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Plasma glial fibrillary acidic protein and tau: predictors of neurological outcome after cardiac arrest.
Arctaedius, Isabelle; Levin, Helena; Thorgeirsdóttir, Bergthóra; Moseby-Knappe, Marion; Cronberg, Tobias; Annborn, Martin; Nielsen, Niklas; Zetterberg, Henrik; Blennow, Kaj; Ashton, Nicholas J; Frigyesi, Attila; Friberg, Hans; Lybeck, Anna; Mattsson-Carlgren, Niklas.
Afiliación
  • Arctaedius I; Department of Clinical Sciences, Anaesthesia and Intensive Care, Skane University Hospital, Lund University, Lund, Sweden. isabelle.arctaedius@med.lu.se.
  • Levin H; Department of Research and Education, Skane University Hospital and Department of Clinical Sciences, Anaesthesia and Intensive Care, Lund University, Lund, Sweden.
  • Thorgeirsdóttir B; Department of Clinical Sciences, Anaesthesia and Intensive Care, Skane University Hospital, Lund University, Malmö, Sweden.
  • Moseby-Knappe M; Neurology and Rehabilitation Medicine, Department of Clinical Sciences Lund, Skane University Hospital, Lund University, Lund, Sweden.
  • Cronberg T; Department of Clinical Sciences, Neurology, Skane University Hospital, Lund University, Lund, Sweden.
  • Annborn M; Department of Clinical Sciences, Anaesthesia and Intensive Care, Helsingborg Hospital, Lund University, Helsingborg, Sweden.
  • Nielsen N; Department of Clinical Sciences, Anaesthesia and Intensive Care, Helsingborg Hospital, Lund University, Helsingborg, Sweden.
  • Zetterberg H; Clinical Neurochemistry Laboratory, Sahlgrenska University Hospital, Mölndal, Sweden.
  • Blennow K; Department of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, The Sahlgrenska Academy at the University of Gothenburg, Mölndal, Sweden.
  • Ashton NJ; Department of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London, UK.
  • Frigyesi A; UK Dementia Research Institute at UCL, London, UK.
  • Friberg H; Hong Kong Center for Neurodegenerative Diseases, Clear Water Bay, Hong Kong, China.
  • Lybeck A; Wisconsin Alzheimer's Disease Research Centre, University of Wisconsin School of Medicine and Public Health, University of Wisconsin-Madison, Madison, WI, USA.
  • Mattsson-Carlgren N; Clinical Neurochemistry Laboratory, Sahlgrenska University Hospital, Mölndal, Sweden.
Crit Care ; 28(1): 116, 2024 04 09.
Article en En | MEDLINE | ID: mdl-38594704
ABSTRACT

BACKGROUND:

The purpose was to evaluate glial fibrillary acidic protein (GFAP) and total-tau in plasma as predictors of poor neurological outcome after out-of-hospital (OHCA) and in-hospital cardiac arrest (IHCA), including comparisons with neurofilament light (NFL) and neuron-specific enolase (NSE).

METHODS:

Retrospective multicentre observational study of patients admitted to an intensive care unit (ICU) in three hospitals in Sweden 2014-2018. Blood samples were collected at ICU admission, 12 h, and 48 h post-cardiac arrest. Poor neurological outcome was defined as Cerebral Performance Category 3-5 at 2-6 months after cardiac arrest. Plasma samples were retrospectively analysed for GFAP, tau, and NFL. Serum NSE was analysed in clinical care. Prognostic performances were tested with the area under the receiver operating characteristics curve (AUC).

RESULTS:

Of the 428 included patients, 328 were OHCA, and 100 were IHCA. At ICU admission, 12 h and 48 h post-cardiac arrest, GFAP predicted neurological outcome after OHCA with AUC (95% CI) 0.76 (0.70-0.82), 0.86 (0.81-0.90) and 0.91 (0.87-0.96), and after IHCA with AUC (95% CI) 0.77 (0.66-0.87), 0.83 (0.74-0.92) and 0.83 (0.71-0.95). At the same time points, tau predicted outcome after OHCA with AUC (95% CI) 0.72 (0.66-0.79), 0.75 (0.69-0.81), and 0.93 (0.89-0.96) and after IHCA with AUC (95% CI) 0.61 (0.49-0.74), 0.68 (0.56-0.79), and 0.77 (0.65-0.90). Adding the change in biomarker levels between time points did not improve predictive accuracy compared to the last time point. In a subset of patients, GFAP at 12 h and 48 h, as well as tau at 48 h, offered similar predictive value as NSE at 48 h (the earliest time point NSE is recommended in guidelines) after both OHCA and IHCA. The predictive performance of NFL was similar or superior to GFAP and tau at all time points after OHCA and IHCA.

CONCLUSION:

GFAP and tau are promising biomarkers for neuroprognostication, with the highest predictive performance at 48 h after OHCA, but not superior to NFL. The predictive ability of GFAP may be sufficiently high for clinical use at 12 h after cardiac arrest.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Paro Cardíaco Extrahospitalario Límite: Humans Idioma: En Revista: Crit Care Año: 2024 Tipo del documento: Article País de afiliación: Suecia

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Paro Cardíaco Extrahospitalario Límite: Humans Idioma: En Revista: Crit Care Año: 2024 Tipo del documento: Article País de afiliación: Suecia