不同器官老化与年龄相关性黄斑变性有关。

IF 8 1区 医学 Q1 CELL BIOLOGY
Aging Cell Pub Date : 2025-01-05 DOI:10.1111/acel.14473
Anastasios Papadam, Arimantas Lionikas, Felix Grassmann
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引用次数: 0

摘要

年龄相关性黄斑变性(AMD)是一种进行性疾病,是中央视力丧失的主要原因。年龄是最重要的风险因素,其次是遗传和吸烟。然而,衰老是一个复杂的过程,个体之间和不同器官系统内的生物年龄可能偏离实足年龄。最初,我们通过分析UK Biobank队列中的各种生理和物理标记物,使用机器学习来预测免疫、心血管、肺、肾、肌肉骨骼、代谢和肝脏系统的生物年龄。然后,我们调查了每个器官的生物年龄与电子健康记录数据得出的AMD事件以及不同AMD遗传风险评分的关系。我们观察到,与对照组相比,招募后发生AMD的参与者的大多数器官系统衰老加速,免疫系统受到的影响最大,尤其是年轻男性。令人惊讶的是,我们发现,与对照组相比,AMD患者的肝脏系统衰老速度较慢,尤其是女性患者。AMD的总体遗传风险评分与除心血管和肺外的所有组织的更快器官衰老相关,而按途径分层的遗传风险评分对每个器官系统的影响不同。总之,我们发现了与AMD相关的不同器官衰老。值得注意的是,AMD的遗传风险变异与不同器官系统的不同衰老有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Differential Organ Ageing Is Associated With Age-Related Macular Degeneration.

Age-related macular degeneration (AMD) is a progressive disorder and the leading cause of central vision loss. Age is the most important risk factor, followed by genetics and smoking. However, ageing is a complex process, and biological age can deviate from chronological age between individuals and within different organ systems. Initially, we used machine learning to predict the biological age of the immune, cardiovascular, pulmonary, renal, musculoskeletal, metabolic and hepatic systems by analysing various physiological and physical markers in the UK Biobank cohort. Then, we investigated the association of each organ's biological age with incident AMD derived from electronic health record data as well as with different AMD genetic risk scores. We observed that most organ systems in participants who developed AMD after recruitment showed accelerated ageing compared with controls, with the immune system being the most affected, especially in younger males. Surprisingly, we found that AMD patients showed slower ageing of their hepatic system compared to controls, particularly in female patients. The overall AMD genetic risk score was associated with faster organ ageing across all tissues except cardiovascular and pulmonary, while genetic risk scores stratified by pathways differently influenced each organ system. In conclusion, we found differential organ ageing associated with AMD. Significantly, genetic risk variants of AMD are associated with differential ageing of various organ systems.

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来源期刊
Aging Cell
Aging Cell Biochemistry, Genetics and Molecular Biology-Cell Biology
自引率
2.60%
发文量
212
期刊介绍: Aging Cell is an Open Access journal that focuses on the core aspects of the biology of aging, encompassing the entire spectrum of geroscience. The journal's content is dedicated to publishing research that uncovers the mechanisms behind the aging process and explores the connections between aging and various age-related diseases. This journal aims to provide a comprehensive understanding of the biological underpinnings of aging and its implications for human health. The journal is widely recognized and its content is abstracted and indexed by numerous databases and services, which facilitates its accessibility and impact in the scientific community. These include: Academic Search (EBSCO Publishing) Academic Search Alumni Edition (EBSCO Publishing) Academic Search Premier (EBSCO Publishing) Biological Science Database (ProQuest) CAS: Chemical Abstracts Service (ACS) Embase (Elsevier) InfoTrac (GALE Cengage) Ingenta Select ISI Alerting Services Journal Citation Reports/Science Edition (Clarivate Analytics) MEDLINE/PubMed (NLM) Natural Science Collection (ProQuest) PubMed Dietary Supplement Subset (NLM) Science Citation Index Expanded (Clarivate Analytics) SciTech Premium Collection (ProQuest) Web of Science (Clarivate Analytics) Being indexed in these databases ensures that the research published in Aging Cell is discoverable by researchers, clinicians, and other professionals interested in the field of aging and its associated health issues. This broad coverage helps to disseminate the journal's findings and contributes to the advancement of knowledge in geroscience.
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