Modeling the involvement of the hypothalamic-pituitary-adrenal and hypothalamic-pituitary-gonadal axes in autoimmune and stress-related rheumatic syndromes in women

Citation
Lj. Crofford et al., Modeling the involvement of the hypothalamic-pituitary-adrenal and hypothalamic-pituitary-gonadal axes in autoimmune and stress-related rheumatic syndromes in women, J WOMENS HE, 8(2), 1999, pp. 203-215
Citations number
58
Categorie Soggetti
Public Health & Health Care Science","General & Internal Medicine
Journal title
JOURNAL OF WOMENS HEALTH
ISSN journal
10597115 → ACNP
Volume
8
Issue
2
Year of publication
1999
Pages
203 - 215
Database
ISI
SICI code
1059-7115(199903)8:2<203:MTIOTH>2.0.ZU;2-2
Abstract
Autoimmune and stress-related rheumatic diseases are significantly more com mon in women than in men. Our group has focused on the role of two principa l neuroendocrine axes, the hypothalamic-pituitary-adrenal (HPA) axis and th e hypothalamic-pituitary-gonadal (HPG) axis, in this increased susceptibili ty to rheumatic disease. We review the physiology of the HPA and HPG axes a nd discuss their reciprocal interactions. Mechanisms by which hormones of t he HPA and HPG axes influence the immune system and modulate the course of autoimmune inflammatory diseases in animal models of rheumatic disease are described. In addition, we review the data suggesting the importance of the se neurohormonal systems in rheumatic diseases. These data provide insights into why women may be at increased risk and how we might better understand the mechanisms that provoke expression of rheumatic diseases in women. To advance research in this area, it is critical to develop methods to evaluat e the function of the neuroendocrine axes. Secretion of both HPA and HPG ax is hormones, particularly the hormones of the hypothalamus and anterior pit uitary, is largely by intermittent pulses. In addition, the HPA axis exhibi ts a profound circadian, or near 24-hour, variation, and HPG axis hormones fluctuate over the monthly cycle. These factors make meaningful analysis of these axes quite complex. We discuss models used in the analyses of neuroe ndocrine axes and the use of challenge testing to assess the integrity of n euroendocrine axes.