Division of Cardiovascular Medicine, Jichi Medical University School of Medicine.
Kumamoto University Hospital.
Circ J. 2019 Feb 25;83(3):622-629. doi: 10.1253/circj.CJ-18-1018. Epub 2019 Feb 13.
SYMPLICITY HTN-Japan is a prospective, randomized, controlled trial comparing renal denervation (RDN) with standard pharmacologic therapy for treatment of uncontrolled hypertension (HTN).
Patients enrolled had uncontrolled HTN, defined as office systolic blood pressure (SBP) ≥160 mmHg and 24-h ambulatory SBP ≥135 mmHg, on ≥3 antihypertensive drugs of maximally tolerated dose for at least 6 weeks prior to enrollment. Randomization was 1:1 to RDN or maintenance of current medical therapy (control). Patients were followed every 6 months post-randomization for up to 36 months. There were 22 patients randomized to RDN and 19 to control, and 11 patients were crossed over and received RDN at 6 months post-randomization. For the RDN group (n=22), office SBP reduction was -32.8±20.1 mmHg and office DBP reduction was -15.8±12.6 mmHg at 36 months post-procedure, both P<0.001. For the combined RDN and crossover group (n=33), office SBP reduction was -26.7±18.9 mmHg and office DBP reduction was -12.7±11.8 mmHg at 30 months post-procedure, both P<0.001. There were no procedural-, device- or treatment-related safety events through 36 months.
SYMPLICITY HTN-Japan is the first randomized controlled trial to evaluate RDN in an Asian population. Despite the small number of enrollments, results show patients who received RDN therapy maintained SBP reduction out to 36 months.
SYMPLICITY HTN-Japan 是一项前瞻性、随机、对照临床试验,比较了肾去神经术(RDN)与标准药物治疗在治疗未控制高血压(HTN)中的疗效。
入选的患者患有未控制的 HTN,定义为诊室收缩压(SBP)≥160mmHg 和 24 小时动态 SBP≥135mmHg,在入组前至少 6 周内服用最大耐受剂量的≥3 种降压药物。随机分为 RDN 组或维持当前药物治疗(对照组),1:1 比例。患者在随机分组后每 6 个月随访一次,最长随访 36 个月。共有 22 例患者被随机分为 RDN 组,19 例患者被随机分为对照组,11 例患者在随机分组后 6 个月交叉接受 RDN 治疗。对于 RDN 组(n=22),术后 36 个月诊室 SBP 降低-32.8±20.1mmHg,诊室 DBP 降低-15.8±12.6mmHg,均 P<0.001。对于 RDN 组和交叉组(n=33),术后 30 个月诊室 SBP 降低-26.7±18.9mmHg,诊室 DBP 降低-12.7±11.8mmHg,均 P<0.001。至 36 个月时无手术、器械或治疗相关的安全性事件。
SYMPLICITY HTN-Japan 是第一项在亚洲人群中评估 RDN 的随机对照试验。尽管入组人数较少,但结果表明接受 RDN 治疗的患者可维持 SBP 降低至 36 个月。