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COVID-19 感染 6 个月后检测到的表观遗传模式、加速的生物衰老和增强的表观遗传漂移:来自全基因组 DNA 甲基化研究的见解。

Epigenetic patterns, accelerated biological aging, and enhanced epigenetic drift detected 6 months following COVID-19 infection: insights from a genome-wide DNA methylation study.

机构信息

Bioinformatics and Statistical Genomics Unit, IRCCS Istituto Auxologico Italiano, Cusano Milanino, Milan, Italy.

Department of Cardiology, S. Luca Hospital, IRCCS, Istituto Auxologico Italiano, Milan, Italy.

出版信息

Clin Epigenetics. 2024 Aug 20;16(1):112. doi: 10.1186/s13148-024-01724-9.

Abstract

BACKGROUND

The epigenetic status of patients 6-month post-COVID-19 infection remains largely unexplored. The existence of long-COVID, or post-acute sequelae of SARS-CoV-2 infection (PASC), suggests potential long-term changes. Long-COVID includes symptoms like fatigue, neurological issues, and organ-related problems, regardless of initial infection severity. The mechanisms behind long-COVID are unclear, but virus-induced epigenetic changes could play a role.

METHODS AND RESULTS

Our study explores the lasting epigenetic impacts of SARS-CoV-2 infection. We analyzed genome-wide DNA methylation patterns in an Italian cohort of 96 patients 6 months after COVID-19 exposure, comparing them to 191 healthy controls. We identified 42 CpG sites with significant methylation differences (FDR < 0.05), primarily within CpG islands and gene promoters. Dysregulated genes highlighted potential links to glutamate/glutamine metabolism, which may be relevant to PASC symptoms. Key genes with potential significance to COVID-19 infection and long-term effects include GLUD1, ATP1A3, and ARRB2. Furthermore, Horvath's epigenetic clock showed a slight but significant age acceleration in post-COVID-19 patients. We also observed a substantial increase in stochastic epigenetic mutations (SEMs) in the post-COVID-19 group, implying potential epigenetic drift. SEM analysis identified 790 affected genes, indicating dysregulation in pathways related to insulin resistance, VEGF signaling, apoptosis, hypoxia response, T-cell activation, and endothelin signaling.

CONCLUSIONS

Our study provides valuable insights into the epigenetic consequences of COVID-19. Results suggest possible associations with accelerated aging, epigenetic drift, and the disruption of critical biological pathways linked to insulin resistance, immune response, and vascular health. Understanding these epigenetic changes could be crucial for elucidating the complex mechanisms behind long-COVID and developing targeted therapeutic interventions.

摘要

背景

COVID-19 感染后 6 个月患者的表观遗传状态在很大程度上仍未得到探索。长 COVID 或 SARS-CoV-2 感染的急性后期后遗症(PASC)的存在表明存在潜在的长期变化。长 COVID 包括疲劳、神经问题和与器官相关的问题等症状,无论初始感染的严重程度如何。长 COVID 的发病机制尚不清楚,但病毒诱导的表观遗传变化可能发挥作用。

方法和结果

我们的研究探讨了 SARS-CoV-2 感染的持久表观遗传影响。我们分析了意大利 96 名 COVID-19 暴露后 6 个月患者的全基因组 DNA 甲基化模式,将其与 191 名健康对照进行比较。我们确定了 42 个具有显著甲基化差异的 CpG 位点(FDR<0.05),主要位于 CpG 岛和基因启动子内。失调的基因突出了与谷氨酸/谷氨酰胺代谢的潜在联系,这可能与 PASC 症状相关。对 COVID-19 感染和长期影响具有潜在意义的关键基因包括 GLUD1、ATP1A3 和 ARRB2。此外,霍瓦特表观遗传时钟在 COVID-19 后患者中显示出轻微但显著的年龄加速。我们还观察到 COVID-19 后组中随机表观遗传突变(SEMs)的大量增加,暗示潜在的表观遗传漂移。SEMs 分析确定了 790 个受影响的基因,表明与胰岛素抵抗、VEGF 信号、细胞凋亡、缺氧反应、T 细胞激活和内皮素信号相关的途径失调。

结论

我们的研究提供了 COVID-19 后表观遗传后果的有价值的见解。结果表明,可能与加速衰老、表观遗传漂移以及与胰岛素抵抗、免疫反应和血管健康相关的关键生物途径的破坏有关。了解这些表观遗传变化对于阐明长 COVID 的复杂机制和开发靶向治疗干预措施可能至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af9d/11337605/48bac1833b14/13148_2024_1724_Fig1_HTML.jpg

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