CIDP/autoimmune nodopathies with nephropathy: a case series study

Author:

Tang Yuwei1ORCID,Liu Jing1,Gao Feng1,Hao Hongjun1,Jia Zhirong1,Zhang Wei1,Shi Xin1,Liang Wei1,Yu Meng1ORCID,Lv He1,Tan Ying2,Li Zhiying2,Wang Yu2,Yuan Yun13,Meng Lingchao13,Wang Zhaoxia13ORCID

Affiliation:

1. Department of Neurology Peking University First Hospital 8 Xishiku Street, Xicheng District Beijing 100034 China

2. Department of Nephrology Peking University First Hospital 8 Xishiku Street, Xicheng District Beijing 100034 China

3. Beijing Key Laboratory of Neurovascular Disease Discovery Beijing 100034 China

Abstract

AbstractObjectiveThe co‐morbidity of chronic inflammatory demyelinating polyradiculoneuropathy (CIDP)/autoimmune nodopathies with nephropathy has been gradually known in recent years. This study was intended to explore the clinical, serological and neuropathological features of seven patients with CIDP/autoimmune nodopathies and nephropathy.MethodsAmong 83 CIDP patients, seven were identified with nephropathy. Their clinical, electrophysiological and laboratory examination data were collected. The nodal/paranodal antibodies were tested. The sural biopsies were performed in all the patients, and renal biopsies were operated in 6 patients.ResultsSix patients had chronic onsets and one had an acute onset. Four patients exhibited peripheral neuropathy preceding nephropathy while two showed concurrent onset of neuropathy and nephropathy, and one started with nephropathy. All the patients showed demyelination in electrophysiological examination. Nerve biopsies showed mild to moderate mixed neuropathies including demyelinating and axonal changes in all patients. Renal biopsies showed membranous nephropathy in all 6 patients. Immunotherapy was effective in all patients, with two patients showing good response to corticosteroid treatment alone. Four of the patients were positive to anti‐CNTN1 antibody. Compared with anti‐CNTN1 antibody‐negative patients, antibody‐positive patients had a higher proportion of ataxia (3/4 vs. 1/3), autonomic dysfunction (3/4 vs. 1/3), less frequent antecedent infections (1/4 vs. 2/3), higher cerebrospinal fluid proteins (3.2 g/L vs. 1.69 g/L), more frequent conduction block on electrophysiological examination (3/4 vs. 1/3), higher myelinated nerve fiber density, and positive CNTN1 expression in the glomeruli of kidney tissues.ConclusionAnti‐CNTN1 antibody was the most frequent antibody in this group of patients with CIDP/autoimmune nodopathies and nephropathy. Our study suggested that there might be some clinical and pathological differences between the antibody positive and negative patients.

Funder

Natural Science Foundation of Beijing Municipality

Publisher

Wiley

Subject

Neurology (clinical),General Neuroscience

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