The CALLY Index May Reflect Systemic Inflammatory Burden Rather than Patient-Reported Disease Activity in Ankylosing

Altuğ Güner1, Taner Dandinoğlu2, Sümeyye Tuna Güner3

  • 1Department of Rheumatology, Bursa City Hospital, 16110 Bursa, Türkiye.

Insights

The C-reactive protein-albumin-lymphocyte (CALLY) index in ankylosing spondylitis (AS) correlates with objective inflammation markers but not patient-reported outcomes. Further research is needed to validate its clinical use.

Area of Science:

  • Rheumatology
  • Biomarker Research
  • Inflammatory Diseases

Background:

  • Ankylosing spondylitis (AS) assessment is challenging, with current indices potentially underestimating systemic inflammation.
  • The C-reactive protein-albumin-lymphocyte (CALLY) index integrates inflammatory, nutritional, and immunological markers.
  • Evaluating novel biomarkers is crucial for improving AS management.

Purpose of the Study:

  • To assess the association of the CALLY index with disease activity, functional status, and quality of life in AS patients.
  • To explore the CALLY index's relationship with established clinical and biochemical markers.
  • To investigate the CALLY index's potential as a comprehensive biomarker in AS.

Main Methods:

  • Cross-sectional study of 65 AS patients using medical records.
  • Calculation of the CALLY index using C-reactive protein (CRP), albumin, and lymphocyte counts.
  • Assessment of disease activity (BASDAI, ASDAS-ESR), function (BASFI), and quality of life (SF-12).

Main Results:

  • The CALLY index showed moderate negative correlations with ESR and ASDAS-ESR.
  • A positive correlation was observed between the CALLY index and lymphocyte count.
  • No significant associations were found between the CALLY index and BASDAI, BASFI, or SF-12, indicating a dissociation.

Conclusions:

  • The CALLY index primarily reflects objective inflammatory markers in AS, not subjective patient experiences.
  • Findings suggest a potential disconnect between biochemical and clinical disease manifestations in AS.
  • Larger, longitudinal studies are required to confirm these preliminary findings and assess clinical utility.