Literature DB >> 26153726

Rationale and Design of the Genomic Research in Alpha-1 Antitrypsin Deficiency and Sarcoidosis Study. Alpha-1 Protocol.

Charlie Strange1, Robert M Senior2, Frank Sciurba3, Scott O'Neal4, Alison Morris3, Stephen R Wisniewski4, Russell Bowler5, Harry S Hochheiser6, Michael J Becich6, Yingze Zhang3,4, Joseph K Leader3, Barbara A Methé7, Naftali Kaminski8, Robert A Sandhaus5.   

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).

Entities:  

Keywords:  COPD; bronchoalveolar lavage; emphysema; lung; microbiome; phenotype

Mesh:

Year:  2015        PMID: 26153726      PMCID: PMC4627425          DOI: 10.1513/AnnalsATS.201503-143OC

Source DB:  PubMed          Journal:  Ann Am Thorac Soc        ISSN: 2325-6621


  64 in total

1.  Inflammatory markers in bacterial exacerbations of COPD.

Authors:  Timothy F Murphy; Sanjay Sethi; Susan L Hill; Robert A Stockley
Journal:  Am J Respir Crit Care Med       Date:  2002-01-01       Impact factor: 21.405

2.  Amplification of inflammation in emphysema and its association with latent adenoviral infection.

Authors:  I Retamales; W M Elliott; B Meshi; H O Coxson; P D Pare; F C Sciurba; R M Rogers; S Hayashi; J C Hogg
Journal:  Am J Respir Crit Care Med       Date:  2001-08-01       Impact factor: 21.405

3.  Sputum sol neutrophil elastase activity in bronchiectasis: differential modulation by syndecan-1.

Authors:  Stanley C H Chan; Daisy K Y Shum; Mary S M Ip
Journal:  Am J Respir Crit Care Med       Date:  2003-04-17       Impact factor: 21.405

4.  Neutrophil inflammation and activation in bronchiectasis: comparison with pneumonia and idiopathic pulmonary fibrosis.

Authors:  B Schaaf; A Wieghorst; S P Aries; K Dalhoff; J Braun
Journal:  Respiration       Date:  2000       Impact factor: 3.580

5.  Comparative loss of activity of recombinant secretory leukoprotease inhibitor and alpha 1-protease inhibitor caused by different forms of oxidative stress.

Authors:  C Vogelmeier; T Biedermann; K Maier; G Mazur; J Behr; F Krombach; R Buhl
Journal:  Eur Respir J       Date:  1997-09       Impact factor: 16.671

6.  Distribution of alpha(1)-antitrypsin alleles in patients with bronchiectasis.

Authors:  A Cuvelier; J F Muir; M F Hellot; D Benhamou; J P Martin; J Bénichou; R Sesboüé
Journal:  Chest       Date:  2000-02       Impact factor: 9.410

7.  Alpha-1-antitrypsin inhibits human immunodeficiency virus type 1.

Authors:  L Shapiro; G B Pott; A H Ralston
Journal:  FASEB J       Date:  2001-01       Impact factor: 5.191

8.  Bronchial inflammation: its relationship to colonizing microbial load and alpha(1)-antitrypsin deficiency.

Authors:  R A Stockley; A T Hill; S L Hill; E J Campbell
Journal:  Chest       Date:  2000-05       Impact factor: 9.410

9.  The effect of augmentation therapy on bronchial inflammation in alpha1-antitrypsin deficiency.

Authors:  Robert A Stockley; Darren L Bayley; Ipek Unsal; Lee J Dowson
Journal:  Am J Respir Crit Care Med       Date:  2002-06-01       Impact factor: 21.405

10.  Predictors of mortality in alpha1-antitrypsin deficiency.

Authors:  P A Dawkins; L J Dowson; P J Guest; R A Stockley
Journal:  Thorax       Date:  2003-12       Impact factor: 9.139

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Journal:  mBio       Date:  2017-02-14       Impact factor: 7.867

5.  Airway Microbiota in Patients With Synchronous Multiple Primary Lung Cancer: The Bacterial Topography of the Respiratory Tract.

Authors:  Kai Qian; Yi Deng; William S Krimsky; Yong-Geng Feng; Jun Peng; Yong-Hang Tai; Hao Peng; Li-Hong Jiang
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  5 in total

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