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临床试验/NCT05914727
NCT05914727招募中不适用

Biomarkers Of Lung InVolvement In ASMD

Eline C. B. Eskes2 个研究点 分布在 1 个国家目标入组 68 人开始时间: 2022年12月5日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
68
试验地点
2
主要终点
Markers of inflammation, fibrosis or sphingolipid accumulation in exhaled breath

研究概览

简要总结

The goal of this study is to characterize ASMD patients' breath profile, exhaled breath and condensate as compared to healthy controls to identify specific volatile and non-volatile compounds that reflect inflammatory processes, fibrotic processes or sphingolipid accumulation in the lungs.

Participants will be provided exhaled breath samples in three ways (breath profile, volatile compounds and condensate). ASMD patients will be compared to age- and sex-matched healthy controls.

详细描述

Rationale: Acid sphingomyelinase deficiency (ASMD) is a lysosomal storage disease in which sphingomyelin accumulates due to a deficiency of the enzyme acid sphingomyelinase. The most common manifestations of the chronic visceral subtype of this disease are hepatosplenomegaly and interstitial lung disease (ILD). Currently, enzyme replacement therapy is under investigation and will likely become available in the near future. The first results indicate that pulmonary involvement may be responsive to treatment. In order to identify those patients that will potentially benefit from therapy, biomarkers for lung injury can be helpful. Compounds measured in exhaled breath and exhaled breath condensate are extensively studied in common lung diseases and increasingly in ILD. These compounds are of interest since they provide information directly form the lung compartment and are collected non-invasively.

Objective: Our aim is to characterize ASMD patients' breath profile, exhaled breath and condensate as compared to healthy controls to identify specific volatile and non-volatile compounds that reflect inflammatory processes, fibrotic processes or sphingolipid accumulation in the lungs.

Study design: This study comprises a cross-sectional case-control part and a prospective cohort part. In the cross-sectional part, exhaled breath samples with volatile and non-volatile compounds of ASMD patients and healthy controls will be collected. After potential biomarkers are identified in the cross-sectional part, patients will enter the longitudinal part in which the prognostic and monitoring value of these markers will be evaluated using clinical parameters.

Study population: ASMD patients ≥ 12 years of age with a confirmed diagnosis of the chronic visceral type will be included as well as age-, sex- and smoking status-matched healthy controls with a ratio of 1:3.

Main study parameters/endpoints: Inflammatory markers, fibrotic markers and markers of sphingolipid accumulation will be measured in exhaled breath. Breath profiles will be measured with eNose, volatile compounds will be measured with GC-MS and non-volatile compounds will be measured in exhaled breath condensates using UPLC-MS/MS.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Other
盲法
None

入排标准

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

入选标准

  • The patient has a biochemical and genetically confirmed diagnosis of the chronic visceral subtype of ASMD
  • The patient is willing and able to provide written informed consent prior to the study-related procedure.
  • The patient is ≥ 12 years of age
  • Healthy controls:
  • The individual is willing and able to provide written informed consent prior to the study-related procedure
  • The individual is ≥ 16 years of age
  • General good health as determined by medical history

排除标准

  • Inability to adhere to the study protocol
  • When a patient is not able to complete a spirometry test, the eNose sample will not be collected.
  • Healthy controls:
  • Medical history of (systemic) disease for which medication was necessary
  • Inability to adhere to the study protocol

结局指标

主要结局

Markers of inflammation, fibrosis or sphingolipid accumulation in exhaled breath

时间窗: 1 year

Markers of inflammation, fibrosis or sphingolipid accumulation in exhaled breath of ASMD patients. Since this is an explorative study these markers cannot be defined in advance.

次要结局

  • Biomarkers with monitoring or prognostic value in ASMD(10 years)

研究者

发起方
Eline C. B. Eskes
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Eline C. B. Eskes

MD

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

研究点 (2)

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