Neurophysiologic assessment of small fibre damage in chemotherapy-induced peripheral neuropathy

被引:5
|
作者
Isak, Baris [1 ,2 ]
Tankisi, Hatice [2 ]
Pugdahl, Kirsten [2 ]
Ventzel, Lise [3 ,4 ]
Finnerup, Nanna Brix [3 ]
Fuglsang-Frederiksen, Anders [2 ]
机构
[1] Marmara Univ Hosp, Dept Neurol, Fevzi Cakmak Sok,Muhsin Yazicioglu Cad 10, Istanbul, Turkey
[2] Aarhus Univ Hosp, Dept Clin Neurophysiol, Aarhus, Denmark
[3] Aarhus Univ, Danish Pain Res Ctr, Dept Clin Med, Aarhus, Denmark
[4] Aarhus Univ Hosp, Dept Oncol, Aarhus, Denmark
关键词
Chemotherapy; Small fibre; Laser; Quantitative sensory testing; Cutaneous silent period; CUTANEOUS SILENT PERIOD; LASER EVOKED-POTENTIALS; SKIN TEMPERATURE; INFRARED-LASER; HAIRY SKIN; PAIN; STIMULATION; AFFERENTS; ABNORMALITIES; SENSITIZATION;
D O I
10.1016/j.clinph.2021.02.406
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: In patients with chemotherapy-induced peripheral neuropathy (CIPN), demonstration of small fibre (SF) damage is important to understand chronic late effects. Methods: Thirty patients having complaints compatible with possible CIPN following treatment with oxaliplatin or docetaxel were compared with 27 healthy subjects. All subjects were evaluated with quantitative sensory testing (QST) assessing SF function and laser evoked potentials (LEP). In addition, SF-damage was assessed using cutaneous silent periods evoked with electrical (El-CSP) and laser (Ls-CSP) stimuli. Results: For LEP, N2P2 amplitudes were significantly smaller in patients than controls in both upper (P = 0.007) and lower extremities (P = 0.002), and the N1 amplitude in upper extremities of patients were significantly smaller than in controls (P = 0.001). SF-QST, LEP, Ls-CSP, and El-CSP were abnormal in 10 (33.3%), 16 (53.3%), 19 (63.3%), and 24 (80%) of CIPN patients, respectively. Conclusions: In patients with possible CIPN, El-CSP and Ls-CSP were more often abnormal than LEP and QST. This is probably because El-CSP and Ls-CSP inform mainly about peripheral nociceptive fibres, while LEP and QST inform about peripheral and central nociceptive pathways together. Significance: LEP and QST are established methods to detect SF-damage. El- and Ls-CSP might help clinicians in diagnosing SF-damage. (C) 2021 International Federation of Clinical Neurophysiology. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:1947 / 1956
页数:10
相关论文
共 50 条
  • [11] Chemotherapy-Induced Peripheral Neuropathy
    Fehrenbacher, Jill C.
    MOLECULAR AND CELL BIOLOGY OF PAIN, 2015, 131 : 471 - 508
  • [12] Chemotherapy-Induced Peripheral Neuropathy
    Desai, Nidhi
    Arora, Nivedita
    Gupta, Arjun
    JAMA INTERNAL MEDICINE, 2022, 182 (07) : 766 - 767
  • [13] Chemotherapy-induced peripheral neuropathy
    Quasthoff, S
    Hartung, HP
    JOURNAL OF NEUROLOGY, 2002, 249 (01) : 9 - 17
  • [14] Chemotherapy-induced Peripheral Neuropathy
    Bobylev, I.
    Elter, T.
    Schneider, C.
    Wunderlich, G.
    Zimmer, P.
    Streckmann, F.
    Fink, G. R.
    Lehmann, H. C.
    FORTSCHRITTE DER NEUROLOGIE PSYCHIATRIE, 2015, 83 (08) : 427 - 436
  • [15] Chemotherapy-induced peripheral neuropathy
    Malik, Bushra
    Stillman, Mark
    CURRENT PAIN AND HEADACHE REPORTS, 2008, 12 (03) : 165 - 174
  • [16] Chemotherapy-Induced Peripheral Neuropathy
    Jain, Ashish
    Hariprasad, M. G.
    Sharique, Mohammad
    Redhwan, Moqbel Ali Moqbel
    INDIAN JOURNAL OF PHARMACEUTICAL EDUCATION AND RESEARCH, 2023, 57 (02) : 342 - 353
  • [17] Chemotherapy-induced peripheral Neuropathy
    Giessen-Jung, Clemens
    von Baumgarten, Louisa
    DEUTSCHE MEDIZINISCHE WOCHENSCHRIFT, 2018, 143 (13) : 970 - 978
  • [18] Chemotherapy-induced peripheral neuropathy
    Bushra Malik
    Mark Stillman
    Current Neurology and Neuroscience Reports, 2008, 8 : 56 - 65
  • [19] Chemotherapy-Induced Peripheral Neuropathy
    Tzatha, Efstathia
    DeAngelis, Lisa M.
    ONCOLOGY-NEW YORK, 2016, 30 (03): : 240 - 244
  • [20] Chemotherapy-induced peripheral neuropathy: A prospective study using methods of small fibre function and structure.
    Venkitaraman, Ramachandran
    Sharma, Sanjeev
    Soomal, Rubin
    Scrase, Christopher D.
    Rayman, Gerry
    JOURNAL OF CLINICAL ONCOLOGY, 2015, 33 (15)