Abstract
Intensive antihypertensive treatment decreases cardiovascular disease and mortality risks in chronic kidney disease (CKD), whereas extremely low systolic blood pressure (SBP) is associated with worsening kidney function and poor prognosis. Although the SBP variation is particularly large in patients with CKD, the optimal lower limit of SBP target is unclear. In a nationwide, multicenter cohort study of patients with an estimated glomerular filtration rate (eGFR) < 45 mL/min/1.73 m2, we evaluated the association between the eGFR slopes and the lower limit of SBP target at ≥110 mmHg using a linear mixed-effects model and an instrumental variable method. The instrumental variable was calculated as the facility-level percentage of nephrologists who answered in the survey that their lower limit of SBP target was 110 mmHg or higher. A total of 1320 patients (mean age 70 years; 66% men) were included. The mean eGFR slope ± standard deviation over the four years to baseline was –2.48 ± 2.15 mL/min/1.73 m2/year. The instrumental variable for the lower limit of SBP target at ≥110 mmHg (vs. ≤100 mmHg) was associated with less eGFR decline (coefficient: +1.05 mL/min/1.73 m2/year; 95% confidence interval: 0.33–1.77), while unassociated with a history of cardiovascular disease. The renoprotective effect was particularly larger in the subgroups of the elderly and those with a history of cardiovascular disease. In conclusion, the lower limit of SBP target at 110 mmHg or higher was associated with improved eGFR slope, suggesting the importance of aiming at avoiding excessively low SBP in patients with advanced CKD.
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Acknowledgements
We thank all the nephrology specialists in Japan who responded to our Reach-J survey, the Scientific Committee: Dr. Kunitoshi Iseki, Dr. Kouichi Asahi, Dr. Junichi Hoshino, the staff members of Department of Nephrology, University of Tsukuba: Dr. Chie Saito, Dr. Hirayasu Kai, Dr. Kei Nagai, Dr. Ryoya Tsunoda, the staff members of Department of Health Care Policy and Health Economics, University of Tsukuba: Dr. Masahide Kondo, Dr. Reiko Okubo, Ms. Yukiko Ito, all the staff members of the Tsukuba Clinical Research & Development Organization (T-CReDO), University of Tsukuba, and Mr. Yoshihiro Ishihara and other staff members of Flexible Inc., for their contribution to our work.
the REACH-J CKD collaborators
Tomoya Hirayama8, Nobuhiko Togashi9, Akira Sugiura10, Kunihiro Yamagata11, Tatsuo Shiigai12, Kazue Ueki13, Ken Kikkawa14, Tsukasa Nakamura15, Eiichi Sato15, Hideki Matsukuma16, Shinsuke Harasawa17, Takehiko Washio17, Yuko Shibuya18, Hitoshi Tagawa19, Takashi Yasuda19, Shuzo Kobayashi20, Masaki Nagasawa21, Minako Wakasugi22, Hajime Yamazaki23, Michio Matsumoto24, Shoichi Maruyama25, Norihiro Suga26, Keiichi Tamagaki27, Taiko Kimura28, Tsutomu Tabata29, Yoshihiro Tsujimoto29, Shinichi Nishi30, Yuriko Yonekura31, Hitoshi Sugiyama32, Naoki Kashihara33, Tadashi Sofue34, Kazuhiko Tsuruya35, Toshiaki Nakano35, Masato Tadokoro36, Shoichi Fujimoto37, Masao Kikuchi37, Kiyoyuki Tokuyama38
Funding
This study was supported by a Grant-in-Aid for Research on Advanced Chronic Kidney Disease (REACH-J), Practical Research Project for Renal Diseases from the Japan Agency for Medical Research and Development (AMED under grant numbers: JP17ek0310005 and JP20ek0310010).
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YY has received honoraria from Astellas, AstraZeneca, Kowa, Mitsubishi Tanabe, and Mochida. SM has received grants and/or research funding from Chugai, Mitsubishi Tanabe, Ono, and ROHTO; honoraria from Alexion, Astellas, AstraZeneca, Bayer, and Mitsubishi Tanabe. HO has received honoraria from Astellas, AstraZeneca, Daiichi Sankyo, Kyowa Kirin, Mitsubishi Tanabe, and Torii. NK has received consulting fees from Kyowa Kirin and Novo Nordisk; honoraria from Astellas, AstraZeneca, Kyowa Kirin, Novartis, Ono, and Otsuka; payment for expert testimony from Kissei and Kyowa Kirin. KY has received grants from Kyowa Kirin and Mitsubishi Tanabe. All other authors reported no conflicts of interest.
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Kurasawa, S., Yasuda, Y., Kato, S. et al. Relationship between the lower limit of systolic blood pressure target and kidney function decline in advanced chronic kidney disease: an instrumental variable analysis from the REACH-J CKD cohort study. Hypertens Res 46, 2478–2487 (2023). https://doi.org/10.1038/s41440-023-01358-z
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DOI: https://doi.org/10.1038/s41440-023-01358-z
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