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Multicenter Cross-Sectional Observational Study Protocol on IgG Glycosylation Modifications in Primary Membranous Nephropathy

Multicenter Cross-Sectional Observational Study Protocol on IgG Glycosylation Modifications in Primary Membranous Nephropathy

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600123145
Enrollment
Unknown
Registered
2026-04-22
Start date
2026-05-01
Completion date
Unknown
Last updated
2026-04-27

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

Conditions

Primary Membranous Nephropath

Interventions

Healthy control group:None
PMN patient group:None

Sponsors

Shanghai East Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: PMN Patient Group: 1. Aged 18-75 years, any gender; 2. Diagnosed with primary membranous nephropathy by renal biopsy pathology (according to the 2012 KDIGO diagnostic criteria); 3. Clear results for serum anti-PLA2R antibody and/or anti-THSD7A antibody tests; 4. No prior treatment with immunosuppressive agents (glucocorticoids, cyclophosphamide, tacrolimus, cyclosporine, etc.); 5. Signed informed consent. Healthy Control Group: 1. Aged 18-75 years, any gender; 2. No history of kidney disease; 3. Normal urinalysis and normal kidney function (eGFR >=90 ml/min/1.73m^2); 4. No history of autoimmune diseases; 5. No history of chronic diseases (diabetes, hypertension, liver disease, etc.); 6. Signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Secondary membranous nephropathy (such as systemic lupus erythematosus, hepatitis B virus-associated nephritis, malignancy-associated membranous nephropathy, etc.); 2. Combined with other primary glomerular diseases; 3. Acute kidney injury or stage 5 chronic kidney disease (eGFR 37.5°C, abnormal infection indicators); 5. History of malignant tumors or currently having malignant tumors; 6. Pregnant or breastfeeding women; 7. Received blood product transfusion within the past 3 months; 8. Having other autoimmune diseases; 9. Severe liver dysfunction (Child-Pugh class C); 10. Other conditions judged by the investigator as unsuitable for participation in this study.

Design outcomes

Primary

MeasureTime frame
Glycosylation profiles of IgG population and subclasses (igg1-4);

Countries

China

Contacts

Public ContactLiu Na

Shanghai East Hospital

naliubrown@163.com+86 18217768587

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 1, 2026