Mishu B, Ilyas A A, Koski C L, Vriesendorp F, Cook S D, Mithen F A, Blaser M J
Infectious Diseases Division, Vanderbilt University School of Medicine, Nashville, TN 37232.
Ann Intern Med. 1993 Jun 15;118(12):947-53. doi: 10.7326/0003-4819-118-12-199306150-00006.
To determine if patients with the Guillain-Barré syndrome are likely to have had Campylobacter jejuni infection before onset of neurologic symptoms.
A case-control study.
Several university medical centers.
Case patients met clinical criteria for the Guillain-Barré 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).
Serum IgA, IgG, and IgM antibodies to C. jejuni were determined by enzyme-linked immunosorbent assays. Assays were done in a blinded manner.
Optical density ratios > or = 2 in two or more immunoglobulin classes were seen in 43 (36%) of patients with the Guillain-Barré 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-Barré 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.
Patients with the Guillain-Barré 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-Barré syndrome in many patients.
确定吉兰-巴雷综合征患者在神经症状出现之前是否有可能感染过空肠弯曲菌。
病例对照研究。
几家大学医学中心。
病例组患者符合1983年至1990年间吉兰-巴雷综合征的临床标准,且在神经症状出现后3周内采集并冷冻了血清样本(n = 118)。疾病对照组为患有其他神经系统疾病的患者(n = 56);健康对照组为医院员工或患者的健康家庭成员(n = 47)。
采用酶联免疫吸附试验测定血清中针对空肠弯曲菌的IgA、IgG和IgM抗体。检测以盲法进行。
吉兰-巴雷综合征患者中有43例(36%)在两种或更多免疫球蛋白类别中光密度比值≥2,而对照组中有10例(10%)出现这种情况(比值比,5.3;95%可信区间,2.4至12.5;P < 0.001)。提高光密度比值或产生阳性结果所需的免疫球蛋白类别数量会增强这种关联强度。吉兰-巴雷综合征患者血清学反应呈阳性的人数在9月至11月最多(P = 0.02)。男性患者出现空肠弯曲菌感染血清学证据的可能性是女性的三倍(P = 0.009);该综合征患者血清学反应呈阳性的比例随年龄增加而升高。
与对照组相比,吉兰-巴雷综合征患者在神经症状出现前数周更有可能出现空肠弯曲菌感染的血清学证据。空肠弯曲菌可能在许多患者吉兰-巴雷综合征的发病过程中起作用。