TY - JOUR
T1 - Statins and atherosclerotic cardiovascular outcomes in patients on incident dialysis and with atherosclerotic heart disease
AU - Shavadia, Jay S.
AU - Wilson, Jonathan
AU - Edmonston, Daniel
AU - Platt, Alyssa
AU - Ephraim, Patti
AU - Hall, Rasheeda
AU - Goldstein, Benjamin A.
AU - Boulware, L. Ebony
AU - Peterson, Eric
AU - Pendergast, Jane
AU - Scialla, Julia J.
N1 - Funding Information:
This work was supported in part by the National Institutes of Health's (NIH's) National Institute for Diabetes and Digestive and Kidney Diseases under R01DK111952 to J. J. Scialla and an educational award from the Duke Clinical Research Institute to J. S. Shavadia. Additional support was provided by the National Center for Advancing Translational Sciences of the NIH under Award Number UL1TR002553 . This work reflects the opinions of the authors and does reflect the official views of the NIH or the National Institute for Diabetes and Digestive and Kidney Diseases.
Funding Information:
The data reported here have been supplied by the USRDS. The interpretation and reporting of these data are the responsibility of the authors and in no way should be seen as an official policy or interpretation of the US government. This work was supported in part by the National Institutes of Health's (NIH's) National Institute for Diabetes and Digestive and Kidney Diseases under R01DK111952 to J. J. Scialla and an educational award from the Duke Clinical Research Institute to J. S. Shavadia. Additional support was provided by the National Center for Advancing Translational Sciences of the NIH under Award Number UL1TR002553. This work reflects the opinions of the authors and does reflect the official views of the NIH or the National Institute for Diabetes and Digestive and Kidney Diseases. All authors report no relevant conflicts of interest.
Publisher Copyright:
© 2020 Elsevier Inc.
PY - 2021/1
Y1 - 2021/1
N2 - Statins failed to reduce cardiovascular (CV) events in trials of patients on dialysis. However, trial populations used criteria that often excluded those with atherosclerotic heart disease (ASHD), in whom statins have the greatest benefit, and included outcome composites with high rates of nonatherosclerotic CV events that may not be modified by statins. Here, we study whether statin use associates with lower atherosclerotic CV risk among patients with known ASHD on dialysis, including in those likely to receive a kidney transplant, a group excluded within trials but with lower competing mortality risks. Methods: Using data from the United States Renal Data System including Medicare claims, we identified adults initiating dialysis with ASHD. We matched statin users 1:1 to statin nonusers with propensity scores incorporating hard matches for age and kidney transplant listing status. Using Cox models, we evaluated associations of statin use with the primary composite of fatal/nonfatal myocardial infarction and stroke (including within prespecified subgroups of younger age [<50 years] and waitlisting status); secondary outcomes included all-cause mortality and the composite of all-cause mortality, nonfatal myocardial infarction, or stroke. Results: Of 197,716 patients with ASHD, 47,562 (24%) were consistent statin users from which we created 46,186 matched pairs. Over a median 662 days, statin users had similar risk of fatal/nonfatal myocardial infarction or stroke overall (hazard ratio [HR] 1.00, 95% CI 0.97-1.02), or in subgroups (age< 50 years [HR = 1.05, 95% CI 0.95-1.17]; waitlisted for kidney transplant [HR 0.99, 95% CI 0.97-1.02]). Statin use was modestly associated with lower all-cause mortality (HR 0.96, 95% CI 0.94-0.98; E value = 1.21) and, similarly, a modest lower composite risk of all-cause mortality, nonfatal myocardial infarction, or stroke over the first 2 years (HR 0.90, 95% CI 0.88-0.91) but attenuated thereafter (HR 0.98, 95% CI 0.96-1.01). Conclusions: Our large observational analyses are consistent with trials in more selected populations and suggest that statins may not meaningfully reduce atherosclerotic CV events even among incident dialysis patients with established ASHD and those likely to receive kidney transplants.
AB - Statins failed to reduce cardiovascular (CV) events in trials of patients on dialysis. However, trial populations used criteria that often excluded those with atherosclerotic heart disease (ASHD), in whom statins have the greatest benefit, and included outcome composites with high rates of nonatherosclerotic CV events that may not be modified by statins. Here, we study whether statin use associates with lower atherosclerotic CV risk among patients with known ASHD on dialysis, including in those likely to receive a kidney transplant, a group excluded within trials but with lower competing mortality risks. Methods: Using data from the United States Renal Data System including Medicare claims, we identified adults initiating dialysis with ASHD. We matched statin users 1:1 to statin nonusers with propensity scores incorporating hard matches for age and kidney transplant listing status. Using Cox models, we evaluated associations of statin use with the primary composite of fatal/nonfatal myocardial infarction and stroke (including within prespecified subgroups of younger age [<50 years] and waitlisting status); secondary outcomes included all-cause mortality and the composite of all-cause mortality, nonfatal myocardial infarction, or stroke. Results: Of 197,716 patients with ASHD, 47,562 (24%) were consistent statin users from which we created 46,186 matched pairs. Over a median 662 days, statin users had similar risk of fatal/nonfatal myocardial infarction or stroke overall (hazard ratio [HR] 1.00, 95% CI 0.97-1.02), or in subgroups (age< 50 years [HR = 1.05, 95% CI 0.95-1.17]; waitlisted for kidney transplant [HR 0.99, 95% CI 0.97-1.02]). Statin use was modestly associated with lower all-cause mortality (HR 0.96, 95% CI 0.94-0.98; E value = 1.21) and, similarly, a modest lower composite risk of all-cause mortality, nonfatal myocardial infarction, or stroke over the first 2 years (HR 0.90, 95% CI 0.88-0.91) but attenuated thereafter (HR 0.98, 95% CI 0.96-1.01). Conclusions: Our large observational analyses are consistent with trials in more selected populations and suggest that statins may not meaningfully reduce atherosclerotic CV events even among incident dialysis patients with established ASHD and those likely to receive kidney transplants.
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U2 - 10.1016/j.ahj.2020.10.055
DO - 10.1016/j.ahj.2020.10.055
M3 - Article
C2 - 33096103
AN - SCOPUS:85095949780
SN - 0002-8703
VL - 231
SP - 36
EP - 44
JO - American Heart Journal
JF - American Heart Journal
ER -