Dysregulation of kynurenine pathway and potential dynamic changes of kynurenine in schizophrenia: A systematic review and meta-analysis

被引:51
作者
Cao, Bing [1 ,2 ]
Chen, Yan [3 ]
Ren, Zhongyu [4 ]
Pan, Zihang [5 ,6 ]
McIntyre, Roger S. [6 ,7 ,8 ,9 ]
Wang, Dongfang [10 ,11 ]
机构
[1] Southwest Univ SWU, Fac Psychol, Key Lab Cognit & Personal, Minist Educ, Chongqing 400715, Peoples R China
[2] Southwest Univ, Natl Demonstrat Ctr Expt Psychol Educ, Chongqing, Peoples R China
[3] Univ Toronto, Dalla Lana Sch Publ Hlth, 155 Coll St, Toronto, ON, Canada
[4] Southwest Univ, Coll Phys Educ, Chongqing, Peoples R China
[5] Duke NUS Med Sch, Singapore, Singapore
[6] Univ Hlth Network, Mood Disorders Psychopharmacol Unit, Toronto, ON, Canada
[7] Univ Toronto, Dept Psychiat, Toronto, ON, Canada
[8] Univ Toronto, Dept Pharmacol, Toronto, ON, Canada
[9] Brain & Cognit Discovery Fdn, Toronto, ON, Canada
[10] Chongqing Med Univ, NHC Key Lab Diag & Treatment Brain Funct Dis, Affiliated Hosp 1, 1 Youyi St, Chongqing 400016, Peoples R China
[11] Chongqing Med Univ, Dept Neurol, Affiliated Hosp 1, Chongqing, Peoples R China
关键词
Schizophrenia; Kynurenine pathway; Kynurenic acid; Antipsychotic treatment; Tryptophan; CEREBROSPINAL-FLUID; AMINO-ACIDS; NMDA-RECEPTOR; TRYPTOPHAN 2,3-DIOXYGENASE; PLASMA TRYPTOPHAN; MEDICATION-NAIVE; SERUM; BRAIN; INDIVIDUALS; GLUTAMATE;
D O I
10.1016/j.neubiorev.2021.01.018
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
The kynurenine (KYN) pathway is postulated to play various roles in immune system dysregulation of schizophrenia (SCZ). We conducted a meta-analysis to explore the association between six key metabolites of KYN pathway (i.e., tryptophan (TRP), KYN, quinolinic acid (QUIN), and kynurenic acid (KYNA)) and SCZ. Priori Bonferroni adjustments were conducted for multiple comparisons. In total, 42 studies that examined the relationship between the metabolites in KYN pathway mentioned above and SCZ in 4217 participants and nine studies that examined alterations of these metabolites after antipsychotic treatments were included. The results demonstrate that (1) subjects with prescribed medication had significantly higher KYN levels when compared to controls; (2) higher KYN levels in cerebrospinal fluid (CSF), lower plasma KYN levels and higher CSF KYNA levels were associated with SCZ; (3) the KYN levels were higher in subjects with SCZ after antipsychotic treatments when compared with baseline. The evidence provides valuable insight of the potential underlying involvement of the KYN pathway in the pathogenesis of SCZ.
引用
收藏
页码:203 / 214
页数:12
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