Hypothalamic-pituitary-adrenal axis function and cytokine production in multiple sclerosis with or without interferon-beta treatment

Acta Neurol Scand. 2002 May;105(5):372-7. doi: 10.1034/j.1600-0404.2002.01155.x.

Abstract

Objectives: Pro-inflammatory cytokines mediate brain damage in multiple sclerosis (MS); they can also influence the hypothalamic-pituitary-adrenal (HPA) axis function. We evaluated the possible abnormalities of HPA axis function in relapsing-remitting MS (RR-MS).

Material and methods: IFN-gamma, TNF-alpha and IL-6 production by ex-vivo lymphocytes from 10 normal volunteers and 10 RR-MS patients before and during IFN-beta therapy was assessed; pituitary-adrenal function was evaluated by means of CRH and ACTH stimulation tests.

Results: In untreated patients the production of IFN-gamma, TNF-alpha, IL-6 was increased, and was significantly decreased by IFN-beta. Neither basal, nor stimulated ACTH, cortisol, DHEA, DHEAs, 17-alpha-OH-progesterone levels differed between controls and RR-MS patients, both before and during treatment. Moreover, no correlation was found between endocrine and immune parameters.

Conclusion: In MS the HPA axis function seems normal and not influenced by IFN-beta treatment. This result is discussed in relation to the increased production of pro-inflammatory cytokines found in this disease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adjuvants, Immunologic / therapeutic use*
  • Adult
  • Female
  • Humans
  • Hypothalamo-Hypophyseal System / metabolism*
  • Hypothalamo-Hypophyseal System / physiopathology*
  • Interferon-beta / therapeutic use*
  • Interferon-gamma / metabolism*
  • Interleukin-6 / metabolism*
  • Male
  • Middle Aged
  • Multiple Sclerosis* / drug therapy
  • Multiple Sclerosis* / metabolism
  • Multiple Sclerosis* / physiopathology
  • Pituitary-Adrenal System / metabolism*
  • Pituitary-Adrenal System / physiopathology*
  • Tumor Necrosis Factor-alpha / metabolism*

Substances

  • Adjuvants, Immunologic
  • Interleukin-6
  • Tumor Necrosis Factor-alpha
  • Interferon-beta
  • Interferon-gamma