Impaired kynurenine metabolism in patients with primary Sjo spacing diaeresis gren's syndrome

被引:4
|
作者
Onmaz, Duygu Eryavuz [1 ,5 ]
Tezcan, Dilek [2 ]
Abusoglu, Sedat [1 ]
Sak, Firdevs [1 ]
Yerlikaya, Fatma Humeyra [1 ]
Yilmaz, Sema [2 ]
Abusoglu, Gulsum [3 ]
Korez, Muslu Kazim [4 ]
Unlu, Ali [1 ]
机构
[1] Selcuk Univ, Fac Med, Dept Biochem, TR-42130 Konya, Turkiye
[2] Selcuk Univ, Fac Med, Div Rheumatol, TR-42130 Konya, Turkiye
[3] Selcuk Univ, Vocat Sch Hlth, Dept Med Lab Tech, TR-42130 Konya, Turkiye
[4] Selcuk Univ, Fac Med, Div Biostat, TR-42130 Konya, Turkiye
[5] Selcuk Univ, Fac Med, Biochem Dept, Alaaddin Keykubat Campus, TR-42075 Konya, Turkiye
关键词
Primary Sjo ?gren?s syndrome; Kynurenine pathway; Immunomudulatory; Inflammation; PRIMARY SJOGRENS-SYNDROME; QUINOLINIC ACID; MECHANISMS; DIAGNOSIS;
D O I
10.1016/j.clinbiochem.2023.01.007
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Objectives: Primary Sjo spacing diaeresis gren's syndrome (pSS) is an autoinflammatory disease characterized by inflammation of the exocrine glands. Elevated inflammation causes an increase in kynurenine pathway (KP) metabolite levels by activating indoleamine 2,3-dioxygenase (IDO). The aim of this study was to measure serum KP metabolite concentrations in patients with pSS and to evaluate the relationship between these metabolites with disease activity score and clinical manifestations.Design & Methods: A total of 80 patients with pSS and 80 healthy controls were enrolled in this study. Serum tryptophan (TRP), kynurenine (KYN), kynurenic acid (KYNA), 3-hydroxyanthranilic acid (3HAA), 3-hydroxyky-nurenine (3HK), quinolinic acid (QUIN) concentrations were quantified with liquid chromatography with tan-dem mass spectrometry (LC-MS/MS). Demographic characteristics, clinical manifestations and disease activity score (ESSDAI) of the participants were recorded.Results: The serum level of KYN and QUIN were significantly higher in patients with pSS with low and moderate activity compared those healthy controls, while the serum level of TRP, KYNA/KYN and 3HK/KYN were lower. In addition, the significant difference for the serum level of KYNA was only in patients with moderate activity from healthy controls, and the difference was higher in favor of pSS patients. Moreover, the KYN/TRP levels were significantly increased with disease activity. The ESSDAI score was positively correlated with KYN/TRP ratio, but negatively correlated with KYNA/KYN ratio.Conclusions: These findings indicated that KP metabolites may play a role in the etiopathogenesis, activation and progression of pSS.
引用
收藏
页码:1 / 10
页数:10
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