Abraham Alon, Alabdali Majed, Alsulaiman Abdulla, Breiner Ari, Barnett Carolina, Katzberg Hans D, Lovblom Leif E, Perkins Bruce A, Bril Vera
Ellen and Martin Prosserman Centre for Neuromuscular Diseases, Division of Neurology, Department of Medicine, University Health Network, University of Toronto, Toronto, Canada.
Department of Neurology, King Fahad Hospital of the University, University of Dammam, Dammam, Saudi Arabia.
PLoS One. 2016 Nov 8;11(11):e0165731. doi: 10.1371/journal.pone.0165731. eCollection 2016.
Small fiber neuropathy might be a part of typical mixed small and large fiber neuropathy, or a distinct entity, affecting exclusively small nerve fibers.
Explore the utility of small nerve fiber testing in patients with clinical presentation suggesting small fiber neuropathy, with and without evidence for concomitant large fiber neuropathy.
Patients attending the neuromuscular clinic from 2012 to 2015 with a clinical presentation suggesting small nerve fiber impairment, who had Laser Doppler flare imaging (LDIFlare) and quantitative thermal testing (QTT) were evaluated for this study. Patients with clinical or electrophysiological evidence for concomitant large fiber neuropathy were not excluded.
The sensitivities of LDIFlare, cooling and heat threshold testing were 64%, 36%, and 0% respectively for clinically highly suggestive small fiber neuropathy, 64%, 56%, and 19% respectively for mixed fiber neuropathy, and 86%, 79%, and 29% respectively for diabetic mixed fiber neuropathy.
LDIFlare and cooling thresholds testing are non-invasive small nerve fiber testing modalities, with moderate performance in patients with small and mixed fiber neuropathy, and excellent performance in diabetic mixed fiber neuropathy.
小纤维神经病变可能是典型的混合性小纤维和大纤维神经病变的一部分,或者是一种仅影响小神经纤维的独特病症。
探讨小神经纤维检测在临床表现提示小纤维神经病变、伴有或不伴有大纤维神经病变证据的患者中的应用价值。
对2012年至2015年在神经肌肉门诊就诊、临床表现提示小神经纤维受损且接受激光多普勒闪烁成像(LDIFlare)和定量热测试(QTT)的患者进行本研究评估。伴有大纤维神经病变临床或电生理证据的患者未被排除。
对于临床高度提示小纤维神经病变,LDIFlare、冷阈值测试和热阈值测试的敏感性分别为64%、36%和0%;对于混合性纤维神经病变,分别为64%、56%和19%;对于糖尿病性混合性纤维神经病变,分别为86%、79%和29%。
LDIFlare和冷阈值测试是非侵入性小神经纤维检测方法,在小纤维和混合性纤维神经病变患者中表现中等,在糖尿病性混合性纤维神经病变患者中表现优异。