Chronic Remote Ischemic Conditioning on Mild Hypertension in the Absence of Antihypertensive Medication: A Multicenter, Randomized, Double-Blind, Proof-of-Concept Clinical Trial

Author:

Guo Wenting1ORCID,Zhao Wenbo12ORCID,Li Dong3,Jia Haiying4,Ren Changhong2,Li Sijie5,Zhao Jing6,Yu Bingxin6,Dong Jian6,Guo Rongfen6,Zhu Kun6,Cao Yu6,Wang Yan2,Wang Ying3,Li Zunshan3,Wang Zhen4,Wang Dan4,Hou Chengbei7,Hausenloy Derek J8910,Chu Xi6ORCID,Ji Xunming11ORCID

Affiliation:

1. Department of Neurology (W.G., W.Z.), Xuanwu Hospital, Capital Medical University, Beijing, China.

2. Beijing Key Laboratory of Hypoxic Conditioning Translational Medicine (W.Z., C.R., Yan Wang), Xuanwu Hospital, Capital Medical University, Beijing, China.

3. Peking University Care Health Management Center, Beijing, China (D.L., Ying Wang, Z.L.).

4. Health Management Center, The 306 Hospital of People’s Liberation Army, Beijing, China (H.J., Z.W., D.W.).

5. Department of Emergency (S.L.), Xuanwu Hospital, Capital Medical University, Beijing, China.

6. Health Management Center (J.Z., B.Y., J.D., R.G., K.Z., Y.C., X.C.), Xuanwu Hospital, Capital Medical University, Beijing, China.

7. Center for Evidence-Based Medicine (C.H.), Xuanwu Hospital of Capital Medical University, Beijing, China.

8. Cardiovascular and Metabolic Disorders Program, Duke-National University of Singapore Medical School (D.J.H.).

9. National Heart Research Institute Singapore, National Heart Centre (D.J.H.).

10. Yong Loo Lin School of Medicine, National University Singapore (D.J.H.).

11. Department of Neurosurgery (X.J.), Xuanwu Hospital, Capital Medical University, Beijing, China.

Abstract

Background: Exploratory studies have shown that remote ischemic conditioning (RIC) has the potential to lower blood pressure (BP). We investigated whether chronic RIC reduces BP for hypertension. Methods: This is a multicenter, randomized, double-blind, parallel-controlled trial. Patients with an office BP of 130/80 to 160/100 mm Hg and a 24-hour average BP ≥125/75 mm Hg not on antihypertensive medications were recruited. After a 1-week compliance screening phase, they were randomly assigned in a 1:1 ratio to receive RIC or sham RIC twice daily for 4 weeks. The primary efficacy outcome was the change in 24-hour average systolic BP from baseline to 4 weeks. Safety events were assessed over the study period. Results: Ninety-five participants were randomly allocated to the RIC (n=49) and sham RIC (n=46) groups. In the intention-to-treat analysis, the reduction in 24-hour average systolic BP was greater in the RIC group than the sham RIC group (−4.6±9.5 versus −0.9±6.8 mm Hg; baseline-adjusted between-group mean difference: −3.6 mm Hg [95% CI, −6.9 to −0.3 mm Hg]; adjusted P =0.035). The per-protocol analysis showed that 24-hour average systolic BP reduced −5.9±8.6 mm Hg in the RIC group and −0.7±6.7 mm Hg in the sham RIC group (baseline-adjusted between-group mean difference: −5.2 mm Hg [95% CI, −8.5 to −1.9 mm Hg]; adjusted P =0.002). No major adverse events were reported in both groups. Conclusions: RIC is safe in patients with mild hypertension and may lower BP in the absence of antihypertensive medications. However, the effects of RIC on clinical outcomes in these patients require further investigation. Registration: URL: https://www.clinicaltrials.gov ; Unique identifier: NCT04915313.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Internal Medicine

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