Key result
Post-transplant kynurenine serum levels increased with the severity of acute rejections (up to 16.9±9.1 nmol/ml in vascular rejections) and during infections.
Why the study?
Does kynurenine serum level have diagnostic value for inflammatory complications in kidney graft recipients?
Observational (n=355)
Does kynurenine serum level have diagnostic value for inflammatory complications in kidney graft recipients?
Serum kynurenine levels may serve as a reliable early diagnostic biomarker for post-transplant inflammatory complications such as acute rejection and infection in kidney allograft recipients.
May indicate inflammatory complications in kidney recipients; hypothesis-generating and requires prospective validation before clinical adoption.
BACKGROUND: Inflammatory events after kidney transplantation (Tx) may lead to activation of the tryptophane-catabolizing enzyme indoleamine 2,3-dioxygenase followed by the formation of kynurenine (KYN). Post-transplant KYN serum levels in kidney allograft recipients were analyzed for their diagnostic value. MATERIAL AND METHODS: This was a retrospective analysis of KYN levels (normal value: 2.7±0.6 nmol/ml) measured in 4083 blood samples collected from 355 kidney graft recipients in connection with uncomplicated courses, acute rejections (ARs), infections, and type of immunosuppression. We performed descriptive data analysis and analysis of variance. RESULTS: In 212 recipients with immediately functioning grafts, the KYN levels dropped from pre-Tx 13.3±5.9 nmol/ml to nearly normal values at day 5 (5.8±3.0 nmol/ml). In patients with delayed graft function, the KYN reduction started only after the last hemodialysis treatment. With respect to ARs in recipients with creatinine values <300 µmol/l pre-AR, the increase of KYN levels depended on the severity of ARs (steroid-sensitive ARs: from 4.5±1.4 to 6.0±6.1 nmol/ml; steroid-resistant ARs: from 6.1±3.1 to 12.9±7.1 nmol/ml; vascular rejections: from 5.8±3.0 to 16.9±9.1 nmol/ml). In patients with creatinine values ≥300 µmol/l pre-AR, a further increase of the KYN level (from 10.1 to 13.2 nmol/ml) was only observed in severe, steroid-resistant ARs. With respect to infections evaluated, the KYN levels before diagnosis/start of treatment were 5.7±3.4 nmol/ml in asymptomatic CMV infections, 7.5±4.4 nmol/ml in CMV diseases, 8.3±3.3 nmol/ml in pneumonia, and 10.4±6.5 nmol/ml in bacterial sepsis. CONCLUSIONS: Serum KYN seems to be a reliable diagnostic tool for the assessment of post-transplant inflammatory complications, already in an early stage, and for monitoring the efficacy of therapeutic interventions. Prospective studies are recommended.
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M. Marzinzig (2015) conducted an observational in Kidney transplantation (n=355). Kynurenine serum levels vs. Baseline or uncomplicated clinical course was evaluated on Kynurenine serum levels during acute rejections and infections. Post-transplant kynurenine serum levels increased with the severity of acute rejections (up to 16.9±9.1 nmol/ml in vascular rejections) and during infections.
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