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Epigenome-Wide Association Studies of Chronic Obstructive Pulmonary Disease and Lung Function: A Systematic Review.
Casas-Recasens, Sandra; Cassim, Raisa; Mendoza, Núria; Agusti, Alvar; Lodge, Caroline; Li, Shuai; Bui, Dinh; Martino, David; Dharmage, Shyamali C; Faner, Rosa.
  • Casas-Recasens S; Fundació Clinic Recerca Biomedica-Institut d'Investigacions Biomediques August Pi i Sunyer (FCRB-IDIBAPS), Barcelona, Spain.
  • Cassim R; Centro de Investigación Biomédica en Red de Enfermedades Respiratorias (CIBERES), Madrid, Spain.
  • Mendoza N; Allergy and Lung Health Unit and.
  • Agusti A; Fundació Clinic Recerca Biomedica-Institut d'Investigacions Biomediques August Pi i Sunyer (FCRB-IDIBAPS), Barcelona, Spain.
  • Lodge C; Centro de Investigación Biomédica en Red de Enfermedades Respiratorias (CIBERES), Madrid, Spain.
  • Li S; Fundació Clinic Recerca Biomedica-Institut d'Investigacions Biomediques August Pi i Sunyer (FCRB-IDIBAPS), Barcelona, Spain.
  • Bui D; Centro de Investigación Biomédica en Red de Enfermedades Respiratorias (CIBERES), Madrid, Spain.
  • Martino D; Respiratory Institute, Hospital Clinic, Barcelona, Spain.
  • Dharmage SC; Catedra Salud Respiratoria and.
  • Faner R; Allergy and Lung Health Unit and.
Am J Respir Crit Care Med ; 210(6): 766-778, 2024 Sep 15.
Article en En | MEDLINE | ID: mdl-38422471
ABSTRACT
Rationale Chronic obstructive pulmonary disease (COPD) results from gene-environment interactions over the lifetime. These interactions are captured by epigenetic changes, such as DNA methylation.

Objectives:

To systematically review the evidence form epigenome-wide association studies related to COPD and lung function.

Methods:

A systematic literature search performed on PubMed, Embase, and Cumulative Index to Nursing and Allied Health Literature (CINAHL) databases identified 1,947 articles that investigated epigenetic changes associated with COPD and/or lung function; 17 of them met our eligibility criteria, from which data were manually extracted. Differentially methylated positions (DMPs) and/or annotated genes were considered replicated if identified by two or more studies with a P < 1 × 10-4. Measurements and Main

Results:

Ten studies profiled DNA methylation changes in blood and seven in respiratory samples, including surgically resected lung tissue (n = 3), small airway epithelial brushings (n = 2), BAL (n = 1), and sputum (n = 1). Main results showed 1) high variability in study design, covariates, and effect sizes, which prevented a formal meta-analysis; 2) in blood samples, 51 DMPs were replicated in relation to lung function and 12 related to COPD; 3) in respiratory samples, 42 DMPs were replicated in relation to COPD but none in relation to lung function; and 4) in COPD versus control studies, 123 genes (2.6% of total) were shared between one or more blood and one or more respiratory samples and associated with chronic inflammation, ion transport, and coagulation.

Conclusions:

There is high heterogeneity across published COPD and/or lung function epigenome-wide association studies. A few genes (n = 123; 2.6%) were replicated in blood and respiratory samples, suggesting that blood can recapitulate some changes in respiratory tissues. These findings have implications for future research. Systematic Review [protocol] registered with Open Science Framework (OSF).
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Metilación de ADN / Enfermedad Pulmonar Obstructiva Crónica / Estudio de Asociación del Genoma Completo / Epigenoma Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Metilación de ADN / Enfermedad Pulmonar Obstructiva Crónica / Estudio de Asociación del Genoma Completo / Epigenoma Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Año: 2024 Tipo del documento: Article