation, and Gilead Sciences.

摘要

背景

未经治疗的 HIV 感染会导致加速的表观遗传衰老,而有效的抗逆转录病毒治疗(ART)可部分逆转这一现象。本研究旨在对未经治疗的 HIV 感染和抑制性 ART 期间 HIV 感染者的表观遗传衰老动态进行长期比较。

方法

在这项长达 17 年的纵向研究中,我们在瑞士 HIV 队列研究参与者的外周血单核细胞(PBMC)中应用了 5 种已建立的表观遗传年龄估算器(表观遗传时钟),这些参与者在接受抑制性 ART 之前或期间接受了治疗。所有参与者都有一组纵向 PBMC 样本,在四个时间点(T1-T4)采集。T1 和 T2 之间必须相隔 3 年或更长时间,T3 和 T4 也是如此。我们评估了表观遗传年龄加速(EAA)和新的表观遗传衰老率。

结果

1990 年 3 月 13 日至 2018 年 1 月 18 日期间,我们从瑞士 HIV 队列研究中招募了 81 名 HIV 感染者。由于一个样本不符合质量检查标准(传播错误),我们排除了一名参与者。80 名患者中,有 52 名(65%)为男性,76 名(95%)为白人,中位患者年龄为 43 岁(IQR 37.5-47)。在未经治疗的 HIV 感染期间,每 1 年的平均 EAA 为:Horvath 时钟为 0.47 岁(95%CI 0.37-0.57),Hannum 时钟为 0.43 岁(0.30-0.57),SkinBlood 时钟为 0.36 岁(0.27-0.44),PhenoAge 时钟为 0.69 岁(0.51-0.86)。在抑制性 ART 期间,每 1 年的平均 EAA 为:Horvath 时钟为-0.35 岁(95%CI-0.44 至-0.27),Hannum 时钟为-0.39 岁(-0.50 至-0.27),SkinBlood 时钟为-0.26 岁(-0.33 至-0.18),PhenoAge 时钟为-0.49 岁(-0.64 至-0.35)。我们的研究结果表明,HIV 感染者的表观遗传年龄平均每年增加 1.47 岁,Horvath 时钟为 1.43 岁,Hannum 时钟为 1.36 岁,SkinBlood 时钟为 1.36 岁,PhenoAge 时钟为 1.69 岁;在抑制性 ART 期间,Horvath 时钟为 0.65 岁,Hannum 时钟为 0.61 岁,SkinBlood 时钟为 0.74 岁,PhenoAge 时钟为 0.51 岁。GrimAge 在未经治疗的 HIV 感染期间的平均 EAA 略有变化(0.10 岁,0.02 至 0.19),在抑制性 ART 期间为-0.05 岁(-0.12 至 0.02)。我们使用表观遗传衰老率得到了非常相似的结果。多种 HIV 相关、抗逆转录病毒和免疫变量以及与 DNA 甲基化相关的多基因风险评分对 EAA 的贡献很小。

结论

在一项超过 17 年的纵向研究中,未经治疗的 HIV 感染期间表观遗传衰老加速,抑制性 ART 期间则减速,这突显了限制未经治疗的 HIV 感染时间的重要性。

资金

瑞士 HIV 队列研究、瑞士国家科学基金会和吉利德科学公司。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验