| Literature DB >> 32612066 |
Masashi Isshiki1, Ichiro Sakuma2, Yasuaki Hayashino3, Takashi Sumita4, Kazuo Hara5, Kazuhisa Takahashi6, Ichiro Shiojima6, Noriko Satoh-Asahara7, Hiroji Kitazato8, Daisuke Ito1,4, Daigo Saito1,4, Masako Hatano1, Yuichi Ikegami1, Shinichiro Iida9, Akira Shimada1, Mitsuhiko Noda1,10.
Abstract
Sodium-glucose cotransporter-2 inhibitors (SGLT2Is) are reported to prevent cardiovascular events by a mechanism possibly including diuresis and sodium excretion. In this respect, diuresis-induced compensatory upregulation of the renin-angiotensin-aldosterone (RAA) system should be clarified and we performed a randomized controlled trial using dapagliflozin, an SGLT2I. Hypertensive diabetic patients taking angiotensin-converting enzyme inhibitors or angiotensin II receptor blockers were randomly assigned to a dapagliflozin group (DAPA) or a control group (CTRL) with the difference in the changes in plasma renin activity (PRA) after 24 weeks of the treatment as the primary outcome. PRA, plasma aldosterone concentration (PAC), age, sex, BMI, blood pressure, pulse rate, eGFRcys, and HbA1c were not different between the groups at baseline. After 24 weeks, the changes in the PRA from the baseline of the DAPA (n = 44) and CTRL (n = 39) groups were 6.30 ± 15.55 and 1.42 ± 11.43 ng/mL/h, respectively (p = 0.11) although the power of detection was too small. However, post hoc nonparametric analyses revealed that there was a definite increase in the PRA and PAC in the DAPA group (p < 0.0001 and p = 0.00025, respectively) but not in the CTRL group. The PRA in the DAPA group after 24 weeks treatment was significantly elevated compared to the CTRL group (p = 0.013) but not for the PAC. Accordingly, it would be suggested that dapagliflozin may not induce a profound increase, if any, in PAC after 24 weeks of treatment in hypertensive type 2 diabetic patients under RAA suppression.Entities:
Keywords: Aldosterone; Hypertension; Plasma renin activity; Renin-angiotensin-alsosterone system; Sodium–glucose cotransporter 2 inhibitors
Year: 2020 PMID: 32612066 DOI: 10.1507/endocrj.EJ20-0222
Source DB: PubMed Journal: Endocr J ISSN: 0918-8959 Impact factor: 2.349