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The kynurenine:tryptophan ratio as a predictor of incident type 2 diabetes mellitus in individuals with coronary artery disease.
Rebnord, Eirik W; Strand, Elin; Midttun, Øivind; Svingen, Gard F T; Christensen, Monika H E; Ueland, Per M; Mellgren, Gunnar; Njølstad, Pål R; Tell, Grethe S; Nygård, Ottar K; Pedersen, Eva R.
Afiliação
  • Rebnord EW; Department of Clinical Science, University of Bergen, Bergen, Norway. Eirik.Rebnord@gmail.com.
  • Strand E; KG Jebsen Centre for Diabetes Research, University of Bergen, Bergen, Norway. Eirik.Rebnord@gmail.com.
  • Midttun Ø; Department of Heart Disease, Haukeland University Hospital, Jonas Lies vei 65, 5021, Bergen, Norway. Eirik.Rebnord@gmail.com.
  • Svingen GFT; Department of Clinical Science, University of Bergen, Bergen, Norway.
  • Christensen MHE; Bevital, Bergen, Norway.
  • Ueland PM; Department of Heart Disease, Haukeland University Hospital, Jonas Lies vei 65, 5021, Bergen, Norway.
  • Mellgren G; Department of Clinical Science, University of Bergen, Bergen, Norway.
  • Njølstad PR; Department of Medicine, Haukeland University Hospital, Bergen, Norway.
  • Tell GS; Department of Clinical Science, University of Bergen, Bergen, Norway.
  • Nygård OK; Laboratory of Clinical Biochemistry, Haukeland University Hospital, Bergen, Norway.
  • Pedersen ER; Department of Clinical Science, University of Bergen, Bergen, Norway.
Diabetologia ; 60(9): 1712-1721, 2017 Sep.
Article em En | MEDLINE | ID: mdl-28612106
AIMS/HYPOTHESIS: The tryptophan metabolite kynurenine has potent immune modulatory and vasoactive properties. Experimental data implicate kynurenine in obesity-related morbidities. Epidemiological studies are, however, sparse. We evaluated associations of the plasma and urine kynurenine:tryptophan ratio (KTR) to incident type 2 diabetes. METHODS: We followed 2519 individuals with coronary artery disease (CAD; 73.1% men) without diabetes at baseline for a median of 7.6 years, during which 173 (6.9%) new incidences of type 2 diabetes were identified. Multivariate Cox regression analyses were applied to investigate the prospective relationships of plasma and urine KTR with new onset type 2 diabetes. RESULTS: At inclusion, mean (SD) age was 61.3 (10.4) years, BMI was 25.9 (3.71) kg/m2 and median (interquartile range) HbA1c was 5.6% (5.0%-6.0%) (38 [31-42] mmol/mol). Plasma KTR was not significantly related to type 2 diabetes risk. By contrast, urine KTR showed a strong positive association. Comparing quartile 4 with quartile 1, the HRs (95% CIs) were 2.59 (1.56, 4.30) and 2.35 (1.39, 3.96) in the age- and sex-adjusted and multivariate models, respectively. CONCLUSIONS/INTERPRETATION: Urine KTR is a strong predictor of incident type 2 diabetes in individuals with CAD. Potential clinical implications and possible pathogenic roles of renal kynurenine excretion in type 2 diabetes development should be further elucidated.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Triptofano / Diabetes Mellitus Tipo 2 / Cinurenina Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Triptofano / Diabetes Mellitus Tipo 2 / Cinurenina Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2017 Tipo de documento: Article