识别诊断前肌萎缩侧索硬化症患者健康记录中的诊断标记。

IF 2.8
Dor Simoni, Marc Gotkine, Iddo Z Ben-Dov, Boaz Lerner
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引用次数: 0

摘要

目的:肌萎缩侧索硬化症(ALS)有一个鲜为人知的临床前阶段,特别是关于诊断血液标志物。我们的目的是确定在临床前阶段是否存在常规收集的临床和实验室标记物的不同模式,并可以合并以促进早期诊断。方法:我们进行了一项纵向、回顾性、病例对照研究,其中包括来自健康维护组织的诊断前ALS患者(PDALS)的健康记录,涵盖了约40%的以色列人口。我们纳入了在诊断日期之前至少有10次临床就诊和至少36个月观察期的PDALS,以测量PDALS与对照组之间的差异,并分析了1,810名成人个体的数据;362名PDALS和1448名年龄和性别匹配的对照组。结果:在诊断日期前数月,PDALS有显著性差异。这些包括生化参数,如尿素、肌酐、CK、钙、铁和肝酶、血液学值和BMI。一些差异在诊断日期前10年就可以检测到。结论:这项研究强调了在临床诊断前几年基于血液标志物早期检测ALS的潜力。这些发现可以显著加快诊断,识别有ALS风险的个体,并揭示未知的疾病机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Identifying diagnostic markers in the health records of prediagnostic amyotrophic lateral sclerosis patients.

Objective: Amyotrophic lateral sclerosis (ALS) has a poorly understood preclinical phase, particularly concerning diagnostic blood markers. Our objective was to determine whether distinct patterns in routinely collected clinical and laboratory markers exist during the preclinical phase and could be incorporated to facilitate early diagnosis. Methods: We conducted a longitudinal, retrospective, case-control study with health records of prediagnostic ALS patients (PDALS) from health maintenance organizations covering approximately 40% of the Israeli population. We included PDALS with at least 10 clinical visits and a minimal observation period of 36 months prior to the diagnosis date to measure differences between PDALS and controls and analyzed data from 1,810 adult individuals; 362 PDALS and 1,448 age- and sex-matched controls. Results: Significant differences were found in PDALS many months before the diagnosis date. These included biochemical parameters such as urea, creatinine, CK, calcium, iron, and liver enzymes, hematological values, and BMI. Some differences were detectable over 10 years prior to the diagnosis date. Conclusions: This study highlights the potential for early detection of ALS based on blood markers in the years preceding clinical diagnosis. These findings could significantly expedite diagnosis, identify individuals at risk for ALS, and uncover unrecognized disease mechanisms.

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