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Blood pressure reduction with empagliflozin in Japanese patients with type 2 diabetes and cardiovascular diseases: a post-hoc sub-analysis of the placebo-controlled randomized EMBLEM trial

  • Atsushi Tanaka,
  • Michio Shimabukuro,
  • Hiroki Teragawa,
  • Hisako Yoshida,
  • Yosuke Okada,
  • Toshinari Takamura,
  • Isao Taguchi,
  • Shigeru Toyoda,
  • Hirofumi Tomiyama,
  • Shinichiro Ueda,
  • Yukihito Higashi,
  • Koichi Node,
  • Junya Ako,
  • Hirohisa Amano,
  • Itaru Hisauchi,
  • Yumi Ikehara,
  • Hideaki Jinnouchi,
  • Yoshiyuki Kawano,
  • Kazuo Kimura,
  • Akira Kurozumi,
  • Takaaki Kusumoto,
  • Noritaka Machii,
  • Tatsuya Maruhashi,
  • Yasushi Matsuzawa,
  • Hirofumi Misu,
  • Manabu Narisawa,
  • Tsuguhito Ota,
  • Jun-ichi Oyama,
  • Masashi Sakuma,
  • Kazuki Shiina,
  • Kosuke R. Shima,
  • Seigo Sugiyama,
  • Kunihiro Suzuki,
  • Naohiko Takahashi,
  • Yasuhiko Takemoto,
  • Yumie Takeshita,
  • Hiroshi Tamaki,
  • Kenichi Tanaka,
  • Akira Tamura,
  • Keiichi Torimoto,
  • Minako Yamaoka-Tojo,
  • Hiroki Uehara,
  • Fumi Uemura,
  • Ken Yamakawa,
  • Kunio Yufu

摘要

Detailed effect of sodium-glucose cotransporter 2 inhibitors on blood pressure (BP) in Japanese patients with type 2 diabetes (T2D) at a high risk of cardiovascular disease (CVD) is not fully understood. In this post-hoc sub-analysis of placebo-controlled randomized EMBLEM trial for Japanese patients with T2D and CVD, 105 participants (empagliflozin N = 52, placebo N = 53) were included, and office systolic/diastolic BPs and mean arterial pressure (MAP) over 24 weeks were estimated using mixed-effects models for repeated measures. Empagliflozin therapy, compared to placebo, reduced systolic/diastolic BPs (mean group difference in change from baseline to week 24; −5.9 [95% confidence interval (CI), −10.4 to −1.4] mmHg/−2.9 [95% CI, −6.2 to 0.4] mmHg) and MAP ( − 3.8 [95% CI, −7.0 to −0.7] mmHg). The systolic BP reduction was almost consistent across differing background clinical characteristics and usage status of anti-hypertensive medications.