The human body responds to inflammation, such as psoriatic skin lesions, by activating the cholinergic anti-inflammatory pathway. In patients with plaque psoriasis, this pathway is not sufficient to clear the skin lesions. Importantly, the vagus nerve, that is part of the anti-inflammatory pathway, also innervates the ear where it can be activated through non-invasive transcutaneous auricular vagus nerve stimulation (taVNS). This raises the research question if taVNS - added to standard of care - improves the symptoms of plaque psoriasis by augmenting the function of the cholinergic anti-inflammatory pathway. Thus, the aim of this project is to test the hypothesis that daily taVNS applied for 3 months results in anti-inflammatory actions and improvements in the Psoriasis Area and Severity Index (PASI). Potential anti-inflammatory actions of taVNS compared to a sham-taVNS control group will be assessed by plasma cytokine levels, flow cytometry, and cell culture experiments. This project is potentially significant, because it may demonstrate that taVNS lessens the symptoms of plaque psoriasis and, therefore, improves the quality of life of millions of patients.
An estimated 20% of psoriasis patients experience treatment failure. Afferent vagal nerve fibers that are part of the anti-inflammatory reflex sense inflammation, such as psoriatic skin lesions. The investigators' pilot data show that transcutaneous auricular vagus nerve stimulation (taVNS) activates afferent nerve fibers within the auricular branch of the vagus nerve to trigger anti-inflammatory reflex responses in healthy individuals. However, it is unknown if taVNS improves plaque psoriasis through the anti-inflammatory reflex. The lack of studies on taVNS in plaque psoriasis constitutes a missed opportunity to reduce treatment failures. The long-term goal of this research is to establish a neuromodulatory approach to activate the anti-inflammatory reflex in patients with plaque psoriasis to lessen treatment failures. The objective of this study is to test the hypothesis that taVNS elicits anti-inflammatory reflex responses and reduces the severity of plaque psoriasis. In a single-blinded randomized controlled clinical trial, participants will self-administer taVNS or sham-taVNS (control) daily for a duration of 3 months, while continuing their standard-of-care treatment. At baseline, 7 days, and 1, 2, and 3 months, clinical , autonomic, and inflammatory responses will be assessed. At the conclusion of this study, the investigators expect to demonstrate anti-inflammatory reflex responses to taVNS and reduced severity of plaque psoriasis. These outcomes are expected to have important positive impact, because they are anticipated to reduce treatment failures in patients with plaque psoriasis.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
50
A bipolar clip electrode is placed at the cymba conchae of the ear. Through this bipolar clip electrode, afferent nerve fibers within the auricular branch of the vagus nerve will be stimulated. Subjects self-administer the stimulation on a daily basis for 3 months.
A bipolar clip electrode is placed at the cymba conchae of the ear. However, active stimulation of the afferent nerve fibers within the auricular branch of the vagus nerve will not occur, because the electrode wire is electrically interrupted. Subjects self-administer the sham taVNS on a daily basis for 3 months.
Burrell College of Osteopathic Medicine
Las Cruces, New Mexico, United States
RECRUITINGChange in Psoriasis Area and Severity Index from Baseline at 1 Week
Clinical assessment of the severity of plaque psoriasis
Time frame: After 1 week of treatment.
Change in Psoriasis Area and Severity Index from Baseline at 1 Month
Clinical assessment of the severity of plaque psoriasis
Time frame: After 1 month of treatment.
Change in Psoriasis Area and Severity Index from Baseline at 2 Months
Clinical assessment of the severity of plaque psoriasis
Time frame: After 2 months of treatment.
Change in Psoriasis Area and Severity Index from Baseline at 3 Months
Clinical assessment of the severity of plaque psoriasis
Time frame: After 3 months of treatment.
Change in Heart Rate Variability from Baseline at 1 Week
Heart rate variability will be determined from ECG recordings
Time frame: After 1 week of treatment.
Change in Heart Rate Variability from Baseline at 1 Month
Heart rate variability will be determined from ECG recordings
Time frame: After 1 month of treatment.
Change in Heart Rate Variability from Baseline at 2 Months
Heart rate variability will be determined from ECG recordings
Time frame: After 2 months of treatment.
Change in Heart Rate Variability from Baseline at 3 Months
Heart rate variability will be determined from ECG recordings
Time frame: After 3 months of treatment.
Change in Plasma Cytokine Levels from Baseline at 1 Week
Plasma concentrations (pg/mL) for 8 different cytokines (GM CSF, IFN-γ, IL-2, IL-4, IL-6, IL-8, IL-10, and TNF-α) will be determined from blood samples.
Time frame: After 1 week of treatment.
Change in Plasma Cytokine Levels from Baseline at 1 Month
Plasma concentrations (pg/mL) for 8 different cytokines (GM CSF, IFN-γ, IL-2, IL-4, IL-6, IL-8, IL-10, and TNF-α) will be determined from blood samples.
Time frame: After 1 month of treatment.
Change in Plasma Cytokine Levels from Baseline at 2 Months
Plasma concentrations (pg/mL) for 8 different cytokines (GM CSF, IFN-γ, IL-2, IL-4, IL-6, IL-8, IL-10, and TNF-α) will be determined from blood samples.
Time frame: After 2 months of treatment.
Change in Plasma Cytokine Levels from Baseline at 3 Months
Plasma concentrations (pg/mL) for 8 different cytokines (GM CSF, IFN-γ, IL-2, IL-4, IL-6, IL-8, IL-10, and TNF-α) will be determined from blood samples.
Time frame: After 3 months of treatment.
Change from baseline in cytokine release from cultured leukocytes at 1 week
Cytokine concentrations (pg/mL) for 8 different cytokines (GM CSF, IFN-γ, IL-2, IL-4, IL-6, IL-8, IL-10, and TNF-α) will be measured in supernatant from LPS-stimulated leukocyte cultures.
Time frame: After 1 week of treatment.
Change from baseline in cytokine release from cultured leukocytes at 1 month
Cytokine concentrations (pg/mL) for 8 different cytokines (GM CSF, IFN-γ, IL-2, IL-4, IL-6, IL-8, IL-10, and TNF-α) will be measured in supernatant from LPS-stimulated leukocyte cultures.
Time frame: After 1 month of treatment.
Change from baseline in cytokine release from cultured leukocytes at 2 months
Cytokine concentrations (pg/mL) for 8 different cytokines (GM CSF, IFN-γ, IL-2, IL-4, IL-6, IL-8, IL-10, and TNF-α) will be measured in supernatant from LPS-stimulated leukocyte cultures.
Time frame: After 2 months of treatment.
Change from baseline in cytokine release from cultured leukocytes at 3 months
Cytokine concentrations (pg/mL) for 8 different cytokines (GM CSF, IFN-γ, IL-2, IL-4, IL-6, IL-8, IL-10, and TNF-α) will be measured in supernatant from LPS-stimulated leukocyte cultures.
Time frame: After 3 months of treatment.
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