# Significance of Systemic Scleroderma-Specific Autoantibodies in Idiopathic Interstitial Pneumonia

**Authors:** Yu Murakami, Hiroki Wakabayashi, Kaichi Kaneko, Kenta Takashima, Atsuhito Saiki, Yasuo Matuzawa

PMC · DOI: 10.7759/cureus.66986 · Cureus · 2024-08-16

## TL;DR

This study explores the role of autoantibodies linked to systemic scleroderma in patients with idiopathic interstitial pneumonia and finds that some antibodies may predict severe lung disease.

## Contribution

Identifies anti-fibrillarin antibodies as a potential predictor of acute exacerbation in idiopathic interstitial pneumonia.

## Key findings

- No significant difference in survival or acute exacerbation rates between SSc-Ab positive and negative IIP patients.
- Anti-fibrillarin antibodies, age, and male sex are significant risk factors for acute exacerbation of IIP.
- SSc-Ab positivity does not correlate with mortality in IIP patients.

## Abstract

Objective

Patients with idiopathic interstitial pneumonia (IIP) often test positive for systemic scleroderma-specific autoantibodies (SSc-Ab), even if they do not meet the diagnostic criteria for systemic scleroderma (SSc). However, the significance of SSc-Ab in IIP is unknown.

Methods

We retrospectively studied the medical records of all patients suspected of interstitial lung disease (ILD) who visited our center between January 2016 and December 2021. We evaluated the association between SSc-Ab subtypes and clinical characteristics, prognosis, and incidence of acute exacerbation (AE) of IIP. Among 571 patients suspected of having IIP and SSc-Ab measured, we excluded cases with clear causes of ILD or those diagnosed with other diseases and analyzed 386 cases diagnosed as IIP.

Results

Among 386 IIP patients, 48 were SSc-Ab positive (platelet-derived growth factor receptor (PDGFR) in 0, Th/To in 10, anti-nucleolar organizer region 90 antibodies (NOR90) in 12, fibrillarin in five, RP155 in 14, RP11 in three, CENP A in seven, CENP B in 10, and Scl-70 in six). There was no significant difference in survival rate or incidence of AE between patients with or without SSc-Ab. Multivariate logistic regression analysis showed that age and malignancy were significant risk factors for death, whereas age, male sex, and anti-fibrillarin antibodies were significant risk factors for AE of IIP.

Conclusion

None of the SSc-Abs were associated with the risk of mortality, and anti-fibrillarin antibodies, along with age and male sex may contribute to the risk of AE of IIP, predicting severe lung involvement and warranting multidisciplinary treatment and careful follow-up.

## Linked entities

- **Proteins:** Fib (Fibrillarin), PRPF31 (pre-mRNA processing factor 31), CENPA (centromere protein A), CENPB (centromere protein B), LOC112003270 (SCARECROW-LIKE protein 7)
- **Diseases:** systemic scleroderma (MONDO:0005100), idiopathic interstitial pneumonia (MONDO:0002429), interstitial lung disease (MONDO:0015925)

## Full-text entities

- **Genes:** UBTF (upstream binding transcription factor) [NCBI Gene 7343] {aka CONDBA, NOR-90, UBF, UBF-1, UBF1, UBF2}, CENPB (centromere protein B) [NCBI Gene 1059], PDGFRB (platelet derived growth factor receptor beta) [NCBI Gene 5159] {aka CD140B, IBGC4, IMF1, JTK12, KOGS, OPDKD}, CENPA (centromere protein A) [NCBI Gene 1058] {aka CENP-A, CenH3}, FBL (fibrillarin rRNA 2'-O-methyltransferase) [NCBI Gene 2091] {aka FIB, FLRN, Nop1, RNU3IP1}, PRPF31 (pre-mRNA processing factor 31) [NCBI Gene 26121] {aka NY-BR-99, PRP31, RP11, SNRNP61}
- **Diseases:** malignancy (MESH:D009369), ILD (MESH:D017563), SSc (MESH:D012595), IIP (MESH:D054988), death (MESH:D003643), AE of IIP (MESH:D000080203), lung involvement (MESH:D008171)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11328454/full.md

## References

29 references — full list in the complete paper: https://tomesphere.com/paper/PMC11328454/full.md

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Source: https://tomesphere.com/paper/PMC11328454