Electroencephalogram Recording in Patients With Systemic Lupus Erythematosus

NCT ID: NCT06378736

Last Updated: 2024-04-29

Basic Information

• Recruitment Status: RECRUITING
• Total Enrollment: 40 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2024-01-22
• Study Completion Date: 2026-03-23

Brief Summary

Patients with systemic lupus erythematosus (SLE) often experience a frustrating decline of their cognitive skills that includes considerable problems in attention, learning, and memory. This lupus-related cognitive dysfunction (termed SLE-CD) is recognized as the most prevalent of the nineteen neuropsychiatric SLE syndromes, as it affects up to 80% of patients and can significantly decrease their quality of life. The goal is to have tools that can be used for diagnosis and for monitoring responses after targeted interventions and therapies. This study will focus on electroencephalographic (EEG) signals, which will be detected noninvasively from scalp placed surface electrodes while the subjects are in a state of wakeful rest. Our hypothesis is that a subset of brain oscillations known as theta and gamma, and their co-modulation or coupling will be disrupted in SLE patients. This research protocol will subject patients with systemic lupus erythematosus (SLE) to scalp electroencephalography (EEG), with the goal of determining whether specific EEG patterns ('theta-gamma coupling') appear abnormal during wakeful-rest periods of 20 minutes. The investigators are interested in using scalp EEG because it is a standard, safe and robust technique for monitoring the electrophysiological activity of neurons in the cerebral cortex.

Detailed Description

Patients will sit comfortably in a quiet room in a wakeful state and perform simple operations with toy blocks and look at three dimensional objects and answer some questions. The EEG electrodes fit into a custom-made cap and will effectively transmit wave activity just by touching the skin surface of the scalp. There is no need for electrode paste so at the end of the experiment the patient can remove the cap and go home. The entire procedure including fitting of the EEG cap will take about an hour.

Conditions

Systemic Lupus Erythematosus

Study Design

• Observational Model Type: CASE_CONTROL
• Study Time Perspective: PROSPECTIVE

Interventions

Electroencephalography (EEG) signals, which will be detected noninvasively from dry scalp surface electrodes while the subjects are in a state of wakeful rest.

The proposed study is to determine whether EEG signals, namely theta-gamma coupling (TGC); The investigators are testing whether TGC can be used as a non-invasive novel biomarker in diagnosis and monitoring of insidious and difficult to detect cognitive dysfunction in SLE patients.

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

1. Must be able to understand and provide informed consent.

2. Must be ≥18 and ≤65years of age.

3. Must be female.

4. Must fulfill the 1997 American College of Rheumatology (ACR) revised criteria for the diagnosis of SLE or the Systemic Lupus Erythematosus International Collaborating Clinics (SLICC) Criteria for SLE.

5. Must have stable disease activity and medication doses for 4 weeks prior to screening. Stable disease activity is defined as no increase in disease activity requiring an increase or change in medications.

6. Must be on a corticosteroid dose that is ≤ prednisone 10 mg daily, or equivalent.

7. Aim 1 ONLY: Must have demonstrated significantly increased metabolism in the hippocampus, temporal or parietal lobes on prior fluoro-deoxy glucose (FDG)-PET imaging.

Exclusion Criteria

1. Inability or unwillingness to give written informed consent or comply with study protocol.

2. History of neurological diseases including, but not limited to, severe head injury or history of brain surgery, stroke, seizure, toxic exposure, mental retardation, migraine headaches, multiple sclerosis, dementia.

3. History of documented transient ischemic attacks within 6 months of screening.

4. History of illicit drug or alcohol dependence/abuse within the past 12 months.

5. Current use of antipsychotic, anticonvulsant, antidepressant (except for selective serotonin reuptake inhibitors) or anxiolytic medications (short acting anxiolytic medications are allowed if taken as needed with > 5 half-lives prior to assessments).

6. History of chronic pain; current and/or chronic use of narcotic analgesia for > 21 days (total) within the last 3 months, or last dose less than 5 days prior to assessment.

7. Increased disease activity within 4 weeks of screening defined by an increase in SLEDAI by 3 points or more, exclusive of points from serologies, which prompts an increase in or new addition of SLE medications.

8. History of a diagnosis of a primary psychiatric disorder preceding SLE diagnosis.

9. Current active acute infections requiring antibiotics within 2 weeks of screening and chronic known infections (eg. hepatitis B, C, and/or HIV).

10. Co-existing other autoimmune disease(s) other than autoimmune thyroid disease and secondary Sjogren's Syndrome.

11. The presence of uncontrolled, severe hypertension, diabetes or heart disease.

12. Impaired renal function with an estimated glomerular filtration rate (eGFR)< 30.

13. Presence of any active medical condition that in the opinion of the investigator may contribute to cognitive and/or behavioral disturbances.

14. Use of investigational drugs within 30 days or 5 half-lives before the study visit, whichever is longer.

15. Past or current medical problems or findings from physical examination or laboratory testing that are not listed above, which, in the opinion of the investigator, may pose additional risks from participation in the study, may interfere with the participant's ability to comply with study requirements or that may impact the quality or interpretation of the data obtained from the study.

16. Current treatment with cyclophosphamide, addition of belimumab within 4 months, addition of any disease modifying drug or biologic within 3 months of screening, and/or rituxan within 6 months.

17. Limited fluency with English or Spanish that in the opinion of the investigator would limit the subject's performance on the assessments.

18. Pregnant and/or lactating women.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: No

Sponsors

Northwell Health

OTHER

Sponsor Role: lead

Responsible Party

Bruce Volpe

Professor, Investigator

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

Northwell Health-Feinstein Insitute

Manhasset, New York, United States

Site Status: RECRUITING

Countries

United States

Central Contacts

Bruce T Volpe, MD

Role: CONTACT

bvolpe1@northwell.edu

5165623384

Facility Contacts

Bruce T Volpe, MD

Role: primary

bvolpe1@northwell.edu

516-562-3384

Celina B. Fernandez, MS

Role: backup

cfernandez14@northwell.edu

5165623646

Other Identifiers

21-1027

Identifier Type: -

Identifier Source: org_study_id