血清 Stanniocalcin-1 作为严重创伤性脑损伤潜在预后生物标志物的前瞻性纵向队列研究。

IF 2.8 3区 医学 Q1 Pharmacology, Toxicology and Pharmaceutics Therapeutics and Clinical Risk Management Pub Date : 2024-06-11 eCollection Date: 2024-01-01 DOI:10.2147/TCRM.S463955
Chunhua Jin, Xiuqin Huang, Yanping Hu, Bing Xu, Jiasen Ma
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引用次数: 0

摘要

背景:Stanniocalcin-1(STC1)可能具有抗炎和抗氧化特性,从而发挥神经保护作用。本研究旨在确定血清 STC1 在严重创伤性脑损伤(sTBI)的严重程度评估和预后预测中的作用:在这项前瞻性纵向队列研究中,对 104 名严重创伤性脑损伤患者和 104 名健康人(对照组)的血清 STC1 水平进行了量化。严重程度指标为格拉斯哥昏迷量表(GCS)和鹿特丹计算机断层扫描分类。随访时间为 180 天,格拉斯哥结果扩展量表(GOSE)1-4 分被视为预后不良。多变量分析用于评估严重程度相关性和预后相关性。根据接收者操作特征曲线下面积(AUC)估算判别效率:结果:患者的血清 STC1 水平明显高于对照组。血清 STC1 水平依次为 GCS 评分 8 分至 3 分、鹿特丹评分 3 分至 6 分和 180 天 GOSE 评分 8 分至 1 分。此外,血清 STC1 水平还与 GCS 评分、鹿特丹评分和 180 天 GOSE 评分独立相关。血清 STC1 水平与 180 天死亡、总生存率和不良预后独立相关,并能有效预测死亡和不良预后。包含 GCS 评分、鹿特丹评分和血清 STC1 水平的预测模型(而非其中任何一项)对死亡和预后不良风险具有更高的判别能力。另外,血清 STC1 水平与死亡风险、总生存率和不良预后呈线性相关。亚组分析表明,血清STC1水平与年龄、性别、高血压、糖尿病等无统计学显著交互作用:结论:血清STC1水平的明显升高与创伤性脑损伤的严重程度和临床预后高度相关,表明血清STC1可能是创伤性脑损伤的潜在预后生物标志物。
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A Prospective Longitudinal Cohort Study of Serum Stanniocalcin-1 as a Potential Prognostic Biomarker of Severe Traumatic Brain Injury.

Background: Stanniocalcin-1 (STC1) may harbor anti-inflammatory and anti-oxidative properties, thereby exerting neuroprotective effects. This study was done with the intent to determine the role of serum STC1 in severity assessment and prognosis prediction of severe traumatic brain injury (sTBI).

Methods: In this prospective longitudinal cohort study of 104 sTBI patients and 104 healthy individuals (controls), serum STC1 levels were quantified. Severity indicators were Glasgow Coma Scale (GCS) and Rotterdam computed tomography classification. Follow-up time was 180 days and extended Glasgow outcome scale (GOSE) score 1-4 was deemed as poor prognosis. Multivariate analyses were applied to assess severity correlations and prognosis associations. Discriminative efficiencies were estimated in terms of area under receiver operating characteristic curve (AUC).

Results: Patients exhibited significantly higher serum STC1 levels than controls. Serum STC1 levels were substantially elevated in order of GCS scores from 8 to 3, Rotterdam scores from 3 to 6 and 180-day GOSE scores from 8 to 1. Also, serum STC1 levels were independently correlated with GCS scores, Rotterdam scores and 180-day GOSE scores. Serum STC1 levels were independently associated with 180-day death, overall survival and poor prognosis, as well as were efficiently predictive of death and poor prognosis. Prediction model containing GCS scores, Rotterdam scores and serum STC1 levels, as opposed to any of them, showed higher discriminative ability for the risks of death and poor prognosis. Alternatively, serum STC1 levels were linearly correlated with risk of death, overall survival and poor prognosis under restricted cubic spline. Subgroup analysis showed that serum STC1 levels non-statistically significantly interacted with age, gender, hypertension, diabetes mellitus, etc.

Conclusion: A significant elevation of serum STC1 levels is highly related to severity and clinical outcome, suggesting that serum STC1 may be a potential prognostic biomarker of sTBI.

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来源期刊
Therapeutics and Clinical Risk Management
Therapeutics and Clinical Risk Management HEALTH CARE SCIENCES & SERVICES-
CiteScore
5.30
自引率
3.60%
发文量
139
审稿时长
16 weeks
期刊介绍: Therapeutics and Clinical Risk Management is an international, peer-reviewed journal of clinical therapeutics and risk management, focusing on concise rapid reporting of clinical studies in all therapeutic areas, outcomes, safety, and programs for the effective, safe, and sustained use of medicines, therapeutic and surgical interventions in all clinical areas. The journal welcomes submissions covering original research, clinical and epidemiological studies, reviews, guidelines, expert opinion and commentary. The journal will consider case reports but only if they make a valuable and original contribution to the literature. As of 18th March 2019, Therapeutics and Clinical Risk Management will no longer consider meta-analyses for publication. The journal does not accept study protocols, animal-based or cell line-based studies.
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