Why the study?
Diabetic nephropathy is the leading cause of end-stage renal disease among patients with CKD, prompting examination of the effects of long-term DPP-4 inhibitor use on all-cause mortality and renal disease progression in veterans.
Does long-term use of DPP-4 inhibitors reduce all-cause mortality and progression of renal disease in U.S. Veterans with type 2 diabetes?
Does long-term use of DPP-4 inhibitors reduce all-cause mortality and progression of renal disease in U.S. Veterans with type 2 diabetes?
Long-term use of DPP-4 inhibitors in U.S. Veterans with type 2 diabetes is associated with a significant reduction in all-cause mortality, incident heart failure, and CABG, independent of glucose control.
DPP-4 inhibitor use was associated with lower mortality in T2D veterans; leaves open causal effects and CKD impact.
OBJECTIVE: The prevalence of chronic kidney disease (CKD) in the United States is 13% of the general population. Among those with CKD, diabetic nephropathy is the leading cause of end-stage renal disease. This is a retrospective study examining the effect of long-term use of dipeptidyl peptidase-4 (DPP-4) inhibitors on all-cause mortality and progression of renal disease in the veteran population. METHODS: Data was extracted using the Veterans Administration Informatics and Computing Infrastructure. A large cohort of veterans diagnosed with type 2 diabetes mellitus were used to identify patients on DPP-4 inhibitors and without DPP-4 inhibitors. Groups were compared to determine the effect of DPP-4 inhibitors on the progression of CKD and all-cause mortality. Data were analyzed using SAS. RESULTS: Subjects in the treatment group (n = 40 558) had baseline variables (age, body mass index, race) similar to the control group (n = 40 558). Diabetes control improved in the treatment group (HgbA1c, 8.3% [67 mmol/mol] to 7.8% [62 mmol/mol]; P < .001) but not in the control group (HgbA1c, 7.4% [57 mmol/mol] to 7.3% [56 mmol/mol]). New diagnoses of heart failure and coronary artery bypass grafts were clinically significant (odds ratios = 0.66 and 0.52). No change in progression of CKD was seen in either group. All-cause mortality was reduced by 59%. CONCLUSION: We conclude that DPP-4 inhibitors are associated with a significant reduction in all-cause mortality independent of glucose control, albeit with no clear cause, including obtainable cardiovascular outcomes. Our data is consistent with prior trials in that DPP-4 inhibitors did not show a significant change in serum creatinine or microalbuminuria.
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Cristiano et al. (2021) studied this question.
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