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Alterations in Hippocampal Subfield Volumes in Systemic Lupus Erythematosus Patients with Cognitive Impairment

Alterations in Hippocampal Subfield Volumes in Systemic Lupus Erythematosus Patients with Cognitive Impairment

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600124396
Enrollment
Unknown
Registered
2026-05-12
Start date
2026-05-15
Completion date
Unknown
Last updated
2026-05-18

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

Conditions

SLE patients with cognitive impairment versus those without cognitive impairment

Interventions

Healthy control group:None
Group SLE:None

Sponsors

First Affiliated Hospital of Kunming Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1. Patients meeting the 2019 EULAR/ACR classification criteria for SLE; 2. Voluntary participation with signed informed consent; 3. Age between 18 and 50 years; 4. Right-handedness. Control group:; 1. Age and gender matched with patients; 2. In good health; 3. Voluntary participation with signed informed consent; 4. Age between 18 and 50 years; 5. Right-handedness.

Exclusion criteria

Exclusion criteria: 1. Comorbid other autoimmune diseases; 2. History of hypertension, diabetes, stroke, renal insufficiency, or other conditions that may cause severe clinical situations such as brain atrophy; 3. History of severe traumatic brain injury or surgery; 4. Severe active psychiatric symptoms, such as severe behavioral disturbance and impaired consciousness; 5. History of substance abuse, alcoholism, or drug abuse; 6. MRI contraindications including claustrophobia or metallic implants; 7. Pregnant or lactating women. Control Group: 1. A history, either past or present, of definite physical diseases or neuropsychiatric disorders (psychiatric symptoms will be assessed/screened by an experienced psychiatrist using the Structured Clinical Interview for DSM-IV, Non-Patient Edition); 2. History of immune system diseases and family history of such diseases; 3. History of substance abuse, alcoholism, or drug abuse; 4. History of severe traumatic brain injury or surgery; 5. Pregnant or lactating women; 6. MRI contraindications including claustrophobia or metallic implants.

Design outcomes

Primary

MeasureTime frame
Structural MRI (sMRI);MRI Conventional Scan;Cognitive Function Assessment;Diffusion Tensor Imaging (DTI);Vascular Function Marker Detection;

Secondary

MeasureTime frame
Demographic Data;Cytokine;Lymphocyte Subset ;Autoantibody;Medical History and Treatment Data;Disease Activity Assessment/Damage Assessment;

Countries

China

Contacts

Public ContactZhang Guofang

First Affiliated Hospital of Kunming Medical University

13987103065@163.com+86 871 6532 4888

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 22, 2026