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Polymyalgia rheumatica and temporal arteritis: the endocrine relations and the pathogenesis. Review
R Imrich1, V Bosak, J Rovensky
1Institute of Experimental Endocrinology, Slovak Academy of Sciences, Bratislava, Slovakia. richard.imrich@savba.sk
Abstract:
Polymyalgia rheumatica (PMR) and giant cell or temporal arteritis (TA) are related chronic inflammatory conditions which typically affect the aged subjects. Typical features of PMR include general symptoms of inflammation as well as severe muscle pain in shoulder and pelvic girdle. The manifestation of TA depends on localization of affected artery, usually branch vessels of the aortic arch. Etiology of PMR and TA remains unclear. The association with HLA system and characteristics of the inflammatory response are discussed in this paper. Age related changes in neuroendocrine system could also represent a pathogenic factor in genetically disposed individuals. Complex bi-directional neuroendocrine-immune relations are further modified by ongoing chronic inflammation. Good clinical response to glucocorticoids in PMR patients supports the assumption that the actual levels of cortisol are lower than would be expected during ongoing inflammation. Moreover, decreased levels of adrenal androgens have been observed in PMR and thus possible adrenal androgens supplementation during glucocorticoid treatment sketches new prospects for the treatment of PMR and TA.
Insights
Polymyalgia rheumatica (PMR) and temporal arteritis (TA) are inflammatory conditions in older adults. Research suggests neuroendocrine-immune interactions and low adrenal androgens may play a role, with potential for androgen supplementation in treatment.
Area of Science:
- Rheumatology
- Immunology
- Endocrinology
Background:
- Polymyalgia rheumatica (PMR) and giant cell/temporal arteritis (TA) are chronic inflammatory conditions primarily affecting the elderly.
- PMR is characterized by inflammation and muscle pain in the shoulder and pelvic girdle.
- TA manifestations vary based on the affected artery, often involving aortic arch branches.
Purpose of the Study:
- To explore the unclear etiology of PMR and TA.
- To discuss the association with the HLA system and inflammatory response characteristics.
- To investigate the role of age-related neuroendocrine changes and neuroendocrine-immune interactions in disease pathogenesis.
Main Methods:
- Review of existing literature on PMR and TA.
- Discussion of genetic predispositions and inflammatory markers.
- Analysis of neuroendocrine-immune system interactions in chronic inflammation.
Main Results:
- The etiology of PMR and TA remains largely unknown.
- Age-related neuroendocrine changes may contribute to pathogenesis in genetically susceptible individuals.
- PMR patients show reduced cortisol levels during inflammation and decreased adrenal androgens.
Conclusions:
- The effectiveness of glucocorticoids in PMR suggests altered cortisol levels.
- Decreased adrenal androgens in PMR indicate potential therapeutic avenues.
- Adrenal androgen supplementation may offer new treatment prospects for PMR and TA.
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