Fath-Elbab Hanaa Khalaf, Ahmed Elham, Mansour Dina Fathy, Soliman Wail Talaat
Minia University Faculty of Medicine, Minia, Egypt.
Egypt J Neurol Psychiatr Neurosurg. 2018;54(1):35. doi: 10.1186/s41983-018-0034-y. Epub 2018 Nov 20.
Chronic infection by hepatitis C virus causes impairment in neurocognitive function in up to 50% of patients which may not be detected by clinical tests.
Early detection of neurocognitive impairment in chronic hepatitis C patients and investigating the cognitive function in HCV patient by p300 and clinical test.
The study included 60 patients with chronic hepatitis C and 30 healthy controls. Participants were subjected to a biochemical, hematological assessment, mini-mental state examination, Montreal Cognitive Assessment, P300, polymerase chain reaction (PCR), and fibroscan made for hepatitis C patients.
The digit span, attention, concentration, and memory were significantly lower in patients than controls. The delayed P300 peak latency and the reduction of its amplitude were significantly evident in patients with liver fibrosis than the controls and patients without fibrosis. These abnormalities were significantly higher with increasing the grade of fibrosis. All patients with cognitive impairment (reduced mini-mental state score) had abnormal P300-evoked responses. P300 could detect neurocognitive impairment in some patients with normal neurocognitive functions by clinical test. P300 had sensitivity (100%), specificity (59.26), positive predictive value (75%), negative predictive value (100%), and accuracy (81.67) in the detection of neurocognitive impairment in HCV patient.
Patients with chronic hepatitis C infection had significant impairment in their cognitive functions. This impairment increases with the increase in grade of hepatic fibrosis. P300 can detect minimal and subclinical impairment of cognitive function at early stages of chronic hepatitis with accuracy (81.67).
PACTR on 19 march 2018 retrospectively. Identification number for the registry is PACTR201804003215168.
丙型肝炎病毒慢性感染导致高达50%的患者出现神经认知功能损害,而临床检测可能无法发现这种损害。
早期检测慢性丙型肝炎患者的神经认知损害,并通过P300和临床检测研究丙型肝炎患者的认知功能。
该研究纳入了60例慢性丙型肝炎患者和30例健康对照。参与者接受了生化、血液学评估、简易精神状态检查、蒙特利尔认知评估、P300、聚合酶链反应(PCR),并对丙型肝炎患者进行了肝脏弹性成像检查。
患者的数字广度、注意力、集中力和记忆力显著低于对照组。与对照组和无肝纤维化的患者相比,肝纤维化患者的P300潜伏期延迟和波幅降低更为明显。随着纤维化程度的增加,这些异常更为显著。所有认知功能受损(简易精神状态评分降低)的患者P300诱发反应均异常。P300可在一些临床检测神经认知功能正常的患者中检测到神经认知损害。P300在检测丙型肝炎患者神经认知损害方面的敏感性为100%,特异性为59.26%,阳性预测值为75%,阴性预测值为100%,准确性为81.67%。
慢性丙型肝炎感染患者存在明显的认知功能损害。这种损害随着肝纤维化程度的增加而加重。P300能够准确检测慢性丙型肝炎早期阶段认知功能的轻微和亚临床损害(准确性为81.67%)。
于2018年3月19日进行回顾性PACTR注册。注册号为PACTR201804003215168。