TY - JOUR
T1 - Motor Cortex Repetitive Transcranial Magnetic Stimulation in Fibromyalgia
T2 - A multicentre Randomised controlled Trial
AU - Silva, Valquíria A.
AU - Fontes Baptista, Abrahão
AU - Fonseca, Alessandra S.
AU - Carneiro, Adriana M.
AU - Brunoni, André Russowsky
AU - Carrilho, Paulo E. M.
AU - Lins, Catarina C.
AU - Kubota, Gabriel T.
AU - Fernandes, Ana Mércia B. L.
AU - Lapa, Jorge D. S.
AU - dos Santos, Lucas M.
AU - Sasso, Ivo
AU - Monte-Silva, Kátia
AU - Poindessous‐Jazat, Frédérique
AU - Mori, Nobuhiko
AU - Miki, Kenji
AU - Baltar do Rêgo Maciel, Adriana
AU - Tanaka, Clarice
AU - Teixeira, Manoel Jacobsen
AU - Hosomi, Koichi
AU - Bouhassira, Didier
AU - Attal, Nadine
AU - de Andrade, Daniel Ciampi
N1 - Copyright © 2025 The Authors. Published by Elsevier Ltd.. All rights reserved.
PY - 2025/6
Y1 - 2025/6
N2 - BackgroundDespite affecting 2–4% of the population worldwide, fibromyalgia often remains refractory to treatment. Here we report the first international randomised double-blind, sham-controlled trial developed to assess the efficacy of repetitive transcranial magnetic stimulation (rTMS) as an add-on therapy for fibromyalgia.MethodsWomen aged ≥18 yr with fibromyalgia refractory to best available treatment were enrolled in Brazil, France, and Japan, and randomised to 10 Hz motor cortex (M1) rTMS, 3000 pulses day−1, or sham stimulation. This included 10 induction sessions over 2 weeks, followed by weekly maintenance (6 weeks), and fortnightly extended maintenance (8 weeks). Primary outcome was ≥50% pain reduction at week 8 compared with baseline. Secondary outcomes included pain interference, mood, global impression of change, and Fibromyalgia Impact Questionnaire (FIQ) scores at weeks 8 and 16.ResultsWe randomised 101 women (mean age 48 [range 25-83] yr) into active (n=52) or sham (n=49) arms. Bayesian analysis revealed a 99.4% probability of ≥50% pain reduction at week 8 in the active group vs sham (odds ratio [OR] 3.04; 95% credible interval [95% CrI] 1.26–8.06), with a number needed to treat of 4.54. Frequentist analysis confirmed that relative pain reduction was higher in the active than in the sham group (40.4% vs 18.4%, P=0.028). At week 16, this probability reduced to 34.2% (OR 0.815; 95% CrI 0.313–2.1), but the likelihood of FIQ score reduction was 79.1%. The intervention appeared safe.ConclusionsAdd-on M1-repetitive transcranial magnetic stimulation reduced pain intensity up to 8 weeks in women with fibromyalgia. Although analgesic effects waned, functional improvements remained during extended maintenance at week 16.
AB - BackgroundDespite affecting 2–4% of the population worldwide, fibromyalgia often remains refractory to treatment. Here we report the first international randomised double-blind, sham-controlled trial developed to assess the efficacy of repetitive transcranial magnetic stimulation (rTMS) as an add-on therapy for fibromyalgia.MethodsWomen aged ≥18 yr with fibromyalgia refractory to best available treatment were enrolled in Brazil, France, and Japan, and randomised to 10 Hz motor cortex (M1) rTMS, 3000 pulses day−1, or sham stimulation. This included 10 induction sessions over 2 weeks, followed by weekly maintenance (6 weeks), and fortnightly extended maintenance (8 weeks). Primary outcome was ≥50% pain reduction at week 8 compared with baseline. Secondary outcomes included pain interference, mood, global impression of change, and Fibromyalgia Impact Questionnaire (FIQ) scores at weeks 8 and 16.ResultsWe randomised 101 women (mean age 48 [range 25-83] yr) into active (n=52) or sham (n=49) arms. Bayesian analysis revealed a 99.4% probability of ≥50% pain reduction at week 8 in the active group vs sham (odds ratio [OR] 3.04; 95% credible interval [95% CrI] 1.26–8.06), with a number needed to treat of 4.54. Frequentist analysis confirmed that relative pain reduction was higher in the active than in the sham group (40.4% vs 18.4%, P=0.028). At week 16, this probability reduced to 34.2% (OR 0.815; 95% CrI 0.313–2.1), but the likelihood of FIQ score reduction was 79.1%. The intervention appeared safe.ConclusionsAdd-on M1-repetitive transcranial magnetic stimulation reduced pain intensity up to 8 weeks in women with fibromyalgia. Although analgesic effects waned, functional improvements remained during extended maintenance at week 16.
KW - fibromyalgia
KW - transcranial magnetic stimulation
KW - chronic pain
KW - neuromodulation
KW - clinical trial
UR - http://www.scopus.com/inward/record.url?scp=86000730951&partnerID=8YFLogxK
U2 - 10.1016/j.bja.2024.12.045
DO - 10.1016/j.bja.2024.12.045
M3 - Journal article
C2 - 40087077
SN - 0007-0912
VL - 134
SP - 1756
EP - 1764
JO - British Journal of Anaesthesia
JF - British Journal of Anaesthesia
IS - 6
ER -