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Rationale and Design of the Genomic Research in Alpha-1 Antitrypsin Deficiency and Sarcoidosis Study. Alpha-1 Protocol.
Strange, Charlie; Senior, Robert M; Sciurba, Frank; O'Neal, Scott; Morris, Alison; Wisniewski, Stephen R; Bowler, Russell; Hochheiser, Harry S; Becich, Michael J; Zhang, Yingze; Leader, Joseph K; Methé, Barbara A; Kaminski, Naftali; Sandhaus, Robert A.
Affiliation
  • Strange C; 1 Division of Pulmonary, Critical Care, Allergy and Sleep Medicine, Medical University of South Carolina, Charleston, South Carolina.
  • Senior RM; 2 Barnes-Jewish Hospital/Washington University, St. Louis, Missouri.
  • Sciurba F; 3 School of Medicine.
  • O'Neal S; 4 Graduate School of Public Health, and.
  • Morris A; 3 School of Medicine.
  • Wisniewski SR; 4 Graduate School of Public Health, and.
  • Bowler R; 5 National Jewish Health, Denver, Colorado.
  • Hochheiser HS; 6 Department of Biomedical Informatics, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Becich MJ; 6 Department of Biomedical Informatics, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Zhang Y; 3 School of Medicine.
  • Leader JK; 4 Graduate School of Public Health, and.
  • Methé BA; 3 School of Medicine.
  • Kaminski N; 7 J. Craig Venter Institute, Rockville, Maryland; and.
  • Sandhaus RA; 8 Section of Pulmonary, Critical Care, and Sleep Medicine, Department of Internal Medicine, Yale School of Medicine, New Haven, Connecticut.
Ann Am Thorac Soc ; 12(10): 1551-60, 2015 Oct.
Article de En | MEDLINE | ID: mdl-26153726
ABSTRACT
Severe deficiency of alpha-1 antitrypsin has a highly variable clinical presentation. The Genomic Research in Alpha-1 Antitrypsin Deficiency and Sarcoidosis α1 Study is a prospective, multicenter, cross-sectional study of adults older than age 35 years with PiZZ or PiMZ alpha-1 antitrypsin genotypes. It is designed to better understand if microbial factors influence this heterogeneity. Clinical symptoms, pulmonary function testing, computed chest tomography, exercise capacity, and bronchoalveolar lavage (BAL) will be used to define chronic obstructive pulmonary disease (COPD) phenotypes that can be studied with an integrated systems biology approach that includes plasma proteomics; mouth, BAL, and stool microbiome and virome analysis; and blood microRNA and blood mononuclear cell RNA and DNA profiling. We will rely on global genome, transcriptome, proteome, and metabolome datasets. Matched cohorts of PiZZ participants on or off alpha-1 antitrypsin augmentation therapy, PiMZ participants not on augmentation therapy, and control participants from the Subpopulations and Intermediate Outcome Measures in COPD Study who match on FEV1 and age will be compared. In the primary analysis, we will determine if the PiZZ individuals on augmentation therapy have a difference in lower respiratory tract microbes identified compared with matched PiZZ individuals who are not on augmentation therapy. By characterizing the microbiome in alpha-1 antitrypsin deficiency (AATD), we hope to define new phenotypes of COPD that explain some of the diversity of clinical presentations. As a unique genetic cause of COPD, AATD may inform typical COPD pathogenesis, and better understanding of it may illuminate the complex interplay between environment and genetics. Although the biologic approaches are hypothesis generating, the results may lead to development of novel biomarkers, better understanding of COPD phenotypes, and development of novel diagnostic and therapeutic trials in AATD and COPD. Clinical trial registered with www.clinicaltrials.gov (NCT01832220).
Sujet(s)
Mots clés

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Emphysème pulmonaire / Plan de recherche / Sarcoïdose / Déficit en alpha-1-antitrypsine / Broncho-pneumopathie chronique obstructive Type d'étude: Clinical_trials / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limites: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Langue: En Journal: Ann Am Thorac Soc Année: 2015 Type de document: Article

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Emphysème pulmonaire / Plan de recherche / Sarcoïdose / Déficit en alpha-1-antitrypsine / Broncho-pneumopathie chronique obstructive Type d'étude: Clinical_trials / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limites: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Langue: En Journal: Ann Am Thorac Soc Année: 2015 Type de document: Article
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