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  4. A randomized controlled trial of dehydroepiandrosterone in postmenopausal women with fibromyalgia
 
  • Détails
Titre

A randomized controlled trial of dehydroepiandrosterone in postmenopausal women with fibromyalgia

Type
article
Institution
UNIL/CHUV/Unisanté + institutions partenaires
Périodique
The Journal of Rheumatology  
Auteur(s)
Finckh, A.
Auteure/Auteur
Berner, I. C.
Auteure/Auteur
Aubry-Rozier, B.
Auteure/Auteur
So, A. K.
Auteure/Auteur
Liens vers les personnes
So, Alexander Kai-Lik  
Liens vers les unités
Rhumatologie et rééducation  
ISSN
0315-162X
Statut éditorial
Publié
Date de publication
2005-07
Volume
32
Numéro
7
Première page
1336
Dernière page/numéro d’article
40
Notes
Clinical Trial
Journal Article
Randomized Controlled Trial
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, P.H.S. --- Old month value: Jul
Résumé
OBJECTIVE: Patients with fibromyalgia (FM) consistently have adrenal hyporesponsiveness and low dehydroepiandrosterone (DHEA) levels. DHEA is promoted for and used by patients with FM. We tested the efficacy and safety of DHEA supplementation in ameliorating the symptoms of FM. METHODS: In a double-blind crossover study, postmenopausal women with FM were randomized to DHEA supplementation (50 mg/day) or placebo for 3 months, with a one-month washout period in between. Patients were assessed monthly for well-being and pain and by medical evaluations at the beginning and the end of each treatment period. The primary outcome was well being; secondary outcomes were pain, fatigue, cognition, sexuality, functional impairment, depression, and anxiety. RESULTS: A total of 52 patients were randomized, 47 patients completed the DHEA treatment period, and 45 the placebo treatment period. After 3 months of treatment with 50 mg of DHEA, median DHEA sulfate blood levels had tripled, but there was no improvement in well-being, pain, fatigue, cognitive dysfunction, functional impairment, depression, or anxiety, nor in objective measurements made by physicians. Androgenic side effects (greasy skin, acne, and increased growth of body hair) were more common during the DHEA treatment period (p = 0.02). CONCLUSION: DHEA does not improve quality of life, pain, fatigue, cognitive function, mood, or functional impairment in FM.
Sujets

Aged Cognition/drug e...

PID Serval
serval:BIB_80AB1DAE653F
PMID
15996074
WOS
000230532000029
Permalien
https://iris.unil.ch/handle/iris/194580
Date de création
2008-01-25T07:39:18.741Z
Date de création dans IRIS
2025-05-21T02:08:02Z
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