Evidence map›Paper›PMID 40757465›Full record

ArticleArthritis care & research2026

International Investigation of the Gut-Lung Axis in Systemic Sclerosis-Interstitial Lung Disease.

Kristofer Andréasson, Arissa Young, Swapna Joshi, Jennifer S Labus, Andrea Hsiu Ling Low, Vanessa Smith, Zsuzsanna McMahan, Susanna Proudman, Antonia Valenzuela, Phoebe Hunter and 6 more

Abstract readMulticenter Study
In one paragraph

Article in Arthritis care & research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
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

16 authors.

Kristofer AndréassonLund University, Lund, Sweden.ORCID 0000-0001-7021-2541
Arissa YoungUniversity of California, Los Angeles.
Swapna JoshiUniversity of California, Los Angeles.
Jennifer S LabusUniversity of California, Los Angeles.
Andrea Hsiu Ling LowSingapore General Hospital, SingHealth Duke-National University of Singapore Academic Medical Centre, Singapore.
Vanessa SmithGhent University, Ghent, Belgium.
Zsuzsanna McMahanThe University of Texas Health Science Center at Houston.
Susanna ProudmanRoyal Adelaide Hospital and University of Adelaide, Adelaide, South Australia, Australia.
Antonia ValenzuelaPontificia Universidad Católica de Chile, Santiago, Chile.ORCID 0000-0003-3357-9402
Phoebe HunterRoyal Adelaide Hospital and University of Adelaide, Adelaide, South Australia, Australia.
Grace Hyun KimUniversity of California, Los Angeles.ORCID 0000-0003-1225-3489
Gracijela BozovicLund University, Lund, Sweden.
Jonathan GoldinUniversity of California, Los Angeles.
Ezinne AjaUniversity of California, Los Angeles.
Jonathan P JacobsUniversity of California, Los Angeles.
Elizabeth R VolkmannUniversity of California, Los Angeles.ORCID 0000-0003-3750-6569

Funding

Functional Response Biomarkers for Systemic Sclerosis-Associated Interstitial Lung DiseaseR01HL174555 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Elizabeth R Volkmann · 2025 to 2026
$1.4M
Identifying predictors of treatment response in systemic sclerosis-related interstitial lung diseaseK23HL150237 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI VOLKMANN, ELIZABETH R · 2020 to 2024
$910k
Anonymous Patient DonationBoehringer IngelheimNHLBI NIH HHS K23 HL150237NHLBI NIH HHS R01 HL174555Ulla och Roland Gustafssons Donationsfond, Alfred Österlunds Stiftelse and Anna-Greta Crafoords Stiftelse
6 · The paper itself

Abstract

objectiveMounting evidence supports an association between the intestinal microbiota and diverse pulmonary pathologies (ie, gut-lung axis). Although intestinal dysbiosis is a feature of systemic sclerosis (SSc), no prior studies have investigated the relationship between intestinal microbiota and SSc-associated interstitial lung disease (ILD) in a multinational cohort. This study aimed to characterize the intestinal microbiota of SSc-ILD and determine whether specific bacterial species and functional pathways are associated with ILD severity.

methodsPatients with SSc with and without ILD from seven SSc Centers across five continents provided a stool sample. Shotgun metagenomic sequencing was performed using the Illumina NovaSeq 6000 to characterize microbial composition at the species level. Quantitative image analysis of high-resolution computed tomography scans of the chest was used to measure radiologic extent of ILD (QILD). Multivariate sparse partial least squares analyses were employed to identify a species signature of ILD and to determine whether specific species and functional pathways are associated with QILD.

resultsAmong 285 participants (mean disease duration of 9.8 years), 62.5% had ILD. In a multivariate analysis of all participants, patients with ILD had a unique microbial signature compared to those without ILD characterized by increased abundance of candidate pathobiont species. In a subgroup of participants with SSc-ILD (n = 103), specific bacterial species and functional pathways were associated with QILD.

conclusionThis multicenter study demonstrates that distinct intestinal bacterial species are linked to the presence and radiologic extent of ILD in SSc. These species and/or their metabolic products may influence ILD pathogenesis and represent novel treatment targets.

Indexed as

BacteriaGastrointestinal MicrobiomeLungLung Diseases, InterstitialScleroderma, SystemicAdultAgedDysbiosisFecesFemaleHumansMaleMiddle AgedSeverity of Illness Index

Identifiers

PMID40757465
PMCPMC13142253

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.