Evaluating the Role of IL-17 as an Orchestrator of Peripheral-central Cross Talk in Depressive Symptoms

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Observational
SUMMARY

The investigators seek clinically actionable understanding of the mechanisms that underlie depression in the context of immune mediated inflammatory diseases (IMIDs), delivered by a focused immune intervention study examining brain circuitry using state of the art imaging in the context of exquisitely specific therapeutic immune interception in human immune disease. Glutamate concentration in the NAcc will be positively correlated with the magnitude of the inflammatory response and will be attenuated by IL-17A inhibition. Ultimately, this will be associated with an improvement in depressive symptoms. The strength of coupling between early and late systems will be attenuated in the context of IL-17A-driven inflammation and will be correlated with less frequent switching behaviour following negative outcomes and ultimately depressive symptoms. This coupling will be re-established following IL-17 antagonism. Patients whose depressive symptoms benefit most from IL-17A antagonism will exhibit greatest resting-state and task-specific functional connectivity between Th-NAcc.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 74
View:

• Adults ≥18 years \< 75years

• Diagnosis of PsO or PsA, made by a dermatologist or rheumatologist.

• Selected to start secukinumab/ bimekizumab/ Ixekizumab as part of their standard clinical care by their usual dermatology team for PsO or rheumatology clinical team for PsA in line with the license for secukinumab/ bimekizumab/ Ixekizumab and NICE/SMC criteria.

• No contraindications to MRI (for example metal fragments or implantable devices not compatible with MRI. (no extra x-ray images will be obtained to check placement of metal fragments or clips insitu. Existing images may be used to check for possible contraindications)

• Satisfactory completion of standard pre-biologic safety screening (including, but not limited to, exclusion of latent TB infection according to local protocol, chest X-ray, negative HIV screen, negative Hepatitis screen antibody, negative Hepatitis B surface antigen \[Hep B sAg\] and negative Hepatitis B anti-core antibody \[Hep B cAb\])

• Recent (but not within 4 weeks prior baseline) use of intra-muscular or intra-articular steroid injections

• Women of Child-Bearing Potential (WoCBP) must be willing to use effective contraception for study duration. Further information is provided in appendix 1.

• Willing to participate and give informed consent

Locations
Other Locations
United Kingdom
Queen Elizabeth University Hospital
RECRUITING
Glasgow
Contact Information
Primary
Maxine Arnott, BSc
maxine.arnott@glasgow.ac.uk
07890 059695
Backup
Neil Basu, MD, PhD
neil.basu@glasgow.ac.uk
Time Frame
Start Date: 2025-06-02
Estimated Completion Date: 2027-04-30
Participants
Target number of participants: 50
Treatments
Psoriatic Disease
Encompasses both Psoriatic Arthritis and and Plague Psoriasis .
Related Therapeutic Areas
Sponsors
Collaborators: Medical Research Council, University of Glasgow
Leads: NHS Greater Glasgow and Clyde

This content was sourced from clinicaltrials.gov

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