Lung Obstruction in Adulthood of Prematurely Born (LUNAPRE)

NCT02923648 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 96

Last updated 2025-04-04

No results posted yet for this study

Summary

Obstructive lung disease is an increasing global health problem of pandemic proportions, with COPD alone affecting \>10% of the population. Smoking is the main and most well studies risk factor for developing COPD. However, chronic airway obstruction also in never-smoking populations has recently been recognized as an increasing health problem. Prematurely born children, particularly survivors of bronchopulmonary dysplasia (BPD), defined as the need for oxygen therapy up to the 28th day of life for children born prior to gestational week 32, have an increased incidence of both airway obstruction and hyper-reactivity, both representing major risk factors for developing COPD, or asthma, later in life. The purpose of this study is to perform in-depth clinical and molecular characterizations of of the lungs of survivors of BPD as they enter adulthood, and compare these profiles to relevant control groups (individuals with mild asthma, healthy prematurely born, and healthy individuals born at full term). Specifically, alterations at the epigenetic, mRNA, microRNA, protein and metabolite level as well as associated molecular pathways critical in the pathological mechanisms of obstructive lung disease related to premature birth and BPD will be identified.

Conditions

  • Premature Birth- and BPD-related Obstructive Lung Disease

Sponsors & Collaborators

  • Swedish Heart Lung Foundation

    collaborator OTHER
  • The Swedish Research Council

    collaborator OTHER_GOV
  • Region Stockholm

    collaborator OTHER_GOV
  • Stockholm South General Hospital

    collaborator OTHER
  • University of California, San Francisco

    collaborator OTHER
  • Kyoto University

    collaborator OTHER
  • Göteborg University

    collaborator OTHER
  • University of Oulu

    collaborator OTHER
  • Karolinska Institutet

    lead OTHER

Principal Investigators

  • Magnus Skold, MD, PhD · Karolinska Institute, Karolinska University Hospital

  • Asa M Wheelock, PhD · Karolinska Institutet

  • Erik Melén, MD, PhD · Karolinska Institute, Stockholm Southern General Hospital

  • Eva Berggren-Brostrom, MD, PhD · Stockholm Southern General Hospital

  • Anders Lindén, MD, PhD · Karolinska Institute, Karolinska University Hospital

  • Sven Nyrén, MD, PhD · Karolinska Institute, Karolinska University Hospital

  • Craig E Wheelock, PhD · Karolinska Institutet

  • Maria J Eriksson, MD, PhD · Karolinska Institute, Karolinska University Hospital

Eligibility

Min Age
18 Years
Max Age
23 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2013-03-01
Primary Completion
2016-09-30
Completion
2035-12-31

Countries

  • Sweden

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02923648 on ClinicalTrials.gov