High Serum sCD40L Levels During the First Week of Malignant Middle Cerebral Artery Infarction and Mortality.


Journal

World neurosurgery
ISSN: 1878-8769
Titre abrégé: World Neurosurg
Pays: United States
ID NLM: 101528275

Informations de publication

Date de publication:
Dec 2019
Historique:
received: 15 03 2019
revised: 08 08 2019
accepted: 09 08 2019
pubmed: 24 8 2019
medline: 25 1 2020
entrez: 24 8 2019
Statut: ppublish

Résumé

Higher circulating soluble cluster of differentiation 40 ligand (sCD40L) levels at admission of an ischemic stroke have been found in nonsurvivor than in survivor patients. The objectives of this study were to determine whether serum sCD40L levels during the first week of a severe malignant middle cerebral artery infarction (MMCAI) are higher in nonsurvivor than in survivor patients and whether they could be used as biomarker of mortality prediction. This multicenter study included patients with severe MMCAI (defined as Glasgow Coma Scale score <9). We determined serum sCD40L concentrations at days 1, 4, and 8 and performed receiver operating characteristic analyses to determine their capacity for 30-day mortality prediction. Nonsurvivors (n = 34) showed higher sCD40L levels on days 1 (P < 0.001), 4 (P = 0.004), and 8 (P < 0.001) than did survivor patients (n = 34). Areas under the curve of serum sCD40L concentrations at days 1, 4, and 8 of severe MMCAI for 30-day mortality prediction were 83% (P < 0.001), 89% (P < 0.001), and 87% (P < 0.001), respectively. The findings that nonsurvivors showed higher serum sCD40L levels during the first week of MMCAI than did survivors and that serum sCD40L levels during the first week of MMCAI could be used as a mortality predictor biomarker are 2 novel findings.

Sections du résumé

BACKGROUND BACKGROUND
Higher circulating soluble cluster of differentiation 40 ligand (sCD40L) levels at admission of an ischemic stroke have been found in nonsurvivor than in survivor patients. The objectives of this study were to determine whether serum sCD40L levels during the first week of a severe malignant middle cerebral artery infarction (MMCAI) are higher in nonsurvivor than in survivor patients and whether they could be used as biomarker of mortality prediction.
METHODS METHODS
This multicenter study included patients with severe MMCAI (defined as Glasgow Coma Scale score <9). We determined serum sCD40L concentrations at days 1, 4, and 8 and performed receiver operating characteristic analyses to determine their capacity for 30-day mortality prediction.
RESULTS RESULTS
Nonsurvivors (n = 34) showed higher sCD40L levels on days 1 (P < 0.001), 4 (P = 0.004), and 8 (P < 0.001) than did survivor patients (n = 34). Areas under the curve of serum sCD40L concentrations at days 1, 4, and 8 of severe MMCAI for 30-day mortality prediction were 83% (P < 0.001), 89% (P < 0.001), and 87% (P < 0.001), respectively.
CONCLUSIONS CONCLUSIONS
The findings that nonsurvivors showed higher serum sCD40L levels during the first week of MMCAI than did survivors and that serum sCD40L levels during the first week of MMCAI could be used as a mortality predictor biomarker are 2 novel findings.

Identifiants

pubmed: 31442656
pii: S1878-8750(19)32215-6
doi: 10.1016/j.wneu.2019.08.060
pii:
doi:

Substances chimiques

Biomarkers 0
CD40 Ligand 147205-72-9

Types de publication

Journal Article Multicenter Study Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

e630-e636

Informations de copyright

Copyright © 2019 Elsevier Inc. All rights reserved.

Auteurs

Leonardo Lorente (L)

Intensive Care Unit, Hospital Universitario de Canarias, La Laguna, Santa Cruz de Tenerife, Spain. Electronic address: lorentemartin@msn.com.

María M Martín (MM)

Intensive Care Unit, Hospital Universitario Nuestra Señora de Candelaria, Tenerife, Santa Cruz de Tenerife, Spain.

Agustín F González-Rivero (AF)

Laboratory Department, Hospital Universitario de Canarias, La Laguna, Santa Cruz de Tenerife, Spain.

Rafael Sabatel (R)

Department of Radiology, Hospital Universitario de Canarias, La Laguna, Santa Cruz de Tenerife, Spain.

Luis Ramos (L)

Intensive Care Unit, Hospital General La Palma, Breña Alta, Santa Cruz de Tenerife, Spain.

Mónica Argueso (M)

Intensive Care Unit, Hospital Clínico Universitario de Valencia, Valencia, Spain.

Juan J Cáceres (JJ)

Intensive Care Unit, Hospital Insular, Las Palmas de Gran Canaria, Spain.

Jordi Solé-Violán (J)

Intensive Care Unit, Hospital Universitario Dr. Negrín, Las Palmas de Gran Canaria, Spain.

Andrea Alvarez-Castillo (A)

Intensive Care Unit, Hospital Universitario de Canarias, La Laguna, Santa Cruz de Tenerife, Spain.

Alejandro Jiménez (A)

Department of Research Unit, Hospital Universitario de Canarias, La Laguna, Santa Cruz de Tenerife, Spain.

Juan M Borreguero-León (JM)

Laboratory Department, Hospital Universitario de Canarias, La Laguna, Santa Cruz de Tenerife, Spain.

Victor García-Marín (V)

Department of Neurosurgery, Hospital Universitario de Canarias, La Laguna, Santa Cruz de Tenerife, Spain.

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Classifications MeSH