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使用应用于外耳的振动触觉装置对类风湿性关节炎进行试验性治疗。

Investigational treatment of rheumatoid arthritis with a vibrotactile device applied to the external ear.

作者信息

Addorisio Meghan E, Imperato Gavin H, de Vos Alex F, Forti Steve, Goldstein Richard S, Pavlov Valentin A, van der Poll Tom, Yang Huan, Diamond Betty, Tracey Kevin J, Chavan Sangeeta S

机构信息

1Center for Biomedical Science and Bioelectronic Medicine, Feinstein Institute for Medical Research, Northwell Health, Manhasset, NY USA.

2Elmezzi Graduate School of Molecular Medicine, Feinstein Institute for Medical Research, Northwell Health, Manhasset, NY USA.

出版信息

Bioelectron Med. 2019 Apr 17;5:4. doi: 10.1186/s42234-019-0020-4. eCollection 2019.

Abstract

BACKGROUND

Rheumatoid arthritis (RA) is a chronic and debilitating inflammatory disease characterized by extensive joint tissue inflammation. Implantable bioelectronic devices targeting the inflammatory reflex reduce TNF production and inflammation in preclinical models of inflammatory disease, and in patients with RA and Crohn's disease. Here, we assessed the effect of applying a vibrotactile device to the cymba concha of the external ear on inflammatory responses in healthy subjects, as well as its effect on disease activity in RA patients.

METHODS

Six healthy subjects received vibrotactile treatment at the cymba concha, and TNF production was analyzed at different time points post-stimulation. In a separate study, nineteen healthy subjects were enrolled in a randomized cross-over study, and effects of vibrotactile treatment at either the cymba concha or gastrocnemius on cytokine levels were assessed. In addition, the clinical efficacy of vibrotactile treatment on disease activity in RA was assessed in nine patients with RA in a prospective interventional study.

RESULTS

Vibrotactile treatment at the cymba concha reduced TNF levels, and the suppressive effect persisted up to 24 h. In the cross-over study with 19 healthy subjects, vibrotactile treatment at the cymba concha but not at the gastrocnemius significantly reduced TNF, IL-1β, and IL-6 levels compared to pre-treatment baseline (TNF  < 0.05, IL-6  < 0.01, IL-1β  < 0.001). In healthy subjects, vibrotactile treatment at the cymba concha inhibited TNF by 80%, IL-6 by 73%, and IL-1β by 50% as compared to pre-treatment baseline levels. In RA patients, a significant decrease in DAS28-CRP scores was observed two days post-vibrotactile stimulation at the cymba concha (DAS28-CRP score pre-treatment = 4.19 ± 0.33 vs post-treatment = 3.12 ± 0.25,  < 0.05). Disease activity remained significantly reduced 7 days following vibrotactile treatment (DAS28-CRP score 7 days post-treatment = 2.79 ± 0.21,  < 0.01). In addition, a persistent improvement in visual analogue scale scores, a patient derived measure of global health assessment, was observed in RA patients following vibrotactile treatment.

CONCLUSION

Application of a vibrotactile device to the cymba concha inhibits peripheral blood production of TNF, IL-1β, and IL-6 in healthy subjects, and attenuates systemic inflammatory responses in RA patients.

TRIAL REGISTRATIONS

ClinicalTrials.gov Identifier: NCT01569789 and NCT00859859. The AMC trial conducted in The Netherlands does not have a ClinicalTrials.gov Identifier.

摘要

背景

类风湿性关节炎(RA)是一种慢性致残性炎症性疾病,其特征为广泛的关节组织炎症。在炎症性疾病的临床前模型以及类风湿性关节炎和克罗恩病患者中,靶向炎症反射的可植入生物电子设备可减少肿瘤坏死因子(TNF)的产生并减轻炎症。在此,我们评估了在外耳耳甲腔应用振动触觉设备对健康受试者炎症反应的影响,以及对类风湿性关节炎患者疾病活动度的影响。

方法

六名健康受试者在耳甲腔接受振动触觉治疗,并在刺激后的不同时间点分析TNF的产生情况。在另一项研究中,19名健康受试者参与了一项随机交叉研究,评估了在耳甲腔或腓肠肌进行振动触觉治疗对细胞因子水平的影响。此外,在一项前瞻性干预研究中,对9名类风湿性关节炎患者评估了振动触觉治疗对疾病活动度的临床疗效。

结果

耳甲腔的振动触觉治疗降低了TNF水平,且抑制作用持续长达24小时。在对19名健康受试者的交叉研究中,与治疗前基线相比,耳甲腔而非腓肠肌的振动触觉治疗显著降低了TNF、白细胞介素-1β(IL-1β)和白细胞介素-6(IL-6)水平(TNF <0.05,IL-6 <0.01,IL-1β <0.001)。与治疗前基线水平相比,在健康受试者中,耳甲腔的振动触觉治疗使TNF降低了80%,IL-6降低了73%,IL-1β降低了50%。在类风湿性关节炎患者中,耳甲腔振动触觉刺激后两天观察到疾病活动评分(DAS28-CRP)显著下降(治疗前DAS28-CRP评分为4.19±0.33,治疗后为3.12±0.25,<0.05)。振动触觉治疗7天后疾病活动度仍显著降低(治疗后7天DAS28-CRP评分为2.79±0.21,<0.01)。此外,在类风湿性关节炎患者中,振动触觉治疗后观察到视觉模拟量表评分持续改善,这是一种由患者得出的整体健康评估指标。

结论

在外耳耳甲腔应用振动触觉设备可抑制健康受试者外周血中TNF、IL-1β和IL-6的产生,并减轻类风湿性关节炎患者的全身炎症反应。

试验注册

ClinicalTrials.gov标识符:NCT01569789和NCT00859859。在荷兰进行的AMC试验没有ClinicalTrials.gov标识符。

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