Hormonal replacement therapy does not affect self-estimated pain or experimental pain responses in post-menopausal women suffering from fibromyalgia: a double-blind, randomized, placebo-controlled trial

被引:25
作者
Stening, Kent D. [1 ,2 ]
Eriksson, Olle [3 ]
Henriksson, Karl G. [4 ]
Brynhildsen, Jan
Lindh-Astrand, Lotta
Berg, Goran
Hammar, Mats
Amandusson, Asa [5 ]
Blomqvist, Anders [1 ]
机构
[1] Linkoping Univ, Fac Hlth Sci, Dept Expt & Clin Med, Div Cell Biol, S-58185 Linkoping, Sweden
[2] Linnaeus Univ, Dept Hlth & Caring Sci, Kalmar, Sweden
[3] Linkoping Univ, Dept Comp & Informat Sci IDA, Div Stat, S-58185 Linkoping, Sweden
[4] Linkoping Univ, Fac Hlth Sci, Dept Expt & Clin Med, Div Rehabil Med, S-58185 Linkoping, Sweden
[5] Uppsala Univ, Dept Neurosci, Div Clin Neurophysiol, Uppsala, Sweden
基金
瑞典研究理事会;
关键词
Oestrogen; Substitution; Pain; Hormonal levels; Quantitative sensory testing; Cold pressor test; ESTROGEN PLUS PROGESTIN; CHRONIC WIDESPREAD PAIN; CLINICAL PAIN; SYMPTOMS; ASSOCIATION; EFFICACY; COLD; PERCEPTION; EXPRESSION; SUBGROUPS;
D O I
10.1093/rheumatology/keq348
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Methods. Twenty-nine post-menopausal women were randomized to either 8 weeks of treatment with transdermal 17 beta-oestradiol (50 mu g/day) or placebo according to a double-blind protocol. A self-estimation of pain, a set of quantitative sensory tests measuring thresholds to temperature, thermal pain, cold pain and pressure pain, and a cold pressor test were performed on three occasions: before treatment, after 8 weeks of treatment and 20 weeks after cessation of treatment. Results. Hormonal replacement treatment significantly increased serum oestradiol levels as expected (P < 0.01). However, no differences in self-estimated pain were seen between treatment and placebo groups, nor were there any differences between the two groups regarding the results of the quantitative sensory tests or the cold pressor test at any of the examined time points. Conclusion. Eight weeks of transdermal oestradiol treatment does not influence perceived pain, pain thresholds or pain tolerance as compared with placebo treatment in post-menopausal women suffering from FM.
引用
收藏
页码:544 / 551
页数:8
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