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Genetic Polymorphism of CHRM2 in COPD: Clinical Significance and Therapeutic Implications.
Cherubini, Emanuela; Esposito, Maria Cristina; Scozzi, Davide; Terzo, Fabrizio; Osman, Giorgia Amira; Mariotta, Salvatore; Mancini, Rita; Bruno, Pierdonato; Ricci, Alberto.
Afiliação
  • Cherubini E; Department of Clinical and Molecular Medicine, Sapienza University of Rome, Rome, Italy.
  • Esposito MC; Department of Clinical and Molecular Medicine, Sapienza University of Rome, Rome, Italy.
  • Scozzi D; Division of Pulmonology, AO Sant' Andrea, Rome, Italy.
  • Terzo F; Department of Clinical and Molecular Medicine, Sapienza University of Rome, Rome, Italy.
  • Osman GA; Department of Clinical and Molecular Medicine, Sapienza University of Rome, Rome, Italy.
  • Mariotta S; Division of Pulmonology, AO Sant' Andrea, Rome, Italy.
  • Mancini R; Department of Clinical and Molecular Medicine, Sapienza University of Rome, Rome, Italy.
  • Bruno P; Division of Pulmonology, AO Sant' Andrea, Rome, Italy.
  • Ricci A; Department of Clinical and Molecular Medicine, Sapienza University of Rome, Rome, Italy.
J Cell Physiol ; 231(8): 1745-51, 2016 Aug.
Article em En | MEDLINE | ID: mdl-26633752
Chronic Obstructive Pulmonary Disease (COPD) is a common preventable and treatable disease, characterized by persistent airflow limitation not fully reversible. However, a number of patients with COPD respond to bronchodilator agents. Some studies have shown polymorphisms in the b2-adrenergic (ADRb2) and muscarinic M2 and M3 receptors (CHRM) that may participate in the modulation of the receptor responses. This study was designed to investigate the existence and the role of adrenergic and muscarinic receptor polymorphisms and their functional impact in COPD. Eighty-two patients with COPD and 17 healthy smokers were recruited and screened for ADRb2 (T164I and R175R), for CHRM2 (rs1824024) and for CHRM3 (-513C/A and -492C/T). Among the polymorphisms studied our results was not able to demonstrate statistically significant association between the polymorphisms studied and COPD risk. Contrarily, we identified, in our COPD population, a significant association with the CHRM2 (rs1824024) polymorphism and disease severity, with lower lung function test values, frequent exacerbations, and poor response to anti-cholinergic drugs. These results suggest the potential role of receptor polymorphism assessment to discriminate newly COPD phenotypes. J. Cell. Physiol. 231: 1745-1751, 2016. © 2015 Wiley Periodicals, Inc.
Assuntos

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Polimorfismo de Nucleotídeo Único / Doença Pulmonar Obstrutiva Crônica / Receptor Muscarínico M2 Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: J Cell Physiol Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Itália

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Polimorfismo de Nucleotídeo Único / Doença Pulmonar Obstrutiva Crônica / Receptor Muscarínico M2 Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: J Cell Physiol Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Itália