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Primary lateral sclerosis: application and validation of the 2020 consensus diagnostic criteria in an expert opinion-based PLS cohort.
Witzel, Simon; Micca, Veronika; Müller, Hans P; Huss, André; Bachhuber, Franziska; Dorst, Johannes; Lulé, Dorothée E; Tumani, Hayrettin; Kassubek, Jan; Ludolph, Albert C.
Affiliation
  • Witzel S; Department of Neurology, Ulm University, Ulm, Germany simon.witzel@uni-ulm.de.
  • Micca V; Department of Neurology, Ulm University, Ulm, Germany.
  • Müller HP; Department of Neurology, Ulm University, Ulm, Germany.
  • Huss A; Department of Neurology, Ulm University, Ulm, Germany.
  • Bachhuber F; Department of Neurology, Ulm University, Ulm, Germany.
  • Dorst J; Department of Neurology, Ulm University, Ulm, Germany.
  • Lulé DE; Department of Neurology, Ulm University, Ulm, Germany.
  • Tumani H; Department of Neurology, Ulm University, Ulm, Germany.
  • Kassubek J; Department of Neurology, Ulm University, Ulm, Germany.
  • Ludolph AC; Department of Neurology, Ulm University, Ulm, Germany.
J Neurol Neurosurg Psychiatry ; 95(8): 737-747, 2024 Jul 15.
Article in En | MEDLINE | ID: mdl-38388486
ABSTRACT

BACKGROUND:

Validation of the 2020 consensus criteria for primary lateral sclerosis (PLS) is essential for their use in clinical practice and future trials.

METHODS:

In a large cohort of patients diagnosed with PLS by expert opinion prior to the new criteria with detailed clinical baseline evaluation (n=107) and longitudinal follow-up (n=63), we applied the new diagnostic criteria and analysed the clinical phenotype, electromyography (EMG), diagnostic accuracy and prognosis, adding neurofilaments and MRI as potential biomarkers.

RESULTS:

The criteria for definite PLS were met by 28% and those for probable PLS by 19%, whereas 53% did not meet the full criteria at baseline, mainly due to the time, EMG and region criteria. Patients not meeting the criteria had less generalised upper motor neuron involvement but were otherwise similar in demographic and clinical characteristics. All patients with definite and probable PLS maintained PLS diagnosis during follow-up, while four patients not meeting the criteria developed clinical lower motor neuron involvement. Definite PLS cases showed improved survival compared with probable PLS and patients who did not meet the criteria. Despite a clinical PLS phenotype, fibrillation potentials/positive sharp waves and fasciculations in one or more muscles were a frequent EMG finding, with the extent and prognostic significance depending on disease duration. Serum neurofilament light and a multiparametric MRI fibre integrity Z-score correlated with clinical parameters and were identified as potential biomarkers.

CONCLUSION:

Validation of the 2020 PLS consensus criteria revealed high diagnostic certainty and prognostic significance, supporting their value for research and clinical practice.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Magnetic Resonance Imaging / Motor Neuron Disease / Consensus / Electromyography Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: J Neurol Neurosurg Psychiatry Year: 2024 Document type: Article Affiliation country: Alemania Country of publication: Reino Unido

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Magnetic Resonance Imaging / Motor Neuron Disease / Consensus / Electromyography Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: J Neurol Neurosurg Psychiatry Year: 2024 Document type: Article Affiliation country: Alemania Country of publication: Reino Unido