跳至主要内容
临床试验/NCT06312774
NCT06312774尚未招募不适用

Feasibility Study for Comparative Analysis of Proteome and Single-cell RNA Sequencing in Chronic Lung Disease Patients With and Without Sarcopenia

University College, London0 个研究点目标入组 49 人开始时间: 2024年4月18日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
49
主要终点
Sarcopenia

研究概览

简要总结

Sarcopenia, the loss of muscle mass and strength with ageing, is a prevalent condition in older adults, particularly those with chronic lung diseases like COPD and interstitial lung disease. The condition exacerbates the decline in physical ability, leading to decreased mobility, impaired quality of life, and increased disability. Sarcopenia's prevalence varies across populations, estimated to affect up to 10% of adults over 60 worldwide, with higher rates reported in studies employing consensus definitions of sarcopenia. The prevalence is even higher in patients with chronic lung diseases, reaching up to 26.6%. Sarcopenia's impact on health-related quality of life has been widely investigated. The condition is associated with various comorbidities, including chronic heart failure, obesity, diabetes, and chronic kidney disease, all negatively impacting the quality of life.

The proposed study's primary aim is to assess the feasibility of the FACS (finding, assessing, confirming, severity) approach in determining sarcopenia's prevalence in the chronic lung disease population. FACS includes screening, strength measurements, and bioelectrical impedance analysis (BIA) to confirm sarcopenia.

The study will also explore potential mechanisms associated with sarcopenia in this population, using proteome and single-cell transcriptome profiles. These multi-omics approaches provide a comprehensive view of the cellular and molecular changes underlying sarcopenia.In particular, the study will evaluate patient acceptance, time efficiency of each test, and recruitment effectiveness. The outcomes will guide the design and execution of subsequent, larger studies and provide preliminary data for power calculation for the full-scale study.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adult patients diagnosed with chronic lung disease (≥ 18years).
  • Only patients who are willing and able to provide informed consent to participate in the study.

排除标准

  • Patients with other major comorbidities that could significantly impact muscle mass and function, such as severe heart failure, advanced liver or kidney disease, uncontrolled diabetes, or malignancies.
  • Patients with acute exacerbations of their chronic lung disease or any other acute illness at the time of the study.
  • Patients with a history of neuromuscular disorders or disability that could significantly affect muscle mass and function.
  • Patients who have undergone recent surgery in the past 6 months or have received specific treatments that could influence muscle mass and function, such as long-term corticosteroid use, chemotherapy, or radiation therapy.
  • Patients with life expectancy of less than 6 months
  • Patients who are unable or unwilling to comply with the study protocol or procedures.
  • Patients that are unable to give informed consent.

结局指标

主要结局

Sarcopenia

时间窗: 3 years

feasibility of using the FACS approach and molecular analyses to investigate the association between sarcopenia and chronic lung disease

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

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