Evidence map›Paper›PMID 32411616›Full record

ArticleFrontiers in cellular and infection microbiology2020

Longitudinal Associations of the Cystic Fibrosis Airway Microbiome and Volatile Metabolites: A Case Study.

Andrea Hahn, Katrine Whiteson, Trenton J Davis, Joann Phan, Iman Sami, Anastassios C Koumbourlis, Robert J Freishtat, Keith A Crandall, Heather D Bean

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cellular and infection microbiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.5field-weighted citation impact, top 20% 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Review
  3. Shallow metagenomic shotgun sequencing improves detection of pathogenic species in cystic fibrosis respiratory samples.Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society · 2025
    Article
  4. The presence of cystic fibrosis-related diabetes modifies the sputum microbiome in cystic fibrosis disease.American journal of physiology. Lung cellular and molecular physiology · 2024
    Article
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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

9 authors at 5 institutions in 1 country.

Andrea HahnDivision of Infectious Diseases, Children's National Health System, Washington, DC, United States.
Katrine WhitesonDepartment of Molecular Biology and Biochemistry, University of California at Irvine, Irvine, CA, United States.
Trenton J DavisSchool of Life Sciences, Arizona State University, Tempe, AZ, United States.
Joann PhanDepartment of Molecular Biology and Biochemistry, University of California at Irvine, Irvine, CA, United States.
Iman SamiDepartment of Pediatrics, George Washington University School of Medicine and Health Sciences, Washington, DC, United States.
Anastassios C KoumbourlisDepartment of Pediatrics, George Washington University School of Medicine and Health Sciences, Washington, DC, United States.
Robert J FreishtatDepartment of Pediatrics, George Washington University School of Medicine and Health Sciences, Washington, DC, United States.
Keith A CrandallComputational Biology Institute and Department of Biostatistics & Bioinformatics, Milken Institute School of Public Health, George Washington University, Washington, DC, United States.
Heather D BeanSchool of Life Sciences, Arizona State University, Tempe, AZ, United States.
Children's National · USArizona State University · USUniversity of California, Irvine · USGeorge Washington University · USMilken Institute · US

Funding

Clinical and Translational Science Institute at Children's NationalUL1TR000075 · NCATS · CHILDREN'S RESEARCH INSTITUTE · PI GUAY-WOODFORD, LISA MARIE · 2012 to 2015
$13.7M
Dynamics of airway microbiota at pulmonary exacerbation in cystic fibrosisR01HL136647 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LIPUMA, JOHN J · 2017 to 2020
$1.3M
K12 Career Development Program: Omics of Pediatric Lung Diseases in DCK12HL119994 · NHLBI · CHILDREN'S RESEARCH INSTITUTE · PI FREISHTAT, ROBERT J · 2013 to 2017
$1.3M
Improving outcomes in CF patients: Toward rapid detection of P. aeruginosaR56HL139846 · NHLBI · DARTMOUTH COLLEGE · PI HILL, JANE · 2018 to 2018
$514k
NCATS NIH HHS UL1 TR000075NHLBI NIH HHS K12 HL119994NHLBI NIH HHS R01 HL136647NHLBI NIH HHS R56 HL139846
6 · The paper itself

Abstract

The identification of 16S rDNA biomarkers from respiratory samples to describe the continuum of clinical disease states within persons having cystic fibrosis (CF) has remained elusive. We sought to combine 16S, metagenomics, and metabolomics data to describe multiple transitions between clinical disease states in 14 samples collected over a 12-month period in a single person with CF. We hypothesized that each clinical disease state would have a unique combination of bacterial genera and volatile metabolites as a potential signature that could be utilized as a biomarker of clinical disease state. Taxonomy identified by 16S sequencing corroborated clinical culture results, with the majority of the 109 PCR amplicons belonging to the bacteria grown in clinical cultures (

Indexed as

Cystic FibrosisMicrobiotaHumansMetagenomicsRNA, Ribosomal, 16SSputumRNA, Ribosomal, 16Scystic fibrosismetabolomemicrobiomepediatricspulmonary medicine

Identifiers

PMID32411616
PMCPMC7198769
OpenAlexW3018786567

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

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.