Predicting prognosis in amyotrophic lateral sclerosis: a simple algorithm.

Predicting prognosis in amyotrophic lateral sclerosis: a simple algorithm.
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DOI:
10.1007/s00415-015-7731-6
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发表时间:
2015-06
影响因子:
6
通讯作者:
Hardiman O
Hardiman O
中科院分区:
医学2区
文献类型:
--
作者:
Elamin M;Bede P;Montuschi A;Pender N;Chio A;Hardiman O

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该研究的目的是利用首次临床咨询时获得的信息,为肌萎缩侧索硬化症 (ALS) 患者制定并验证实用的预后指数。我们询问了两个基于人口的项目(位于爱尔兰共和国和意大利)生成的数据集。爱尔兰患者队列分为训练和测试子队列。 Kaplan-Meier 方法和 Cox 比例风险回归用于识别训练集中预后的显着预测因子。使用加权分级系统,得出了区分三个风险组的预后指数。指数的有效性在爱尔兰测试子队列中进行了测试,并在意大利复制队列中得到了外部确认。在训练子队列 (n = 117) 中,预后的重要预测因素是疾病发作部位 (HR = 1.7,p = 0.012);首次评估之前的 ALSFRS-R 斜率(HR = 2.8,p < 0.0001)和执行功能障碍(HR = 2.11,p = 0.001)。使用这些结果生成的风险组系统预测了训练集、测试集 (n = 87) 和意大利队列 (n = 122) 中的中位生存时间,95% CI 没有重叠 (p < 0.0001)。在验证队列中,高风险分类与不良预后的阳性预测值(73.3-85.7%)相关,与良好预后的阴性预测值(NPV)相关(93.3-100%)。分类为低风险组与 100% 不良预后的 NPV 相关。一种简单的算法使用可以在第一次遇到患者时收集的变量,并在独立的患者系列中进行验证,可以可靠地预测 ALS 患者的预后。
The objective of the study was to develop and validate a practical prognostic index for patients with amyotrophic lateral scleroses (ALS) using information available at the first clinical consultation. We interrogated datasets generated from two population-based projects (based in the Republic of Ireland and Italy). The Irish patient cohort was divided into Training and Test sub-cohorts. Kaplan–Meier methods and Cox proportional hazards regression were used to identify significant predictors of prognoses in the Training set. Using a weighted grading system, a prognostic index was derived that separated three risk groups. The validity of index was tested in the Irish Test sub-cohort and externally confirmed in the Italian replication cohort. In the Training sub-cohort (n = 117), significant predictors of prognoses were site of disease onset (HR = 1.7, p = 0.012); ALSFRS-R slope prior to first evaluation (HR = 2.8, p < 0.0001), and executive dysfunction (HR = 2.11, p = 0.001). The risk group system generated using these results predicted median survival time in the Training set, the Test set (n = 87) and the Italian cohort (n = 122) with no overlap of the 95 % CI (p < 0.0001). In the validation cohorts, a high-risk classification was associated with a positive predictive value for poor prognosis of 73.3–85.7 % and a negative predictive value (NPV) for good prognosis of 93.3–100 %. Classification into the low-risk group was associated with an NPV for bad prognosis of 100 %. A simple algorithm using variables that can be gathered at first patient encounter, validated in an independent patient series, reliably predicts prognoses in ALS patients.
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