Biomarkers Of Lung InVolvement In ASMD

Not Applicable

Recruiting

• Conditions: Asmd, Visceral Type
• Interventions: Diagnostic Test: eNose; Diagnostic Test: Volatile exhaled breath sample; Diagnostic Test: Condensate sample

• Registration Number: NCT05914727
• Lead Sponsor: Eline C. B. Eskes

Brief Summary

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.

Detailed Description

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.

Nature and extent of the burden and risks associated with participation, benefit and group relatedness: Sampling of exhaled breath yields no risk: at most, patients might suffer from dizziness or mild dyspnea. Patients will not directly benefit from participation in the study. We aim to identify biomarkers reflecting lung involvement of ASMD and in that respect the results of the study may improve clinical care in the future for the patients participating in the study or any ASMD patient with similar characteristics.

Study Timeline

• Study Start: 2022-12-05
• Status Verified: 2023-06
• Study First Submitted: 2023-06-06
• Study First Submitted QC: 2023-06-19
• Last Update Submitted: 2023-06-19
• Study First Posted: 2023-06-22
• Last Update Posted: 2023-06-22
• Primary Completion: 2024-04-01
• Study Completion: 2024-09-01

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 68

Inclusion Criteria

Patients:

• 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

Exclusion Criteria

Patients:

• 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

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
ASMD patients	Volatile exhaled breath sample	ASMD patients
ASMD patients	Condensate sample	ASMD patients
Healthy controls	eNose	Healthy controls
Healthy controls	Condensate sample	Healthy controls
Healthy controls	Volatile exhaled breath sample	Healthy controls
ASMD patients	eNose	ASMD patients

Primary Outcome Measures

Name	Time	Method
Markers of inflammation, fibrosis or sphingolipid accumulation in exhaled breath	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.

Secondary Outcome Measures

Name	Time	Method
Biomarkers with monitoring or prognostic value in ASMD	10 years	Biomarkers with monitoring or prognostic value in ASMD patients in a longitudinal study design. Since this is an explorative study these markers cannot be defined in advance.

Trial Locations

Locations (1)

Amsterdam UMC; 🇳🇱 Amsterdam, Noord-Holland, Netherlands