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Mayo Test Catalog, (Sorted By Test Name) - Mayo Medical ...

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GANC<br />

80140<br />

GM1B<br />

83189<br />

Ganciclovir, Serum<br />

Clinical Information: Ganciclovir, an analog of acylcovir, demonstrates inhibitory action against<br />

some viruses including herpes virus, cytomegalovirus, and HIV. Therapeutic ranges have not been<br />

well-established for ganciclovir; current ranges are based on typical values seen during ganciclovir<br />

therapy and do not correlate well to toxicity or outcome. Monitoring of ganciclovir serum concentrations<br />

may be most useful in guiding therapy in patients with renal dysfunction. Myelosuppression is the major<br />

dose-limiting side effect of ganciclovir. Valcyte (valganciclovir) is an oral pro-drug of ganciclovir ester. It<br />

is immediately converted to ganciclovir once it enters the bloodstream. The oral dose is designed to<br />

deliver ganciclovir equivalent to intravenous ganciclovir at 5 mg/kg.<br />

Useful For: Monitoring patients on ganciclovir<br />

Interpretation: Serum concentrations of ganciclovir do not correlate well to toxicity or efficacy. Peak<br />

and trough levels provided are representative of typical serum concentrations seen during therapy, but<br />

individual values must be interpreted in conjunction with the clinical status of the individual patient and<br />

the specific characteristics of the infecting microorganism.<br />

Reference Values:<br />

Trough: 1.0-3.0 mcg/mL<br />

Peak: 3.0-12.5 mcg/mL<br />

Clinical References: 1. Perrottet N, Decosterd LA, Meylan P, et al: Valganciclovir in adult solid<br />

organ transplant recipients: paharmacokinetic and pharmacodynamic characteristics and clinical<br />

interpretation of plasma concentration measurements. Clin Pharmacokinet 2009;48(6):399-418 2. Uges D:<br />

Therapeutic and toxic drug concentrations, The International Association of Forensic Toxicologists. Dec<br />

2009. Retrieved 12/09; Available from URL: www.tiaft.org<br />

Ganglioside Antibody Panel, Serum<br />

Clinical Information: Peripheral neuropathies are a group of disorders that results from lesions on<br />

peripheral nerves. Patients with a peripheral neuropathy can have symptoms of weakness, sensory loss,<br />

and/or autonomic dysfunction. The causes of acquired peripheral neuropathies are varied, and include<br />

vitamin deficiencies, metabolic abnormalities, infections, malignancies (paraneoplastic disorders), and<br />

autoimmune diseases. A subset of the autoimmune-mediated peripheral neuropathies is associated with<br />

the presence of circulating autoantibodies that bind to specific gangliosides. Gangliosides are<br />

glycosphingolipids that contain sialic acid residues. Although present in the plasma membranes of many<br />

cell types, gangliosides are particularly abundant in neural tissue. Guillain-Barre syndrome is one class of<br />

autoimmune peripheral neuropathies, and comprises a spectrum of disorders including acute inflammatory<br />

demyelinating polyradiculoneuropathy, acute motor axonal neuropathy, and acute motor and sensory<br />

axonal neuropathy. This class of autoimmune neuropathies is generally characterized by an acute onset.<br />

Although the diagnosis of these disorders is based significantly on clinical evaluation and<br />

electrophysiologic studies, assessment of ganglioside antibodies, particularly against GM1, asialo GM1,<br />

and GD1b, can provide useful information. It is thought that the Guillain-Barre syndrome disorders are<br />

triggered by an infection, which results in production of infection-associated lipooligosaccharide-specific<br />

antibodies. These antibodies subsequently bind to endogenous gangliosides, due to molecular mimicry,<br />

which leads to immune-mediate damage to the peripheral nerves, ultimately resulting in the clinical<br />

symptoms associated with the disorders.(1)<br />

Useful For: Supporting diagnosis of neurological diseases-primarily motor neuron disease and motor<br />

neuropathies<br />

Interpretation: High titers (>1:2,000) have been found only in patients with multifocal motor<br />

neuropathy and not with motor neuron disease. About 30% to 50% of patients with these clinical<br />

syndromes or the pure motor variant of chronic inflammatory demyelinating polyneuropathy have<br />

increased antibody titers. Increased antibody titers, therefore, appear to be a specific but not sensitive<br />

marker of those related disorders. For IgG and IgM antibodies directed against monosialo GM1 and<br />

Current as of January 3, 2013 2:22 pm CST 800-533-1710 or 507-266-5700 or <strong>Mayo</strong><strong>Medical</strong>Laboratories.com Page 804

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