Suppr超能文献

成人 1 型戈谢病中的周围神经病:一项为期 2 年的前瞻性观察研究。

Peripheral neuropathy in adult type 1 Gaucher disease: a 2-year prospective observational study.

机构信息

Department of Neurology, Academic Medical Centre, Amsterdam, The Netherlands.

出版信息

Brain. 2010 Oct;133(10):2909-19. doi: 10.1093/brain/awq198. Epub 2010 Aug 7.

Abstract

Type 1 Gaucher disease is currently categorized as non-neuronopathic, although recent studies suggest peripheral neurological manifestations. We report prevalence and incidence data for peripheral neuropathy and associated conditions from a multinational, prospective, longitudinal, observational cohort study in patients with type 1 Gaucher disease, either untreated or receiving enzyme replacement therapy. The primary outcome parameters were the prevalence and incidence of polyneuropathy, evaluated by standardized assessments of neurological symptoms and signs, and electrophysiological studies. All diagnoses of polyneuropathy were adjudicated centrally. Secondary outcome parameters included the prevalence and incidence of mononeuropathy, other neurological or electrophysiological abnormalities not fulfilling the criteria for a mono- or polyneuropathy and general type 1 Gaucher disease symptoms. Furthermore, a literature search was performed to identify all studies reporting on prevalence and incidence of polyneuropathy in the general population. One hundred and three patients were enrolled [median (range) age: 42 (18-75) years; disease duration: 15 (0-56) years; 52% female]; 14 (13.6%) were untreated and 89 (86.4%) were on enzyme replacement therapy. At baseline, 11 patients [10.7%; 95% confidence interval (CI): 5.9-18.3] were diagnosed with sensory motor axonal polyneuropathy. Two (1.9%; 95% CI: 0.1-7.2) had a mononeuropathy of the ulnar nerve. The 2-year follow-up period revealed another six cases of polyneuropathy (2.9 per 100 person-years; 95% CI: 1.2-6.3). Patients with polyneuropathy were older than those without (P<0.001). Conditions possibly associated with polyneuropathy were identified in four patients only, being monoclonal gammopathy, vitamin B(1) deficiency, folic acid deficiency, type 2 diabetes mellitus, renal insufficiency, alcohol abuse and exposure to toxins related to profession. The 11 cases of polyneuropathy found at baseline were confirmed during follow-up. According to the literature, the prevalence of polyneuropathy in the general population was estimated between 0.09 and 1.3% and the incidence was estimated between 0.0046 and 0.015 per 100 person-years. Thus, we conclude that the prevalence and incidence of polyneuropathy in patients with type 1 Gaucher disease is increased compared with the general population.

摘要

1 型戈谢病目前被归类为非神经病变型,但最近的研究表明其存在周围神经病变表现。我们报告了一项多国、前瞻性、纵向、观察性队列研究中 1 型戈谢病患者的周围神经病及相关疾病的患病率和发病率数据,这些患者要么未接受治疗,要么接受酶替代治疗。主要结局参数是通过标准化评估神经症状和体征以及电生理研究评估的多发性神经病的患病率和发病率。所有多发性神经病的诊断均由中心进行裁定。次要结局参数包括单神经病、其他不符合单神经病或多神经病标准的神经或电生理异常以及一般 1 型戈谢病症状的患病率和发病率。此外,还进行了文献检索,以确定所有报告一般人群中多发性神经病患病率和发病率的研究。共纳入 103 例患者[中位(范围)年龄:42(18-75)岁;病程:15(0-56)年;52%为女性];14 例(13.6%)未接受治疗,89 例(86.4%)接受酶替代治疗。基线时,11 例患者[10.7%;95%置信区间(CI):5.9-18.3]被诊断为感觉运动轴索多发性神经病。2 例(1.9%;95%CI:0.1-7.2)患有尺神经单神经病。在 2 年的随访期间,又发现 6 例多发性神经病(每 100 人年 2.9 例;95%CI:1.2-6.3)。患有多发性神经病的患者比未患有多发性神经病的患者年龄更大(P<0.001)。仅在 4 例患者中确定了可能与多发性神经病相关的情况,即单克隆丙种球蛋白病、维生素 B1 缺乏、叶酸缺乏、2 型糖尿病、肾功能不全、酒精滥用和接触与职业相关的毒素。基线时发现的 11 例多发性神经病在随访期间得到了证实。根据文献,一般人群中多发性神经病的患病率估计为 0.09%至 1.3%,发病率估计为每 100 人年 0.0046 至 0.015。因此,我们得出结论,1 型戈谢病患者的多发性神经病患病率和发病率高于一般人群。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验