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 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 <60 ml/min/1.73m 2 , only those with MS+/hs-CRP− had an increased risk of coronary artery disease adjusted HR 2.00 (1.06–3.77). Chronic low-grade inflammation is associated with the MS in type 1 diabetes, irrespective of kidney disease severity. Hs-CRP adds to the coronary artery disease risk associated with the MS only in those without diabetic kidney disease. • Hs-CRP is linked to metabolic syndrome (MS) in type 1 diabetes. • The association between hs-CRP and MS was irrespective of kidney disease severity. • Hs-CRP and MS add to the coronary artery disease (CAD) risk in type 1 diabetes. • Their additive impact on CAD risk was confined to those without kidney disease. • Hs-CRP and MS in type 1 diabetes might offer improved risk-stratification for CAD.
Blomqvist et al. (Wed,) studied this question.