Prognostic value of anti-IFI16 autoantibodies in pulmonary arterial hypertension and mortality in patients with systemic sclerosis

Med Clin (Barc). 2024 Apr 26;162(8):370-377. doi: 10.1016/j.medcli.2023.11.020. Epub 2024 Feb 1.
[Article in English, Spanish]

Abstract

Objectives: To determine the diagnostic value of anti-interferon gamma inducible protein 16 (IFI16) autoantibodies in systemic sclerosis (SSc) patients negative for all tested SSc-specific autoantibodies (SSc-seronegative patients) and to evaluate the clinical significance of these autoantibodies, whether isolated or in the presence of anti-centromere autoantibodies (ACA).

Methods: Overall, 58 SSc-seronegative and 66 ACA-positive patients were included in the study. All patients were tested for anti-IFI16 autoantibodies by an in-house direct ELISA. Associations between clinical parameters and anti-IFI16 autoantibodies were analysed.

Results: Overall, 17.2% of SSc-seronegative and 39.4% of ACA-positive patients were positive for anti-IFI16 autoantibodies. Anti-IFI16 autoantibodies were found only in patients within the limited cutaneous SSc (lcSSc) subset. A positive association between anti-IFI16 positivity and isolated pulmonary arterial hypertension (PAH) was found (odds ratio [OR]=5.07; p=0.014) even after adjusting for ACA status (OR=4.99; p=0.019). Anti-IFI16-positive patients were found to have poorer overall survival than negative patients (p=0.032). Cumulative survival rates at 10, 20 and 30 years were 96.9%, 92.5% and 68.7% for anti-IFI16-positive patients vs. 98.8%, 97.0% and 90.3% for anti-IFI16-negative-patients, respectively. Anti-IFI16-positive patients also had worse overall survival than anti-IFI16-negative patients after adjusting for ACA status in the multivariate Cox analysis (hazard ratio [HR]=3.21; p=0.043).

Conclusion: Anti-IFI16 autoantibodies were associated with isolated PAH and poorer overall survival. Anti-IFI16 autoantibodies could be used as a supplementary marker of lcSSc in SSc-seronegative patients and for identifying ACA-positive patients with worse clinical outcome.

Keywords: Autoantibodies; Autoanticuerpos; Esclerodermia sistémica; Factores pronósticos; Hipertensión arterial pulmonar; Interferon gamma inducible protein 16; Mortalidad; Mortality; Prognostic factors; Pulmonary arterial hypertension; Systemic sclerosis.

MeSH terms

  • Autoantibodies
  • Humans
  • Nuclear Proteins
  • Phosphoproteins
  • Prognosis
  • Proportional Hazards Models
  • Pulmonary Arterial Hypertension*
  • Scleroderma, Systemic* / complications
  • Scleroderma, Systemic* / diagnosis

Substances

  • Autoantibodies
  • IFI16 protein, human
  • Nuclear Proteins
  • Phosphoproteins