Expression of SLC25A48 in Chronic Obstructive Pulmonary Disease
Association Between SLC25A48 Expression and Chronic Obstructive Pulmonary Disease Progression
1 other identifier
observational
180
1 country
2
Brief Summary
This study aims to investigate the expression level of SLC25A48, a mitochondrial choline transporter, in peripheral blood mononuclear cells of patients with chronic obstructive pulmonary disease, and to analyze its correlation with inflammatory markers and choline metabolic byproducts.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Jun 2026
Shorter than P25 for all trials
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
March 11, 2026
CompletedFirst Posted
Study publicly available on registry
March 16, 2026
CompletedStudy Start
First participant enrolled
June 29, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 31, 2026
July 6, 2026
March 1, 2026
6 months
March 11, 2026
July 1, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
expression of SLC25A48
the expression level of SLC25A48 in mitochondria isolated from peripheral blood mononuclear cells
one day
Study Arms (2)
Case group
Pre-COPD or COPD stages I-IV as per the 2023 GOLD guidelines
Control group
healthy controls
Eligibility Criteria
patient of hospital
You may qualify if:
- pre-COPD or COPD stages I-IV as per the 2023 GOLD guidelines (case group)
- healthy individuals without chronic diseases or major medical conditions
You may not qualify if:
- diagnosed with neuromuscular diseases
- experienced respiratory disease exacerbation requiring emergency care or hospitalization in the past three months
- assessed by a physician to have severe malnutrition or a significantly low BMI
- continuously taking folic acid supplements
- willing to receive or have already received self-paid nutrition clinic services at this hospital
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (2)
Cardinal Tien Hospital
New Taipei City, 23148, Taiwan
Fu Jen Catholic University Hospital, Fu Jen Catholic University
New Taipei City, 24352, Taiwan
Biospecimen
Peripheral venous blood samples will be collected. Plasma, isolated peripheral blood mononuclear cells will be retained.
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Ke-Yun Chao, PhD
Fu Jen Catholic University
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
March 11, 2026
First Posted
March 16, 2026
Study Start
June 29, 2026
Primary Completion (Estimated)
December 31, 2026
Study Completion (Estimated)
December 31, 2026
Last Updated
July 6, 2026
Record last verified: 2026-03
Data Sharing
- IPD Sharing
- Will not share