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ARTICLE

Serologic Evidence of Previous Campylobacter jejuni Infection in Patients with the Guillain-Barre Syndrome

right arrow Ban Mishu; Amjad A. Ilyas; Carol L. Koski; Francine Vriesendorp; Stuart D. Cook; Francis A. Mithen; and Martin J. Blaser

15 June 1993 | Volume 118 Issue 12 | Pages 947-953

Objective: To determine if patients with the Guillain-Barre syndrome are likely to have had Campylobacter jejuni infection before onset of neurologic symptoms.

Design: A case–control study.

Setting: Several university medical centers.

Patients: Case patients met clinical criteria for the Guillain-Barre syndrome between 1983 and 1990 and had a serum sample collected and frozen within 3 weeks after onset of neurologic symptoms (n = 118). Disease controls were patients with other neurologic illnesses (n = 56); healthy controls were hospital employees or healthy family members of patients (n = 47).

Measurements: Serum IgA, IgG, and IgM antibodies to C. jejuni were determined by enzyme-linked immunosorbent assays. Assays were done in a blinded manner.

Results: Optical density ratios ≥ 2 in two or more immunoglobulin classes were seen in 43 (36%) of patients with the Guillain-Barre syndrome and in 10 (10%) of controls (odds ratio, 5.3; 95% CI, 2.4 to 12.5; P < 0.001). Increasing the optical density ratio or the number of immunoglobulin classes necessary to yield a positive result increased the strength of the association. The number of patients with the Guillain-Barre syndrome who had positive serologic responses was greatest from September to November (P = 0.02). Male patients were three times more likely to have serologic evidence of C. jejuni infection (P = 0.009); the proportion of patients with the syndrome who had a positive serologic response increased with age.

Conclusions: Patients with the Guillain-Barre syndrome are more likely than controls to have serologic evidence of C. jejuni infection in the weeks before onset of neurologic symptoms. Campylobacter jejuni may play a role in the initiation of the Guillain-Barre syndrome in many patients.

Author and Article Information
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From Vanderbilt University School of Medicine and Veterans Affairs Medical Center, Nashville, Tennessee; University of Medicine and Dentistry of New Jersey Newark, New Jersey; University of Maryland School of Medicine, Baltimore, Maryland; St. Louis University, St. Louis, Missouri.
Grant Support: In part by the Muscular Dystrophy Association, the U.S. Army Medical Research and Development Command, the Thrasher Research Fund, and the Medical Research Service of the Department of Veterans Affairs.




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