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Mechanistic Role of Skull Bone Marrow-Mediated Neuro-Immune Axis in Drug-Resistant Epilepsy

Mechanistic Role of Skull Bone Marrow-Mediated Neuro-Immune Axis in Drug-Resistant Epilepsy

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500111673
Enrollment
Unknown
Registered
2025-11-04
Start date
2025-11-13
Completion date
Unknown
Last updated
2025-11-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Drug-resistant epilepsy

Interventions

Case Group (Drug-Resistant Epilepsy):None
Control Group (Non-Epilepsy):None

Sponsors

The second affiliated hospital of Army medical university
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 90 Years

Inclusion criteria

Inclusion criteria: 1. Case Group (Drug-Resistant Epilepsy): Patients diagnosed with drug-resistant epilepsy and scheduled for epileptogenic focus resection. Inclusion criteria for the case group: (1) Age >=1 month and =18 years). 2. Control Group (Non-Epilepsy): Patients undergoing surgery for other neurosurgical conditions (e.g., acute intracranial hemorrhage within 24 hours, craniotomy with aneurysm clipping for non-epilepsy reasons) and without systemic immune system diseases, matched for age and gender with the case group. Inclusion criteria for the control group: (1) Age >=1 month and <=90 years. (2) Undergoing craniotomy for non-epilepsy-related reasons (e.g., acute intracranial hemorrhage within 24 hours, craniotomy with aneurysm clipping for non-epilepsy reasons). (3) No history of epilepsy, no other neurological disease diagnosis, and no diseases affecting immune function. (4) The patient or family member is able to understand and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Exclusion criteria for the case group (drug-resistant epilepsy group): (1) Coexisting other severe neurological diseases (such as brain tumor, stroke, multiple sclerosis, etc.). (2) Coexisting severe immune system diseases or autoimmune disorders. (3) Suffering from severe systemic infection or inflammatory disease. (4) Receiving treatments that may affect immune response (such as chemotherapy, radiotherapy, immunosuppressive therapy, etc.). (5) Pregnant or lactating women. (6) History of psychiatric illness, unable to cooperate with the study. 2. Exclusion criteria for the control group (non-epilepsy): (1) Coexisting severe immune system diseases or autoimmune disorders. (2) Suffering from severe systemic infection or inflammatory disease. (3) Receiving treatments that may affect immune response. (4) Pregnant or lactating women. (5) History of psychiatric illness, unable to cooperate with the study.

Design outcomes

Primary

MeasureTime frame
Composition of immune cell subsets and enriched molecular signaling pathways in skull bone marrow;

Secondary

MeasureTime frame
Composition, quantity, and activation status of B cells, T cells, and myeloid cells in meninges;Immune cell infiltration and functional status in choroid plexus;Expression levels of inflammatory cytokines and chemokines, and activation status of microglia and astrocytes in epileptogenic focus;Differentially expressed key genes and proteins in skull bone marrow, meninges, choroid plexus, and epileptogenic focus (especially related to cell migration, adhesion, and immune regulation);Statistical correlation between key immune cell subset proportions or core molecular pathway features in skull bone marrow and seizure frequency, seizure severity, and drug-resistant status;Levels of inflammatory cytokines, chemokines, and cell damage markers in peripheral blood;

Countries

China

Contacts

Public ContactZhang Chunqing

The second affiliated hospital of Army medical university

cqzhang@tmmu.edu.cn+86 189 8320 4130

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026