Wake Forest APOLLO Scientific and Data Research Center

维克森林阿波罗科学与数据研究中心

• 批准号: 9440610
• 负责人: DONALD W BOWDEN
• 金额: $ 75万
• 依托单位: WAKE FOREST UNIVERSITY HEALTH SCIENCES
• 依托单位国家: 美国
• 财政年份: 2017
• 资助国家: 美国
• 起止时间: 2017-09-25 至 2022-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9440610
• 关键词: APOL1 gene; Acute; Adult; African; African American; Allografting; American; Ancillary Study; Antibodies; Apolipoproteins; Archives; Area; Biometry; Characteristics; Childhood; Clinical; Clinical Data; Cohort Studies; Collection; Communication; Country; Creatinine; DNA; Data; Data Analyses; Data Quality; Data Security; Development; End stage renal failure; Ensure; Ethicists; Ethics; Ethnic group; European; Evaluation; Failure; Funding; Genes; Genetic; Genotype; Glomerular Filtration Rate; Health; Health Care Costs; Histologic; Human Resources; Informed Consent; Kidney; Kidney Transplantation; Laboratories; Lead; Leadership; Link; Living Donors; Manuals; Monitor; Multicenter Studies; National Institute of Diabetes and Digestive and Kidney Diseases; Nephrology; Online Systems; Operative Surgical Procedures; Organ; Organ Procurements; Outcome; Patients; Physicians; Population; Predisposition; Preparation; Procedures; Process; Prospective Studies; Proteinuria; Protocols documentation; Quality of life; Race; Renal function; Reporting; Request for Applications; Research; Research Personnel; Resources; Retrospective Studies; Risk; Risk Estimate; Safety; Sampling; Serum; Sickle Hemoglobin; Specimen; Statistical Data Interpretation; Structure; System; Time; Transplant Recipients; Transplantation; United Network for Organ Sharing; United States National Institutes of Health; Variant; Virus Diseases; Vital Status; base; biobank; design; ethnic disparity; forest; genetic information; improved; improved outcome; indexing; kidney allograft; non-diabetic; organ allocation; precision medicine; primary outcome; programs; prospective; racial and ethnic; racial disparity; repository; response; risk variant; screening; skills; tool; web site

The NIH APOL1 Long-term Transplantation Outcomes Network (APOLLO) Collaborative U01 will perform a national prospective evaluation of donor and recipient APOL1 renal-risk variants in all US kidney transplants from African American kidney donors to determine their effect on transplant outcomes. In addition, the post- donation health and kidney function of African American living kidney donors will be assessed. We are applying to be the APOLLO Scientific and Data Research Center (SDRC) for this NIH Funding Announcement. Shorter renal allograft survival is observed for transplantations from deceased African American kidney donors, relative to deceased European American kidney donors. Reasons for this are unknown, but retrospective reports suggest that presence of two apolipoprotein L1 gene (APOL1) renal-risk variants in kidney donors may contribute to the disparity. These variants are common in populations with recent African ancestry (such as African Americans), where they are strongly associated with non-diabetic end-stage kidney disease, but rare in other racial/ethnic groups. APOL1 genotype data may provide more accurate assessment of the likelihood for long-term renal allograft function in donor kidneys, thereby improving the matching of donor kidneys with potential recipients in order to optimize renal allograft and patient survival. This information may better inform physicians about organ quality prior to decisions on allocation are made and regarding the safety of living kidney donation. Before this genotypic data can be used clinically, a prospective national study is required to evaluate all kidney transplantation outcomes from African American donors and recipients of their kidneys based on APOL1 genotypes. Information lacking from retrospective studies needs to be collected, including recipient APOL1 genotypes, renal histologic data in failed allografts and presence or development of BK viral infections, donor specific antibodies, and acute rejections after kidney transplantation. We will perform the following activities for the APOLLO Network: overall study coordination, assist with preparation of the final protocol and Manual of Procedures, develop data tracking tools and the study website, collect and archive clinical and outcomes data, perform genotyping, statistical analyses, assessment of the primary outcome “time to allograft failure in transplanted kidneys from African American donors, based on donor APOL1 genotypes” and create a bio-repository. We will longitudinally assess vital status, kidney function and proteinuria in living African American kidney donors based on APOL1 genotypes. Prospective assessment of the effects of kidney donor APOL1 genotypes on serum creatinine concentration, estimated glomerular filtration rate, and proteinuria in transplant recipients with functioning allografts will also be performed. Results have the potential to transform the organ allocation and informed consent processes in kidney transplantation, optimize renal allograft survival, reduce the discard of good-quality kidneys, and protect the health of living kidney donors.

NIH APOL1长期移植结果网络（APOLLO）合作U01将执行一项研究