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Cerebrospinal fluid markers of central nervous system injury in decompression illness - a case-controlled pilot study.
Shahim, Pashtun; Arnell, Per; Kvarnström, Andreas; Rosén, Anders; Bremell, Daniel; Hagberg, Lars; Blennow, Kaj; Zetterberg, Henrik.
Afiliación
  • Shahim P; Clinical Neurochemistry Laboratory, Institute of Neuroscience and Physiology, Sahlgrenska Academy at University of Gothenburg, Sahlgrenska University Hospital SE-43180 Mölndal, Sweden, Phone (mobile): +46-(0)762-704584, E-mail: pashtun.shahim@neuro.gu.se.
  • Arnell P; Department of Anaesthesia and Intensive Care, Sahlgrenska University Hospital, Gothenburg, Sweden.
  • Kvarnström A; Department of Anaesthesia and Intensive Care, Sahlgrenska University Hospital, Gothenburg, Sweden.
  • Rosén A; Department of Anaesthesia and Intensive Care, Sahlgrenska University Hospital, Gothenburg, Sweden.
  • Bremell D; Department of Infectious Diseases, Institute of Biomedicine, The Sahlgrenska Academy at the University of Gothenburg, Gothenburg, Sweden.
  • Hagberg L; Department of Infectious Diseases, Institute of Biomedicine, The Sahlgrenska Academy at the University of Gothenburg, Gothenburg, Sweden.
  • Blennow K; Clinical Neurochemistry Laboratory, Institute of Neuroscience and Physiology, Sahlgrenska Academy at University of Gothenburg, Sahlgrenska University Hospital,Mölndal, Sweden.
  • Zetterberg H; Clinical Neurochemistry Laboratory, Institute of Neuroscience and Physiology, Sahlgrenska Academy at University of Gothenburg, Sahlgrenska University Hospital,Mölndal, Sweden, Department of Molecular Neuroscience, Reta Lila Weston Laboratories, UCL Institute of Neurology, London, UK.
Diving Hyperb Med ; 45(4): 240-3, 2015 Dec.
Article en En | MEDLINE | ID: mdl-26687311
ABSTRACT

INTRODUCTION:

Decompression sickness (DCS) may cause a wide variety of symptoms, including central nervous system (CNS) manifestations. The main objective of this study was to examine whether DCS is associated with neuronal injury, and whether DCS could result in altered amyloid metabolism.

METHODS:

Seven, male divers with DCS and seven age-matched controls were included in the study. All the divers were treated by recompression but the controls did not receive hyperbaric oxygen. Cerebrospinal fluid (CSF) samples were collected 7-10 days after the diving injury and at three months follow-up. CSF biomarkers of neuronal injury, astroglial Injury/activation, and a range of markers of amyloid ß (Aß) metabolism, as well as two proinflammatory interleukins, were analysed using immunochemical methods.

RESULTS:

There were no significant differences in the best-established CSF markers of neuronal injury, total tau (T-tau) and neurofilament light, between DCS patients and controls or between the two sampling time points. Also, there were no significant changes in the astroglial or amyloid (Aß)-related markers between DCS patients and controls. However, the only diver with CNS symptoms had the highest levels of CSF T-tau, Aß38, Aß40 and Aß42.

CONCLUSION:

The results of our study speak against subclinical CNS injury or induction of inflammation or amyloid build-up in the brain among the six DCS patients without neurological symptoms. Further research, including on divers with CNS DCS, is justified.
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Biomarcadores / Sistema Nervioso Central / Enfermedad de Descompresión / Buceo Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Adult / Humans / Male Idioma: En Revista: Diving Hyperb Med Año: 2015 Tipo del documento: Article
Buscar en Google
Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Biomarcadores / Sistema Nervioso Central / Enfermedad de Descompresión / Buceo Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Adult / Humans / Male Idioma: En Revista: Diving Hyperb Med Año: 2015 Tipo del documento: Article