首页> 美国卫生研究院文献>Frontiers in Aging Neuroscience >Association of Circulating Apolipoprotein AI Levels in Patients With Alzheimers Disease: A Systematic Review and Meta-Analysis
【2h】

Association of Circulating Apolipoprotein AI Levels in Patients With Alzheimers Disease: A Systematic Review and Meta-Analysis

机译:阿尔茨海默病患者循环载脂蛋白 AI 水平的关联:系统评价和荟萃分析

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

With the development of medicine, our research on Alzheimer's disease (AD) has been further deepened, but the mechanism of its occurrence and development has not been fully revealed, and there is currently no effective treatment method. Several studies have shown that apolipoprotein AI (ApoA-I) can affect the occurrence and development of Alzheimer's disease by binding to amyloid β (Aβ). However, the association between circulating levels of ApoA-I and AD remains controversial. We conducted a meta-analysis of 18 studies published between 1992 and 2017 to determine whether the ApoA-I levels in the blood and cerebrospinal fluid (CSF) are abnormal in AD. Literatures were searched in PubMed, EMBASE and Web of Science databases without language limitations. A pooled subject sample including 1,077 AD patients and 1,271 healthy controls (HCs) was available to assess circulating ApoA-I levels; 747 AD patients and 680 HCs were included for ApoA-I levels in serum; 246 AD patients and 456 HCs were included for ApoA-I levels in plasma; 201 AD patients and 447 HCs were included for ApoA-I levels in CSF. It was found that serum and plasma levels of ApoA-I were significantly reduced in AD patients compared with HCs {[standardized mean difference (SMD) = −1.16; 95% confidence interval (CI) (−1.72, −0.59); P = 0.000] and [SMD = −1.13; 95% CI (−2.05, −0.21); P = 0.016]}. Patients with AD showed a tendency toward higher CSF ApoA-I levels compared with HCs, although this difference was non-significant [SMD = 0.20; 95% CI (−0.16, 0.56); P = 0.273]. In addition, when we analyzed the ApoA-I levels of serum and plasma together, the circulating ApoA-I levels in AD patients was significantly lower [SMD = −1.15; 95% CI (−1.63, −0.66); P = 0.000]. These results indicate that ApoA-I deficiency may be a risk factor of AD, and ApoA-I has the potential to serve as a biomarker for AD and provide experimental evidence for diagnosis of AD.Systematic Review Registration: PROSPERO, identifier: 325961.
机译:随着医学的发展,我们对阿尔茨海默病 (AD) 的研究进一步深化,但其发生和发展的机制尚未完全揭示,目前尚无有效的治疗方法。几项研究表明,载脂蛋白 AI (ApoA-I) 可通过与淀粉样蛋白 β (Aβ) 结合来影响阿尔茨海默病的发生和发展。然而,ApoA-I 和 AD 循环水平之间的关联仍然存在争议。我们对 1992 年至 2017 年间发表的 18 项研究进行了荟萃分析,以确定 AD 患者血液和脑脊液 (CSF) 中 ApoA-I 水平是否异常。包括 1,077 名 AD 患者和 1,271 名健康对照 (HCs) 的合并受试者样本可用于评估循环 ApoA-I 水平;血清中 ApoA-I 水平纳入 747 例 AD 患者和 680 例 HCs;血浆中 ApoA-I 水平包括 246 例 AD 患者和 456 例 HCs;包括 201 例 AD 患者和 447 例 HCs 的 CSF 中 ApoA-I 水平。发现与 HCs 相比,AD 患者的血清和血浆 ApoA-I 水平显著降低 {[标准化平均差 (SMD) = -1.16;95% 置信区间 (CI) (-1.72, -0.59);P = 0.000] 和 [SMD = -1.13;95% CI (-2.05, -0.21);P = 0.016]}。与 HCs 相比,AD 患者表现出更高的 CSF ApoA-I 水平倾向,尽管这种差异不显著 [SMD = 0.20;95% CI (-0.16, 0.56);P = 0.273]。此外,当我们一起分析血清和血浆的 ApoA-I 水平时,AD 患者的循环 ApoA-I 水平显着降低 [SMD = -1.15;95% CI (-1.63, -0.66);P = 0.000]。这些结果表明,ApoA-I 缺乏可能是 AD 的危险因素,ApoA-I 有可能作为 AD 的生物标志物,并为 AD 的诊断提供实验证据。系统综述注册:PROSPERO,标识符:325961。

著录项

代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号