Veterans with familial ALS and bulbar and respiratory presentations at onset had shorter survival.

IF 2.6 4区 综合性期刊 Q2 MULTIDISCIPLINARY SCIENCES Science Progress Pub Date : 2024-07-01 DOI:10.1177/00368504241262902
Meheroz H Rabadi, Kimberly A Russell, Chao Xu
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Abstract

Objective: We sought to characterize the clinical prognostic factors in veterans with amyotrophic lateral sclerosis (ALS) followed in our ALS clinic.

Background: ALS is a rare, progressive neurodegenerative condition associated with decreased survival compared to that in the normal population.

Method: The electronic medical records of 105 veterans diagnosed with ALS who are followed in our ALS clinic between 2010 and 2021 were reviewed. Approval from the institutional review board was obtained from the study protocol. Demographic and clinical variables included age at symptom onset, age at initial evaluation, survival (from symptom onset to death), gender, site of onset (appendicular, bulbar, and respiratory), initial amyotrophic lateral sclerosis functional-related score-revised (ALSFRS-R), total functional independence measure (TFIM) scores, initial forced vital capacity (FVC), and interventions (Riluzole, gastrostomy, noninvasive ventilation [NIV], and tracheostomy). Normally distributed data was expressed as mean ± standard deviation. Fischer's exact analysis of the distribution differences of categorical data. The Kaplan-Meier plot analyzed the time-to-event.

Results: The mean (SD) age at symptom onset was 62.0 (11.1) years, age at diagnosis was 65 (11) years, with 72% of the patients being over 60 years at diagnosis. The median survival time from symptom onset was 4.12 (3) years. Limb-onset ALS (appendicular) was the most frequent (52%) followed by bulbar-onset ALS (43%). The mean ALSFRS-R and TFIM scores were 31 (8) and 91 (25), respectively. Family history (familial), bulbar, and respiratory presentation at diagnosis were associated with shorter survival times.

Conclusion: This study suggests that of the clinical prognostic factors veterans with familial ALS, bulbar, and respiratory onset at presentations had shorter survival. The presence of Agent Orange, PEG placement, and NIV did not affect survival.

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患有家族性肌萎缩性脊髓侧索硬化症的退伍军人在发病时出现球部和呼吸道症状,存活时间较短。
摘要背景:ALS是一种罕见的渐进性神经退行性疾病,与正常人相比存活率较低:背景:肌萎缩侧索硬化症是一种罕见的进行性神经退行性疾病,与正常人群相比存活率较低:方法:对 2010 年至 2021 年期间在我院 ALS 诊所接受随访的 105 名确诊为 ALS 的退伍军人的电子病历进行审查。研究方案获得了机构审查委员会的批准。人口统计学和临床变量包括发病年龄、初始评估年龄、存活率(从发病到死亡)、性别、发病部位(阑尾、球部和呼吸道)、初始肌萎缩侧索硬化症功能相关评分-修订版(ALSFRS-R)、总功能独立性测量(TFIM)评分、初始强迫生命容量(FVC)和干预措施(利鲁唑、胃造口术、无创通气[NIV]和气管造口术)。正态分布数据以均数±标准差表示。对分类数据的分布差异进行费舍尔精确分析。Kaplan-Meier 图分析了事件发生的时间:症状出现时的平均(标准差)年龄为 62.0(11.1)岁,确诊时的年龄为 65(11)岁,72% 的患者确诊时年龄超过 60 岁。自症状出现起的中位生存时间为 4.12 (3) 年。最常见的是肢端渐进性脊髓侧索硬化症(阑尾)(52%),其次是球部渐进性脊髓侧索硬化症(43%)。ALSFRS-R 和 TFIM 的平均得分分别为 31(8)分和 91(25)分。诊断时的家族史(家族性)、球部和呼吸道表现与较短的存活时间有关:这项研究表明,在临床预后因素中,患有家族性 ALS 的退伍军人在确诊时出现肺部和呼吸道症状的存活时间较短。橘剂、PEG 植入和 NIV 对存活率没有影响。
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来源期刊
Science Progress
Science Progress Multidisciplinary-Multidisciplinary
CiteScore
3.80
自引率
0.00%
发文量
119
期刊介绍: Science Progress has for over 100 years been a highly regarded review publication in science, technology and medicine. Its objective is to excite the readers'' interest in areas with which they may not be fully familiar but which could facilitate their interest, or even activity, in a cognate field.
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