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Prolactin deficiency in rheumatoid arthritis
E Nagy1, I M Chalmers, F D Baragar
1Department of Immunology, Faculty of Medicine, University of Manitoba, Winnipeg, Canada.
The Journal of Rheumatology
|November 1, 1991
Summary
Rheumatoid arthritis (RA) patients show significantly reduced prolactin (PRL) bioactivity, not just lower levels. This indicates a functional deficiency of PRL in RA, impacting its biological effects.
Area of Science:
- Endocrinology
- Immunology
- Rheumatology
Background:
- Rheumatoid arthritis (RA) is a chronic autoimmune disease.
- Hormonal imbalances, including prolactin (PRL) dysfunction, may play a role in RA pathogenesis.
- Previous studies have yielded conflicting results regarding PRL levels in RA patients.
Purpose of the Study:
- To investigate the bioactivity and immunoactivity of circulating prolactin (PRL) in patients with rheumatoid arthritis (RA).
- To compare PRL levels and function between RA patients and healthy controls.
- To explore the relationship between PRL status and clinical features of RA, such as anemia.
Main Methods:
- Sera from 48 RA patients and 23 controls were analyzed.
- Radioimmunoassay (RIA) was used to measure immunoactive PRL levels.
- Nb2 lymphoma cell proliferation bioassay was employed to assess PRL bioactivity.
Main Results:
- RA patients exhibited significantly diminished PRL bioactivity compared to controls, despite near-normal immunoactive PRL levels.
- A subset of male RA patients showed lower serum PRL levels by RIA.
- PRL bioactivity in RA patients with anemia and high reticulocyte counts was elevated, while those with low reticulocyte counts showed decreased bioactivity.
- Isolated PRL from RA patients' sera demonstrated reduced bioactivity.
Conclusions:
- Rheumatoid arthritis is associated with a deficiency in prolactin bioactivity.
- The discrepancy between immunoactive and bioactive PRL suggests post-translational modification or inhibitory serum factors in RA.
- PRL dysfunction may contribute to the pathophysiology of rheumatoid arthritis.