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Biomarkers of DNA damage in COPD patients undergoing pulmonary rehabilitation: Integrating clinical parameters with genomic profiling.
Russo, Patrizia; Lamonaca, Palma; Milic, Mirta; Rojas, Emilio; Prinzi, Giulia; Cardaci, Vittorio; Vitiello, Laura; Proietti, Stefania; Santoro, Alessia; Tomino, Carlo; Fini, Massimo; Bonassi, Stefano.
Afiliação
  • Russo P; Unit of Clinical and Molecular Epidemiology, IRCCS San Raffaele Pisana, Roma, Italy.
  • Lamonaca P; Unit of Clinical and Molecular Epidemiology, IRCCS San Raffaele Pisana, Roma, Italy.
  • Milic M; Institute for Medical Research and Occupational Health, Zagreb, Croatia.
  • Rojas E; Departamento de Medicina Genòmica y Toxicologìa Ambiental, Instituto de Investigaciones Biomédicas, Universidad Nacional Autònoma de México, Ciudad Universitaria, Mexico.
  • Prinzi G; Unit of Clinical and Molecular Epidemiology, IRCCS San Raffaele Pisana, Roma, Italy.
  • Cardaci V; Unit of Pulmonary Rehabilitation, IRCCS San Raffaele Pisana, Rome, Italy.
  • Vitiello L; Unit of Flow Cytometry IRCCS San Raffaele Pisana, Rome, Italy.
  • Proietti S; Scientific Direction, IRCCS San Raffaele Pisana, Rome, Italy.
  • Santoro A; Unit of Clinical and Molecular Epidemiology, IRCCS San Raffaele Pisana, Roma, Italy.
  • Tomino C; Scientific Direction, IRCCS San Raffaele Pisana, Rome, Italy.
  • Fini M; Scientific Direction, IRCCS San Raffaele Pisana, Rome, Italy.
  • Bonassi S; Unit of Clinical and Molecular Epidemiology, IRCCS San Raffaele Pisana, Roma, Italy; Department of Human Sciences and Quality of Life Promotion, San Raffaele University, Rome, Italy. Electronic address: stefano.bonassi@sanraffaele.it.
Article em En | MEDLINE | ID: mdl-31421732
ABSTRACT
Chronic obstructive pulmonary disease (COPD) is a progressive lung disease characterized by severe respiratory symptoms. COPD shows several hallmarks of aging, and an increased oxidative stress, which is responsible for different clinical and molecular COPD features, including an increased frequency of DNA damage. The current pharmacological treatment options for COPD are mostly symptomatic, and generally do not influence disease progression and survival. In this framework, pulmonary rehabilitation is the most effective therapeutic strategy to improve physical performance, reducing hospital readmissions and mortality. Response to rehabilitation may greatly differ among patients calling for a personalized treatment. In this paper we will investigate in a group of COPD patients those variables that may predict the response to a program of pulmonary rehabilitation, integrating clinical parameters with cellular and molecular measurements, offering the potential for more effective and individualized treatment options. A group of 89 consecutive COPD patients admitted to a 3-weeks Pulmonary Rehabilitation (PR) program were evaluated for clinical and biological parameters at baseline and after completion of PR. DNA fragmentation in cryopreserved lymphocytes was compared by visual scoring and using the Comet Assay IV analysis system. The comparison of DNA damage before and after PR showed a highly significant increase from 19.6 ± 7.3 at admission to 21.8 ± 7.2 after three weeks of treatment, with a significant increase of 2.46 points (p < 0.001). Higher levels of DNA damage were observed in the group of non- responders and in those patients receiving oxygen therapy. The overall variation of %TI during treatment significantly correlated with the level of pCO2 at admission and negatively with the level of IL-6 at admission. Measuring the frequency of DNA damage in COPD patients undergoing pulmonary rehabilitation may provide a meaningful biological marker of response and should be considered as additional diagnostic and prognostic criterion for personalized rehabilitation programs.
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Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 6_ODS3_enfermedades_notrasmisibles Base de dados: MEDLINE Assunto principal: Terapia Respiratória / Dano ao DNA / Proteína C-Reativa / Interleucina-6 / Ensaio Cometa / Doença Pulmonar Obstrutiva Crônica / Instabilidade Genômica Tipo de estudo: Prognostic_studies Limite: Aged / Aged80 / Female / Humans / Male Idioma: En Revista: Mutat Res Genet Toxicol Environ Mutagen Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 6_ODS3_enfermedades_notrasmisibles Base de dados: MEDLINE Assunto principal: Terapia Respiratória / Dano ao DNA / Proteína C-Reativa / Interleucina-6 / Ensaio Cometa / Doença Pulmonar Obstrutiva Crônica / Instabilidade Genômica Tipo de estudo: Prognostic_studies Limite: Aged / Aged80 / Female / Humans / Male Idioma: En Revista: Mutat Res Genet Toxicol Environ Mutagen Ano de publicação: 2019 Tipo de documento: Article