Study of Genetic Anomalies of Complement Related Proteins in Patients With IgA Glomerulonephritis
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Purpose
OBJECTIVES: I. Determine whether allelic differences associated with the fourth component of complement, type-1 complement receptor expressed on erythrocytes, and Fc receptor FcgRIII contribute to the pathogenesis of IgA glomerulonephritis (IgA-N).
II. Compare genetic anomalies of these key components in immune complex processing and clearance between juvenile vs adult onset IgA-N vs normal controls.
| Condition |
|---|
|
IGA Glomerulonephritis |
| Study Type: | Observational |
| Study Design: | Primary Purpose: Screening |
| Estimated Enrollment: | 105 |
| Study Start Date: | January 1998 |
PROTOCOL OUTLINE:
Participants undergo qualitative genetic analysis of complement-related proteins. Studies include: genomic re-arrangement of 4-gene unit, C4 DNA sequence and RNA expression, type-1 complement receptor DNA sequence, Fc-gamma receptor IIIA isoform analysis, classical and alternative complement activation pathway assays, plasma C4 and C4d protein levels, and immunoglobulin patterns in glomerular deposits.
Eligibility| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
- IgA glomerulonephritis
Contacts and Locations
More Information
No publications provided
| ClinicalTrials.gov Identifier: | NCT00004305 History of Changes |
| Other Study ID Numbers: | 199/11791, OSU-94H0338 |
| Study First Received: | October 18, 1999 |
| Last Updated: | June 23, 2005 |
| Health Authority: | United States: Federal Government |
Keywords provided by National Center for Research Resources (NCRR):
|
IgA glomerulonephritis rare disease renal and genitourinary disorders |
Additional relevant MeSH terms:
|
Glomerulonephritis Glomerulonephritis, IGA Nephritis Kidney Diseases |
Urologic Diseases Autoimmune Diseases Immune System Diseases |
ClinicalTrials.gov processed this record on May 22, 2013