Membranous Nephropathy-associated Serological Antibody Predict the Prognosis of Idiopathic Membranous Nephropathy

Sponsor
Guangdong Provincial People's Hospital (Other)
Overall Status
Terminated
CT.gov ID
NCT03475602
Collaborator
(none)
85
1
26.3
3.2

Study Details

Study Description

Brief Summary

Idiopathic membranous nephropathy (IMN) remains a common cause of the nephrotic syndrome in adults and one of the leading known causes of end-stage renal disease. Identification of circulating autoantigens provide potential biomarkers for diagnosis and therapy of idiopathic membranous nephropathy. M-type phospholipase A2 receptor (PLA2R) and Thrombospondin type-I domain-containing 7A (THSD7A) were identified as the target antigen in membranous nephropathy with high specificity and the concentration of serum anti-PLA2R antibody and anti-TSHD7A antibody were helpful for predicting disease activity. In our prospective cohort study, hospitalized patients diagnosed as IMN are prospectively studied. Circulating anti-PLA2R antibody and anti-THSD7A antibodies were recently screened by using enzyme-linked sorbent assay(ELISA). This study aims to analyse the difference of clinicopathological characteristics for different concentrations of serum anti PLA2R antibody and anti TSHD7A antibody, and analyze the association between baseline concentrations of serum antibody and disease activity. This study also explored the prediction effects of serum antibody concentrations with different types of therapeutic regimen in IMN and compare the curative effects of different types of therapeutic regimen in different serum antibody concentrations.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: PLA2R
  • Diagnostic Test: TSHD7A

Study Design

Study Type:
Observational [Patient Registry]
Actual Enrollment :
85 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
A Prospective Cohort Study of Membranous Nephropathy-associated Serological Antibody in Prediction of the Prognosis of Idiopathic Membranous Nephropathy
Actual Study Start Date :
Mar 1, 2018
Actual Primary Completion Date :
May 10, 2020
Actual Study Completion Date :
May 10, 2020

Arms and Interventions

Arm Intervention/Treatment
Cyclophosphamide

Drug: Cyclophosphamide,CTX Determination of serum concentration of anti PLA2R antibody and anti TSHD7A antibody

Diagnostic Test: PLA2R
Determination of serum concentration of anti PLA2R antibody

Diagnostic Test: TSHD7A
Determination of serum concentration of anti TSHD7A antibody

Cyclosporin

Drug: Cyclosporin Determination of serum concentration of anti PLA2R antibody and anti TSHD7A antibody

Diagnostic Test: PLA2R
Determination of serum concentration of anti PLA2R antibody

Diagnostic Test: TSHD7A
Determination of serum concentration of anti TSHD7A antibody

Outcome Measures

Primary Outcome Measures

  1. Complete Remission [after treatment for 6 months]

    Urinary protein excretion<0.3 g/d (uPCR<300 mg/g or <30 mg/mmol), confirmed by two values at least 1 week apart, accompanied by a normal serum albumin concentration, and a normal SCr.

  2. Partial Remission [after treatment for 6 months]

    Urinary protein excretion <3.5 g/d (uPCR <3500 mg/g or <350 mg/mmol) and a 50% or greater reduction from peak values;confirmed by two values at least 1 week apart, accompanied by an improvement or normalization of the serum albumin concentration and stable SCr.

Secondary Outcome Measures

  1. estimated Glomerular filtration rate and serum creatinine [after treatment for 6 months]

    time to a 50% reduction in baseline estimated Glomerular filtration rate (according to CK-EPI) and to doubling of baseline creatinine

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • (1) Patients who provided informed consent

  • (2) Patients who are diagnosed as membranous nephropathy by renal biopsy

  • (3) 18 years of age or older, male or female

Exclusion Criteria:
  • (1) identification of Secondary factors such as infectious diseases, rheumatic diseases, tumors, drugs and so on

  • (2) Previous medicine history of immunosuppressive medication and corticosteroids

  • (3) Patients who are not expected to complete 6 months of follow-up

Contacts and Locations

Locations

Site City State Country Postal Code
1 Nephrology Dept,Guangdong General Hospital Guangzhou Guangdong China

Sponsors and Collaborators

  • Guangdong Provincial People's Hospital

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Guangdong Provincial People's Hospital
ClinicalTrials.gov Identifier:
NCT03475602
Other Study ID Numbers:
  • GDREC2017318H
First Posted:
Mar 23, 2018
Last Update Posted:
Jun 18, 2020
Last Verified:
Feb 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 18, 2020