Abstract
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.

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Acknowledgements
The authors thank all participants, investigators, board members, and medical staff involved in the EMBLEM trial.
on behalf of the EMBLEM Investigators
Junya Ako12, Hirohisa Amano13, Itaru Hisauchi14, Yumi Ikehara15, Hideaki Jinnouchi16, Yoshiyuki Kawano17, Kazuo Kimura18, Akira Kurozumi19, Takaaki Kusumoto20, Noritaka Machii21, Tatsuya Maruhashi22, Yasushi Matsuzawa18, Hirofumi Misu23, Manabu Narisawa19, Tsuguhito Ota23, Jun-ichi Oyama24, Masashi Sakuma13, Kazuki Shiina25, Kosuke R. Shima23, Seigo Sugiyama16, Kunihiro Suzuki13, Naohiko Takahashi26, Yasuhiko Takemoto27, Yumie Takeshita23, Hiroshi Tamaki28, Kenichi Tanaka19, Akira Tamura17, Keiichi Torimoto19, Minako Yamaoka-Tojo12, Hiroki Uehara29, Fumi Uemura19, Ken Yamakawa30, Kunio Yufu26
Funding
The EMBLEM trial was funded by Boehringer Ingelheim and Eli Lilly and Company. The funders of the trial had no role in the study design, data collection, data analysis, or data interpretation, or writing of the paper. Boehringer Ingelheim was given the opportunity to review the manuscript for medical and scientific accuracy as it relates to Boehringer Ingelheim substances, as well as intellectual property considerations.
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A.T. received honoraria from Nippon Boehringer Ingelheim and Mochida and research funding from GlaxoSmithKline, Takeda, Bristol-Myers Squibb, and Novo Nordisk Pharma. M.S. received honorarium and an endowed chair from Boehringer Ingelheim. H.Te. received lecture fees from Bayer, Boehringer Ingelheim, Daiichi Sankyo, Kowa, Takeda, Mitsubishi Tanabe, and Sanwa Kagaku Kenkyusyo. Y.O. received lecture fees from MSD, Mitsubishi Tanabe, Novo Nordisk Pharma, Eli Lilly Japan, Novartis Pharma, Kissei, Kowa, and Sumitomo Pharma and research fund from Kissei. T.T. received lecture fees from Kowa and Taisho and research grants from Kowa and Taisho. S.T. received honoraria from Daiichi Sankyo, AstraZeneca, Bayer, Nippon Boehringer Ingelheim, TSUMURA, and Novo Nordisk Pharma. Y.H. received grants from Mitsubishi Tanabe Pharma Corporation, Teijin Pharma Limited, Boehringer Ingelheim GmbH, Merck Sharp & Dohme Corporation, Sanofi Kabushiki Kaisya, AstraZeneca Kabushiki Kaisya, Kyowa Hakko Kirin Company Limited, Takeda Pharmaceutical Company Limited, Astellas Pharma Incorporated, Daiichi Sankyo Company Limited, Mochida Pharmaceutical Company Limited, Nihon Kohden Corporation, Shionogi Company Limited, Nippon Sigmax Company Limited, Sanwa Kagaku Kenkyusho Company Limited, Unex Corporation, and Kao Corporation, and honoraria from Radiometer Limited, Omron Corporation, Sumitomo Dainippon Pharma Company Limited, Otsuka Pharmaceutical Company Limited, Torii Pharmaceutical Company Limited, Kowa Company Limited, Fujiyakuhin Company Limited, Amgen Astellas BioPharma Kabushiki Kaisya, Nippon Shinyaku Company Limited, Itamar Medical Limited, Bayer Holding Limited, Eli Lilly Kabushiki Kaisya, and Ono Pharmaceutical Company Limited. K.N. received honoraria from AstraZeneca, Bayer Yakuhin, Nippon Boehringer Ingelheim, Daiichi Sankyo, Eli Lilly Japan, Kowa, Mitsubishi Tanabe Pharma, MSD, Novartis Pharma, Novo Nordisk Pharma, Ono Pharmaceutical, Otsuka, and Takeda Pharmaceutical, research grants from Asahi Kasei, Astellas, Nippon Boehringer Ingelheim, Fuji Yakuhin, Mitsubishi Tanabe Pharma, Mochida Pharmaceutical, Novartis Pharma, and Teijin Pharma, and scholarship from Bayer Yakuhin, Medtronic, and Teijin Pharma. Other authors declare no competing interests.
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Tanaka, A., Shimabukuro, M., Teragawa, H. et al. 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. Hypertens Res 47, 2295–2302 (2024). https://doi.org/10.1038/s41440-024-01725-4
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DOI: https://doi.org/10.1038/s41440-024-01725-4
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