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Selective beta 1-Blockers Are Not Associated With New-onset Diabetes Mellitus in Hypertensive Patients

Authors
Park, YoonjeeChoi, Byoung GeolRha, Seung-WoonBaek, Man JongRyu, Yang GiChoi, Se YeonByun, Jae KyeongShim, Min SukMashaly, AhmedLi, HuJang, Won YoungKim, WoohyeunKang, Jun HyukChoi, Jah YeonPark, Eun JinPark, Sung HunLee, SunkiNa, Jin OhChoi, Cheol UngLim, Hong EuyKim, Eung JuPark, Chang GyuSeo, Hong SeogOh, Dong Joo
Issue Date
1월-2018
Publisher
LIPPINCOTT WILLIAMS & WILKINS
Keywords
selective ss 1-blockers; nonselective ss-blockers; new-onset diabetes mellitus; carvedilol; bisoprolol; hypertension
Citation
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, v.71, no.1, pp.38 - 45
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY
Volume
71
Number
1
Start Page
38
End Page
45
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/78539
ISSN
0160-2446
Abstract
Background: Although ss-blockers are known to increase new-onset diabetes mellitus (DM), previous evidence have been controversial. It has been suggested that newer vasodilatory ss-blockers yield better glycemic control than older nonselective agents. The aim of this study was to evaluate the diabetogenicity of currently used newer ss-blockers based on ss 1 receptor selectivity in a series of Asian population. Methods: We investigated a total of 65,686 hypertensive patients without DM from 2004 to 2014. Patients with hemoglobin (Hb) A1c <= 6.0%, fasting blood glucose <= 110 mg/dL, and no history of diabetes or diabetic treatment were enrolled for analysis. Patients were divided into the ss-blockers group and non-ss-blockers group. Propensity score matching (PSM) analysis using a logistic regression model was performed to adjust for potential confounders. The primary end point was the cumulative incidence of new-onset DM, defined as a fasting blood glucose >= 126 mg/dL or HbA1c >= 6.5%, and major adverse cardiac and cerebral events (MACCE), defined as a composite of total death, nonfatal myocardial infarction, and cerebrovascular accidents. We investigated predictors of new-onset DM and MACCE based on 2 models, including clinical risk factors and co-medications, respectively. Results: Mean follow-up duration was 30.91 +/- 23.14 months in the entire group before adjustment. The ss-blockers group had a significantly higher incidence of new-onset DM and MACCE than the non-ss-blockers group. After PSM, analysis of a total of 2284 patients (1142 pairs, C-statistic = 0.752) showed no difference between the 2 groups in new-onset DM or MACCE. In multivariate analysis after PSM, baseline HbA1c, stroke, heart failure, nonselective ss-blockers, and age were independent predictors of new-onset DM. Selective ss 1-blockers did not increase new-onset DM after adjustment for other antihypertensive medication and statins. Conclusions: In the era of newer ss-blockers, selective ss 1-blockers were not associated with new-onset DM. More evidence is needed to verify this relationship and the underlying mechanisms.
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