Evidence map›Paper›PMID 26153726›Full record

Observational studyAnnals of the American Thoracic Society2015

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

Charlie Strange, Robert M Senior, Frank Sciurba, Scott O'Neal, Alison Morris, Stephen R Wisniewski, Russell Bowler, Harry S Hochheiser, Michael J Becich, Yingze Zhang and 5 more

Registry-linked trialOpen access · greenAbstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Annals of the American Thoracic Society, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01832220 (Genomic Research in Alpha-1 Antitrypsin Deficiency and Sarcoidosis), which is not on this map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.2field-weighted citation impact, top 41% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT01832220 completednot on this map

Genomic Research in Alpha-1 Antitrypsin Deficiency and Sarcoidosis (GRADS) - Alpha-1 Protocol

TypeobservationalSponsorUniversity of PittsburghRan2013 to 2015Enrolled140ConditionsAlpha 1 Antitrypsin Deficiency, AATD
3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 15 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Alpha-1 antitrypsin inhibits fractalkine-mediated monocyte-lung endothelial cell interactions.American journal of physiology. Lung cellular and molecular physiology · 2023
    Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Exacerbations of Lung Disease in Alpha-1 Antitrypsin Deficiency.Chronic obstructive pulmonary diseases (Miami, Fla.) · 2021
    Article
  10. Observational
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors at 9 institutions in 1 country.

Charlie Strange1 Division of Pulmonary, Critical Care, Allergy and Sleep Medicine, Medical University of South Carolina, Charleston, South Carolina.ORCID http://orcid.org/0000-0002-8109-8067
Robert M Senior2 Barnes-Jewish Hospital/Washington University, St. Louis, Missouri.
Frank Sciurba3 School of Medicine.
Scott O'Neal4 Graduate School of Public Health, and.
Alison Morris3 School of Medicine.
Stephen R Wisniewski4 Graduate School of Public Health, and.
Russell Bowler5 National Jewish Health, Denver, Colorado.
Harry S Hochheiser6 Department of Biomedical Informatics, University of Pittsburgh, Pittsburgh, Pennsylvania.
Michael J Becich6 Department of Biomedical Informatics, University of Pittsburgh, Pittsburgh, Pennsylvania.
Yingze Zhang3 School of Medicine.
Joseph K Leader3 School of Medicine.
Barbara A Methé7 J. Craig Venter Institute, Rockville, Maryland; and.
Naftali Kaminski8 Section of Pulmonary, Critical Care, and Sleep Medicine, Department of Internal Medicine, Yale School of Medicine, New Haven, Connecticut.
Robert A Sandhaus5 National Jewish Health, Denver, Colorado.
GRADS Alpha-1 Study Group
Washington School of Psychiatry · USGraduate School USA · USNational Jewish Health · USUniversity of Pittsburgh · USBarnes-Jewish Hospital · USIndiana University School of MedicineJ. Craig Venter Institute · USMedical University of South Carolina · USYale University · US

Funding

CTSA INFRASTRUCTURE FOR PEDIATRIC RESEARCHUL1RR025780 · NCRR · UNIVERSITY OF COLORADO DENVER · PI SOKOL, RONALD J. · 2008 to 2011
$61.3M
University of Pittsburgh Clinical and Translational Science InstituteUL1TR000005 · NCATS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI REIS, STEVEN E · 2012 to 2015
$50.8M
Colorado Clinical and Translational Sciences InstituteUL1TR001082 · NCATS · UNIVERSITY OF COLORADO DENVER · PI SOKOL, RONALD J. · 2013 to 2017
$48.0M
The internship in Biomedical Research, Informatics, and Computer Science (iBRIC): Biomedical Informatics and Data Science research experiences for students from Minority Serving InstitutionsT15LM007059 · NLM · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI HARRY S HOCHHEISER · 1987 to 2026
$23.9M
Sustaining the Expansion of the National Mesothelioma Virtual Bank (NMVB)U24OH009077 · OH · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI BECICH, MICHAEL JOHN, DACIC, SANJA · 2008 to 2025
$18.0M
SOUTH CAROLINA CLINICAL & TRANSLATIONAL RESEARCH INSTITUTE (SCTR)UL1RR029882 · NCRR · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI BRADY, KATHLEEN T. · 2009 to 2011
$10.1M
Sarcoidosis and A1AT Genomics & Informatics CenterU01HL112707 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI BECICH, MICHAEL JOHN, KAMINSKI, NAFTALI · 2012 to 2015
$8.5M
Genetic Risk for Granulomatous Interstitial Lung DiseaseR01HL114587 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI FINGERLIN, TASHA E. · 2013 to 2018
$3.2M
Epigenetic Regulation of Immunity in Alpha-1 Anti-trypsin DeficiencyR01HL126600 · NHLBI · NATIONAL JEWISH HEALTH · PI HAMZEH, NABEEL, O'CONNOR, BRIAN P · 2015 to 2018
$1.6M
Ancillary T Cell Based Studies in SPIROMICSR01HL110883 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI KHERADMAND, FARRAH · 2012 to 2015
$1.6M
Significance Circulating Semaphorin 7a+ve Cells in Pulmonary SarcoidosisU01HL112702 · NHLBI · YALE UNIVERSITY · PI HERZOG, ERICA L · 2012 to 2014
$488k
GRADS Cooperative Research Project: JHU Clinical CenterU01HL112708 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI MOLLER, DAVID R · 2012 to 2014
$481k
NCATS NIH HHS U54 9 UL1 TR000005NCATS NIH HHS UL1 TR000005NCATS NIH HHS UL1 TR001082NCRR NIH HHS UL1 RR025780NCRR NIH HHS UL1 RR029882NHLBI NIH HHS R01 HL110883NHLBI NIH HHS R01 HL114587NHLBI NIH HHS R01 HL126600NHLBI NIH HHS U01 HL112694NHLBI NIH HHS U01 HL112695NHLBI NIH HHS U01 HL112696NHLBI NIH HHS U01 HL112702NHLBI NIH HHS U01 HL112707NHLBI NIH HHS U01 HL112708NHLBI NIH HHS U01 HL112711NHLBI NIH HHS U01 HL112712NIOSH CDC HHS 5 U24 OH009077NIOSH CDC HHS U19 OH009077NIOSH CDC HHS U24 OH009077NLM NIH HHS T15 LM007059
6 · The paper itself

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).

Indexed as

Research DesignAdultAgedAged, 80 and overalpha 1-Antitrypsin DeficiencyBronchoalveolar LavageCross-Sectional StudiesExercise ToleranceFemaleGenomicsGenotypeHumansMaleMicrobiotaMiddle AgedPhenotypebronchoalveolar lavageCOPDemphysemalungmicrobiomephenotype

Identifiers

PMID26153726
PMCPMC4627425
OpenAlexW2175079504

What OpenQuestion holds

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Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.