Evidence map›Paper›PMID 42228224›Full record

Observational studyClinical rheumatology2026

High frequency of interstitial lung disease in Indian patients with adult- onset idiopathic inflammatory myopathy: Insights from a prospective observational cohort.

Harikrishnan Gangadharan, Anusree Prasad Seetha, Sajitha Musthafa, Sandra Pulickal Babu, Sandra Krishnan, Sonia John, Sajitha Krishnadas

Abstract readObservational Study
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In one paragraph

Observational study in Clinical rheumatology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Harikrishnan GangadharanDepartment of Rheumatology, Government Medical College Kottayam, Gandhinagar, 686008, Kerala, India. drharikrishnang@gmail.com.ORCID http://orcid.org/0000-0001-5313-7316
Anusree Prasad SeethaDepartment of Pulmonary Medicine, Marian Medical Center Pala, Kottayam, Kerala, India.ORCID http://orcid.org/0009-0000-4580-4617
Sajitha MusthafaDepartment of Pulmonary Medicine, Government Medical College Kottayam, Gandhinagar, Kerala, India.ORCID http://orcid.org/0000-0002-0751-8537
Sandra Pulickal BabuDepartment of Rheumatology, Government Medical College Kottayam, Gandhinagar, 686008, Kerala, India.ORCID http://orcid.org/0009-0005-6670-0661
Sandra KrishnanDepartment of Rheumatology, Government Medical College Kottayam, Gandhinagar, 686008, Kerala, India.ORCID http://orcid.org/0009-0002-6550-4800
Sonia JohnDepartment of Pulmonary Medicine, Government Medical College Kottayam, Gandhinagar, Kerala, India.
Sajitha KrishnadasDepartment of Radiodiagnosis, Government Medical College Kottayam, Gandhinagar, Kerala, India.ORCID http://orcid.org/0009-0007-7220-0895

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesData on interstitial lung disease (ILD) in Indian patients with idiopathic inflammatory myopathy (IIM) is limited. We aimed to determine the characteristics of ILD, and factors associated with the progression of ILD in Indian patients with IIM.

methodsA prospective single centre cohort of 86 consecutive adult-onset IIM patients recruited between October 2020 and December 2025 were studied. The diagnosis of IIM related ILD (IIM-ILD) was made after high resolution CT Thorax. Progression of ILD was defined as per the 2022 ATS/ERS/JRS/ALAT guidelines for progressive pulmonary fibrosis (PPF). Multivariate logistic regression was done to identify independent factors associated IIM-ILD. Comparisons were made between patients with PPF and those without PPF.

resultsOf the 86 IIM patients, ILD was seen in 59.3% of patients (n = 51). The most common radiological patterns were non-specific interstitial pneumonia (58.8%), organizing pneumonia (21.6%), usual interstitial pneumonia (13.7%), and overlap of NSIP-OP (5.9%). The most common subsets were anti synthetase syndrome (66.6%, 34/51), dermatomyositis (23.5%, 12/51) and overlap myositis (7.8%, 4/51). The most common myositis specific autoantibody was anti-Jo1 (27.4%, 14/51) and the most common myositis associated autoantibody was anti-Ro52 (58.8%, 30/51). On multivariate logistic regression, heliotrope rash (OR 0.25, 95% CI 0.06-0.96, p = 0.04), arthritis (OR 3.57, 95% CI 1.15-11.07, p = 0.03) and anti-Ro52 (OR 4.37, 95% CI 1.40-13.40, p = 0.01) were associated with ILD. Of the 37 patients with IIM-ILD evaluated for progression, 18.9% (n = 7) developed PPF within 1 year of follow up. Amyopathic presentation and NSIP/OP pattern were associated with PPF (p = 0.02, p = 0.03 respectively).

conclusionThe frequency of ILD is high in Indian patients with IIM (59.3%, 51/86) and of the IIM-ILD evaluated for progression, around one fifth developed PPF (18.9%, 7/37). A baseline screening for ILD is mandatory in IIM and close monitoring of IIM-ILD is required for early detection of PPF. Key Points •The frequency of ILD in Indian patients with IIM is high (59.3%, 51/86), higher than the global prevalence of ILD in IIM. •Arthritis, heliotrope rash and anti-Ro52 antibody were identified as significant factors associated with IIM-ILD. •Around 1/5th of evaluable IIM-ILD (18.9%, 7/37) developed progressive pulmonary fibrosis within 1 year of follow up.

Indexed as

Lung Diseases, InterstitialMyositisAdultAgedAutoantibodiesDisease ProgressionFemaleHumansIndiaMaleMiddle AgedProspective StudiesTomography, X-Ray ComputedAutoantibodiesInterstitial; prognosisMyositis; Lung diseases

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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.