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Design of the SPIROMICS Study of Early COPD Progression: SOURCE Study.
Curtis, Jeffrey L; Bateman, Lori A; Murray, Susan; Couper, David J; Labaki, Wassim W; Freeman, Christine M; Arnold, Kelly B; Christenson, Stephanie A; Alexis, Neil E; Kesimer, Mehmet; Boucher, Richard C; Kaner, Robert J; Barjaktarevic, Igor; Cooper, Christopher B; Hoffman, Eric A; Barr, R Graham; Bleecker, Eugene R; Bowler, Russell P; Comellas, Alejandro; Dransfield, Mark T; Freedman, Michael B; Hansel, Nadia N; Krishnan, Jerry A; Marchetti, Nathaniel; Meyers, Deborah A; Ohar, Jill; O'Neal, Wanda K; Ortega, Victor E; Paine Iii, Robert; Peters, Stephen P; Smith, Benjamin M; Wedzicha, Jadwiga A; Wells, J Michael; Woodruff, Prescott G; Han, MeiLan K; Martinez, Fernando J.
Afiliação
  • Curtis JL; Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, United States.
  • Bateman LA; Medical Service, VA Ann Arbor Healthcare System, Ann Arbor, Michigan, United States.
  • Murray S; Graduate Program in Immunology, University of Michigan, Ann Arbor, Michigan, United States.
  • Couper DJ; Collaborative Studies Coordinating Center, Department of Biostatistics, Gillings School of Global Public Health, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States.
  • Labaki WW; Department of Biostatistics, University of Michigan School of Public Health, Ann Arbor, Michigan, United States.
  • Freeman CM; Collaborative Studies Coordinating Center, Department of Biostatistics, Gillings School of Global Public Health, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States.
  • Arnold KB; Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, United States.
  • Christenson SA; Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, United States.
  • Alexis NE; Graduate Program in Immunology, University of Michigan, Ann Arbor, Michigan, United States.
  • Kesimer M; Research Service, VA Ann Arbor Healthcare System, Ann Arbor, Michigan, United States.
  • Boucher RC; Department of Biomedical Engineering, University of Michigan, Ann Arbor, Michigan, United States.
  • Kaner RJ; Division of Pulmonary, Critical Care, Sleep and Allergy, Department of Medicine, University of California San Francisco, San Francisco, California, United States.
  • Barjaktarevic I; Division of Allergy Immunology and Infectious Disease, Department of Pediatrics, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States.
  • Cooper CB; Marsico Lung Institute, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States.
  • Hoffman EA; Marsico Lung Institute, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States.
  • Barr RG; Weill Cornell Medicine, New York-Presbyterian Hospital, New York City, New York, United States.
  • Bleecker ER; Division of Pulmonary, Critical Care and Sleep Medicine, University of California Los Angeles, Los Angeles, California, United States.
  • Bowler RP; Division of Pulmonary, Critical Care and Sleep Medicine, University of California Los Angeles, Los Angeles, California, United States.
  • Comellas A; Department of Radiology, University of Iowa, Iowa City, Iowa, United States.
  • Dransfield MT; Department of Medicine and Department of Epidemiology, Columbia University Medical Center, New York City, New York, United States.
  • Freedman MB; Division of Pulmonary and Critical Care Medicine, Mayo Clinic, Scottsdale, Arizona, United States.
  • Hansel NN; Division of Pulmonary, Critical Care and Sleep Medicine, National Jewish Health, Denver, Colorado, United States.
  • Krishnan JA; Department of Medicine, University of Iowa, Iowa City, Iowa, United States.
  • Marchetti N; Division of Pulmonary, Allergy and Critical Care Medicine, University of Alabama at Birmingham, Birmingham, Alabama, United States.
  • Meyers DA; Division of Pulmonary, Critical Care, Sleep and Allergy, University of Illinois at Chicago, Chicago, Illinois, United States.
  • Ohar J; Department of Medicine, Johns Hopkins University, Baltimore, Maryland, United States.
  • O'Neal WK; Division of Pulmonary, Critical Care, Sleep and Allergy, University of Illinois at Chicago, Chicago, Illinois, United States.
  • Ortega VE; Department of Thoracic Medicine and Surgery, Lewis Katz School of Medicine at Temple University, Philadelphia, Pennsylvania, United States.
  • Paine Iii R; Division of Pulmonary, Critical Care and Sleep Medicine, National Jewish Health, Denver, Colorado, United States.
  • Peters SP; Section of Pulmonary, Critical Care, Allergy and Immunologic Diseases, Wake Forest University, Winston-Salem, North Carolina, United States.
  • Smith BM; Marsico Lung Institute, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States.
  • Wedzicha JA; Division of Pulmonary and Critical Care Medicine, Mayo Clinic, Scottsdale, Arizona, United States.
  • Wells JM; Division of Respiratory, Critical Care, and Occupational Pulmonary Medicine, University of Utah Health Sciences Center, Salt Lake City, Utah, United States.
  • Woodruff PG; Section of Pulmonary, Critical Care, Allergy and Immunologic Diseases, Wake Forest University, Winston-Salem, North Carolina, United States.
  • Han MK; Department of Medicine and Department of Epidemiology, Columbia University Medical Center, New York City, New York, United States.
  • Martinez FJ; National Heart and Lung Institute, Imperial College, London, United Kingdom.
Article em En | MEDLINE | ID: mdl-39159077
ABSTRACT
The biological mechanisms leading some tobacco-exposed individuals to develop early-stage chronic obstructive pulmonary disease (COPD) are poorly understood. This knowledge gap hampers development of disease-modifying agents for this prevalent condition. Accord-ingly, with National Heart, Lung and Blood Institute support, we initiated the SPIROMICS Study of Early COPD Progression (SOURCE), a multicenter observational cohort study of younger individuals with a history of cigarette smoking and thus at-risk for, or with, early-stage COPD. Our overall objectives are to identify those who will develop COPD earlier in life, characterize them thoroughly, and by contrasting them to those not developing COPD, define mechanisms of disease progression. SOURCE utilizes the established SPIROMICS clinical network. Its goal is to enroll n=649 participants, ages 30-55 years, all races/ethnicities, with ≥10 pack-years cigarette smoking, in either Global Initiative for Chronic Obstructive Lung Disease (GOLD) groups 0-2 or with Preserved Ratio Impaired Spirometry (PRISm); and an additional n=40 never-smoker controls. Participants undergo baseline and three-year follow-up visits, each including high-resolution computed tomography; respiratory oscillometry and spirometry (pre- and post-bronchodilator administration), exhaled breath condensate (baseline only); and extensive biospecimen collection, including sputum induction. Symptoms, interim healthcare utilization, and exacerbations are captured every six months via follow-up phone calls. An embedded bronchoscopy sub-study involving n=100 participants (including all never-smokers) will allow collection of lower airway samples for genetic, epigenetic, genomic, immunological, microbiome, mucin analyses, and basal cell culture. SOURCE should provide novel insights into the natural history of lung disease in younger individuals with a smoking history, and its biological basis.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Chronic Obstr Pulm Dis Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Chronic Obstr Pulm Dis Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos