Use este identificador para citar ou linkar para este item: http://hdl.handle.net/11690/3835
Autor(es): Paula, Tania Maria Hendges de
Castro, Mariane Schäffer
Medeiros, Liciane Fernandes
Paludo, Rodrigo Hernandes
Couto, Fabricia Fritz
Costa, Tainá Ramires da
Fortes, Juliana Pereira
Salbego, Maiara de Oliveira
Behnck, Gabriel Schardosim
Moura, Thielly Amaral Mesquita de
Tarouco, Mariana Lenz
Caumo, Wolnei
Souza, Andressa de
Título: Association of low-dose naltrexone and transcranial direct current stimulation in fibromyalgia: a randomized, double-blinded, parallel clinical trial
Palavras-chave: Fibromyalgia;Naltrexone;Pain;Transcranial direct current stimulation
Data do documento: 2022
Editor: BRAZILIAN JOURNAL OF ANESTHESIOLOGY
Citação: CASTRO, M. S. et al. Association of low-dose naltrexone and transcranial direct current stimulation in fibromyalgia: a randomized, double-blinded, parallel clinical trial. BRAZILIAN JOURNAL OF ANESTHESIOLOGY, p. xx, 2022. Disponível em: https://www.sciencedirect.com/science/article/pii/S010400142200104X?via%3Dihub Acesso em: 22 fev. 2024.
Resumo: Introduction: Fibromyalgia is a complex, generalized, and diffuse chronic musculoskeletal pain. Pharmacological approaches are widely used to relieve pain and increase quality of life. LowDose Naltrexone (LDN) was shown to increase the nociceptive threshold in patients with fibromyalgia. Transcranial Direct Current Stimulation (tDCS) is effective for pain management. Objective: The purpose of this study was to evaluate the analgesic and neuromodulatory effects of a combination of LDN and tDCS in patients with fibromyalgia. Methods: This was a randomized, double-blinded, parallel, placebo/sham-controlled trial (NCT04502251; RBR-7HK8N) in which 86 women with fibromyalgia were included, and written informed consent was obtained from them. The patients were allocated into four groups: LDN + tDCS (n = 21), LDN + tDCS Sham (n = 22), placebo + tDCS (n = 22), and placebo+tDCS Sham (n = 21). The LDN or placebo (p.o.) intervention lasted 26 days; in the last five sessions, tDCS was applied (sham or active, 20 min, 2 mA). The following categories were assessed: sociodemographic, Visual Analog Pain Scale (VAS), Pain Catastrophizing Scale (PCS), State-Trait Anxiety Inventory (STAI), Fibromyalgia Impact Questionnaire (FIQ), Beck Depression Inventory (BDI-II), Profile of Chronic Pain Scale (PCP:S), Pain Pressure Threshold (PPT), and Conditioned Pain Modulation (CPM). Blood samples were collected to analyze BDNF serum levels. Results: At baseline, no significant difference was found regarding all measurements. VAS pain was significantly reduced in the LDN + tDCS (p = 0.010), LDN + tDCS Sham (p = 0.001), and placebo+tDCS Sham (p = 0.009) groups. In the PCP:S, the LDN+tDCS group showed reduced pain frequency and intensity (p = 0.001), effect of pain on activities (p = 0.014) and emotions (p = 0.008). Depressive symptoms reduced after all active interventions (p > 0.001). Conclusion: Combined LDN+tDCS has possible benefits in reducing pain frequency and intensity; however, a placebo effect was observed in pain using VAS, and further studies should be performed to analyze the possible association.
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