Aims: To investigate whether metabolic syndrome (MetS) could predict renal outcome in patients with established chronic kidney disease (CKD).
Materials and Methods:We enroled 2500 patients with CKD stage 1-4 from the Integrated CKD care programme, Kaohsiung for delaying Dialysis (ICKD) prospective observational study. 66.9% and 49.2% patients had MetS and diabetes (DM), respectively. We accessed three clinical outcomes, including all-cause mortality, RRT, and 50% decline in estimated glomerular filtration rate events.
Results:The MetS score was positively associated with proteinuria, inflammation, and nutrition markers. In fully adjusted Cox regression, the hazard ratio (HR) (95% confidence interval) of MetS for composite renal outcome (renal replacement therapy, and 50% decline of renal function) in the DM and non-DM subgroups was 1.56 (1.15-2.12) and 1.31 (1.02-1.70), respectively, while that for all-cause mortality was 1.00 (0.71-1.40) and 1.27 (0.92-1.74). Blood pressure is the most important component of MetS for renal outcomes. In the 2 by 2 matrix, compared with the non-DM/non-MetS group, the DM/MetS group (HR: 1.62 (1.31-2.02)) and the non-DM/MetS group (HR: 1.33 (1.05-1.69)) had higher risks for composite renal outcome, whereas the DM/MetS group had higher risk for all-cause mortality (HR:1.43 (1.09-1.88)).
Conclusions: MetS could predict renal outcome in patients withCKD stage 1-4 independent of DM. K E Y W O R D S chronic kidney disease, diabetes mellitus, metabolic syndrome, renal outcomes 1 | INTRODUCTION Metabolic syndrome (MetS) is a cluster of medical conditions, including hypertension (HTN), impaired glucose tolerance, central obesity, and dyslipidaemia. 1 MetS increments the risk of diabetes (DM), cardiovascular disease, and chronic kidney disease (CKD) 2 and is the trigger of cardiorenal metabolic disease. Patients with MetS may progress from normoglycaemia to overt DM resulting from a gradual β-cell function decline. DM is one of the most relevant risk factors for both heart failure and end-stage renal disease (ESRD) and