Association between chronic low-grade inflammation and metabolic syndrome and their impact on the risk of coronary artery disease in type 1 diabetes

Evaluate the interplay between metabolic syndrome (MS) and chronic low-grade inflammation in type 1 diabetes at different stages of diabetic kidney disease, and to assess whether chronic low-grade inflammation, determined by high-sensitivity C-reactive protein (hs-CRP) increases coronary artery disease risk linked to MS. We included 4014 participants with type 1 diabetes from the Finnish Diabetic Nephropathy Study. Hs-CRP was dichotomized by the kidney disease group median for the survival analyses (above median indicated hs-CRP+ and below hs-CRP−). MS-/hs-CRP− was used as the reference category. Follow-up data on coronary artery disease were retrieved from hospital discharge registries and death certificates. Hs-CRP increased with the number of MS components, irrespective of diabetic kidney disease severity ( p < 0.001). In those with normal kidney status, the adjusted HR for coronary artery disease was 1.23 (0.87–1.75) for MS−/hs-CRP+, 1.28 (0.83–1.99) for MS+/hs-CRP−, and 1.53 (1.06–2.21) for MS+/hs-CRP+. In the group with albuminuria and eGFR >60 ml/min/1.73m 2 , neither MS+, hs-CRP+, nor their combinations were associated with increased risk of coronary artery disease. In the group with albuminuria and eGFR