Evidence map›Paper›PMID 42699467›Full record

ArticleEJIFCC2026

Autoantibody Profiles and Clinical Correlations in Systemic Sclerosis: A Cross-Sectional Study.

Debamita Datta, Sushil Kumar, Lekha Priyadharshini Kamarajan, Mala Mahto, Bandana Kumari, Ayan Banerjee, Swetalina Pradhan, Bijay Nanda Naik

Abstract read
In one paragraph

Article in EJIFCC, 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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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

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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

8 authors.

Debamita DattaDepartment of Biochemistry, Tripura Santiniketan Medical College, Agartala, Tripura, India.
Sushil KumarDepartment of Biochemistry, All India Institute of Medical Sciences (AIIMS), Patna, Bihar, India.
Lekha Priyadharshini KamarajanDepartment of Biochemistry, All India Institute of Medical Sciences (AIIMS), Patna, Bihar, India.
Mala MahtoDepartment of Biochemistry, All India Institute of Medical Sciences (AIIMS), Patna, Bihar, India.
Bandana KumariDepartment of Biochemistry, All India Institute of Medical Sciences (AIIMS), Patna, Bihar, India.
Ayan BanerjeeDepartment of Biochemistry, All India Institute of Medical Sciences (AIIMS), Patna, Bihar, India.
Swetalina PradhanDepartment of Dermatology, All India Institute of Medical Sciences (AIIMS), Patna, Bihar, India.
Bijay Nanda NaikDepartment of Community and Family Medicine, All India Institute of Medical Sciences (AIIMS), Patna, Bihar, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Systemic sclerosis (SSc) is a rare autoimmune disease marked by immune dysregulation, vascular injury, and fibrosis. Antinuclear antibodies (ANA) are pivotal for diagnosis and prognosis, yet Indian data remain scarce. This study assessed ANA patterns and autoantibody profiles in SSc and their clinical relevance. Methods: A cross-sectional study was conducted in the Department of Dermatology, AIIMS Patna, from September 2022 to September 2023. Eighty-five patients fulfilling ACR/EULAR criteria for SSc were enrolled. Clinical features were documented using a structured proforma, and patients were classified into diffuse cutaneous (dcSSc) and limited cutaneous (lcSSc) subsets. ANA screening was performed by indirect immunofluorescence (IIF) on HEp2 cells, followed by autoantibody profiling with line immunoassay (LIA). Statistical analyses were performed using JAMOVI v2.3.28, with p<0.05 considered significant. Results: Of 85 patients, 70 (82.4%) were female (ratio of 5:1), with a mean age of 34.7 ± 10.7 years. dcSSc accounted for 55.3%. Common manifestations included arthralgia (69.4%), respiratory symptoms (68.2%), and interstitial lung disease (ILD) (64.1%). Homogeneous ANA was the predominant IIF pattern (41.2%), followed by centromere (10.6%) and speckled (8.2%). LIA revealed anti-Scl70 as the most frequent autoantibody (58.3%), significantly associated with ILD and Raynaud's phenomenon. Anti-U1 snRNP and anti-PMScl antibodies correlated with musculoskeletal involvement. Conclusion: SSc in this cohort showed female predominance with frequent arthralgia and respiratory symptoms. Anti-Scl-70 antibodies were most common, strongly linked to diffuse disease and ILD. ANA profiling provides disease characterization in Indian SSc.

Indexed as

Antinuclear antibodiesAnti-Scl-70Interstitial lung diseaseSystemic sclerosis

Identifiers

PMID42699467
PMCPMC13543460

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