We prospectively evaluated patients with idiopathic polyneuropathy (PN
) and motor neuron disease (MND) with commercial antibody (Ab) panels.
Patients with sensorimotor PN received a ''sensorimotor neuropathy pr
ofile'' [3-sulfated glucuronyl paragloboside (SGPG)/myelin-associated
glycoprotein (MAG), GM1, asialo-GM1, GD1b, Hu, sulfatide]. Motor neuro
pathy or MND patients underwent a ''motor neuropathy profile'' (SGPG/M
AG, GM1, asialo-GM1). Seven of 78 patients (9.0%) with sensorimotor PN
and 3 of 44 patients (6.8%) with MND had abnormal panels. None of 60
patients with axonal sensory or sensorimotor PN had antisulfatide Ab.
Seven of 13 patients (54%) with multifocal motor neuropathy had abnorm
al panels, with 6 seropositive to GM1. We found abnormal Ab panels in
fewer than 10% of patients with idiopathic sensorimotor PN and MND. Mo
reover, abnormal Ab tests often did not relate to the clinical context
. Our data do not support the use of commercial Ab panels in the evalu
ation of patients with idiopathic PN or MND. (C) 1997 John Wiley & Son
s, Inc.