Using serum s100-β protein as a biomarker for comparing silent brain injury in carotid endarterectomy and carotid artery stenting.


Journal

International angiology : a journal of the International Union of Angiology
ISSN: 1827-1839
Titre abrégé: Int Angiol
Pays: Italy
ID NLM: 8402693

Informations de publication

Date de publication:
Apr 2019
Historique:
pubmed: 18 1 2019
medline: 19 9 2019
entrez: 18 1 2019
Statut: ppublish

Résumé

S100-β protein has been introduced as a sensitive biomarker of silent cerebral injury. This study compares its serum levels before, during, and 24 hours after carotid artery stenting (CAS) and carotid endarterectomy (CEA). We measured serum level of S100-β in arterial blood before (S100Ba), during (S100Bb), and 24 hours after (S100Bc) CAS and CEA. We assessed differences in S100-β levels using non-parametric tests. We analyzed the relationship between carotid plaque type (echolucency) and S100-β protein level. We also examined its relation to the oximetry results in the CEA group (ipsilateral and contralateral). Thirty patients were enrolled, including 15 CAS and 15 CEA patients, with no significant differences in baseline atherosclerotic characteristics. There was no significant difference in S100Ba or S100Bb levels between CAS and CEA patients. However, a significant difference was found in S100Bc: 331.3 pg/mL (IQ range 56.4-583.5) for CAS vs. 76.3 pg/mL (IQ range 29.7-117.4) for CEA (P=0.01). Type I and II plaques were associated with the higher S100Bc levels in CAS (P=0.048). S100Bc was higher in CEA patients when the contralateral cerebral hemisphere had oximetry values less than 60% (P=0.043). Our study suggests that CAS might produce silent brain injury. Moreover, vulnerable plaques might be associated with higher levels of S100-β protein, especially in CAS. This pilot study demonstrates that S100-β is a useful biomarker for silent brain injury in carotid revascularization. Large scale studies are still needed to confirm these findings.

Sections du résumé

BACKGROUND BACKGROUND
S100-β protein has been introduced as a sensitive biomarker of silent cerebral injury. This study compares its serum levels before, during, and 24 hours after carotid artery stenting (CAS) and carotid endarterectomy (CEA).
METHODS METHODS
We measured serum level of S100-β in arterial blood before (S100Ba), during (S100Bb), and 24 hours after (S100Bc) CAS and CEA. We assessed differences in S100-β levels using non-parametric tests. We analyzed the relationship between carotid plaque type (echolucency) and S100-β protein level. We also examined its relation to the oximetry results in the CEA group (ipsilateral and contralateral).
RESULTS RESULTS
Thirty patients were enrolled, including 15 CAS and 15 CEA patients, with no significant differences in baseline atherosclerotic characteristics. There was no significant difference in S100Ba or S100Bb levels between CAS and CEA patients. However, a significant difference was found in S100Bc: 331.3 pg/mL (IQ range 56.4-583.5) for CAS vs. 76.3 pg/mL (IQ range 29.7-117.4) for CEA (P=0.01). Type I and II plaques were associated with the higher S100Bc levels in CAS (P=0.048). S100Bc was higher in CEA patients when the contralateral cerebral hemisphere had oximetry values less than 60% (P=0.043).
CONCLUSIONS CONCLUSIONS
Our study suggests that CAS might produce silent brain injury. Moreover, vulnerable plaques might be associated with higher levels of S100-β protein, especially in CAS. This pilot study demonstrates that S100-β is a useful biomarker for silent brain injury in carotid revascularization. Large scale studies are still needed to confirm these findings.

Identifiants

pubmed: 30650951
pii: S0392-9590.19.04079-3
doi: 10.23736/S0392-9590.19.04079-3
doi:

Substances chimiques

Antiplatyhelmintic Agents 0
Biomarkers 0
S100 Calcium Binding Protein beta Subunit 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

136-142

Auteurs

Ayman H Alserr (AH)

Department of Vascular Surgery, Attikon University Hospital, Athens, Greece - ayman_elsir@hotmail.com.
Division of Vascular Surgery, Department of General Surgery, Cairo University Hospital, Cairo, Egypt - ayman_elsir@hotmail.com.

Hussein Elwan (H)

Division of Vascular Surgery, Department of General Surgery, Cairo University Hospital, Cairo, Egypt.

Constantine N Antonopoulos (CN)

Department of Vascular Surgery, Attikon University Hospital, Athens, Greece.

Amr Abdelreheem (A)

Division of Vascular Surgery, Department of General Surgery, Cairo University Hospital, Cairo, Egypt.

Hossam Elmahdy (H)

Division of Vascular Surgery, Department of General Surgery, Cairo University Hospital, Cairo, Egypt.

Ahmed Sayed (A)

Division of Vascular Surgery, Department of General Surgery, Cairo University Hospital, Cairo, Egypt.

Ahmed Taha (A)

Division of Vascular Surgery, Department of General Surgery, Cairo University Hospital, Cairo, Egypt.

Eirini Maratou (E)

Hellenic National Center for Research, Prevention and Treatment of Diabetes Mellitus and its Complications (HNCDC), Athens, Greece.

Elias Brountzos (E)

Department of Interventional Radiology, Attikon University Hospital, Athens, Greece.

Hussein Khairy (H)

Division of Vascular Surgery, Department of General Surgery, Cairo University Hospital, Cairo, Egypt.

Christos D Liapis (CD)

Department of Vascular Surgery, Attikon University Hospital, Athens, Greece.

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Classifications MeSH