AI Article Synopsis

  • - The systematic review investigates how DNA methylation in peripheral blood could serve as a potential biomarker for lung function and chronic obstructive pulmonary disease (COPD) by analyzing data from population-based studies.
  • - Out of 1155 screened articles, only six met the criteria for inclusion, revealing that though most studies reported significant findings, there was no consistent identification of specific CpG sites related to COPD or lung function.
  • - The review suggests that while DNA methylation patterns might differ in those with reduced lung function or COPD compared to healthy individuals, further large-scale studies are needed to clarify these associations and explore potential reverse causality.

Article Abstract

Background: Epigenetic variations in peripheral blood have potential as biomarkers for disease. This systematic review assesses the association of lung function and chronic obstructive pulmonary disease (COPD) with DNA methylation profiles in peripheral blood from population-based studies.

Methods: Online databases Medline, Embase, and Web of Science were searched. Google Scholar was searched to identify grey literature. After removing duplicate articles, 1155 articles were independently screened by two investigators. Peer reviewed reports on population-based studies that examined peripheral blood DNA methylation in participants with measured lung function (FEV1, FEV1/FVC ratio) or known COPD status were selected for full-text review. Six articles were suitable for inclusion. Information regarding study characteristics, designs, methodologies and conclusions was extracted. A narrative synthesis was performed based on published results.

Results: Three of the six articles assessed the association of COPD with DNA methylation, and two of these also included associations with lung function. Overall, five reports examined the association of lung function with DNA methylation profiles. Five of the six articles reported 'significant' results. However, no consistent CpG sites were identified across studies for COPD status or lung function values.

Conclusions: DNA methylation patterns in peripheral blood from individuals with reduced lung function or COPD may be different to those in people with normal lung function. However, this systematic review did not find any consistent associations of lung function or COPD with differentially methylated CpG sites. Large studies with a longitudinal design to address reverse causality may prove a more fruitful area of research.

Trial Registration: PROSPERO 2016: CRD42016037352 .

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5360084PMC
http://dx.doi.org/10.1186/s12890-017-0397-3DOI Listing

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