Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease (Oct 2024)

Low‐Level Tragus Stimulation Attenuates Blood Pressure in Young Individuals With Hypertension: Results From a Small‐Scale Single‐Blind Controlled Randomized Clinical Trial

  • Muisha B. Mbikyo,
  • Ai Wang,
  • Qun Ma,
  • Linlin Miao,
  • Nan Cui,
  • Yiqing Yang,
  • Haoran Fu,
  • Yingxian Sun,
  • Zhao Li

DOI
https://doi.org/10.1161/JAHA.123.032269
Journal volume & issue
Vol. 13, no. 19

Abstract

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Background Hypertension is a significant risk factor for cardiovascular and chronic kidney diseases. Its management in young people remains limited. Device‐based therapies, such as low‐level tragus stimulation (LL‐TS), a noninvasive method that reduces sympathetic activity, have recently been explored for resistant hypertension. Methods and Results This trial involved patients with Grade 1 hypertension with no other medical history. LL‐TS (20 Hz, 1 mA, 1 h/day) was applied for 3 months on the tragus (Intervention group [IG]) or earlobe (Control group [CG]). Blood pressure and outcomes were assessed at the first, second, and third months. Among 40 patients, 21 were in IG and 19 in CG. Baseline systolic blood pressure was similar between IG (142.62±8.18 mm Hg) and CG (143.00±8.61 mm Hg), P=0.89. Post‐LL‐TS, systolic blood pressure showed significant reductions in IG compared with CG at the first (IG: 134.47±5.95 mm Hg, CG: 141.28±6.78 mm Hg, P=0.002), second (IG: 132.50±7.51 mm Hg, CG: 140.62±7.15 mm Hg, P=0.001), and third months (IG: 128.81±7.13 mm Hg, CG: 136.51±7.96 mm Hg, P=0.003). diastolic blood pressure also differed significantly: first month (IG: 85.34±5.81 mm Hg, CG: 89.74±6.32 mm Hg, P=0.03), second month (IG: 82.12±5.22 mm Hg, CG: 88.57±7.11 mm Hg, P=0.002), and third month (IG: 80.71±5.96 mm Hg, CG: 87.55±5.26 mm Hg, P=0.001). Heart rate was unchanged (P>0.05). Only 0.01% of IG subjects reported site irritation, with no serious adverse events. Conclusions LL‐TS led to significant blood pressure reductions in young patients with essential hypertension. Further larger trials are needed to confirm the safety and efficacy of LL‐TS. Registration URL: https://www.chictr.org.cn/; Unique identifier: ChiCTR2000038448.

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