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空肠弯曲菌感染与吉兰 - 巴雷综合征

Campylobacter jejuni infection and Guillain-Barré syndrome.

作者信息

Rees J H, Soudain S E, Gregson N A, Hughes R A

机构信息

Department of Neurology, United Medical School, Guy's Hospital, London, United Kingdom.

出版信息

N Engl J Med. 1995 Nov 23;333(21):1374-9. doi: 10.1056/NEJM199511233332102.

Abstract

BACKGROUND

Although infection with Campylobacter jejuni is recognized as a common antecedent of the Guillain-Barré syndrome, the clinical and epidemiologic features of this association are not well understood.

METHODS

We performed a prospective case-control study in a cohort of patients with Guillain-Barré syndrome (96 patients) or Miller Fisher syndrome (7 patients) who were admitted to hospitals throughout England and Wales between November 1992 and April 1994. Bacteriologic and serologic techniques were used to diagnose preceding C. jejuni infection.

RESULTS

There was evidence of recent C. jejuni infection in 26 percent of the patients with Guillain-Barré or Miller Fisher syndrome, as compared with 2 percent of household controls and 1 percent of age-matched hospital controls (P < 0.001). Of the 27 patients with C. jejuni infection, 19 (70 percent) reported having had a diarrheal illness within 12 weeks before the onset of the neurologic illness. No specific serotypes were associated with Guillain-Barré syndrome. C. jejuni infection was slightly more common in men (P = 0.14) and was more likely to be associated with a pure motor syndrome and a slower recovery (P = 0.03). The patients with preceding C. jejuni infection were more likely to have acute axonal neuropathy or axonal degeneration in association with acute inflammatory demyelinating polyradiculoneuropathy, and they had greater disability after one year (P = 0.02). C. jejuni infection was significantly associated with a poor outcome even after correction for other factors associated with a poor prognosis.

CONCLUSIONS

Infection with C. jejuni often precedes the Guillain-Barré syndrome and is associated with axonal degeneration, slow recovery, and severe residual disability.

摘要

背景

尽管空肠弯曲菌感染被认为是吉兰 - 巴雷综合征常见的前驱因素,但这种关联的临床和流行病学特征尚未完全明确。

方法

我们对1992年11月至1994年4月期间在英格兰和威尔士各医院住院的吉兰 - 巴雷综合征患者(96例)或米勒 - 费希尔综合征患者(7例)进行了一项前瞻性病例对照研究。采用细菌学和血清学技术诊断先前的空肠弯曲菌感染。

结果

在患有吉兰 - 巴雷或米勒 - 费希尔综合征的患者中,有26%的人有近期空肠弯曲菌感染的证据,相比之下,家庭对照者中有2%,年龄匹配的医院对照者中有1%(P < 0.001)。在27例有空肠弯曲菌感染的患者中,19例(70%)报告在神经系统疾病发病前12周内有腹泻病史。没有特定血清型与吉兰 - 巴雷综合征相关。空肠弯曲菌感染在男性中略为常见(P = 0.14),并且更可能与单纯运动综合征和恢复较慢相关(P = 0.03)。先前有空肠弯曲菌感染的患者更可能同时患有急性轴索性神经病或轴索变性以及急性炎症性脱髓鞘性多发性神经根神经病,并且一年后他们的残疾程度更高(P = 0.02)。即使校正了其他与预后不良相关的因素后,空肠弯曲菌感染仍与不良预后显著相关。

结论

空肠弯曲菌感染常先于吉兰 - 巴雷综合征发生,并与轴索变性、恢复缓慢和严重的残留残疾相关。

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