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Novel inflammatory markers for incident pre-diabetes and type 2 diabetes: the Rotterdam Study.

Adela BrahimajSymen LigthartMohsen GhanbariMohammad Arfan IkramAlbert HofmanOscar H FrancoMaryam KavousiAbbas Dehghan
Published in: European journal of epidemiology (2017)
During a follow-up of up to 14.7 years (between April 1, 1997, and Jan 1, 2012) 139 cases of pre-diabetes, 110 cases of T2D and 26 cases of insulin initiation were identified. In age and sex adjusted Cox models, IL13 (HR = 0.78), EN-RAGE (1.30), CFH (1.24), IL18 (1.22) and CRP (1.32) were associated with incident pre-diabetes. IL13 (0.62), IL17 (0.75), EN-RAGE (1.25), complement 3 (1.44), IL18 (1.35), TNFRII (1.27), IL1ra (1.24) and CRP (1.64) were associated with incident T2D. In multivariate models, IL13 (0.77), EN-RAGE (1.23) and CRP (1.26) remained associated with pre-diabetes. IL13 (0.67), IL17 (0.76) and CRP (1.32) remained associated with T2D. IL13 (0.55) was the only marker associated with initiation of insulin therapy in diabetics. Various inflammatory markers are associated with progression from normoglycemia to pre-diabetes (IL13, EN-RAGE, CRP), T2D (IL13, IL17, CRP) or insulin therapy start (IL13). Among them, EN-RAGE is a novel inflammatory marker for pre-diabetes, IL17 for incident T2D and IL13 for pre-diabetes, incident T2D and insulin therapy start.
Keyphrases
  • type diabetes
  • cardiovascular disease
  • glycemic control
  • rheumatoid arthritis
  • stem cells
  • mesenchymal stem cells
  • insulin resistance
  • oxidative stress
  • skeletal muscle
  • disease activity