4.1 Article

Association of Serum Triglycerides and Renal Outcomes among 1.6 Million US Veterans

Journal

NEPHRON
Volume 146, Issue 5, Pages 457-468

Publisher

KARGER
DOI: 10.1159/000522388

Keywords

Triglycerides; End-stage renal disease; Chronic kidney disease; Metabolic syndrome; Renal function decline

Funding

  1. NIH/NIDDK mid-career award [K24-DK091419]
  2. Office of Research and Development of the Department of VAs [IK2- CX 001266-01, 1IK- CX 001043-01A2]

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The study suggests that elevated triglycerides (TGs) levels are associated with a higher incidence of chronic kidney disease (CKD) and a faster decline in renal function, independent of other components of metabolic syndrome (MetS). However, in CKD stages 4-5, the association between TGs and time to end-stage renal disease (ESRD) is null or inverse.
Background: Previous studies have suggested that metabolic syndrome (MetS) components are associated with renal outcomes, defined as a decline in kidney function or reaching end-stage renal disease (ESRD). Elevated triglycerides (TGs) are a component of MetS that have been reported to be associated with renal outcomes. However, the association of TGs with renal outcomes in chronic kidney disease (CKD) patients independent of the other components of the MetS remains understudied. Methods: We examined 1,657,387 patients with data on TGs and other components of MetS in 2004-2006 and followed up until 2014. Patients with ESRD on renal replacement therapy were excluded. We examined time to ESRD, estimated glomerular filtration rate (eGFR) slope (renal function decline), and time to incident CKD (eGFR <60 mL/min/1.73 m(2)) among baseline normal kidney function (non-CKD) patients, using Cox or logistic regression, adjusted for clinical characteristics and MetS components. We also stratified analyses by the number of MetS components. Results: The cohort was on average 64 years old and comprised 5% females, 15% African Americans, and 24% with nondialysis-dependent CKD. Among non-CKD patients, the adjusted relationship of TGs with time to incident CKD was strong and linear. Compared to TGs 120-<160 mg/dL, higher TGs were associated with a faster renal function decline across all CKD stages. Elevated TGs >= 240 mg/dL were associated with a faster time to ESRD among non-CKD and CKD stages 3A-3B, while the risk gradually declined to null or lower in CKD stages 4-5. Models were robust after MetS component adjustment and stratification. Conclusion: Independent of MetS components, high TGs levels were associated with a higher incidence of CKD and a faster renal function decline, yet showed no or inverse associations with time to ESRD in CKD stages 4-5. Examining the effects of TGs-lowering interventions on incident CKD and kidney preserving therapy warrants further studies including clinical trials.

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