Volatile Organic Compounds (VOCs) as a Biomarker in Immune-mediated Pulmonary Arterial Hypertension (PAH)

Pulmonary Arterial Hypertension Clinical Trial

— VOC-PAH  

Official title:

Volatile Organic Compounds as a Biomarker in Immune-mediated Pulmonary Arterial Hypertension

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03819777
• Other study ID #: NL57351.068.17
• Status: Recruiting
• Start date: March 1, 2018
• Est. completion date: January 31, 2023

Study information

• Verified date: August 2021
• Source: Maastricht University Medical Center
• Contact: Judith Potjewijd, MD
• Phone: +31 (0) 433871198
• Email: pah.uitademingslucht.int[@]mumc.nl
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

Aim: to investigate the role of inflammation and auto-immunity in pulmonary arterial hypertension by using the profile of volatile organic compounds. Hypothesis: first, the investigators hypothesize that at time of diagnosis the VOC profiles will discriminate patients with PAH-CTD and idiopathic PAH (IPAH) from patients with systemic sclerosis or systemic lupus erythematosus (CTD) without PAH, supporting the contention that there is a overlapping inflammatory and auto-immune pathway in PAH. During follow-up, the investigators will measure the VOC profiles of patients in all three groups who will be treated according standard clinical care. The hypothesis is that VOC profiles are affected by therapy.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 150
• Est. completion date: January 31, 2023
• Est. primary completion date: October 31, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. PAH-CTD patients, inclusion criteria:

• classification as definite systemic sclerosis or systemic lupus erythematosus according to respectively the ACR-EULAR criteria (16) and SLICC criteria (17)
• minimal age of 18 year
• diagnosis of pulmonary arterial hypertension: mean pulmonary artery pressure (mPAP) of =25 mmHg, pulmonary capillary wedge pressure (PCWP) =15 mmHg, and a pulmonary vascular resistance (PVR) =240 dynes.s.cm-5 measured by right heart catherization.

2. IPAH patients, inclusion criteria:

• diagnosis of pulmonary arterial hypertension: mean pulmonary artery pressure (mPAP) of =25 mmHg, pulmonary capillary wedge pressure (PCWP) =15 mmHg, and a pulmonary vascular resistance (PVR) =240 dynes.s.cm-5 measured by right heart catherization.
• no family history of PAH
• triggering factor is excluded: connective tissue disease, drugs or toxins, human immunodeficiency virus, congenital heart disease, portal hypertension, schistosomiasis (2)
• minimal age of 18 year

3. SSc and SLE (CTD) patients without PAH, inclusion criteria:

• classification as definite systemic sclerosis or systemic lupus erythematosus according to respectively the ACR-EULAR criteria (16) and SLICC criteria (17)
• minimal age of 18 year
• no signs of PAH at screening visit

Exclusion Criteria:

• active or treated malignancy
• tuberculosis or hepatitis B/C infection in case of start immunosuppressive therapy
• need to start immediately with therapy
• already use of immune suppression

Related Conditions & MeSH terms

• Familial Primary Pulmonary Hypertension
• Hypertension
• Pulmonary Arterial Hypertension
• Scleroderma, Diffuse
• Scleroderma, Systemic
• Systemic Lupus
• Systemic Sclerosis

Locations

Country	Name	City	State
Netherlands	Maastricht University Medical Center	Maastricht

Sponsors (1)

Lead Sponsor	Collaborator
Maastricht University Medical Center

Country where clinical trial is conducted

Netherlands, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Determining unique inflammatory VOC profiles in exhaled air in three groups of patients: IPAH, PAH-CTD and CTD without PAH.	Exhaled air samples will be analyzed on inflammatory VOC profiles in the diagnostic phase of the study. Three measurements over a period of two weeks will be done. Statistically analysis will report one average VOC profile of the three measurements.; Procedure: the patient is asked to exhale via a sterile mask into the ReCIVA breath sampler (Owlstone Medical, Cambridge, UK) in which mixed total exhaled air is immediately trapped and stored onto stainless-steel two-bed sorption tubes, filled with carbograph 1TD/Carbopack X (Markes International, Wales, UK). The tubes will be analyzed with GC-TOF-MS for the presence of VOCs after which multivariate statistical analysis will be used to select those VOCs unique for the various patient groups.	3 measurements in 2 weeks
Secondary	Correlation between unique inflammatory VOCs to well-established biomarkers of immune activation and inflammation in PAH-CTD and idiopathic PAH.	The correlation analysis by means of bivariate (Spearman correlation) and multivariate analysis (canonical correlation analysis) will be performed.	1 measurement at baseline
Secondary	Change (?, delta) from baseline in selective inflammatory VOC profiles after 3, 6 and 12 months in all patients treated with PAH and/or immunsuppressive medication.	Wilcoxon signed-rank test will be utilized to see if the individual, selective inflammatory VOCs after treatment significantly differ with the baseline measurements.	Changes (?, delta) between baseline, 3 months, 6 months, 9 months and 12 months