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Association of hematological inflammatory indices with disease activity and interstitial lung disease in systemic sclerosis
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Association of hematological inflammatory indices with disease activity and interstitial lung disease in systemic sclerosis

Clinical Rheumatology·August 17
RheumatologyLimited evidenceInterstitial Lung DiseaseSystemic SclerosisCross-Sectional StudyHematological BiomarkerAdultMean Platelet VolumeNeutrophil-To-Lymphocyte RatioPlatelet-To-Lymphocyte RatioRed Cell Distribution WidthSystemic Immune-Inflammation Index

Summary

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What was studied

This cross-sectional study evaluated whether hematological inflammatory indices (NLR, PLR, SII, RDW, MPV) are associated with disease activity (EUSTAR index) and ILD in 51 SSc patients compared to 106 healthy controls.

Key findings

NLR and SII were significantly elevated in SSc-ILD vs. non-ILD patients; on multivariable logistic regression, NLR remained independently associated with ILD (OR 2.63, 95% CI 1.01–6.85, p = 0.047), while anti-Scl-70 was the strongest independent predictor. ROC analysis showed moderate discrimination: SII AUC 0.72, NLR AUC 0.68. SII lost significance in the adjusted model.

Study limitations

- Small SSc sample (n=51) limits statistical power and generalizability. - Cross-sectional design prevents causal inference or assessment of longitudinal changes. - Full-text not available for review; details on ILD ascertainment method (e.g., HRCT criteria) are not reported in the abstract.

Clinical implications

In SSc patients, a routinely available NLR from a standard CBC may help flag higher ILD risk, particularly alongside anti-Scl-70 serology. However, its moderate AUC (0.68) means it should supplement—not replace—established clinical and serological evaluation.

Caveats

  • Full text was not accessible; summary is based solely on the abstract and publisher page content.
  • ILD ascertainment method (e.g., HRCT protocol, radiologist criteria) is not described in the available abstract text, which limits appraisal of the ILD classification validity.
  • Sex distribution of the study population is not explicitly reported in the abstract; 'mixed' sex tag is inferred from the typical SSc demographic.
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  • The sample_size tag reflects total participants (51 SSc + 106 controls = 157); the SSc-only cohort is small (n=51), which may limit the reliability of multivariable regression findings.

Related Questions

Explore related topics

What is the role of NLR in predicting ILD severity and progression in systemic sclerosis?How does anti-Scl-70 antibody status influence ILD risk and outcomes in scleroderma?Which hematological or serological biomarkers best identify early pulmonary involvement in connective tissue diseases?

Publication Details

Year
2026
Journal
Clinical Rheumatology
Sample Size
n=157
Source
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