Emerging biomarkers to predict clinical outcomes in Guillain-Barré syndrome

Expert Rev Neurother. 2023 Jul-Dec;23(12):1201-1215. doi: 10.1080/14737175.2023.2273386. Epub 2023 Dec 15.

Abstract

Introduction: Guillain-Barré syndrome (GBS) is an immune-mediated poly(radiculo)neuropathy with a variable clinical outcome. Identifying patients who are at risk of suffering from long-term disabilities is a great challenge. Biomarkers are useful to confirm diagnosis, monitor disease progression, and predict outcome.

Areas covered: The authors provide an overview of the diagnostic and prognostic biomarkers for GBS, which are useful for establishing early treatment strategies and follow-up care plans.

Expert opinion: Detecting patients at risk of developing a severe outcome may improve management of disease progression and limit potential complications. Several clinical factors are associated with poor prognosis: higher age, presence of diarrhea within 4 weeks of symptom onset, rapid and severe weakness progression, dysautonomia, decreased vital capacity and facial, bulbar, and neck weakness. Biological, neurophysiological and imaging measures of unfavorable outcome include multiple anti-ganglioside antibodies elevation, increased serum and CSF neurofilaments light (NfL) and heavy chain, decreased NfL CSF/serum ratio, hypoalbuminemia, nerve conduction study with early signs of demyelination or axonal loss and enlargement of nerve cross-sectional area on ultrasound. Depicting prognostic biomarkers aims at predicting short-term mortality and need for cardio-pulmonary support, long-term patient functional outcome, guiding treatment decisions and monitoring therapeutic responses in future clinical trials.

Keywords: Autoimmune; Miller-Fisher syndrome; electroneuromyography; immunoglobulins; mechanical ventilation; peripheral nervous system.

Publication types

  • Review

MeSH terms

  • Autonomic Nervous System Diseases*
  • Biomarkers
  • Disease Progression
  • Guillain-Barre Syndrome* / diagnosis
  • Guillain-Barre Syndrome* / therapy
  • Humans
  • Infant, Newborn

Substances

  • Biomarkers