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Association between Beta2-Adrenergic Receptor Agonists and the Risk of Vascular Complications in Diabetic Patients: A Population-Based Cohort Study

Authors :
Dong Cheol Han
Hyunjin Noh
Song Hee Oh
Jin Seok Jeon
Suyeon Park
Hee Jeong Lee
Hyoungnae Kim
Haekyung Lee
Kwang-Young Jung
Soon Hyo Kwon
Source :
Journal of Clinical Medicine, Volume 8, Issue 8, Journal of Clinical Medicine, Vol 8, Iss 8, p 1145 (2019)
Publication Year :
2019
Publisher :
MDPI AG, 2019.

Abstract

Beta2-adrenergic receptor (&beta<br />2AR) agonists can have protective effects targeting macrophage activation, but research on human subjects has not been done. This study was designed to assess the relationship between the use of &beta<br />2AR agonists and diabetic vascular complications. Using data from the Korean National Health Insurance Service, adults first diagnosed with diabetes in 2004 (n = 249,222) were followed up until 31 December 2015. Propensity score matching was performed between case and control groups (n = 5179 in each), and multivariate analysis was conducted. The &beta<br />2AR agonist group was divided into quartiles according to the duration of &beta<br />2AR agonist use. During the follow-up, the incidence of vascular complications gradually decreased as the duration of &beta<br />2AR agonist administration increased. Multivariate analysis revealed that the hazard ratio for all composite vascular complications was 0.80 (95% CI, 0.75&ndash<br />0.86, p &lt<br />0.001) in the longest quartile of &beta<br />2AR agonist use as compared with the control group after adjusting for confounding variables. The association between the duration of &beta<br />2AR agonist use and the risk of each vascular complication including cerebrovascular, peripheral vascular, peripheral neural, renal, and ophthalmic complications was consistent, and the risks were significantly lower in the longest users than the control group. Long-term use of &beta<br />2AR agonists may exert a protective effect against diabetic vascular complications.

Details

ISSN :
20770383
Volume :
8
Database :
OpenAIRE
Journal :
Journal of Clinical Medicine
Accession number :
edsair.doi.dedup.....96d5eef5d1eddd2f9334091152f4c113
Full Text :
https://doi.org/10.3390/jcm8081145