A diagnostic score for anti-myelin-associated-glycoprotein neuropathy or chronic inflammatory demyelinating polyradiculoneuropathy in patients with anti-myelin- associated-glycoprotein antibody

被引:9
作者
Doneddu, Pietro E. [1 ]
Ruiz, Marta [1 ]
Bianchi, Elisa [2 ]
Liberatore, Giuseppe [1 ]
Manganelli, Fiore [3 ]
Cocito, Dario [4 ]
Cosentino, Giuseppe [5 ]
Benedetti, Luana [6 ,7 ]
Marfia, Girola A. [8 ]
Filosto, Massimiliano [9 ]
Briani, Chiara [10 ]
Giannotta, Claudia [1 ]
Nobile-Orazio, Eduardo [1 ,11 ]
机构
[1] IRCCS Humanitas Res Hosp, Neuromuscular & Neuroimmunol Serv, Milan, Italy
[2] IRCCS Ist Mario Negri, Lab Malattie Neurol, Milan, Italy
[3] Univ Naples Federico II, Dept Neurosci Reprod Sci & Odontostomatol, Naples, Italy
[4] Ist Clin Sci Maugeri, Presidio Sanitario Major, Turin, Italy
[5] IRCCS Fdn C Mondino Natl Neurol Inst, Pavia, Italy
[6] Univ Genoa, Dept Neurosci Rehabil Ophthalmol Genet Maternal &, Genoa, Italy
[7] IRCCS AOU San Martino IST, Genoa, Italy
[8] Tor Vergata Univ Rome, Dept Syst Med, Dysimmune Neuropathies Unit, Rome, Italy
[9] Univ Brescia, NeMO Brescia Clin Ctr Neuromuscular Dis, Dept Clin & Expt Sci, Brescia, Italy
[10] Univ Padua, Dept Neurosci, Neurol Unit, Padua, Italy
[11] Milan Univ, Dept Med Biotechnol & Translat Med, Milan, Italy
关键词
chronic inflammatory demyelinating polyradiculoneuropathy; antibody; diagnostic criteria; CIDP; MAG; neuropathy; TERMINAL LATENCY INDEX; PLACEBO-CONTROLLED TRIAL; NERVE SOCIETY GUIDELINE; INTRAVENOUS IMMUNOGLOBULIN; MAG ANTIBODIES; POLYNEUROPATHY; RITUXIMAB;
D O I
10.1111/ene.15296
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and purpose: A diagnostic score was developed to discriminate anti-myelinassociated-glycoprotein (MAG) neuropathy from chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) and applied it to patients with atypical anti-MAG neuropathy. Methods: The clinical and electrophysiological features of patients with a diagnosis of typical anti-MAG neuropathy were compared to those of patients with a diagnosis of CIDP. The association of each feature with the diagnosis was assessed in the two groups. Features showing a significant association with the diagnosis were included in a multivariable logistic regression model and adjusted odds ratios were estimated for each feature. A score ranging from 1 to 3 was applied to each feature based on the magnitude of the estimated odds ratios. The score was then applied to patients with a clinical diagnosis of CIDP who also had high anti-MAG antibody titers (CIDP- MAG). Results: Thirty-one anti-MAG neuropathy patients, 45 typical CIDP patients and 16 CIDP-MAG patients were included. Scores in anti-MAG antibody patients ranged from 1 to 5 and in CIDP patients from -7 to -1. Using the score, 4/16 CIDP-MAG patients were diagnosed to have anti-MAG neuropathy and 12/16 patients to have CIDP. Response to intravenous immunoglobulin in the CIDP-MAG patients classified as CIDP was similar to that of definite CIDP patients and higher than that of anti-MAG neuropathy patients. Conclusions: Our score allowed an accurate discrimination to be made, amongst patients with anti-MAG antibodies, of those affected by CIDP and the patients with anti-MAG neuropathy. This score may help proper treatment to be chosen for patients with anti-MAG antibodies with a CIDP-like presentation.
引用
收藏
页码:501 / 510
页数:10
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