Institute of Acu-Mox, China Academy of Chinese Medical Sciences, 16# Nanxiao Street, Dongzhimennei, Beijing 100700, China.
BMC Complement Altern Med. 2014 Jun 26;14:203. doi: 10.1186/1472-6882-14-203.
BACKGROUND: Impaired glucose tolerance (IGT) is a pre-diabetic state of hyperglycemia that is associated with insulin resistance, increased risk of type II diabetes, and cardiovascular pathology. Recently, investigators hypothesized that decreased vagus nerve activity may be the underlying mechanism of metabolic syndrome including obesity, elevated glucose levels, and high blood pressure. METHODS: In this pilot randomized clinical trial, we compared the efficacy of transcutaneous auricular vagus nerve stimulation (taVNS) and sham taVNS on patients with IGT. 72 participants with IGT were single-blinded and were randomly allocated by computer-generated envelope to either taVNS or sham taVNS treatment groups. In addition, 30 IGT adults were recruited as a control population and not assigned treatment so as to monitor the natural fluctuation of glucose tolerance in IGT patients. All treatments were self-administered by the patients at home after training at the hospital. Patients were instructed to fill in a patient diary booklet each day to describe any side effects after each treatment. The treatment period was 12 weeks in duration. Baseline comparison between treatment and control group showed no difference in weight, BMI, or measures of systolic blood pressure, diastolic blood pressure, fasting plasma glucose (FPG), 2-hour plasma glucose (2hPG), or glycosylated hemoglobin (HbAlc). RESULTS: 100 participants completed the study and were included in data analysis. Two female patients (one in the taVNS group, one in the sham taVNS group) dropped out of the study due to stimulation-evoked dizziness. The symptoms were relieved after stopping treatment. Compared with sham taVNS, taVNS significantly reduced the two-hour glucose tolerance (F(2) = 5.79, p = 0.004). In addition, we found that taVNS significantly decreased (F(1) = 4.21, p = 0.044) systolic blood pressure over time compared with sham taVNS. Compared with the no-treatment control group, patients receiving taVNS significantly differed in measures of FPG (F(2) = 10.62, p < 0.001), 2hPG F(2) = 25.18, p < 0.001) and HbAlc (F(1) = 12.79, p = 0.001) over the course of the 12 week treatment period. CONCLUSIONS: Our study suggests that taVNS is a promising, simple, and cost-effective treatment for IGT/ pre-diabetes with only slight risk of mild side-effects.
背景:糖耐量受损(IGT)是一种高血糖的糖尿病前期状态,与胰岛素抵抗、II 型糖尿病风险增加和心血管病理有关。最近,研究人员假设迷走神经活动的减少可能是包括肥胖、血糖升高和高血压在内的代谢综合征的潜在机制。
方法:在这项初步的随机临床试验中,我们比较了经皮耳迷走神经刺激(taVNS)和假 taVNS 对 IGT 患者的疗效。72 名 IGT 患者进行了单盲,并通过计算机生成的信封随机分配到 taVNS 或 sham taVNS 治疗组。此外,还招募了 30 名 IGT 成年人作为对照组,不给予治疗,以监测 IGT 患者血糖耐量的自然波动。所有治疗均由患者在家中自行进行,在医院接受培训后进行。患者每天填写患者日记手册,描述每次治疗后的任何副作用。治疗期为 12 周。治疗组和对照组的基线比较显示,体重、BMI 或收缩压、舒张压、空腹血糖(FPG)、2 小时血糖(2hPG)或糖化血红蛋白(HbAlc)的测量值无差异。
结果:100 名参与者完成了研究并纳入数据分析。两名女性患者(一名在 taVNS 组,一名在 sham taVNS 组)因刺激诱发的头晕而退出研究。停止治疗后症状缓解。与 sham taVNS 相比,taVNS 显著降低了两小时糖耐量(F(2) = 5.79,p = 0.004)。此外,我们发现 taVNS 与 sham taVNS 相比,收缩压随时间的变化显著降低(F(1) = 4.21,p = 0.044)。与无治疗对照组相比,接受 taVNS 的患者在 FPG(F(2) = 10.62,p < 0.001)、2hPG F(2) = 25.18,p < 0.001)和 HbAlc(F(1) = 12.79,p = 0.001)方面有显著差异。在 12 周的治疗过程中。
结论:我们的研究表明,taVNS 是一种有前途的、简单的、具有成本效益的 IGT/糖尿病前期治疗方法,只有轻微的轻度副作用风险。
BMC Complement Altern Med. 2014-6-26
Bioelectron Med. 2025-4-30
Front Endocrinol (Lausanne). 2025-3-27
Clin Auton Res. 2024-12
Bioelectron Med. 2023-4-27
BMC Complement Altern Med. 2012-12-14
Nat Rev Endocrinol. 2012-12
J Neural Transm (Vienna). 2012-11-2
Lancet. 2012-6-9
Clin Sci (Lond). 2012-4
Eur J Pharmacol. 2011-10-12
Can J Cardiol. 2009-6