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

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CLYWB<br />

83857<br />

spirochete. Lyme disease exhibits a variety of symptoms that may be confused with immune and<br />

inflammatory disorders. Inflammation around the tick bite causes skin lesions. Erythema chronicum<br />

migrans (ECM), a unique expanding skin lesion with central clearing that results in a ring-like<br />

appearance, is the first stage of the disease. Any of the following clinical manifestations may be present in<br />

patients with Lyme disease: arthritis, neurological or cardiac disease, or skin lesions. Neurologic and<br />

cardiac symptoms may appear with stage 2 and arthritic symptoms with stage 3 of Lyme disease. In some<br />

cases, a definitive distinction between stages is not always seen. Further, secondary symptoms may occur<br />

even though the patient does not recall having a tick bite or a rash. Early antibiotic treatment of Lyme<br />

disease can resolve clinical symptoms and prevent progression of the disease to later stages. However, the<br />

early administration of antibiotics may suppress the antibody response to levels that are undetectable by<br />

current laboratory tests. The Second National Conference on the Serologic Diagnosis of Lyme Disease<br />

(1994) recommended that laboratories use a 2-test approach for the serologic diagnosis of Lyme disease.<br />

Accordingly, specimens are first tested by the more sensitive EIA. A Western blot (WB) assay is used to<br />

supplement positive or equivocal Lyme (EIA). WB identifies the specific proteins to which the patient's<br />

antibodies bind. Although there are no proteins that specifically diagnose Borrelia burgdorferi infection,<br />

the number of proteins recognized in the WB assay is correlated with diagnosis. Culture or PCR of skin<br />

biopsies obtained near the margins of ECM are frequently positive. In late (chronic) stages of the disease,<br />

serology is often positive and the diagnostic method of choice. PCR testing also may be of use in these<br />

late stages if performed on synovial fluid or cerebrospinal fluid (CSF).<br />

Useful For: Diagnosing Lyme disease IgM assay is useful for confirming stage 1 (acute) Lyme<br />

disease IgG assay is useful for confirming stage 2 and stage 3 Lyme disease<br />

Interpretation: IgM IgM antibodies to Borrelia burgdorferi may be detectable within 1 to 2 weeks<br />

following the tick bite; they usually peak during the third to sixth week after disease onset, and then<br />

demonstrate a gradual decline over a period of months. IgM antibody may persist for months even<br />

though antimicrobial agents are given. The IgM assay is more likely to be useful during early disease,<br />

and should only be tested during the first 4 to 6 weeks after disease onset. Negative specimens typically<br />

demonstrate antibodies to less than 2 of the 3 significant Borrelia burgdorferi proteins. Additional<br />

specimens should be submitted in 2 to 3 weeks if Borrelia burgdorferi exposure has not been ruled out.<br />

Individuals who have recently seroconverted due to infection with Borrelia burgdorferi may display<br />

incomplete banding patterns, but may develop increased reactivity (both in band intensity and number)<br />

when followed for a period of 4 to 6 months. IgG Serum IgG is detected as early as 2 weeks after onset<br />

of disease. Significant concentrations of antibody and Western blot banding patterns for Borrelia<br />

burgdorferi can be found years after onset. Normal specimens and false-positive EIA specimens<br />

generally have antibodies to 4 or fewer proteins. Except for early patients, antibodies from patients with<br />

Lyme disease generally bind to 5 or more proteins. For persons who have received recombinant OspA<br />

vaccine and who are not infected with Borrelia burgdorferi, an intense band representing antibody to the<br />

OspA protein (band 30) should be visible on the Western blot.<br />

Reference Values:<br />

IgG: negative<br />

IgM: negative<br />

Clinical References: 1. Dressler F, Whalen JA, Reinhardt BN, Steere AC: Western blotting in the<br />

serodiagnosis of Lyme disease. J Infect Dis 1993;167(2):392-400 2. Brown SL, Hansen SL, Langone JJ:<br />

Role of serology in the diagnosis of Lyme disease. JAMA 1999;282:62-66 3. Anonymous: Lyme<br />

disease-United States, 1995. MMWR Morb Mortal Wkly Rep 1996;June 14;45(23):481-484<br />

Lyme Disease Antibody, Western Blot, Spinal Fluid<br />

Clinical Information: Lyme disease is caused by the spirochete Borrelia burgdorferi. The<br />

spirochete is transmitted to humans through the bite of Ixodes species ticks. Endemic areas for Lyme<br />

disease in the United States (U.S.) correspond with the distribution of 2 tick species, Ixodes dammini<br />

(Northeastern and Upper Midwestern U.S.) and Ixodes pacificus (West Coast U.S.). In Europe, Ixodes<br />

ricinus transmits the spirochete. Lyme disease exhibits a variety of symptoms that may be confused with<br />

immune and inflammatory disorders. Any of the following clinical manifestations may be present in<br />

patients with Lyme disease: skin lesions or cardiac or neurological disease. In the first stage of disease,<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 1135

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