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1.
J Peripher Nerv Syst ; 29(3): 329-338, 2024 09.
Artigo em Inglês | MEDLINE | ID: mdl-39164223

RESUMO

AIMS: To develop a standardised, automated protocol for detecting protein gene product 9.5 (PGP9.5) positive intra-epidermal nerve fibres (IENFs) in skin biopsies, transitioning from the established manual technique to an automated platform. This automated method, although currently intended for research applications, may improve the accessibility of this diagnostic test for small fibre neuropathy in clinical settings. METHODS: Skin biopsies (n = 274) from 100 participants (fibromyalgia syndrome n = 62; idiopathic small fibre neuropathy: n = 16; healthy volunteers: n = 22) were processed using an automated immunohistochemistry platform. IENF quantification was performed by blinded examiners, with reliability assessed via a two-way mixed-effects model to evaluate inter- and intra-observer variability. RESULTS: The automated staining system reproduced intra-epidermal nerve fibre density (IENFD) counts consistent with free-floating sections (mean ± standard deviation: free-floating: 5.6 ± 3.4 fibres/mm; automated: 5.9 ± 3.2 fibres/mm). A median difference of 0.3 with a lower bound 95% Confidence Interval (CI) at -0.00005 established non-inferiority against a margin of -0.4 (p = .08). Specifically, the inter-class correlation coefficient (class denotes consistency in measured observations) was 99% (95% CI: 0.9-1), indicating excellent agreement between free-floating and automated methods. The inter- and intra-class coefficient between examiners were both 99% (95% CI: 0.9-0.1) for IENFD, demonstrating high reliability using sections stained using the automated method. INTERPRETATION: Automated immunohistochemistry provides high-throughput reliable and reproducible intra-epidermal nerve fibre quantification. This method, although currently proof-of-concept, for research use only, may be more widely deployed in histopathology laboratories to increase the adoption of IENFD assessment for the diagnosis of peripheral neuropathies.


Assuntos
Imuno-Histoquímica , Fibras Nervosas , Estudo de Prova de Conceito , Pele , Neuropatia de Pequenas Fibras , Humanos , Fibras Nervosas/patologia , Feminino , Masculino , Adulto , Pessoa de Meia-Idade , Pele/inervação , Pele/patologia , Neuropatia de Pequenas Fibras/diagnóstico , Neuropatia de Pequenas Fibras/patologia , Biópsia , Epiderme/inervação , Epiderme/patologia , Idoso , Ubiquitina Tiolesterase/metabolismo , Ubiquitina Tiolesterase/análise , Reprodutibilidade dos Testes
2.
ASN Neuro ; 2(4): e00042, 2010 Sep 09.
Artigo em Inglês | MEDLINE | ID: mdl-20842208

RESUMO

It is becoming apparent that a number of pathogenic mechanisms contribute to diabetic neuropathy, so that therapeutic interventions that target one particular mechanism may have limited success. A recently published preclinical study has adopted an alternative approach by using a novel small molecule to induce heat-shock protein 70. This confers upon neurons, and perhaps other cells of the nervous system, the ability to better tolerate the diverse stresses associated with diabetes rather than intervening in their production.


Assuntos
Diabetes Mellitus Experimental/metabolismo , Neuropatias Diabéticas/tratamento farmacológico , Neuropatias Diabéticas/metabolismo , Proteínas de Choque Térmico HSP90/antagonistas & inibidores , Medição da Dor , Células Receptoras Sensoriais/metabolismo , Animais , Humanos
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