Background: In this clinical and psychophysical study, we aimed to verify whether patients with fibromyalgia with and without small-fibre pathology and patients with pure small-fibre neuropathy share common sensory phenotypes. Methods: Using an algorithm based on quantitative sensory testing variables, we grouped 64 consecutive patients with fibromyalgia (20 with small-fibre pathology, 44 without) and 30 patients with pure small-fibre neuropathy into different sensory phenotypes: sensory loss, thermal hyperalgesia, mechanical hyperalgesia and healthy phenotypes. Results: We found that the frequency of the different sensory phenotypes differed markedly between patients with fibromyalgia and patients with small-fibre neuropathy. In patients with fibromyalgia, with and without small-fibre pathology, healthy and hyperalgesia phenotypes (both thermal and mechanical) were similarly represented, whilst sensory loss and mechanical hyperalgesia phenotypes were the most frequent phenotypes in patients with small-fibre neuropathy. Conclusions: Our findings indicate that small-fibre damage is associated with distinct sensory phenotypes in patients with fibromyalgia and in patients with small-fibre neuropathy. The lack of phenotype differences between patients with fibromyalgia with and without small-fibre pathology and the relatively high frequency of the healthy phenotype in these patients highlight a complex relationship between small-fibre pathology and pain in patients with fibromyalgia.

Small‐fibre damage is associated with distinct sensory phenotypes in patients with fibromyalgia and small‐fibre neuropathy / Leone, CATERINA MARIA; Galosi, Eleonora; Esposito, Nicoletta; Falco, Pietro; Fasolino, Alessandra; DI PIETRO, Giuseppe; DI STEFANO, Giulia; Camerota, Filippo; Vollert, Jan; Truini, Andrea. - In: EUROPEAN JOURNAL OF PAIN. - ISSN 1090-3801. - (2023). [10.1002/ejp.2049]

Small‐fibre damage is associated with distinct sensory phenotypes in patients with fibromyalgia and small‐fibre neuropathy

Caterina Leone;Eleonora Galosi;Nicoletta Esposito;Pietro Falco;Alessandra Fasolino;Giuseppe Di Pietro;Giulia Di Stefano;Andrea Truini
2023

Abstract

Background: In this clinical and psychophysical study, we aimed to verify whether patients with fibromyalgia with and without small-fibre pathology and patients with pure small-fibre neuropathy share common sensory phenotypes. Methods: Using an algorithm based on quantitative sensory testing variables, we grouped 64 consecutive patients with fibromyalgia (20 with small-fibre pathology, 44 without) and 30 patients with pure small-fibre neuropathy into different sensory phenotypes: sensory loss, thermal hyperalgesia, mechanical hyperalgesia and healthy phenotypes. Results: We found that the frequency of the different sensory phenotypes differed markedly between patients with fibromyalgia and patients with small-fibre neuropathy. In patients with fibromyalgia, with and without small-fibre pathology, healthy and hyperalgesia phenotypes (both thermal and mechanical) were similarly represented, whilst sensory loss and mechanical hyperalgesia phenotypes were the most frequent phenotypes in patients with small-fibre neuropathy. Conclusions: Our findings indicate that small-fibre damage is associated with distinct sensory phenotypes in patients with fibromyalgia and in patients with small-fibre neuropathy. The lack of phenotype differences between patients with fibromyalgia with and without small-fibre pathology and the relatively high frequency of the healthy phenotype in these patients highlight a complex relationship between small-fibre pathology and pain in patients with fibromyalgia.
2023
neuropathic pain
01 Pubblicazione su rivista::01a Articolo in rivista
Small‐fibre damage is associated with distinct sensory phenotypes in patients with fibromyalgia and small‐fibre neuropathy / Leone, CATERINA MARIA; Galosi, Eleonora; Esposito, Nicoletta; Falco, Pietro; Fasolino, Alessandra; DI PIETRO, Giuseppe; DI STEFANO, Giulia; Camerota, Filippo; Vollert, Jan; Truini, Andrea. - In: EUROPEAN JOURNAL OF PAIN. - ISSN 1090-3801. - (2023). [10.1002/ejp.2049]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1671088
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