Skip to content

DNA Methylation and Lung Disease in Cystic Fibrosis

DNA Methylation and Lung Disease in Cystic Fibrosis

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02884622
Acronym
METHYLCF
Enrollment
72
Registered
2016-08-31
Start date
2013-06-01
Completion date
2016-08-01
Last updated
2026-04-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cystic Fibrosis

Keywords

Lung disease, Epigenetics, DNA methylation, Modifier genes

Brief summary

Lung disease progression is variable among cystic fibrosis (CF) patients and depends on DNA mutations in the CFTR gene, polymorphic variations in disease-modifier genes and environmental exposure. The contribution of genetic factors has been extensively investigated, whereas the mechanism whereby environmental factors modulate the lung disease is unknown. Because these factors can affect the epigenome, investigators hypothesized that DNA methylation variations at disease-modifier genes modulate the lung function in CF patients.

Detailed description

Lung disease progression is variable among cystic fibrosis (CF) patients and depends on DNA mutations in the CFTR gene, polymorphic variations in disease-modifier genes and environmental exposure. The contribution of genetic factors has been extensively investigated, whereas the mechanism whereby environmental factors modulate the lung disease is unknown. Because these factors can affect the epigenome, investigators hypothesized that DNA methylation variations at disease-modifier genes modulate the lung function in CF patients. The investigators analyzed DNA methylation levels in the promoter of fourteen lung disease-modifier genes and showed that DNA methylation levels are altered in nasal epithelial and blood cell samples from CF patients. This study disclosed slightly, but significantly differentially methylated regions that collectively may modulate lung disease severity. It also highlighted that complex relationships between genetic and epigenetic factors contribute to the phenotypic variability of CF patients.

Interventions

OTHERnasal epithelial

CF patients with the same procedures as in the usual management of routine care, only the sampling nasal epithelial cells will be added

OTHERBlood sampling

CF patients with the same procedures as in the usual management of routine care, only the sampling 5ml additional blood will be taken

Sponsors

University Hospital, Montpellier
Lead SponsorOTHER
Vaincre la Mucoviscidose
CollaboratorOTHER
Institut National de la Santé Et de la Recherche Médicale, France
CollaboratorOTHER_GOV

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
Yes

Inclusion criteria

* \>18 years old * homozygous for the F508del mutation

Exclusion criteria

* subjects who have an active CF exacerbation or a recent viral infection on the day of biological samples collection; * pregnant women; * patients who are included in interventional medical trials; * patients who had lung transplantation.

Design outcomes

Primary

MeasureTime frameDescription
DNA methylation levels (chemical changes)D0 (day of inclusion)DNA methylation levels (chemical changes)

Countries

France

Contacts

PRINCIPAL_INVESTIGATORRaphaël CHIRON, MD

University Hospital, Montpellier

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 7, 2026