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The cross-sectional area of the median nerve: An independent prognostic biomarker in amyotrophic lateral sclerosis.
Martínez-Payá, J J; Ríos-Díaz, J; Del Baño-Aledo, M E; Hervás, D; Tembl-Ferrairó, J I; Sevilla-Mantecón, T; Vázquez-Costa, J F.
Affiliation
  • Martínez-Payá JJ; Physiotherapy Department, Facultad de Medicina, Universidad de Murcia, Murcia, Spain.
  • Ríos-Díaz J; Campus San Rafael, Escuela de Enfermería y Fisioterapia San Juan de Dios, Universidad Pontificia de Comillas, Madrid, Spain. Electronic address: jriosmetinv@gmail.com.
  • Del Baño-Aledo ME; Physiotherapy Department, Facultad de Medicina, Universidad de Murcia, Murcia, Spain.
  • Hervás D; Department of Applied Statistics and Operations Research, and Quality, Universitat Politècnica de València, Valencia, Spain; Medicine Department, Facultad de Medicina, Universitat de València, Valencia, Spain.
  • Tembl-Ferrairó JI; Neurosonology Unit, Department of Neurology, Hospital Universitario y Politécnico La Fe, Valencia, Spain.
  • Sevilla-Mantecón T; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Spain; ALS Unit, Department of Neurology, Hospital Universitario y Politécnico La Fe, Valencia, Spain; Medicine Department, Facultad de Medicina, Universitat de València, Valencia, Spain.
  • Vázquez-Costa JF; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Spain; ALS Unit, Department of Neurology, Hospital Universitario y Politécnico La Fe, Valencia, Spain; Medicine Department, Facultad de Medicina, Universitat de València, Valencia, Spain. Electronic address: juan.vazquez.neuro
Neurologia (Engl Ed) ; 39(7): 564-572, 2024 Sep.
Article in En | MEDLINE | ID: mdl-39232594
ABSTRACT

INTRODUCTION:

Ultrasound changes in the cross-sectional area of the median nerve (CSAmn) could be of interest as biomarkers in patients with amyotrophic lateral sclerosis (ALS).

METHODS:

Eighty-four ALS patients (51 men [60.7%]; mean 62.0 [SD 11.46] years old) and forty-six controls (27 men [58.7%]; mean 59.9 [SD 8.08] years old) of two different cohorts were recruited between September 2013 and February 2018. The CSAmn was measured bilaterally in each cohort, by two different examiners with two different ultrasound machines (one in each cohort). Its association with clinical variables (disease duration, muscle strength, disability, progression rate and tracheostomy-free survival) was assessed.

RESULTS:

The CSAmn was smaller in patients than in controls, and the study cohort did not influence its values. A mild correlation between the strength of the wrist flexor and the CSAmn was found. In the multivariable analysis, the probability of this association being true was 90%. In the cox regression, both a faster progression rate and a larger CSAmn independently predicted poor survival (HR=4.29, [Cr.I95% 2.71-6.80], p<0.001; and HR=1.14, [Cr.I95% 1.03-1.25], p=0.01), after adjusting by age, body mass index, bulbar onset, and diagnostic delay.

CONCLUSIONS:

The CSAmn is an easy to assess biomarker that seems reliable and reproducible. Our data also suggest that it could act as a progression and prognostic biomarker in ALS patients. Longitudinal studies with repeated measures are warranted to confirm its usefulness in the clinical practice.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Biomarkers / Ultrasonography / Amyotrophic Lateral Sclerosis / Median Nerve Limits: Aged / Female / Humans / Male / Middle aged Language: En Journal: Neurologia (Engl Ed) Year: 2024 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Biomarkers / Ultrasonography / Amyotrophic Lateral Sclerosis / Median Nerve Limits: Aged / Female / Humans / Male / Middle aged Language: En Journal: Neurologia (Engl Ed) Year: 2024 Document type: Article Affiliation country: Country of publication: