Department of Laboratory Diagnostics, University Hospital Center Zagreb, Zagreb, Croatia.
Faculty of Pharmacy and Biochemistry, University of Zagreb, Zagreb, Croatia.
Lab Med. 2024 Jul 3;55(4):492-497. doi: 10.1093/labmed/lmad116.
Diagnostic accuracy of glial fibrillary acidic protein (GFAP) and ubiquitin C-terminal hydrolase L1 (UCH-L1) in identification of intracranial abnormalities detected by computed tomography (CT) in mild traumatic brain injury (mTBI), and in patients with mild neurological symptoms not caused by head trauma but suspected with a neurological disorder, was examined.
GFAP and UCH-L1 were determined using the chemiluminescence immunoassays on the Alinity i analyzer (Abbott Laboratories).
Significantly higher GFAP (median 53.8 vs 25.7 ng/L, P < .001) and UCH-L1 (median 350.9 vs 153.9 ng/L, P < .001) were found in mTBI compared to non-head trauma patients. In mTBI diagnostic sensitivity (Se) and specificity (Sp) for the combination of GFAP and UCH-L1 were 100% and 30.9%, respectively, with area under the curve (AUC) 0.655. GFAP alone yielded Se 85.7%, Sp 41.8%, and AUC 0.638, while UCH-L1 yielded Se 57.1%, Sp 56.4%, and AUC 0.568. In non-head trauma patients, the combination of GFAP and UCH-L1 showed Se 100%, Sp 87.9%, and AUC 0.939, while GFAP alone demonstrated Se 100%, Sp 90.9%, and AUC 0.955.
If these results are reproduced on a larger sample, GFAP and UCH-L1 may reduce CT use in patients with mild neurological symptoms after systemic causes exclusion and neurologist's evaluation.
在轻度创伤性脑损伤(mTBI)患者和有轻度神经症状但无头部外伤且疑似神经疾病的患者中,检测到 CT 检测到的颅内异常时,胶质纤维酸性蛋白(GFAP)和泛素 C 端水解酶 L1(UCH-L1)的诊断准确性。
使用 Abbott Laboratories 的 Alinity i 分析仪上的化学发光免疫分析测定 GFAP 和 UCH-L1。
与非头部外伤患者相比,mTBI 患者的 GFAP(中位数 53.8 比 25.7ng/L,P<0.001)和 UCH-L1(中位数 350.9 比 153.9ng/L,P<0.001)明显升高。GFAP 和 UCH-L1 联合检测对 mTBI 的诊断敏感性(Se)和特异性(Sp)分别为 100%和 30.9%,曲线下面积(AUC)为 0.655。GFAP 单独检测的 Se 为 85.7%,Sp 为 41.8%,AUC 为 0.638,UCH-L1 的 Se 为 57.1%,Sp 为 56.4%,AUC 为 0.568。在非头部外伤患者中,GFAP 和 UCH-L1 联合检测的 Se 为 100%,Sp 为 87.9%,AUC 为 0.939,而 GFAP 单独检测的 Se 为 100%,Sp 为 90.9%,AUC 为 0.955。
如果在更大的样本中得到重现,GFAP 和 UCH-L1 可能会减少对有轻度神经症状且排除全身性病因和神经科医生评估后的患者进行 CT 检查。