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Survival and prognostic factors of motor neuron disease in a multi-ethnic Asian population

机译:亚洲多族裔人群运动神经元疾病的生存和预后因素

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摘要

Our objective was to determine the survival and prognostic factors of motor neuron disease (MND) in a multi-ethnic cohort of Malaysian patients. All patients seen at a university medical centre between January 2000 and December 2009 had their case records reviewed for demographic, clinical and follow-up data. Mortality data, if unavailable from records, were obtained by telephone interview of relatives or from the national mortality registry. Of the 73 patients, 64.4% were Chinese, 19.2% Malays and 16.4% Indians. Male: female ratio was 1.43: 1. Mean age at onset was 51.5 + 11.3 years. Onset was spinal in 75.3% and bulbar in 24.7% of the patients; 94.5% were ALS and 5.5% were progressive muscular atrophy (PMA). Overall median survival was 44.9 + 5.8 months. Ethnic Indians had shorter interval from symptom onset to diagnosis and shorter median survival compared to non-Indians. On Cox proportional hazards analysis, poor prognostic factors were bulbar onset, shorter interval from symptom onset to diagnosis and worse functional score at presentation. In conclusion, age of onset and median survival duration are similar to previous reports in Asians. Clinical features and prognostic factors are similar to other populations. In our cohort, ethnic Indians had more rapid disease course accounting for their shorter survival.
机译:我们的目标是确定马来西亚多种族人群中运动神经元疾病(MND)的存活率和预后因素。 2000年1月至2009年12月在大学医学中心就诊的所有患者均对其病例记录进行了人口统计学,临床和随访数据审查。如果无法从记录中获得死亡率数据,则可以通过对亲属的电话采访或从国家死亡率登记处获得。在73名患者中,华人占64.4%,马来人占19.2%,印度人占16.4%。男女之比为1.43:1。平均发病年龄为51.5 + 11.3岁。脊柱发炎的患者占75.3%,延髓的发病率为24.7%。 ALS为94.5%,进行性肌萎缩症(PMA)为5.5%。总体中位生存期为44.9 + 5.8个月。与非印第安人相比,印第安人从症状发作到诊断的间隔时间较短,中位生存期较短。在Cox比例风险分析中,不良预后因素为延髓发作,从症状发作到诊断的间隔时间较短,以及表现较差的功能评分。总之,发病年龄和中位生存期与亚洲人以前的报道相似。临床特征和预后因素与其他人群相似。在我们的队列中,印第安人的疾病进程较快,原因是其生存期较短。

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