Department of Cardiovascular Science and Medicine, Chiba University Graduate School of Medicine, Chuo-ku, Chiba, Japan.
Clin Exp Hypertens. 2012;34(2):86-91. doi: 10.3109/10641963.2011.628729. Epub 2012 Jan 17.
The Candesartan Cooperative Research of Therapy Design for Early Morning Hypertension in CHIBA was designed to investigate whether switching from angiotensin II receptor blockers (ARBs) except candesartan to candesartan might be effective in Japanese patients with morning hypertension. Seventy-eight mild to moderate hypertensive patients, who were treated with the standard doses of ARBs except candesartan (losartan, 50 mg; valsartan, 80 mg; telmisartan, 40 mg; or olmesartan, 20 mg), were entered into 12-week treatment period with candesartan 8 mg according to a multicenter, open-label design. Morning and office blood pressures (BPs) were significantly reduced (morning, -10.1 ± 10.5/-4.5 ± 8.4 mm Hg; office, -13.1 ± 17.3/-6.2 ± 11.3 mm Hg) after medication change. Target BPs (morning BPs ≤ 135/85 mm Hg and office BPs ≤ 140/90 mm Hg) achievement rates were 42.9% in the morning and 64.3% at office. No adverse events were recognized in all patients. Candesartan treatment significantly reduced the morning and office BPs compared with other ARBs in Japanese patients with morning hypertension.
Candesartan 协作研究治疗清晨高血压的设计旨在探讨是否将除坎地沙坦以外的血管紧张素 II 受体阻滞剂(ARB)转换为坎地沙坦对日本清晨高血压患者有效。78 名轻度至中度高血压患者,使用除坎地沙坦(氯沙坦 50mg;缬沙坦 80mg;替米沙坦 40mg;奥美沙坦 20mg)以外的标准剂量 ARB 治疗,根据多中心、开放标签设计进入为期 12 周的坎地沙坦 8mg 治疗期。服药后,清晨和诊室血压(BP)显著降低(清晨:-10.1±10.5/-4.5±8.4mmHg;诊室:-13.1±17.3/-6.2±11.3mmHg)。目标 BP(清晨 BP≤135/85mmHg,诊室 BP≤140/90mmHg)的达标率分别为 42.9%和 64.3%。所有患者均未出现不良反应。与其他 ARB 相比,坎地沙坦治疗可显著降低日本清晨高血压患者的清晨和诊室 BP。