gms | German Medical Science

65. Jahrestagung der Deutschen Gesellschaft für Neurochirurgie (DGNC)

Deutsche Gesellschaft für Neurochirurgie (DGNC) e. V.

11. - 14. Mai 2014, Dresden

Regulation of Neuropeptide Y in cerebrospinal fluid and in serum after spontaneous subarachnoid hemorrhage

Meeting Abstract

  • Karl-Michael Schebesch - Klinik und Poliklinik für Neurochirurgie am Universitätsklinikum Regensburg
  • Elisabeth Bründl - Klinik und Poliklinik für Neurochirurgie am Universitätsklinikum Regensburg
  • Andreas Hochreiter - Klinik und Poliklinik für Neurochirurgie am Universitätsklinikum Regensburg
  • Judith Scheitzach - Klinik und Poliklinik für Neurochirurgie am Universitätsklinikum Regensburg
  • Alexander Brawanski - Klinik und Poliklinik für Neurochirurgie am Universitätsklinikum Regensburg
  • Petra Schödel - Klinik und Poliklinik für Neurochirurgie am Universitätsklinikum Regensburg

Deutsche Gesellschaft für Neurochirurgie. 65. Jahrestagung der Deutschen Gesellschaft für Neurochirurgie (DGNC). Dresden, 11.-14.05.2014. Düsseldorf: German Medical Science GMS Publishing House; 2014. DocMO.02.03

doi: 10.3205/14dgnc003, urn:nbn:de:0183-14dgnc0038

Veröffentlicht: 13. Mai 2014

© 2014 Schebesch et al.
Dieser Artikel ist ein Open Access-Artikel und steht unter den Creative Commons Lizenzbedingungen (http://creativecommons.org/licenses/by-nc-nd/3.0/deed.de). Er darf vervielfältigt, verbreitet und öffentlich zugänglich gemacht werden, vorausgesetzt dass Autor und Quelle genannt werden.


Gliederung

Text

Objective: The abundantly expressed vasoconstrictive Neuropeptide Y (NPY) has been shown to have the potential to significantly influence the development of vasospasm-related cerebral ischemia and functional outcome, subsequently after spontaneous subarachnoid hemorrhage (SAH). Here, we present the results of a prospectively designed observational study concerning the nuances of regulation of endogenous NPY in cerebrospinal fluid (CSF) and in serum according to location of aneurysm, modality of treatment and development of cerebral ischemia during the acute phase after SAH.

Method: Prospectively, we collected CSF and serum over ten days in 34 patients (18 female, 16 male) who received a ventricular drainage within 24 hours after onset of the SAH. All patients were graded 3 or 4 according to Fisher. The levels of NPY in serum and in CSF were determined using an enzyme-immunosorbent assay (EIA). The population was dichotomized due to aneurysmal location, treatment modality and development of vasospasm-related ischemia during the first 10 days.

Results:

1.
Patients with radiological assessable ischemia had significantly higher levels of NPY in CSF, p=0.037.
2.
The levels of NPY in CSF in anterior circulation aneurysms were significantly higher compared to those of the posterior circulation, p=0.021.
3.
A strong correlation between serum levels and CSF levels of NPY was detected in anterior circulation aneurysms, p=0.014.
4.
The levels of NPY in CSF ranged significantly higher in surgically or endovascularily approached aneurysms than in those without treatment, p=0.024.

Conclusions: The release of endogenous NPY is significantly correlated to cerebral ischemia. We found strong evidence that the anatomical location of the aneurysm and the manipulation of cerebral arteries potentially influenced the release of NPY into serum and CSF after SAH.