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A new potential therapeutic approach for ALS: A case report with NGS analysis.
Hu, Chaur-Jong; Chen, Po-Chih; Padmanabhan, Neeraj; Zahn, Andre; Ho, Chih-Ming; Wang, Kuan; Yen, Yun.
Affiliation
  • Hu CJ; Department of Neurology, School of Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan.
  • Chen PC; Department of Neurology, Shuang Ho Hospital, Taipei Medical University, New Taipei City, Taiwan.
  • Padmanabhan N; Department of Neurology, School of Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan.
  • Zahn A; Department of Neurology, Shuang Ho Hospital, Taipei Medical University, New Taipei City, Taiwan.
  • Ho CM; Department of Chemical and Biomolecular Engineering Henry Samueli School of Engineering at the University of California Los Angeles, Los Angeles, CA.
  • Wang K; Department of General Medicine, Taipei Medical University Hospital, Taipei City, Taiwan.
  • Yen Y; Mechanical and Aerospace Engineering Henry Samueli School of Engineering University of California, Los Angeles, CA.
Medicine (Baltimore) ; 103(9): e37401, 2024 Mar 01.
Article in En | MEDLINE | ID: mdl-38428880
ABSTRACT
RATIONALE Amyotrophic lateral sclerosis (ALS) poses a significant clinical challenge due to its rapid progression and limited treatment options, often leading to deadly outcomes. Looking for effective therapeutic interventions is critical to improve patient outcomes in ALS. PATIENT CONCERNS The patient, a 75-year-old East Asian male, manifested an insidious onset of right-hand weakness advancing with dysarthria. Comprehensive Next-generation sequencing analysis identified variants in specific genes consistent with ALS diagnosis. DIAGNOSES ALS diagnosis is based on El Escorial diagnostic criteria.

INTERVENTIONS:

This study introduces a novel therapeutic approach using artificial intelligence phenotypic response surface (AI-PRS) technology to customize personalized drug-dose combinations for ALS. The patient underwent a series of phases of AI-PRS-assisted trials, initially incorporating a 4-drug combination of Ibudilast, Riluzole, Tamoxifen, and Ropinirole. Biomarkers and regular clinical assessments, including nerve conduction velocity, F-wave, H-reflex, electromyography, and motor unit action potential, were monitored to comprehensively evaluate treatment efficacy.

OUTCOMES:

Neurophysiological assessments supported the ALS diagnosis and revealed the co-presence of diabetic polyneuropathy. Hypotension during the trial necessitated an adaptation to a 2-drug combinational trial (ibudilast and riluzole). Disease progression assessment shifted exclusively to clinical tests of muscle strength, aligning with the patient's well-being. LESSONS The study raises the significance of personalized therapeutic strategies in ALS by AI-PRS. It also emphasizes the adaptability of interventions based on patient-specific responses. The encountered hypotension incident highlights the importance of attentive monitoring and personalized adjustments in treatment plans. The described therapy using AI-PRS, offering personalized drug-dose combinations technology is a potential approach in treating ALS. The promising outcomes warrant further evaluation in clinical trials for searching a personalized, more effective combinational treatment for ALS patients.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Amyotrophic Lateral Sclerosis / Hypotension Limits: Aged / Humans / Male Language: En Journal: Medicine (Baltimore) Year: 2024 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Amyotrophic Lateral Sclerosis / Hypotension Limits: Aged / Humans / Male Language: En Journal: Medicine (Baltimore) Year: 2024 Document type: Article Affiliation country: