APOL1 Gene Variants in African American Kidney Transplant Recipients



Status:Completed
Conditions:Renal Impairment / Chronic Kidney Disease
Therapuetic Areas:Nephrology / Urology
Healthy:No
Age Range:18 - Any
Updated:4/2/2016
Start Date:June 2011
End Date:June 2014
Contact:Anil K Chandraker, MD
Email:achandraker@rics.bwh.harvard.edu
Phone:617-732-7412

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Impact of APOL1 Gene Variants in African American Kidney Transplant Recipients: A Study of Clinical Outcomes and Molecular Mechanisms

Aim 1:

Determine if there is an association between the APOL1 risk variants and allograft survival
and function in African Americans

Aim 2:

Determine if there is an association between the presence of APOL1 risk variants in an
African American kidney transplant recipient and the risk of recurrent disease

Aim 3:

Investigate mechanisms of APOL1 associated kidney disease by prospectively following African
American kidney transplant recipients throughout their clinical course.


Aim 1:

Inclusion Criteria:

- self-reported African American

- 18 years or older

- kidney transplant within 12 years

Aim 2:

Inclusion Criteria for patients with recurrent disease:

- self-reported African American

- 18 years or older

- kidney transplant within 12 years

- recurrent or de novo glomerular disease on allograft kidney biopsy

Inclusion Criteria for control group:

- self-reported African American

- 18 years or older

- kidney transplant within 12 years

- end stage kidney disease due to glomerular nephritis, clinically diagnosed or by
native kidney biopsy

Exclusion Criteria for control group:

- clinical evidence of recurrent disease (presence of proteinuria, hematuria,
Creatinine >2)

Aim 3:

Inclusion Criteria:

- self-reported African American

- 18 years or older

- scheduled living kidney transplant
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