Association of low-dose naltrexone and transcranial direct current stimulation in fibromyalgia: a randomized, double-blinded, parallel clinical trial

被引:18
作者
de Paula, Tania Maria Hendges [1 ]
Castro, Mariane Schaffer [1 ,2 ]
Medeiros, Liciane Fernandes [1 ,3 ]
Paludo, Rodrigo Hernandes [1 ,2 ]
Couto, Fabricia Fritz [1 ,2 ]
da Costa, Taina Ramires [1 ,2 ]
Fortes, Juliana Pereira [1 ,2 ]
Salbego, Maiara de Oliveira [1 ,2 ]
Behnck, Gabriel Schardosim [1 ,2 ]
de Moura, Thielly Amaral Mesquita [1 ,2 ]
Tarouco, Mariana Lenz [1 ,2 ]
Caumo, Wolnei [3 ]
de Souza, Andressa [1 ,3 ,4 ]
机构
[1] Univ La Salle, Programa Posgrad Saude & Desenvolvimento Humano, Canoas, RS, Brazil
[2] Univ La Salle, Canoas, RS, Brazil
[3] Univ Fed Rio Grande do Sul, Programa Posgrad Ciencias Biol Farmacol & Terapeut, Porto Alegre, RS, Brazil
[4] Univ Fed Rio Grande do Sul, Programa Posgrad Ciencias Med Med, Porto Alegre, RS, Brazil
来源
BRAZILIAN JOURNAL OF ANESTHESIOLOGY | 2023年 / 73卷 / 04期
关键词
Fibromyalgia; Naltrexone; Pain; Transcranial direct current stimulation; PAIN; DISEASE; BDNF;
D O I
10.1016/j.bjane.2022.08.003
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Introduction: Fibromyalgia is a complex, generalized, and diffuse chronic musculoskeletal pain. Pharmacological approaches are widely used to relieve pain and increase quality of life. Low-Dose Naltrexone (LDN) was shown to increase the nociceptive threshold in patients with fibromy-algia. 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: sociodemo-graphic, 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.& COPY; 2022 Sociedade Brasileira de Anestesiologia. Published by Elsevier Editora Ltda. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/ 4.0/).
引用
收藏
页码:409 / 417
页数:9
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