Volta U, De Giorgio R, Petrolini N, Stangbellini V, Barbara G, Granito A, De Ponti F, Corinaldesi R, Bianchi F B
Dept. of Internal Medicine, Cardioangiology, Hepatology, University of Bologna, Italy.
Scand J Gastroenterol. 2002 Nov;37(11):1276-81. doi: 10.1080/003655202761020542.
Little is known about the clinical and immunological features of coeliac disease patients with neurological disorders. In a large series of adult coeliac disease patients, we investigated the prevalence of neurological disorders and anti-neuronal antibodies, along with the clinical course.
Neurological symptoms were investigated in 160 consecutive patients (120 F, 40 M) with biopsy-proven coeliac disease. Anti-neuronal antibodies to central/enteric nervous systems were investigated in all neurological patients, 20 unaffected ones and 20 controls.
Thirteen (8%) patients had neurological disorders, including epilepsy (n = 3), attention/memory impairment (n = 3), cerebellar ataxia (n = 2), peripheral neuropathy (n = 2), multiple sclerosis (n = 1), Moyamoya disease (n = 1) and Steinert's disease (n = 1). No significant demographic or clinical differences (gastrointestinal or other gluten-related signs) were found between patients with and without neurological involvement. In all but 2 of the 13 cases, the neurological disorder preceded diagnosis ofcoeliac disease. Neurological symptoms improved or disappeared in 7 patients who started a gluten-free diet within 6 months after neurological onset, and in none of 4 patients who began later. Prevalence of central nervous system anti-neuronal antibodies was significantly higher in neurological (61%) than in other patients (5%) (P = 0.0007) or controls (0%) (P = 0.00001).
Coeliac disease can sometimes present in the guise of a neurological disorder, which may greatly improve when a gluten-free diet is started promptly. Therefore, the possible presence of coeliac disease needs to be carefully considered in patients with cerebellar ataxia, epilepsy, attention/memory impairment or peripheral neuropathy.
关于患有神经系统疾病的乳糜泻患者的临床和免疫学特征,人们所知甚少。在一大系列成年乳糜泻患者中,我们调查了神经系统疾病和抗神经元抗体的患病率以及临床病程。
对160例经活检证实为乳糜泻的连续患者(120例女性,40例男性)进行神经系统症状调查。对所有有神经系统症状的患者、20例未受影响的患者和20例对照进行中枢/肠神经系统抗神经元抗体检测。
13例(8%)患者患有神经系统疾病,包括癫痫(3例)、注意力/记忆力损害(3例)、小脑共济失调(2例)、周围神经病变(2例)、多发性硬化(1例)、烟雾病(1例)和斯坦纳特病(1例)。有神经系统受累和无神经系统受累的患者之间在人口统计学或临床方面(胃肠道或其他与麸质相关的体征)未发现显著差异。在13例病例中,除2例之外,其余病例的神经系统疾病均先于乳糜泻的诊断。7例在神经系统症状出现后6个月内开始无麸质饮食的患者,其神经系统症状得到改善或消失,而4例较晚开始无麸质饮食的患者症状均未改善。神经系统疾病患者中中枢神经系统抗神经元抗体的患病率(61%)显著高于其他患者(5%)(P = 0.0007)或对照(0%)(P = 0.00001)。
乳糜泻有时可能以神经系统疾病的形式出现,及时开始无麸质饮食后病情可能会大为改善。因此,对于患有小脑共济失调、癫痫、注意力/记忆力损害或周围神经病变的患者,需要仔细考虑是否可能存在乳糜泻。