Kong Yu, Chen Zhongyun, Shi Qi, Zuo Ya, Zhang Jing
Department of Neurology, Xuanwu Hospital, Capital Medical University, Beijing, China.
State Key Laboratory of Infectious Disease Prevention and Control, NHC Key Laboratory of Medical Virology and Viral Diseases, National Institute for Viral Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing, China.
J Alzheimers Dis. 2023;91(1):263-272. doi: 10.3233/JAD-220718.
The 14-3-3 protein in cerebrospinal fluid (CSF) is a suitable biomarker for the diagnosis of Creutzfeldt-Jakob disease (CJD). However, it has also been detected in various non-prion-related rapidly progressive dementia (RPD), which affected its diagnostic performance and clinical utilization.
To investigate the general disease distribution with positive 14-3-3 result and to evaluate the association between CSF 14-3-3 protein and the clinical features in patients with non-prion RPD.
A total of 150 patients with non-prion RPD were enrolled. The clinical data were collected and CSF 14-3-3 test was performed for all patients. The distribution of various diseases with a positive 14-3-3 result was analyzed and the association of CSF 14-3-3 with clinical features was tested.
The CSF 14-3-3 protein was detected in 23.3% of non-prion RPD patients, and the most frequent diagnoses were autoimmune encephalitis (22.9%) and neurodegenerative disease (22.9%). CSF 14-3-3 protein was more common in older patients (p = 0.028) and those presenting myoclonus (p = 0.008). In subgroup analysis, the positive 14-3-3 test was more common in neurodegenerative disease with a long time from the symptom onset to CSF 14-3-3 test (p = 0.014).
CSF 14-3-3 protein could be detected in a broad spectrum of non-prion RPD. In particular, patients with autoimmune encephalitis and rapidly progressive neurodegenerative diseases and those with myoclonus have a greater likelihood of a positive 14-3-3 result. These results could help clinicians interpret the results of CSF 14-3-3 protein more reasonably.
脑脊液(CSF)中的14-3-3蛋白是诊断克雅氏病(CJD)的合适生物标志物。然而,在各种非朊病毒相关的快速进展性痴呆(RPD)中也检测到了该蛋白,这影响了其诊断性能和临床应用。
调查14-3-3结果为阳性的疾病总体分布情况,并评估非朊病毒RPD患者脑脊液14-3-3蛋白与临床特征之间的关联。
共纳入150例非朊病毒RPD患者。收集所有患者的临床资料并进行脑脊液14-3-3检测。分析14-3-3结果为阳性的各种疾病的分布情况,并检测脑脊液14-3-3与临床特征的关联。
23.3%的非朊病毒RPD患者检测到脑脊液14-3-3蛋白,最常见的诊断是自身免疫性脑炎(22.9%)和神经退行性疾病(22.9%)。脑脊液14-3-3蛋白在老年患者(p = 0.028)和出现肌阵挛的患者中更常见(p = 0.008)。在亚组分析中,14-3-3检测阳性在症状出现到脑脊液14-3-3检测间隔时间较长的神经退行性疾病中更常见(p = 0.014)。
在广泛的非朊病毒RPD中可检测到脑脊液14-3-3蛋白。特别是,自身免疫性脑炎、快速进展性神经退行性疾病患者以及出现肌阵挛的患者14-3-3结果为阳性的可能性更大。这些结果有助于临床医生更合理地解读脑脊液14-3-3蛋白的检测结果。