Leucine-Rich Glioma-Inactivated 1 versus Contactin-Associated Protein-like 2 Antibody Neuropathic Pain: Clinical and Biological Comparisons

被引:25
|
作者
Ramanathan, Sudarshini [1 ,2 ,3 ,4 ,5 ]
Tseng, Mandy [6 ]
Davies, Alexander J. [7 ]
Uy, Christopher E. [1 ,8 ]
Paneva, Sofija [1 ]
Mgbachi, Victor C. [1 ]
Michael, Sophia [1 ]
Varley, James A. [1 ]
Binks, Sophie [1 ]
Themistocleous, Andreas C. [6 ]
Fehmi, Janev [7 ]
Anziska, Yaacov [1 ]
Soni, Anushka [9 ]
Hofer, Monika [10 ]
Waters, Patrick [1 ]
Brilot, Fabienne [2 ,3 ,4 ,11 ]
Dale, Russell C. [2 ,3 ,4 ,12 ]
Dawes, John [6 ]
Rinaldi, Simon [7 ]
Bennett, David L. [6 ]
Irani, Sarosh R. [1 ]
机构
[1] Univ Oxford, John Radcliffe Hosp, Nuffield Dept Clin Neurosci, Oxford Autoimmune Neurol Grp, Level 3 West Wing, Oxford OX3 9DU, England
[2] Childrens Hosp Westmead, Kids Neurosci Ctr, Neuroimmunol & Brain Autoimmun Grp, Westmead, NSW, Australia
[3] Univ Sydney, Brain & Mind Ctr, Sydney, NSW, Australia
[4] Univ Sydney, Sydney Med Sch, Fac Med & Hlth, Sydney, NSW, Australia
[5] Concord Hosp, Dept Neurol, Sydney, NSW, Australia
[6] Univ Oxford, John Radcliffe Hosp, Nuffield Dept Clin Neurosci, Neural Injury Grp, Oxford, England
[7] Univ Oxford, John Radcliffe Hosp, Nuffield Dept Clin Neurosci, Inflammatory Neuropathy Grp, Oxford, England
[8] Univ British Columbia, Dept Med, Div Neurol, Vancouver, BC, Canada
[9] Univ Oxford, John Radcliffe Hosp, Wellcome Ctr Integrat Neuroimaging, Nuffield Dept Clin Neurosci, Oxford, England
[10] Natl Hlth Serv Fdn Trust, Oxford Univ Hosp, Dept Neuropathol, Oxford, England
[11] Univ Sydney, Sch Med Sci, Sydney, NSW, Australia
[12] Childrens Hosp Westmead, Dept Paediat Neurol, Sydney, NSW, Australia
基金
澳大利亚国家健康与医学研究理事会; 英国医学研究理事会; 英国惠康基金;
关键词
D O I
10.1002/ana.26189
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Pain is a under-recognized association of leucine-rich glioma-inactivated 1 (LGI1) and contactin-associated protein-like 2 (CASPR2) antibodies. Of 147 patients with these autoantibodies, pain was experienced by 17 of 33 (52%) with CASPR2- versus 20 of 108 (19%) with LGI1 antibodies (p = 0.0005), and identified as neuropathic in 89% versus 58% of these, respectively. Typically, in both cohorts, normal nerve conduction studies and reduced intraepidermal nerve fiber densities were observed in the sampled patient subsets. In LGI1 antibody patients, pain responded to immunotherapy (p = 0.008), often rapidly, with greater residual patient-rated impairment observed in CASPR2 antibody patients (p = 0.019). Serum CASPR2 antibodies, but not LGI1 antibodies, bound in vitro to unmyelinated human sensory neurons and rodent dorsal root ganglia, suggesting pathophysiological differences that may underlie our clinical observations. ANN NEUROL 2021
引用
收藏
页码:683 / 690
页数:8
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