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HLA DR antigens and gold toxicity
Annals of the Rheumatic Diseases
|February 1, 1983
Summary
Patients with rheumatoid arthritis treated with gold experienced more adverse reactions if they had the HLA DR3 antigen. This included an 11-fold increased risk of proteinuria, while DR7 positives showed fewer side effects.
Area of Science:
- Immunogenetics
- Rheumatology
- Pharmacogenetics
Background:
- Rheumatoid arthritis (RA) is a chronic autoimmune disease.
- Gold therapy has been used for RA treatment.
- Human Leukocyte Antigen (HLA) DR antigens are associated with immune responses and drug reactions.
Purpose of the Study:
- To investigate the association between HLA DR antigens and adverse reactions to gold therapy in rheumatoid arthritis patients.
- To identify specific HLA DR types that may predict risk for side effects during gold treatment.
Main Methods:
- A cohort of 132 rheumatoid arthritis patients treated with gold was analyzed.
- Patients were genotyped for HLA DR antigens.
- Frequencies of adverse reactions were compared between different HLA DR antigen groups.
Main Results:
- Patients with the HLA DR3 antigen showed a significantly higher frequency of adverse reactions to gold therapy compared to those without DR3.
- HLA DR3-positive patients had an 11-fold increased risk of developing proteinuria.
- The lowest incidence of side effects was observed in patients positive for HLA DR7.
- No significant differences in skin eruptions, liver reactions, or leucopenia were found across DR antigen groups.
Conclusions:
- HLA DR3 is a significant risk factor for adverse reactions, particularly proteinuria, during gold therapy for rheumatoid arthritis.
- HLA DR7 may be associated with a lower risk of side effects.
- HLA DR genotyping could aid in predicting and managing gold therapy-related adverse events in RA patients.