Kynurenine pathway dysregulation in cognitive impairment and dementia: a systematic review and meta-analysis

IF 5.3 2区 医学 Q1 GERIATRICS & GERONTOLOGY
Kyonghwan Choe, Lieke Bakker, Daniel L. A. van den Hove, Simone J. P. M. Eussen, Gunter Kenis, Inez H. G. B. Ramakers, Frans R. J. Verhey, Bart P. F. Rutten, Sebastian Köhler
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引用次数: 0

Abstract

The kynurenine pathway (KP) might be involved in pathophysiological processes associated with dementia, but clinical studies reported contradictory results. This systematic review and meta-analysis summarized the available evidence for (i) differences in KP metabolites in patients with cognitive impairment compared to cognitively healthy individuals and (ii) associations between KP metabolites and cognitive functioning. English, full-length articles with prospective, cross-sectional, or case–control study designs, published in Pubmed, Embase, PsychINFO, or the Cochrane Database of Systematic Reviews up to October 2023, were included. Random-effects meta-analyses of standardized mean differences (SMD) were performed. Heterogeneity, meta-regression, small study bias, and study quality assessments were carried out. Of 8797 retrieved studies, 98 were eligible for the systematic review. Meta-analyses comparing Alzheimer’s disease (AD) dementia patients to controls (n = 27 studies) indicated lower CSF levels of tryptophan (SMD = − 0.26 [95% CI − 0.41, − 0.12]), 3-hydroxykynurenine (− 0.21 [− 0.39, − 0.04]), anthranilic acid (− 0.28 [− 0.48, − 0.08]), and quinolinic acid (− 0.38 [− 0.56, − 0.21]) in AD dementia, while CSF levels of kynurenic acid were higher (0.18 [0.01, 0.35]). Blood levels of tryptophan (− 0.39 [− 0.51, − 0.28]), kynurenic acid (− 0.31 [− 0.47, − 0.15]), xanthurenic acid (− 0.34 [− 0.54, − 0.15]), and 3-hydroxyanthranilic acid (− 0.42 [− 0.61, − 0.22]) were lower in AD dementia. For some of these metabolites, similar directions were observed in meta-analyses comparing individuals with mild cognitive impairment with controls, although the number of included studies in these analyses was relatively small (n = 11). Associations with cognitive test scores were inconclusive and generally non-significant. These results suggest that AD dementia is associated with lower blood levels of several KP metabolites. Findings challenge current assumptions of neurotoxic quinolinic acid levels being associated with dementia. 

认知障碍和痴呆中犬尿氨酸通路失调:系统回顾和荟萃分析
摘要犬尿氨酸通路(KP)可能参与痴呆相关的病理生理过程,但临床研究结果相互矛盾。本系统综述和荟萃分析总结了现有证据:(1)认知障碍患者与认知健康个体相比KP代谢物的差异;(2)KP代谢物与认知功能之间的关联。纳入了2023年10月前发表于Pubmed、Embase、PsychINFO或Cochrane系统评价数据库的前瞻性、横断面或病例对照研究设计的英文全文文章。对标准化平均差异(SMD)进行随机效应荟萃分析。异质性、meta回归、小研究偏倚和研究质量评估进行了评估。在检索到的8797项研究中,有98项符合系统评价。meta分析显示,阿尔茨海默病(AD)痴呆患者与对照组(n = 27项研究)的脑脊液中色氨酸(SMD = - 0.26 [95% CI - 0.41, - 0.12])、3-羟基犬尿氨酸(- 0.21[- 0.39,- 0.04])、苯胺酸(- 0.28[- 0.48,- 0.08])和喹啉酸(- 0.38[- 0.56,- 0.21])水平较低,而犬尿酸水平较高(0.18[0.01,0.35])。AD痴呆患者血液中色氨酸(- 0.39[- 0.51,- 0.28])、犬尿酸(- 0.31[- 0.47,- 0.15])、黄嘌呤酸(- 0.34[- 0.54,- 0.15])和3-羟基苯甲酸(- 0.42[- 0.61,- 0.22])水平较低。对于其中一些代谢物,在比较轻度认知障碍个体与对照组的荟萃分析中观察到类似的方向,尽管这些分析中纳入的研究数量相对较少(n = 11)。与认知测试成绩的关联不确定,通常不显著。这些结果表明AD痴呆与血液中几种KP代谢物水平降低有关。研究结果挑战了目前关于神经毒性喹啉酸水平与痴呆有关的假设。
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来源期刊
GeroScience
GeroScience Medicine-Complementary and Alternative Medicine
CiteScore
10.50
自引率
5.40%
发文量
182
期刊介绍: GeroScience is a bi-monthly, international, peer-reviewed journal that publishes articles related to research in the biology of aging and research on biomedical applications that impact aging. The scope of articles to be considered include evolutionary biology, biophysics, genetics, genomics, proteomics, molecular biology, cell biology, biochemistry, endocrinology, immunology, physiology, pharmacology, neuroscience, and psychology.
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