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Metabolites related to purine catabolism and risk of type 2 diabetes incidence; modifying effects of the TCF7L2-rs7903146 polymorphism.

Christopher PapandreouJun LiLiming LiangMònica BullóYan ZhengMiguel Ruiz-CanelaEdward YuMarta Guasch-FerréCristina RazquinAndrew T ChanDolores CorellaRamon EstruchEmilio RosMontserrat FitóFernando ArósLluís Serra-MajemNuria RosiqueMiguel A Martínez-GonzálezFrank B HuJordi Salas Salvadó
Published in: Scientific reports (2019)
Studies examining associations between purine metabolites and type 2 diabetes (T2D) are limited. We prospectively examined associations between plasma levels of purine metabolites with T2D risk and the modifying effects of transcription factor-7-like-2 (TCF7L2) rs7903146 polymorphism on these associations. This is a case-cohort design study within the PREDIMED study, with 251 incident T2D cases and a random sample of 694 participants (641 non-cases and 53 overlapping cases) without T2D at baseline (median follow-up: 3.8 years). Metabolites were semi-quantitatively profiled with LC-MS/MS. Cox regression analysis revealed that high plasma allantoin levels, including allantoin-to-uric acid ratio and high xanthine-to-hypoxanthine ratio were inversely and positively associated with T2D risk, respectively, independently of classical risk factors. Elevated plasma xanthine and inosine levels were associated with a higher T2D risk in homozygous carriers of the TCF7L2-rs7903146 T-allele. The potential mechanisms linking the aforementioned purine metabolites and T2D risk must be also further investigated.
Keyphrases
  • uric acid
  • type diabetes
  • risk factors
  • ms ms
  • transcription factor
  • metabolic syndrome
  • adipose tissue
  • high resolution
  • dna binding