Non-invasive Brain Stimulation Normalizes Dopaminergic Transmission in the Frontostriatal Circuit to Alleviate Depression With Metabolic Disorders.

NCT05117983 | Unknown

• 1 other identifier: A-BR-110-005
• Study Type: interventional
• Target: 90
• Locations: 1 country
• Sites: 1

Brief Summary

Depression and metabolic disorder (MetD) are two of the most common and debilitating disorders worldwide, occurring with significant rates of comorbidity. This is a major clinical challenge as the outcomes of both conditions are worsened. Studies have uncovered that depression and metabolic disorder are associated with chronic, low-grade inflammation. In brain circuit level, patients with depression are characterized with aberrant frontostriatal (FS) circuit connectivity and reduced activity level that also associated with metabolic comorbidity. In neurotransmitter level, the dopaminergic pathway, that could be feedback regulated by immune and metabolic factors, has long been known to involve in emotional and metabolic homeostasis. More importantly, this dopamine (DA) input is critical to shaping the FS circuit-level dynamic connectivity and plasticity. Therefore, this study hypothesizes that inflammatory and metabolic dysregulations on DA transmission link to the aberrant FS function that cause mood and metabolic syndromes. To clarify the underlying mechanisms, 90 patients who meet the DSM-5 diagnostic criteria of major depressive episode in either major depressive disorder or bipolar disorder are planned to be recruit. FS functional connectivity and activation, before and after receiving 10 Hz repetitive transcranial magnetic stimulation (rTMS) to left dorsolateral prefrontal cortex will be measured. Then systemically analyze participants' clinical symptomology, neurocognitive function, inflammation and metabolic status. Possible correlations between indices, the effects of rTMS and differences between groups will be tested. Results could provide a chance for further understanding the pathophysiology of depression with MetD and comparing between unipolar and bipolar depression, and developing brain circuit based non-invasive brain stimulation personalized treatment for depression with MetD to achieve a better outcome.

Conditions

Depression

Keywords

Depression; Dopamine (DA); Frontostriatal (FS) circuit; Metabolic disorder; Repetitive transcranial magnetic stimulation (rTMS)

Outcome Measures

Primary Outcomes (12)

• Change from baseline mood symptom severity at several timepoints over 3 months

  Evaluation for disease severity by using the Hamilton Rating Scale for Depression (HAM-D) by trained senior psychiatrists. The same rater administers the scale for each patient.

  Week 0, Week 1, Week 2, Week 3, Week 4, Week 8, Week 12.

• Iowa gambling task (IGT) with functional MR imaging

  The subject will be asked to turn a card from 4-decks voluntarily, and maximize gains and minimize losses during the game.

  Week 0

• Change from baseline functional connectivity maps at 3 months

  A 2-sample independent t-test will be employed to analyze the functional connectivity maps using SPM 12. Statistical maps will be computed to identify changes in striatum-seeded functional connectivity for between-group comparisons. The age will be regressed out as a covariate of non-interest. Significance will be threshold at the uncorrected voxel level p=0.001, followed by the FWE- corrected cluster level p=0.05.

  Week 0, Week 12

• Change from baseline homeostasis model assessment-estimated insulin resistance (HOMA-IR) index at several timepoints within 3 months

  The homeostasis model assessment-estimated insulin resistance (HOMA-IR) index is calculated as the product of the fasting plasma insulin level (uIn/ml) and the fasting plasma glucose level (mg/dl), divided by 405. Insulin resistance is defined as HOMA-IR ≥2.5.

  Week 0, Week 4, Week 8, Week 12

• Change from baseline body mass index (BMI) at several timepoints within 3 months

  Body weight (to the nearest 0.1 kg), body height (to the nearest 0.1 cm) will be measured and BMI (kg/m2) will be calculated accordingly.

  Week 0, Week 4, Week 8, Week 12

• Change from baseline waist and hip circumference at several timepoints within 3 months

  Waist and hip circumference (to the nearest 0.1 cm) will be measured.

  Week 0, Week 4, Week 8, Week 12

• Change from baseline fasting serum leptin level at several timepoints within 3 months

  Measured using ELISA method (Linco Research, USA). The limit of detection was 0.5 ng/mL, and the intra- and interassay coefficients of variation were 7% and 9%, respectively.

  Week 0, Week 4, Week 8, Week 12

• Change from baseline fasting serum lipid level at several timepoints within 3 months

  Fasting total cholesterol, high density lipoprotein cholesterol (HDL), low-density lipoprotein cholesterol (LDL) and triglyceride (TG) concentrations will be measured.

  Week 0, Week 4, Week 8, Week 12

• Change from baseline immunological markers at several timepoints within 3 months

  The fasting plasma CRP level will be assessed using an high-sensitivity CRP ELISA kit (Bender MedSystems, USA), for which the limit of detection was 3 pg/mL and the intra- and inter-assay coefficients of variation were 6.9% and 13.1%, respectively. The other immunological parameters to be analyzed include TNF-α, TGF-β1, IL-1, IL-8 and IL-10.

  Week 0, Week 2, Week 3, Week 4, Week 8, Week 12

• Change from baseline neurocognitive performance at 3 months

  Neurocognitive performance will be assessed using Continuous Performance Test (CPT), Finger-Tapping Test (FTT) and Wisconsin Card-Sorting Test (WCST).

  Week 0, Week 12

• Change from baseline social cognitive function at 3 months

  Mayer-Salovey-Caruso emotional Intelligent Test (MSCEIT): four branches: perceiving emotion (consisting of two tasks: face and picture tasks), facilitating emotion, understanding emotion, and managing emotion (Mayer, Salovey, Caruso, \& Sitarenios, 2003). The results will be scaled to a standard score based on the weight from the representative adult population (regarding age, gender, and ethnicity) in an extremely large sample of people (5,000). The reliability and validity of MSCEIT V2.0 have been proved before.

  Week 0, Week 12

• Change from baseline autonomic nervous system performance at several timepoints within 3 months

  Cardiac autonomic function will be calculated by the geometric method, which is based on short-term measurements of the interbeat interval (IBI) \[82\]. Power spectral density analysis of HRV will be performed by fast Fourier transformation \[83\].

  Week 0, Week 4, Week 12

Study Arms (2)

MDD patient with HRSD score of at least 18

ACTIVE COMPARATOR

MDD patients who meet the DSM-5 diagnostic criteria of MDD and their current episode show a Hamilton Rating Scale for Depression (HRSD) score of at least 18

Device: Repetitive transcranial magnetic stimulation (rTMS)

BD patient with HRSD score of at least 18

ACTIVE COMPARATOR

BD patients who meet the DSM-5 diagnostic criteria of BD and their current depression episode show a Hamilton Rating Scale for Depression (HRSD) score of at least 18

Device: Repetitive transcranial magnetic stimulation (rTMS)

Interventions

Repetitive transcranial magnetic stimulation (rTMS) DEVICE

Real-time MRI-guided neuronavigation with a Visor neuronavigation system (ANT Neuro, Enschede, Netherlands) will be used for coil positioning. Left dorsolateral prefrontal cortex target is located in each participant.

Also known as: Antidepressants

BD patient with HRSD score of at least 18; MDD patient with HRSD score of at least 18

Eligibility Criteria

• Age: 20 Years - 70 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• (1)Signed informed consent by patient or legal representative;
• (2) male or female patient aged ≧20 and ≦70 years;
• (3) a diagnosis of MDD or BD according to DSM criteria made by a specialist in psychiatry;
• (4) a total score of at least 18 in the Hamilton Rating Scale for Depression (HDRS) at the screening stage;
• (5) patient or a reliable caregiver can be expected to ensure acceptable compliance and visit attendance for the duration of the study.

You may not qualify if:

• (1) women of childbearing potential, not using adequate contraception as per investigator judgment or not willing to comply with contraception for the duration of the study;
• (2) females who are pregnant or breast-feeding;
• (3) other major DSM 5 diagnoses other than mood disorders, except for tobacco use disorder and anxiety disorder;
• (4) current evidence of an uncontrolled and/or clinically significant medical condition, e.g. patients with extensive area of ischemic bruise, multiple sclerosis, cardiac, hepatic and renal failure that would compromise patient safety or preclude study participation;
• (5) history of seizure or epilepsy;
• (6) history of neurological diseases or traumatic brain injury;
• (7) history of brain lesion, having received neurosurgery, meningitis or encephalitis;
• (8) exacerbation of symptom severity, presenting severe suicidal ideation or self harm behavior during the screen or study period;
• (9) presence of devices, e.g. pacemakers, cochlear prosthesis, neuro-stimulators, magnetic cochlear prosthesis, intracranial/intraocular metallic fragments;
• (10) patient has received electroconvulsive therapy (ECT) within 3 months prior to the first intervention of the treatment;
• (11) skin lesion at local site receiving rTMS stimulation;
• (12) those who cannot tolerate the side effects or ever developed sleep disorder while receiving rTMS therapy.

Sponsors & Collaborators

• National Cheng-Kung University Hospital: lead
• Ministry of Science and Technology, Taiwan: collaborator
• Ministry of Health and Welfare, Taiwan: collaborator

Study Sites (1)

National Cheng-Kung University

Tainan, 704, Taiwan

RECRUITING

MeSH Terms

Conditions

Depression; Metabolic Diseases

Interventions

Transcranial Magnetic Stimulation

Condition Hierarchy (Ancestors)

Behavioral Symptoms; Behavior; Nutritional and Metabolic Diseases

Intervention Hierarchy (Ancestors)

Magnetic Field Therapy; Therapeutics

Central Study Contacts

Po See Chen, MD, PhD

CONTACT

06-2353535; chenps@mail.ncku.edu.tw

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: NON RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: September 28, 2021
• First Posted: November 11, 2021
• Study Start: August 12, 2021
• Primary Completion: July 31, 2024
• Study Completion: July 31, 2024
• Last Updated: November 11, 2021

Record last verified: 2021-09

Locations

TW (1)