Evidence map›Paper›PMID 41316278›Full record

Observational studyRespiratory research2025

Antiphospholipid antibodies and subclinical interstitial lung disease in the MESA cohort.

Claire F McGroder, Mary M Salvatore, John Newell, Jubal Watts, P Hrudaya Nath, Sushilkumar K Sonavane, Eric A Hoffman, Ganesh Raghu, R Graham Barr, John S Kim and 3 more

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Respiratory research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Claire F McGroderDivision of Pulmonary, Allergy, and Critical Care Medicine, Columbia University Irving Medical Center, New York, NY, USA.
Mary M SalvatoreDepartment of Radiology, Albert Einstein College of Medicine, New York, NY, USA.
John NewellDepartment of Radiology, University of Iowa Carver College of Medicine, Iowa City, IA, USA.
Jubal WattsDepartment of Radiology, University of Alabama, Birmingham, AL, USA.
P Hrudaya NathDepartment of Radiology, University of Alabama, Birmingham, AL, USA.
Sushilkumar K SonavaneDepartment of Radiology, Mayo Clinic at Jacksonville, Jacksonville, FL, USA.
Eric A HoffmanDepartment of Radiology, University of Iowa Carver College of Medicine, Iowa City, IA, USA.
Ganesh RaghuDepartment of Medicine, University of Washington, Seattle, WA, USA.
R Graham BarrDivision of Pulmonary, Allergy, and Critical Care Medicine, Columbia University Irving Medical Center, New York, NY, USA.
John S KimDivision of Pulmonary, Allergy, and Critical Care Medicine, Columbia University Irving Medical Center, New York, NY, USA.
Anna J PodolanczukDivision of Pulmonary and Critical Care Medicine, Weill Cornell Medical College, New York, NY, USA.
Christine Kim GarciaDivision of Pulmonary, Allergy, and Critical Care Medicine, Columbia University Irving Medical Center, New York, NY, USA.
Elana J BernsteinDivision of Rheumatology, Columbia University Irving Medical Center, 630 W 168th St, Suite 3-450, New York, NY, 10032, USA. ejb2153@cumc.columbia.edu.

Funding

Pulmonary Toxicology Facility CoreP30ES005605 · NIEHS · UNIVERSITY OF IOWA · PI PATRICK T O'SHAUGHNESSY · 1990 to 2026
$40.5M
Pulmonary microvascular perfusion in the Multi-Ethnic Study of AtherosclerosisR01HL077612 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI R Graham BARR · 2004 to 2026
$18.8M
Pulmonary Vascular Changes in Early Chronic Obstructive Pulmonary Disease (COPD)R01HL093081 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI R Graham BARR · 2008 to 2026
$17.2M
The Columbia University Training Program in Lung ScienceT32HL105323 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Jahar Bhattacharya, Wellington V. Cardoso · 2011 to 2026
$4.7M
Vasculopathy and Systemic Sclerosis-Associated Interstitial Lung DiseaseR01HL164758 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Elana J. Bernstein · 2022 to 2026
$3.5M
Role of polyunsaturated fatty acids in pulmonary fibrosisK23HL150301 · NHLBI · UNIVERSITY OF VIRGINIA · PI KIM, JOHN S · 2021 to 2025
$858k
Role of High Density Lipoproteins in Interstitial Lung DiseaseK23HL140199 · NHLBI · WEILL MEDICAL COLL OF CORNELL UNIV · PI PODOLANCZUK, ANNA · 2018 to 2022
$858k
Screening Chest CT to Detect Interstitial Lung Disease in Systemic SclerosisK23AR075112 · NIAMS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI BERNSTEIN, ELANA · 2019 to 2023
$794k
Congressionally Directed Medical Research Programs W81XWH2210163NHLBI NIH HHS K23 HL140199NHLBI NIH HHS K23 HL150301NHLBI NIH HHS K23-HL-150301NHLBI NIH HHS R01 HL077612NHLBI NIH HHS R01 HL093081NHLBI NIH HHS R01 HL164758NHLBI NIH HHS R01-HL-164758NHLBI NIH HHS T32 HL105323NIAMS NIH HHS K23 AR075112NIAMS NIH HHS K23-AR-075112NIEHS NIH HHS P30 ES005605
6 · The paper itself

Abstract

backgroundInterstitial lung disease (ILD) is a rare complication of antiphospholipid syndrome (APS), but circulating antiphospholipid antibodies have been detected in patients with ILD without APS. Whether antiphospholipid antibodies are associated with subclinical ILD phenotypes is unknown. We aim to examine the associations between anticardiolipin (aCL) and B-2 glycoprotein-1 (B2GP1) isotypes and high attenuation areas (HAA) and interstitial lung abnormalities (ILA) on CT scans in the Multi-Ethnic Study of Atherosclerosis (MESA).

methodsWe measured serum aCL and B2GP1 isotypes and calculated proportion of HAA on cardiac CT scan in 6623 MESA participants at baseline. The presence of ILAs were assessed on full lung CT scans at Exam 5. We used linear and logistic regression to examine these associations. We examined interactions by age, race, and smoking status.

resultsIn adjusted models, every doubling of aCL IgA, IgG, and IgM was associated with 0.36% (95% CI 0.03 to 0.70), 0.31% (95% CI 0.08 to 0.54), and 0.30% (95% CI 0.10 to 0.50) higher HAA in White participants, respectively. No association was found in participants of other races/ethnicities. Smoking modified the association between B2GP1 isotypes and HAA: in individuals with moderate smoking history, every doubling of B2GP1 IgA, IgG and IgM was associated with 0.84% (95% CI 0.30 to 1.38), 0.97% (95% CI 0.43 to 1.52) and 0.65% (95% CI 0.11 to 1.20) higher HAA, respectively. There was no association between antiphospholipid antibodies and ILA.

conclusionsAntiphospholipid antibodies are associated with HAA, a quantitative measure of lung injury, inflammation and fibrosis.

Indexed as

Antibodies, AntiphospholipidLung Diseases, InterstitialAgedAged, 80 and overAntibodies, AnticardiolipinBiomarkersCohort StudiesFemaleHumansMaleMiddle AgedProspective StudiesTomography, X-Ray ComputedUnited StatesAntibodies, AnticardiolipinAntibodies, AntiphospholipidBiomarkersAutoimmune diseaseBiomarkersInterstitial lung diseasePulmonary fibrosisRadiology and other imaging

Identifiers

PMID41316278
PMCPMC12664236

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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.