Evaluation of the mechanisms of sarcopenia in chronic inflammatory disease: protocol for a prospective cohort study.

IF 5.3 2区 医学 Q2 CELL BIOLOGY Skeletal Muscle Pub Date : 2021-12-11 DOI:10.1186/s13395-021-00282-5
Amritpal Dhaliwal, Felicity R Williams, Jonathan I Quinlan, Sophie L Allen, Carolyn Greig, Andrew Filer, Karim Raza, Subrata Ghosh, Gareth G Lavery, Philip N Newsome, Surabhi Choudhary, Leigh Breen, Matthew J Armstrong, Ahmed M Elsharkawy, Janet M Lord
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引用次数: 4

Abstract

Background: Several chronic inflammatory diseases co-exist with and accelerate sarcopenia (reduction in muscle strength, function and mass) and negatively impact on both morbidity and mortality. There is currently limited research on the extent of sarcopenia in such conditions, how to accurately assess it and whether there are generic or disease-specific mechanisms driving sarcopenia. Therefore, this study aims to identify potential mechanisms driving sarcopenia within chronic inflammatory disease via a multi-modal approach; in an attempt to help define potential interventions for future use.

Methods: This prospective cohort study will consist of a multi-modal assessment of sarcopenia and its underlying mechanisms. Recruitment will target three chronic inflammatory diseases: chronic liver disease (CLD) (n=50), with a subset of NAFLD (n=20), inflammatory bowel disease (IBD) (n=50) and rheumatoid arthritis (RA) (n=50) both before and after therapeutic intervention. In addition, 20 age and sex matched healthy individuals will be recruited for comparison. Participants will undergo 4 assessment visits at weeks 0, 2, 12 and 24. Visits will consist of the following assessments: blood tests, anthropometrics, functional assessment, quadriceps muscle imaging, actigraphy, quality of life questionnaires, food diary collection and muscle biopsy of the vastus lateralis (at weeks 2 and 24 only). In addition, stool and urine samples will be collected for future microbiome and metabolomics analysis.

Discussion: This is the first study to use a multi-modal assessment model to phenotype sarcopenia in these chronic inflammatory diseases. We hope to identify generic as well as disease-specific mechanisms driving sarcopenia. We appreciate that these cohorts do require separate standards of care treatments which limit comparison between groups.

Ethics and dissemination: The study is approved by the Health Research Authority - West Midlands Solihull Research Ethics Service Committee Authority (REC reference: 18/WM/0167). Recruitment commenced in January 2019 and will continue until July 2021. The study was halted in March 2020 and again in January 2021 with the COVID-19 pandemic. The findings will be disseminated through peer-reviewed publications and conference presentations. All data will be stored on a secure server.

Trial registration: ClinicalTrials.gov Identifier: NCT04734496.

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慢性炎症性疾病中肌肉减少的机制评价:一项前瞻性队列研究方案
背景:几种慢性炎症性疾病与肌肉减少症(肌肉力量、功能和质量下降)并存并加速其发生,对发病率和死亡率都有负面影响。目前关于这种情况下肌肉减少症的程度、如何准确评估以及是否存在一般性或疾病特异性机制驱动肌肉减少症的研究有限。因此,本研究旨在通过多模式方法确定慢性炎症疾病中驱动肌肉减少症的潜在机制;试图帮助确定未来使用的潜在干预措施。方法:这项前瞻性队列研究将包括对肌肉减少症及其潜在机制的多模式评估。招募将针对三种慢性炎症性疾病:慢性肝病(CLD) (n=50), NAFLD (n=20)的一个子集,炎症性肠病(IBD) (n=50)和类风湿性关节炎(RA) (n=50)在治疗干预前后。此外,还将招募20名年龄和性别匹配的健康个体进行比较。参与者将在第0、2、12和24周接受4次评估访问。访问将包括以下评估:血液检查、人体测量、功能评估、股四头肌成像、活动成像、生活质量问卷调查、食物日记收集和股外侧肌活检(仅在第2周和第24周)。此外,将收集粪便和尿液样本,用于未来的微生物组学和代谢组学分析。讨论:这是第一个使用多模态评估模型对这些慢性炎症性疾病中的肌肉减少症进行表型分析的研究。我们希望确定驱动肌肉减少症的一般机制以及疾病特异性机制。我们认识到,这些队列确实需要单独的护理治疗标准,这限制了组间的比较。伦理和传播:该研究得到了卫生研究管理局-西米德兰兹索利赫尔研究伦理服务委员会管理局(REC参考:18/WM/0167)的批准。招聘于2019年1月开始,将持续到2021年7月。该研究于2020年3月和2021年1月因COVID-19大流行而再次停止。研究结果将通过同行评议的出版物和会议报告进行传播。所有数据将被存储在一个安全的服务器上。试验注册:ClinicalTrials.gov标识符:NCT04734496。
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来源期刊
Skeletal Muscle
Skeletal Muscle CELL BIOLOGY-
CiteScore
9.10
自引率
0.00%
发文量
25
审稿时长
12 weeks
期刊介绍: The only open access journal in its field, Skeletal Muscle publishes novel, cutting-edge research and technological advancements that investigate the molecular mechanisms underlying the biology of skeletal muscle. Reflecting the breadth of research in this area, the journal welcomes manuscripts about the development, metabolism, the regulation of mass and function, aging, degeneration, dystrophy and regeneration of skeletal muscle, with an emphasis on understanding adult skeletal muscle, its maintenance, and its interactions with non-muscle cell types and regulatory modulators. Main areas of interest include: -differentiation of skeletal muscle- atrophy and hypertrophy of skeletal muscle- aging of skeletal muscle- regeneration and degeneration of skeletal muscle- biology of satellite and satellite-like cells- dystrophic degeneration of skeletal muscle- energy and glucose homeostasis in skeletal muscle- non-dystrophic genetic diseases of skeletal muscle, such as Spinal Muscular Atrophy and myopathies- maintenance of neuromuscular junctions- roles of ryanodine receptors and calcium signaling in skeletal muscle- roles of nuclear receptors in skeletal muscle- roles of GPCRs and GPCR signaling in skeletal muscle- other relevant aspects of skeletal muscle biology. In addition, articles on translational clinical studies that address molecular and cellular mechanisms of skeletal muscle will be published. Case reports are also encouraged for submission. Skeletal Muscle reflects the breadth of research on skeletal muscle and bridges gaps between diverse areas of science for example cardiac cell biology and neurobiology, which share common features with respect to cell differentiation, excitatory membranes, cell-cell communication, and maintenance. Suitable articles are model and mechanism-driven, and apply statistical principles where appropriate; purely descriptive studies are of lesser interest.
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