Evidence map›Paper›PMID 30466159›Full record

ReviewIUBMB life2019

Lung inflammation and disease: A perspective on microbial homeostasis and metabolism.

Roberto Mendez, Sulagna Banerjee, Sanjoy K Bhattacharya, Santanu Banerjee

Open access · bronzeAbstract readReview
In one paragraph

Review in IUBMB life, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

47 citing papers in PubMed, 83 citations in OpenAlex.

  1. Article
  2. Review
  3. Observational
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Frontiers in public health · 2025
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. Article
  20. Article
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

4 authors at 1 institution in 1 country.

Roberto MendezDepartment of Surgery, Miller School of Medicine, University of Miami, Miami, FL, USA.
Sulagna BanerjeeDepartment of Surgery, Miller School of Medicine, University of Miami, Miami, FL, USA.
Sanjoy K BhattacharyaMiami Integrative Metabolomics Research Center, University of Miami, Miami, FL, USA.
Santanu BanerjeeDepartment of Surgery, Miller School of Medicine, University of Miami, Miami, FL, USA.ORCID 0000-0002-3749-0387
University of Miami · US

Funding

Shared Equipment ModuleP30EY014801 · NEI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI Dmitry V Ivanov · 2004 to 2026
$12.2M
HIV and Morphine Increase Susceptibility to Lung Opportunistic Infections by Modulating TLR2/IL17A Mediated Lung InflammationR21HL125021 · NHLBI · UNIVERSITY OF MINNESOTA · PI BANERJEE, SANTANU · 2015 to 2016
$420k
NEI NIH HHS P30 EY014801NHLBI NIH HHS R21 HL125021
6 · The paper itself

Abstract

It is now well appreciated that the human microbiome plays a significant role in a number of processes in the body, significantly affecting its metabolic, inflammatory, and immune homeostasis. Recent research has revealed that almost every mucosal surface in the human body is associated with a resident commensal microbiome of its own. While the gut microbiome and its role in regulation of host metabolism along with its alteration in a disease state has been well studied, there is a lacuna in understanding the resident microbiota of other mucosal surfaces. Among these, the scientific information on the role of lung microbiota in pulmonary diseases is currently severely limited. Historically, lungs have been considered to be sterile and lung diseases have only been studied in the context of bacterial pathogenesis. Recently however, studies have revealed a resilient microbiome in the upper and lower respiratory tracts and there is increased evidence on its central role in respiratory diseases. Knowledge of lung microbiome and its metabolic fallout (local and systemic) is still in its nascent stages and attracting immense interest in recent times. In this review, we will provide a perspective on lung-associated metabolic disorders defined for lung diseases (e.g., chronic obstructive pulmonary disease, asthma, and respiratory depression due to infection) and correlate it with lung microbial perturbation. Such perturbations may be due to altered biochemical or metabolic stress as well. Finally, we will draw evidence from microbiome and classical microbiology literature to demonstrate how specific lung morbidities associate with specific metabolic characteristics of the disease, and with the role of microbiome in this context. © 2018 IUBMB Life, 71(1):152-165, 2019.

Indexed as

ActinobacteriaAsthmaBacillotaCystic FibrosisHomeostasisHumansLungLung NeoplasmsMicrobiotaPneumonia, BacterialProteobacteriaPulmonary Disease, Chronic ObstructiveRespiratory Mucosa16s rRNA sequencingcommensal floradysbiosislungmetabolomemucosapulmonary microbiome

Identifiers

PMID30466159
PMCPMC6352907
OpenAlexW2900743864

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.