Motor and Sensory Neuropathy Profile II includes 456, 464, 500, 501, 502, 506

Specimen need not be refrigerated or frozen. Collect 2-3 ml of blood in a red top or serum
separator tube. If possible, separate serum from clot and place into white tube provided with
Immco Diagnostics’ collection kits. If separation facilities are not available, the blood can be sent
in the tube used for collection.

Sample is stable at ambient temperature during shipment. If sample is stored prior to shipment, it
is stable refrigerated (2-8°C) up to five days and frozen (-20°C or lower) up to one year.

Cause for rejection: Specimens other than serum. Grossly hemolyzed, lipemic or icteric samples.
Clinical Relevance: GM1, GD1b, GQ1b, Asialo GM1, GD1a Antibodies against glycolipids (GM1,
GD1a, GD1b, GQ1b, Asialo GM1 and sulfatides) are present in Guillain- Barre syndrome(GBS),
IgM paraproteinemic neuropathy, and chronic demyelinating polyneuropathy. Antibodies to one or
more glycolipids are present in 60-70% of patients with GBS. The titers of antiglycolipid
antibodies are higher in acute phase and decrease with clinical improvement. Antibodies to GM1
and/or GD1b are frequently found in acute phase GBS. The two antibodies together occur in 20%
of these cases, anti-GM1 without GD1b antibodies in about 10% and anti-GD1b without GM1
antibodies in about 10% of GBS patients.Antibodies to GQ1b of IgG isotype are present in 95%
of patients with Miller Fisher syndrome (MFS). The titers of these antibodies fluctuate with disease
activity. IgM paraproteinemia is often associated with peripheral neuropathies. These antibodies
are present in one half of patients with specificity for SGPG, GD1b and other gangliosides. Anti-
GM1 IgM are usually associated with motor dominant or sensorimotor neuropathies. These
antibodies are also elevated in multifocal neuropathies such as GBS, CIDP and other
immunological diseases.