Schulich School of Medicine and Dentistry, University of Western Ontario, London, ON, Canada.
Sandra Black Centre for Brain Resilience and Recovery, Sunnybrook Research Institute, Toronto, ON, Canada.
J Alzheimers Dis. 2022;88(4):1279-1292. doi: 10.3233/JAD-220360.
The endosomal-lysosomal and autophagy (ELA) pathway may be implicated in the progression of Alzheimer's disease (AD); however, findings thus far have been inconsistent.
To systematically summarize differences in endosomal-lysosomal and autophagy proteins in the cerebrospinal fluid (CSF) of people with AD and healthy controls (HC).
Studies measuring CSF concentrations of relevant proteins in the ELA pathway in AD and healthy controls were included. Standardized mean differences (SMD) with 95% confidence intervals (CI) between AD and healthy controls in CSF concentrations of relevant proteins were meta-analyzed using random-effects models.
Of 2,471 unique studies, 43 studies were included in the systematic review and meta-analysis. Differences in ELA protein levels in the CSF between AD and healthy controls were observed, particularly in lysosomal membrane (LAMP-1: NAD/NHC = 348/381, SMD [95% CI] = 0.599 [0.268, 0.930], I2 = 72.8%; LAMP-2: NAD/NHC = 401/510, SMD [95% CI] = 0.480 [0.134, 0.826], I2 = 78.7%) and intra-lysosomal proteins (GM2A: NAD/NHC = 390/420, SMD [95% CI] = 0.496 [0.039, 0.954], I2 = 87.7%; CTSB: NAD/NHC = 485/443, SMD [95% CI] = 0.201 [0.029, 0.374], I2 = 28.5%; CTSZ: NAD/NHC = 535/820, SMD [95% CI] = -0.160 [-0.305, -0.015], I2 = 24.0%) and in proteins involved in endocytosis (AP2B1:NAD/NHC = 171/205, SMD [95% CI] = 0.513 [0.259, 0.768], I2 = 27.4%; FLOT1: NAD/NHC = 41/45, SMD [95% CI] = -0.489 [-0.919, -0.058], I2 <0.01). LC3B, an autophagy marker, also showed a difference (NAD/NHC = 70/59, SMD [95% CI] = 0.648 [0.180, 1.116], I2 = 38.3%)), but overall there was limited evidence suggesting differences in proteins involved in endosomal function and autophagy.
Dysregulation of proteins in the ELA pathway may play an important role in AD pathogenesis. Some proteins within this pathway may be potential biomarkers for AD.
内体溶酶体和自噬(ELA)途径可能与阿尔茨海默病(AD)的进展有关;然而,迄今为止的研究结果并不一致。
系统总结 AD 患者和健康对照者(HC)脑脊液中 ELA 途径相关蛋白的差异。
纳入了测量 ELA 途径相关蛋白在 AD 和健康对照者脑脊液中浓度的研究。使用随机效应模型对 AD 和健康对照者脑脊液中相关蛋白浓度的标准化均数差(SMD)及其 95%置信区间(CI)进行荟萃分析。
在 2471 篇独特的研究中,有 43 篇研究被纳入系统评价和荟萃分析。AD 和 HC 之间 ELA 蛋白水平在脑脊液中存在差异,尤其是在溶酶体膜(LAMP-1:NAD/NHC=348/381,SMD[95%CI]=0.599[0.268, 0.930],I2=72.8%;LAMP-2:NAD/NHC=401/510,SMD[95%CI]=0.480[0.134, 0.826],I2=78.7%)和溶酶体内蛋白(GM2A:NAD/NHC=390/420,SMD[95%CI]=0.496[0.039, 0.954],I2=87.7%;CTSB:NAD/NHC=485/443,SMD[95%CI]=0.201[0.029, 0.374],I2=28.5%;CTSZ:NAD/NHC=535/820,SMD[95%CI]=-0.160[-0.305, -0.015],I2=24.0%)和参与内吞作用的蛋白(AP2B1:NAD/NHC=171/205,SMD[95%CI]=0.513[0.259, 0.768],I2=27.4%;FLOT1:NAD/NHC=41/45,SMD[95%CI]=-0.489[-0.919, -0.058],I2<0.01))中也存在差异。自噬标志物 LC3B 也存在差异(NAD/NHC=70/59,SMD[95%CI]=0.648[0.180, 1.116],I2=38.3%)),但总体而言,只有有限的证据表明内体功能和自噬相关蛋白存在差异。
ELA 途径中蛋白的失调可能在 AD 发病机制中起重要作用。该途径中的一些蛋白可能是 AD 的潜在生物标志物。