Identifying diagnostic markers in the health records of prediagnostic amyotrophic lateral sclerosis patients

<i>Objective</i>: 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. <i>Methods</i>: 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. <i>Results</i>: 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. <i>Conclusions</i>: 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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Publication Details

Journal
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
Published
2025-09-05
DOI
https://doi.org/10.1080/21678421.2025.2539898
Primary Topic
Amyotrophic Lateral Sclerosis Research
Type
article
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article

Identifying diagnostic markers in the health records of prediagnostic amyotrophic lateral sclerosis patients

David Simoni, Iddo Z. Ben‐Dov, Marc Gotkine, Boaz Lerner
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
Amyotrophic Lateral Sclerosis Research
article

Identifying diagnostic markers in the health records of prediagnostic amyotrophic lateral sclerosis patients

David Simoni, Iddo Z. Ben‐Dov, Marc Gotkine, Boaz Lerner
article en

Abstract

<i>Objective</i>: 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. <i>Methods</i>: 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. <i>Results</i>: 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. <i>Conclusions</i>: 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.

Amyotrophic Lateral Sclerosis and Frontotemporal DegenerationVol. 27(1-2)
Ben-Gurion University of the Negev (IL), Hebrew University of Jerusalem (IL), Hadassah Medical Center (IL)
Openalex Percentile: Top 66%
Amyotrophic Lateral Sclerosis Research
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Identifying diagnostic markers in the health records of prediagnostic amyotrophic lateral sclerosis patients — David Simoni, Iddo Z. Ben‐Dov, et al. · Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration (2025) | TGRS Research Map | TGRS