Study Analysis of Serum Phosphorylated Tau (P-Tau) Levels with Severity and Outcome in Traumatic Brain Injury Patients: A Single Center Observational Study at Dr. M. Djamil General Hospital, Padang, Indonesia

Istiqomah, Yuliarni Syafrita, Fanny Adhy Putri, Syarif Indra, Restu Susanti, Reno Bestari
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Abstract

Background: Traumatic brain injury (TBI) is a global health problem that can cause death and disability in people of productive age. The diagnosis and assessment of TBI severity currently still rely on clinical examination and neuroimaging. However, limited access and cost of neuroimaging are obstacles in many health facilities. Therefore, blood-based biomarkers are needed that can help the diagnosis and prognosis of TBI. Phosphorylated Tau (p-tau) is a potential biomarker that can be measured in serum. This study aims to assess the relationship between serum p-tau levels and severity and outcome in TBI patients. Methods: This research is a comparative study with a cross-sectional design involving 70 TBI patients who came to the emergency room (ER) of Dr. M. Djamil General Hospital Padang. TBI severity was assessed using the Glasgow coma scale (GCS) and grouped into mild (GCS 13-15) and moderate to severe (GCS 3-12). Outcomes were assessed using the Glasgow outcome scale (GOS) and grouped into good (GOS 4-5) and poor (GOS 1-3). Serum p-tau levels were measured using the ELISA method. Data analysis was carried out using SPSS. Results: The median serum p-tau level in the mild TBI group was 165.84 ng/L (IQR 126.18-463.85), while in the moderate to severe TBI group, it was 177.68 ng/L (IQR 87.62-591 .93). There was a significant difference between serum p-tau levels in the mild and moderate to severe TBI groups (p=0.029). The median serum p-tau level in the good outcome group was 167.21 ng/L (IQR 87.62-463.85), while in the poor outcome group it was 187.04 ng/L (IQR 137.75-591.93). There was a significant difference between serum p-tau levels in the good and bad outcome groups (p=0.014). Conclusion: Serum p-tau levels have a significant relationship with severity and outcome in TBI patients. Elevated serum p-tau levels are associated with increased severity of TBI and poor outcomes. Further research is needed to confirm these findings and explore the potential of p-tau as a biomarker in TBI management.
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创伤性脑损伤患者血清磷酸化 Tau (P-Tau) 水平与严重程度和预后的研究分析:印度尼西亚巴东 M. Djamil 医生综合医院单中心观察研究
背景:创伤性脑损伤(TBI)是一个全球性的健康问题,可导致生产年龄段的人死亡和残疾。目前,对创伤性脑损伤严重程度的诊断和评估仍依赖于临床检查和神经影像学检查。然而,在许多医疗机构中,神经影像学检查的可及性有限且费用高昂。因此,需要能帮助诊断和预后创伤性脑损伤的血液生物标志物。磷酸化 Tau(p-tau)是一种可在血清中测量的潜在生物标志物。本研究旨在评估 TBI 患者血清 p-tau 水平与严重程度和预后之间的关系。研究方法本研究是一项横断面比较研究,涉及 70 名到巴东 M. Djamil 医生综合医院急诊室(ER)就诊的创伤性脑损伤患者。创伤性脑损伤的严重程度使用格拉斯哥昏迷量表(GCS)进行评估,并分为轻度(GCS 13-15)和中度至重度(GCS 3-12)。预后采用格拉斯哥预后量表(GOS)进行评估,分为良好(GOS 4-5)和较差(GOS 1-3)两组。血清 p-tau 水平采用 ELISA 方法进行测量。使用 SPSS 进行数据分析。结果轻度创伤性脑损伤组的血清 p-tau 水平中位数为 165.84 ng/L(IQR 126.18-463.85),而中重度创伤性脑损伤组的血清 p-tau 水平中位数为 177.68 ng/L(IQR 87.62-591.93)。轻度和中重度创伤性脑损伤组的血清 p-tau 含量有明显差异(p=0.029)。预后良好组的血清 p-tau 水平中位数为 167.21 纳克/升(IQR 87.62-463.85),预后不良组为 187.04 纳克/升(IQR 137.75-591.93)。结果良好组和结果不佳组的血清 p-tau 水平存在明显差异(P=0.014)。结论血清 p-tau 水平与创伤性脑损伤患者的严重程度和预后有显著关系。血清 p-tau 水平升高与创伤性脑损伤严重程度增加和预后不良有关。需要进一步研究来证实这些发现,并探索 p-tau 作为生物标志物在创伤性脑损伤管理中的潜力。
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