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The effects of DPP4 inhibitors on the levels of plasma catecholamines and their metabolites in patients with type 2 diabetes

Authors
Kim, Tae HunLee, KiyoungPark, Ie ByungChoi, Cheol SooAhn, Tae HoonLee, Dae Ho
Issue Date
Oct-2019
Publisher
ELSEVIER IRELAND LTD
Keywords
Dipeptidyl peptidase 4; Catecholamines; Sympathetic nervous system; Dipeptidyl peptidase 4 inhibitors; Type 2 diabetes mellitus
Citation
DIABETES RESEARCH AND CLINICAL PRACTICE, v.156
Journal Title
DIABETES RESEARCH AND CLINICAL PRACTICE
Volume
156
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/18109
DOI
10.1016/j.diabres.2019.107832
ISSN
0168-8227
Abstract
Aims: Dipeptidyl peptidase 4 inhibitors (DPP4Is) can increase sympathetic activity. We aimed to evaluate the direct association between serum DPP4 activity and sympathetic activity in humans. Methods: Fasting serum DPP4 activity and plasma levels of catecholamines and their metabolites were measured in 211 patients with type 2 diabetes mellitus (T2DM) treated with DPP4I (n = 146) or non-DPP4I therapy (n = 65) and in healthy control subjects (n = 30). Results: Although there were no differences in plasma levels of catecholamines and their metabolites between the DPP4I and non-DPP4I groups, the levels in both of these groups were lower than those in the healthy control group. In DPP4I-treated patients, serum DPP4 activity showed an inverse correlation with plasma levels of norepinephrine (NE) (r = -0.339, p < 0.01), metanephrine (MET) (r = -0.251, p < 0.01) and normetanephrine (r = -0.312, p < 0.001). In addition, plasma MET level showed a weak inverse correlation with serum DPP4 activity in the combined T2DM group. In DPP4I-treated patients, the inverse correlation between DPP4 activity and plasma NE remained significant even after multiple adjustments. Conclusions: Our results suggest that although sympathetic activity is lower in patients with T2DM, the greater the suppression of DPP4 activity by DPP4I therapy, the greater the increase in sympathetic activity is, which may have clinical implications in high risk T2DM patients. (C) 2019 Elsevier B.V. All rights reserved.
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