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Sorted By Test Name - Mayo Medical Laboratories

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LYWB<br />

9535<br />

> or = 1.3 Positive<br />

Control Antibody Index: < or = 1.0<br />

Albumin Ratio: 1.2), accompanied by a Control Antibody Index of less than 1.0 and an<br />

Albumin Ratio of less than 0.0078, is strong evidence for intrathecal synthesis of organism-specific<br />

antibody, and thus CNS B. burgdorferi infection. Elevation of either the control antibody index, the<br />

Albumin Ratio, or both may indicate leakage of antibody across the blood-brain barrier which may falsely<br />

elevate the Lyme Disease Antibody Index.<br />

<strong>Test</strong> Performed by: Focus Diagnostics, Inc.<br />

5785 Corporate Avenue<br />

Cypress, CA 90630-4750<br />

Lyme Disease Antibody, Western Blot, Serum<br />

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

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

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

upper Midwestern U.S.) and Ixodes pacificus (West Coast U.S.). In Europe, Ixodes ricinus transmits the<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 disease<br />

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 though<br />

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

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

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

submitted in 2 to 3 weeks if Borrelia burgdorferi exposure has not been ruled out. Individuals who have<br />

recently seroconverted due to infection with Borrelia burgdorferi may display incomplete banding<br />

patterns, but may develop increased reactivity (both in band intensity and number) when followed for a<br />

period of 4 to 6 months. IgG Serum IgG is detected as early as 2 weeks after onset of disease. Significant<br />

concentrations of antibody and Western blot banding patterns for Borrelia burgdorferi can be found years<br />

Current as of January 4, 2013 7:15 pm CST 800-533-1710 or 507-266-5700 or <strong>Mayo</strong><strong>Medical</strong><strong>Laboratories</strong>.com Page 1129

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