Department of Neuroscience, S. Agostino-Estense Hospital, Azienda Ospedaliero-Universitaria di Modena, University of Modena and Reggio Emilia, Modena.
'Rita Levi Montalcini' Department of Neuroscience, University of Torino, Torino.
Eur J Neurol. 2018 Jun;25(6):861-868. doi: 10.1111/ene.13620. Epub 2018 Apr 15.
Only a few studies have considered the role of comorbidities in the prognosis of amyotrophic lateral sclerosis (ALS) and have provided conflicting results.
Our multicentre, retrospective study included patients diagnosed from 1 January 2009 to 31 December 2013 in 13 referral centres for ALS located in 10 Italian regions. Neurologists at these centres collected a detailed phenotypic profile and follow-up data until death in an electronic database. Comorbidities at diagnosis were recorded by main categories and single medical diagnosis, with the aim of investigating their role in ALS prognosis.
A total of 2354 incident cases were collected, with a median survival time from onset to death/tracheostomy of 43 months. According to univariate analysis, together with well-known clinical prognostic factors (age at onset, diagnostic delay, site of onset, phenotype, Revised El Escorial Criteria and body mass index at diagnosis), the presence of dementia, hypertension, heart disease, chronic obstructive pulmonary disease, haematological and psychiatric diseases was associated with worse survival. In multivariate analysis, age at onset, diagnostic delay, phenotypes, body mass index at diagnosis, Revised El Escorial Criteria, dementia, hypertension, heart diseases (atrial fibrillation and heart failure) and haematological diseases (disorders of thrombosis and haemostasis) were independent prognostic factors of survival in ALS.
Our large, multicentre study demonstrated that, together with the known clinical factors that are known to be prognostic for ALS survival, hypertension and heart diseases (i.e. atrial fibrillation and heart failure) as well as haematological diseases are independently associated with a shorter survival. Our findings suggest some mechanisms that are possibly involved in disease progression, giving new interesting clues that may be of value for clinical practice and ALS comorbidity management.
仅有少数研究探讨了合并症在肌萎缩侧索硬化症(ALS)预后中的作用,且结果相互矛盾。
我们的多中心回顾性研究纳入了 2009 年 1 月 1 日至 2013 年 12 月 31 日期间在意大利 10 个地区的 13 个 ALS 转诊中心诊断的患者。这些中心的神经病学家在电子数据库中收集详细的表型特征和随访数据,直至死亡。根据主要类别和单一医疗诊断记录诊断时的合并症,旨在研究其在 ALS 预后中的作用。
共收集了 2354 例首发病例,发病至死亡/气管切开的中位生存时间为 43 个月。根据单因素分析,除了众所周知的临床预后因素(发病年龄、诊断延迟、发病部位、表型、修订版 El Escorial 标准和诊断时的体重指数)外,痴呆、高血压、心脏病、慢性阻塞性肺疾病、血液和精神疾病的存在与更差的生存相关。多因素分析显示,发病年龄、诊断延迟、表型、诊断时的体重指数、修订版 El Escorial 标准、痴呆、高血压、心脏病(心房颤动和心力衰竭)和血液疾病(血栓和止血紊乱)是 ALS 生存的独立预后因素。
我们的大型多中心研究表明,除了已知的与 ALS 生存相关的临床因素外,高血压和心脏病(即心房颤动和心力衰竭)以及血液疾病也与较短的生存时间独立相关。我们的研究结果表明了一些可能与疾病进展相关的机制,为临床实践和 ALS 合并症管理提供了新的有趣线索。