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Persistent eosinophilia in rheumatoid arthritis: a prospective observational study
Dantis Emmanuel1,2, Subhash Chandra Parija3,4, Ankit Jain1,5
1Department of Clinical Immunology, Jawaharlal Institute of Postgraduate Medical Education and Research (JIPMER), Puducherry, 605006, India.
Eosinophilia in Rheumatoid arthritis (RA) is often secondary to causes like intestinal helminthiasis. Persistent eosinophilia in RA patients did not correlate with a more severe disease phenotype.
Area of Science:
- Rheumatology
- Immunology
- Infectious Diseases
Background:
- Eosinophilia is an infrequent finding in Rheumatoid arthritis (RA).
- Limited data exists on the association between eosinophilia and RA disease characteristics.
- Understanding the causes and implications of eosinophilia in RA is crucial.
Purpose of the Study:
- To prospectively investigate the clinical and disease-specific factors associated with eosinophilia in Rheumatoid arthritis patients.
- To identify the causes of eosinophilia in RA patients and assess the impact of treatment.
Main Methods:
- Prospective evaluation of RA patients with absolute eosinophil count ≥ 500/mm³.
- Investigation for parasitic infestation, with targeted therapy or empirical albendazole treatment.
- Comparison of disease-specific characteristics between RA patients with persistent eosinophilia and those without.
Main Results:
- Intestinal helminthiasis was identified as the most common cause (21%) of eosinophilia in this RA cohort.
- Eosinophilia resolved in approximately two-thirds of patients after empirical albendazole therapy.
- No significant difference in disease-related characteristics was observed between RA patients with persistent eosinophilia and those without.
Conclusions:
- Secondary causes, predominantly intestinal helminthic infections, account for most cases of eosinophilia in Rheumatoid arthritis patients.
- Empirical albendazole therapy can be effective in resolving eosinophilia of unknown origin in RA.
- Persistent eosinophilia in RA does not appear to indicate a more severe disease phenotype.
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