|
|
Expression and significance of P-tau-181, IL-1β and AD7c-NTP in patients with Alzheimer′s disease |
LI Min1 YE Lijun2 YU Changfa3 FU Pan1 XUE Yufeng1▲ |
1.Department of Neurology, the First People′s Hospital of Taizhou, Zhejiang Province, Taizhou 318020, China;
2.Department of Blood Transfusion, the First People′s Hospital of Taizhou, Zhejiang Province, Taizhou 318020, China;
3.Department of Laboratory, the First People′s Hospital of Taizhou, Zhejiang Province, Taizhou 318020, China |
|
|
Abstract Objective To explore the expression and clinical significance of serum phosphorylated tau protein (P-tau-181), interleukin-1β (IL-1β) and urinary Alzheimer′s disease (AD) associated neurofilament protein (AD7c-NTP) in patients with AD. Methods A total of 76 patients with AD were selected as the AD group who were hospitalized in the Department of Neurology, Taizhou First People′s Hospital from January 2017 to June 2019. According to the clinical dementia scale score, they were divided into 26 cases in mild group, 29 cases in moderate group and 21 cases in severe group. A total of 35 healthy people who underwent physical examination at the same time were selected as the control group. Serum P-tau-181, IL-1β and AD7c-NTP in urine were detected by enzyme-linked immunosorbent assay. The expression levels of P-tau-181, IL-1β and AD7c-NTP were compared in each group, and the diagnostic efficacy of P-tau-181, IL-1β and AD7c-NTP in AD were analyzed. Results The expressions of P-tau-181, IL-1β, and AD7c-NTP in AD group were higher than those in control group (all P < 0.05). The expression levels of P-tau-181, IL-1β, and AD7c-NTP in the severe group were higher than those in the moderate and mild groups. The expression levels of P-tau-181, IL-1β, and AD7c-NTP in the moderate group were higher than those in the mild group (all P < 0.05). The area under curve (AUC) of P-tau181 in the diagnosis of AD was 0.898, the AUC of IL-1β was 0.851, and the AUC of AD7c-NTP was 0.847. Conclusion The expression of P-tau-181, IL-1β and AD7c-NTP in AD patients is elevated, which can be used as a detection index for clinical diagnosis of AD, and it can also classify the severity of lesions, which has important clinical significance.
|
|
|
|
|
[1] Vergallo A,Carlesi C,Pagni C,et al. A single center study:Aβ42/p-Tau181 CSF ratio to discriminate AD from FTD in clinical setting [J]. Neurol Sci,2017,38(10):1791-1797.
[2] Dayon L,Wojcik J,Nunez Galindo A,et al. Plasma proteomic profiles of cerebrospinal fluid-defined Alzheimer′s Disease pathology in older adults [J]. J Alzheimers Dis,2017,60(4):1641-1652.
[3] Ma L,Wang R,Han Y,et al. Development of a novel urine Alzheimer-associated neuronal thread protein ELISA kit and its potential use in the diagnosis of Alzheimer′s Disease [J]. J Clin Lab Anal,2016,30(4):308-314.
[4] 张兰.同型半胱氨酸和C反应蛋白对阿尔茨海默病与血管性痴呆的鉴别诊断价值[J].中国实用医药,2016,11(11):113-114.
[5] 彭丹涛,张占军.神经心理认知量表操作指南[M].北京:人民卫生出版社,2015:5-9.
[6] Muller S,Preische O,Gopfert JC,et al. Tau plasma levels in subjective cognitive decline:Results from the DELCODE study [J]. Sci Rep,2017,7(1):9529-9537.
[7] Yang CC,Chiu MJ,Chen TF,et al. Assay of plasma phosphorylated tau protein (threonine 181) and total tau protein in early-stage Alzheimer′s Disease [J]. J Alzheimers Dis,2018,61(4):1323-1332.
[8] Santangelo R,Dell Edera A,Sala A,et al. The CSF p-tau181/Aβ42 ratio offers a good accuracy “In Vivo” in the differential diagnosis of Alzheimer′s Dementia [J]. Curr Alzheimer Res,2019,16(7):587-595.
[9] Schaeverbeke J,Gille B,Adamczuk K,et al. Cerebrospinal fluid levels of synaptic and neuronal integrity correlate with gray matter volume and amyloid load in the precuneus of cognitively intact older adults [J]. J Neurochem,2019,149(1):139-157.
[10] Babic Leko M,Krbot Skoric M,Klepac N,et al. Event-related potentials improve the efficiency of cerebrospinal fluid biomarkers for differential diagnosis of Alzheimer′s Disease [J]. Curr Alzheimer Res,2018,15(13):1244-1260.
[11] Vergallo A,Bun RS,Toschi N,et al. Association of cerebrospinal fluid α-synuclein with total and phospho-tau181 protein concentrations and brain amyloid load in cognitively normal subjective memory complainers stratified by Alzheimer′s disease biomarkers [J]. Alzheimers Dement,2018,14(12):1623-1631.
[12] Shekhar S,Kumar R,Rai N,et al. Estimation of tau and phosphorylated tau181 in serum of Alzheimer′s Disease and mild cognitive impairment patients [J]. PLoS One,2016,11(7):e0159099.
[13] Tatebe H,Kasai T,Ohmichi T,et al. Quantification of plasma phosphorylated tau to use as a biomarker for brain Alzheimer pathology:pilot case-control studies including patients with Alzheimer′s disease and down syndrome [J] .Mol Neurodegener,2017,12(1):63-72.
[14] 郝建华,肖利佳,靳亮,等.磷酸化Tau-181蛋白在阿尔茨海默病患者临床诊断中的应用价值[J].江西科学,2016,34(2):190-193.
[15] 黄若燕,任建娟,韩海英,等.代谢综合征与阿尔茨海默病的相关性研究[J].精神医学杂志,2013,26(3):175-177.
[16] Gelman CR. Familismo and its impact on the family caregiving of latinos with Alzheimer′s disease: a complex narrative [J]. Rese Aging,2014,36(1):40-71.
[17] D′Anna L,Abu-Rumeileh S,Fabris M,et al. Serum interleukin-10 levels correlate with cerebrospinal fluid amyloid beta deposition in Alzheimer disease patients [J]. Neurodegener Dis,2017,17(4):227-234.
[18] 吴琼,闫荣.阿尔茨海默病病人瘦素、空腹血糖、胰岛素及炎性因子水平分析[J].实用老年医学,2018,32(6):527-530.
[19] 伏彩霞,尚天明,马宝山.阿尔茨海默病患者炎症因子、氧化应激与胰岛素抵抗的相关性分析[J].检验医学与临床,2019,16(7):939-942.
[20] 李晓佳,杨丽莉,肖军,等.探讨胰岛素及胰岛素抵抗在不同ApoE基因型轻中度阿尔茨海默病中的作用[J].成都医学院学报,2018,13(6):715-719.
[21] 仲丽丽,张维嘉,刘旭,等.通天草醇提物对阿尔茨海默病小鼠行为学及海马炎症介质的影响[J].中国医药导报,2018,15(25):17-20.
[22] 梁子涌,武雅静,邓远飞,等.阿尔茨海默病的研究进展[J].中国医药科学,2018,8(16):42-45.
[23] Ma L,Chen J,Wang R,et al. The level of Alzheimer-associated neuronal thread protein in urine may be an important biomarker of mild cognitive impairment [J]. J Clin Neurosci,2015,22(4):649-652.
[24] Wang N,Chen J,Xiao H,et al. Application of artificial neural network model in diagnosis of Alzheimer′s disease [J]. BMC Neurol,2019,19(1):154-164.
[25] 李爱东,陈曦,陈建良,等.不同类型认知障碍患者的尿液AD7c-NTP与头部MRI、MRS的相关性研究[J].国际精神病学杂志,2017,44(4):643-645.
[26] 王静,王霆,韩智涛,等.薄荷醇抑制β淀粉样蛋白聚合保护神经细胞的实验研究[J].中国医药,2018,13(2):227-230. |
|
|
|