骨关节炎的遗传学和功能基因组学。

IF 7.7 2区 生物学 Q1 GENETICS & HEREDITY Annual review of genomics and human genetics Pub Date : 2024-08-01 DOI:10.1146/annurev-genom-010423-095636
Ana Luiza Arruda, Georgia Katsoula, Shibo Chen, Ene Reimann, Peter Kreitmaier, Eleftheria Zeggini
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引用次数: 0

摘要

骨关节炎是最常见的全关节退行性疾病,其特点是关节软骨和下层骨结构退化。全世界约有 6 亿人受到骨关节炎的影响。目前尚无根治性治疗方法,治疗策略主要集中于缓解疼痛。在此,我们全面概述了迄今为止针对骨关节炎开展的人类遗传学和功能基因组学研究,并阐述了这些研究是如何帮助揭示疾病病因的。我们重点介绍了全基因组关联研究中的基因发现,并详细概述了骨关节炎组织中的分子水平研究,包括甲基化、转录组学和蛋白质组学水平分析。我们回顾了来自不同分子水平的功能基因组学数据如何帮助确定效应基因的优先次序,从而将其作为药物靶点或药物再利用的机会。最后,我们讨论了有可能推动骨关节炎研究发生重大变革的未来方向。
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The Genetics and Functional Genomics of Osteoarthritis.

Osteoarthritis is the most prevalent whole-joint degenerative disorder, and is characterized by the degradation of articular cartilage and the underlying bone structures. Almost 600 million people are affected by osteoarthritis worldwide. No curative treatments are available, and management strategies focus mostly on pain relief. Here, we provide a comprehensive overview of the available human genetic and functional genomics studies for osteoarthritis to date and delineate how these studies have helped shed light on disease etiopathology. We highlight genetic discoveries from genome-wide association studies and provide a detailed overview of molecular-level investigations in osteoarthritis tissues, including methylation-, transcriptomics-, and proteomics-level analyses. We review how functional genomics data from different molecular levels have helped to prioritize effector genes that can be used as drug targets or drug-repurposing opportunities. Finally, we discuss future directions with the potential to drive a step change in osteoarthritis research.

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来源期刊
CiteScore
14.90
自引率
1.10%
发文量
29
期刊介绍: Since its inception in 2000, the Annual Review of Genomics and Human Genetics has been dedicated to showcasing significant developments in genomics as they pertain to human genetics and the human genome. The journal emphasizes genomic technology, genome structure and function, genetic modification, human variation and population genetics, human evolution, and various aspects of human genetic diseases, including individualized medicine.
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