Genotype-Phenotype Correlations in Patients With Alport Syndrome

  • STATUS
    Recruiting
  • End date
    Dec 31, 2030
  • participants needed
    8165
  • sponsor
    Xinhua Hospital, Shanghai Jiao Tong University School of Medicine
Updated on 11 July 2021

Summary

Alport syndrome (AS) is caused by pathogenic variants in the type IV collagen genes COL4A3, COL4A4, and COL4A5. This study aims to enroll families and patients with a history of renal hematuria in 27 hospitals and detect these three genes for AS screening. This study also aims to analysis the effect of COL4A3/COL4A4/COL4A5 genotype on the development of kidney disease.

Description

Alport syndrome (AS) is a genetically and phenotypically heterogeneous disorder caused by the mutations in the type IV collagen genes COL4A3, COL4A4, and COL4A5. In this study, next generation sequencing is used to screen AS on 8165 participants enrolled from families and patients with a history of renal hematuria in 27 hospitals of China Huadong Region. Genotype (variants in COL4A3/COL4A4/COL4A5)-phenotype (onset age of hearing loss, nephroticrange proteinuria, decline of eGFR, kidney survival and onset age of CKD5) correlations in AS were evaluated.

Details
Condition Collagen disease, Alport's Syndrome, Nephritis
Clinical Study IdentifierNCT04947813
SponsorXinhua Hospital, Shanghai Jiao Tong University School of Medicine
Last Modified on11 July 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Age: up to 99 Years (Child, Adult, Older Adult)
Sex: All
Families and patients with a history of renal hematuria
Those who signed the informed consent

Exclusion Criteria

Polycystic kidney disease, hypertensive nephropathy, etc
Kidney biopsy is diagnosed as other primary/secondary kidney disease without type IV collagen-related kidney disease, including IgA nephropathy, membranous nephropathy, lupus nephritis, etc
Incomplete medical history or clinical data
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