TY - JOUR
T1 - Statin Use and Risk of Diabetes by Subclinical Atherosclerosis Burden (from a Multi-Ethnic Study of Atherosclerosis Report)
AU - Al Rifai, Mahmoud
AU - Szklo, Moyses
AU - Patel, Jaideep
AU - Blaha, Michael J.
AU - Ballantyne, Christie M.
AU - Bittner, Vera
AU - Morris, Pamela
AU - McEvoy, John W.
AU - Shapiro, Michael D.
AU - Al-Mallah, Mouaz H.
AU - Greenland, Philip
AU - Virani, Salim S.
N1 - Funding Information:
The Multi-Ethnic Study of Atherosclerosis ( MESA) projects are conducted and supported by the National Heart, Lung, and Blood Institute, Bethesda, Maryland , in collaboration with MESA investigators. Support for MESA is provided by contracts 75N92020D00001 , HHSN268201500003I , N01-HC-95159 , 75N92020D00005 , N01-HC-95160 , 75N92020D00002 , N01-HC-95161 , 75N92020D00003 , N01-HC-95162 , 75N92020D00006 , N01-HC-95163 , 75N92020D00004 , N01-HC-95164 , 75N92020D00007 , N01-HC-95165 , N01-HC-95166 , N01-HC-95167 , N01-HC-95168 , N01-HC-95169 , UL1-TR-000040 , UL1-TR-001079 , and UL1-TR-001420 . This study is also supported in part by the National Center for Advancing Translational Sciences, Bethesda, Maryland, Clinical and Translational Science Institute grant UL1TR001881 and the National Institute of Diabetes and Digestive and Kidney Disease, Bethesda, Maryland, Diabetes Research Center grant DK063491 to the Southern California Diabetes Endocrinology Research Center.
Funding Information:
Dr. Virani reports research support from Department of Veterans Affairs, World Heart Federation, and Tahir and Jooma Family; honorarium from American College of Cardiology (associate editor for innovations, acc.org). Dr. Greenland reports grants from National Institute of Health and American Heart Association. Dr. Bittner reports funding through contracts between UAB and the sponsor, VB was National Coordinator for the STRENGTH Trial (AstraZeneca) and the Dalgene trial (DalCor); is the national coordinator for the CLEAR Outcomes trial and a steering committee member for the ODYSSEY OUTCOMES trial (Sanofi/Regeneron); serves as site principal investigator for the ORION IV trial (Novartis); completed a consultantship with Pfizer in 2021 and currently serves on a Data Safety and Monitoring Board for Verve Therapeutics. Dr. Shapiro reports institutional research support from National Institutes of Health, Amgen, Novartis, Ionis, Regeneron; is part of the scientific advisory boards for Amgen, Novartis, Novo Nordisk; and is a consultant from Regeneron. Dr. Ballantyne reports grant/research support from (all paid to the institution and not to the individual): Abbott Diagnostic, Akcea, Amgen, Arrowhead, Esperion, Ionis, Merck, Novartis, Novo Nordisk, Regeneron, Roche Diagnostic, National Institutes of Health, American Heart Association and the American Diabetes Association. Consultant- 89Bio, Abbott Diagnostics, Alnylam Pharmaceuticals, Althera, Amarin, Amgen, Arrowhead, Astra Zeneca, Denka Seiken*, Esperion, Genentech, Gilead, Illumina, Matinas BioPharma Inc, Merck, New Amsterdam*, Novartis, Novo Nordisk, Pfizer, Regeneron, Roche Diagnostic, and Sanofi-Synthelabo. The remaining authors have no conflicts of interest to declare.
Funding Information:
The Multi-Ethnic Study of Atherosclerosis (MESA) projects are conducted and supported by the National Heart, Lung, and Blood Institute, Bethesda, Maryland, in collaboration with MESA investigators. Support for MESA is provided by contracts 75N92020D00001, HHSN268201500003I, N01-HC-95159, 75N92020D00005, N01-HC-95160, 75N92020D00002, N01-HC-95161, 75N92020D00003, N01-HC-95162, 75N92020D00006, N01-HC-95163, 75N92020D00004, N01-HC-95164, 75N92020D00007, N01-HC-95165, N01-HC-95166, N01-HC-95167, N01-HC-95168, N01-HC-95169, UL1-TR-000040, UL1-TR-001079, and UL1-TR-001420. This study is also supported in part by the National Center for Advancing Translational Sciences, Bethesda, Maryland, Clinical and Translational Science Institute grant UL1TR001881 and the National Institute of Diabetes and Digestive and Kidney Disease, Bethesda, Maryland, Diabetes Research Center grant DK063491 to the Southern California Diabetes Endocrinology Research Center.
Publisher Copyright:
© 2022 Elsevier Inc.
PY - 2022/12/1
Y1 - 2022/12/1
N2 - Although there is a significant reduction in atherosclerotic cardiovascular disease risk with statins, a higher risk of diabetes mellitus has been demonstrated in randomized clinical trials. The risk of incident diabetes with statins may be heterogeneous by presence of coronary artery calcium (CAC). We evaluated participants without prevalent diabetes at baseline from the MESA (Multi-Ethnic Study of Atherosclerosis), a prospective cohort study of subjects free of clinical cardiovascular disease at baseline. We used multivariable-adjusted Cox proportional hazards models to study the association between statin use and incident diabetes, adjusting for sociodemographic and cardiovascular risk factors, including time-varying statin use and stratifying by baseline CAC (0, 1 to 100, ≥100). The study population included 5,943 participants with a mean (SD) age of 62 (10) years, 54% women, 41% White, 26% Black, 12% Chinese-American, and 21% Hispanic. In the unadjusted analyses, statin use was associated with a higher risk of incident diabetes (hazard ratio [HR] 1.62, 95% confidence interval [CI] 1.27 to 2.06). After adjustment, this risk was no longer significant (HR 1.13, 95% CI 0.83 to 1.54). Although imprecise, the HR expressing the association of statins with diabetes was lower for those with CAC = 0 (HR 0.80, 95% CI 0.45 to 1.40) than for those with a higher CAC burden (HR 1.30, 95% CI 0.71 to 2.39 for CAC 1 to 100 and HR 1.39, 95% CI 0.85 to 2.28 for CAC ≥100), but this heterogeneity was not statistically significant. In conclusion, statin therapy was not significantly associated with incident diabetes mellitus in this observational study. The risk of incident diabetes did not significantly differ by baseline CAC.
AB - Although there is a significant reduction in atherosclerotic cardiovascular disease risk with statins, a higher risk of diabetes mellitus has been demonstrated in randomized clinical trials. The risk of incident diabetes with statins may be heterogeneous by presence of coronary artery calcium (CAC). We evaluated participants without prevalent diabetes at baseline from the MESA (Multi-Ethnic Study of Atherosclerosis), a prospective cohort study of subjects free of clinical cardiovascular disease at baseline. We used multivariable-adjusted Cox proportional hazards models to study the association between statin use and incident diabetes, adjusting for sociodemographic and cardiovascular risk factors, including time-varying statin use and stratifying by baseline CAC (0, 1 to 100, ≥100). The study population included 5,943 participants with a mean (SD) age of 62 (10) years, 54% women, 41% White, 26% Black, 12% Chinese-American, and 21% Hispanic. In the unadjusted analyses, statin use was associated with a higher risk of incident diabetes (hazard ratio [HR] 1.62, 95% confidence interval [CI] 1.27 to 2.06). After adjustment, this risk was no longer significant (HR 1.13, 95% CI 0.83 to 1.54). Although imprecise, the HR expressing the association of statins with diabetes was lower for those with CAC = 0 (HR 0.80, 95% CI 0.45 to 1.40) than for those with a higher CAC burden (HR 1.30, 95% CI 0.71 to 2.39 for CAC 1 to 100 and HR 1.39, 95% CI 0.85 to 2.28 for CAC ≥100), but this heterogeneity was not statistically significant. In conclusion, statin therapy was not significantly associated with incident diabetes mellitus in this observational study. The risk of incident diabetes did not significantly differ by baseline CAC.
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U2 - 10.1016/j.amjcard.2022.08.040
DO - 10.1016/j.amjcard.2022.08.040
M3 - Article
C2 - 36192199
AN - SCOPUS:85139075695
SN - 0002-9149
VL - 184
SP - 7
EP - 13
JO - American Journal of Cardiology
JF - American Journal of Cardiology
ER -