期刊论文详细信息
Frontiers in Neurology
Association Between Copeptin and Six-Month Neurologic Outcomes in Patients With Moderate Traumatic Brain Injury
Jeong Jin Park1  Suk Hyung Kang2  Jin Pyeong Jeon2  Jun Hyong Ahn2  Jong Kook Rhim3  Seonghyeon Kim4  Heung Cheol Kim5  Dong Hyuk Youn6  Chan Hum Park6  Jong-Tae Kim6  Sung Woo Han6  Seung Hyuk Lim6  Bong Jun Kim6  Eun Pyo Hong6  Tae Yeon Kim6 
[1] Department of Neurology, Konkuk Medical Center, Seoul, South Korea;Department of Neurosurgery, Hallym University College of Medicine, Chuncheon, South Korea;Department of Neurosurgery, Jeju National University College of Medicine, Jeju, South Korea;Department of Orthopaedic Surgery, Hallym University College of Medicine, Chuncheon, South Korea;Department of Radioilogy, Hallym University College of Medicine, Chuncheon, South Korea;Institute of New Frontier Research, Hallym University College of Medicine, Chuncheon, South Korea;
关键词: biomarkers;    traumatic brain injury;    copeptin;    outcome;    cohort study;   
DOI  :  10.3389/fneur.2021.749110
来源: DOAJ
【 摘 要 】

BackgroundCopeptin has been reported as a predictive biomarker for the prognosis after traumatic brain injury (TBI). However, most of them were in patients with severe TBI and limited value in predicting outcomes in patients with moderate TBI defined as Glasgow Coma Scale (GCS) score from 9 to 12. We aimed to investigate the predictive value of copeptin in assessing the neurologic outcome following moderate TBI.MethodsPatients were prospectively enrolled between May 2017 and November 2020. We consecutively measured plasma copeptin within 24 h after trauma, days 3, 5, and 7 using ELISA. The primary outcome was to correlate plasma copeptin levels with poor neurologic outcome at 6 months after moderate TBI. The secondary outcome was to compare the prognostic accuracy of copeptin and C-reactive protein (CRP) in assessing the outcome of patient.ResultsA total of 70 patients were included for the final analysis. The results showed that 29 patients (41.4%) experienced a poor neurologic outcome at 6 months. Multivariable logistic regression analysis revealed that increased copeptin (odds ration [OR] = 1.020, 95% CI: 1.005–1.036), GCS score of 9 or 10 (OR = 4.507, 95% CI: 1.266–16.047), and significant abnormal findings on CT (OR = 4.770; 95% CI: 1.133–20.076) were independent risk factors for poor outcomes. Consecutive plasma copeptin levels were significantly different according to outcomes (p < 0.001). Copeptin on day 7 exhibited better prognostic performance than CRP with an area under receiver operating characteristic curve (AUROC) difference of 0.179 (95% CI: 0.032–0.325) in predicting 6-month poor outcomes.ConclusionPlasma copeptin level can be a useful marker in predicting 6-month outcomes in patients with moderate TBI.

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