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Comparison of the serum brain-derived neurotrophic factor (BDNF) between fibromyalgia and nociceptive pain groups; and effect of duloxetine on the BDNF level.
Bidari, Ali; Ghavidel-Parsa, Banafsheh; Gharibpoor, Faeze.
Afiliação
  • Bidari A; Department of Rheumatology, Iran University of Medical Sciences, Tehran, Iran.
  • Ghavidel-Parsa B; Rheumatology Research Center, Razi Hospital, School of Medicine, Guilan University of Medical Science, Rasht, Iran.
  • Gharibpoor F; Student Research Committee, Deputy of Research and Technology, Faculty of Medicine, Guilan University of Medical Sciences, Namjoo St, Rasht, Guilan, 41446-66949, Iran. faezegharibpoor@gmail.com.
BMC Musculoskelet Disord ; 23(1): 411, 2022 May 02.
Article em En | MEDLINE | ID: mdl-35501732
ABSTRACT

BACKGROUND:

The primary objective was to compare the serum brain-derived neurotrophic factor (BDNF) level in the patients with two types of pain fibromyalgia (FM) and non-FM nociceptive pain (non-FM NP). The secondary objective was to investigate the effect of duloxetine on serum BDNF in FM patients and assess the direction of BDNF changes' relation to clinical parameters' alterations.

METHODS:

This is a study on 73 patients (50 FM and 23 non-FM chronic non-inflammatory pain patients). Serum BDNF was first compared between both groups. Patients with FM, then prospectively, underwent standardized FM treatment with duloxetine maximized to 60 mg/day. The Revised Fibromyalgia Impact Questionnaire (FIQR), Short-Form Health Survey (SF-12), pain visualized analog scale (pain VAS), Beck Depression Inventory-II (BDI-II), polysymptomatic distress scale (PSD) and serum BDNF were measured and compared at baseline and 4 weeks after treatment in FM group.

RESULTS:

The mean of adjusted BDNF level in the FM group had no significant difference than the non-FM NP group ((5293.5 ± 2676.3 vs. 6136.3 ± 4037.6; P value = 0.77). Using linear mixed model, we showed that duloxetine reduced BDNF level significantly in FM patients, even after adjusting for depression, pain and severity of the disease (P < 0.01). The FIQR, BDI-II, PSD, and pain VAS improved significantly after duloxetine treatment.

CONCLUSIONS:

Non-significant BDNF level difference between FM and non-FM nociceptive pain suggested that peripheral BDNF is not a pathophysiological feature of FM. The decreased BDNF level parallel with improvement of PSD/pain scores after duloxetine treatment indicates BDNF alteration in the pain modulation process, regardless of cause and effect.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fibromialgia / Fator Neurotrófico Derivado do Encéfalo / Dor Nociceptiva / Cloridrato de Duloxetina Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fibromialgia / Fator Neurotrófico Derivado do Encéfalo / Dor Nociceptiva / Cloridrato de Duloxetina Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article