Long-term outcomes among living kidney donors with isolated medical abnormalities

患有孤立性医学异常的活体肾脏捐献者的长期结果

• 批准号: 9110989
• 负责人: JAYME ELIZABETH LOCKE
• 金额: $ 17.95万
• 依托单位: UNIVERSITY OF ALABAMA AT BIRMINGHAM
• 依托单位国家: 美国
• 财政年份: 2015
• 资助国家: 美国
• 起止时间: 2015-07-15 至 2020-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9110989
• 关键词: Address; African American; Alabama; American; Anatomy; Ancillary Study; Award; Caring; Categories; Characteristics; Chronic Disease; Chronic Kidney Failure; Cohort Studies; Comorbidity; Coronary artery; Data; Decision Making; Development; Diabetes Mellitus; Disease; Disease-Free Survival; Donor Selection; Epidemiologic Methods; Epidemiology; Equilibrium; European; Evaluation; Exposure to; Family; Fatty acid glycerol esters; Fostering; Foundations; Funding; General Population; Goals; Growth; Health; Hypertension; Image; Individual; Informed Consent; Kidney; Kidney Transplantation; Knowledge; Life; Living Donors; Measures; Medical; Mentors; Metabolic syndrome; Methodology; Methods; Minority; Morbidity - disease rate; Obesity; Organ; Outcome; Parents; Population; Postoperative Period; Race; Recording of previous events; Relaxation; Research; Research Infrastructure; Research Personnel; Resources; Risk; Risk Estimate; Risk Factors; Safety; Scientist; Selection Criteria; Source; Stratification; Surgeon; Techniques; Time; Training; Transplantation; Universities; Vascular calcification; Weight; X-Ray Computed Tomography; base; cardiovascular risk factor; career; cohort; demographics; disorder risk; hazard; health disparity; high risk; improved; innovation; loved ones; mortality; novel; outcome prediction; predictive tools; prehypertension; prognostic; racial difference; racial disparity; response; social; tool; tool development; young adult

 DESCRIPTION (provided by applicant): The demand for kidney transplantation continues to exceed the supply. Increasing the number of living kidney donors is a major priority. Historically, living donors were healthy and free of isolated medical abnormalities (IMA) at the time of donation. Recently, general US population demographics have changed, and in response, transplant centers now include donors with IMAs such as pre-hypertension (pre-HTN), obesity, and metabolic syndrome. At a general population level, individuals with IMAs, particularly African Americans (AA), are more likely to develop comorbidities, such as diabetes, HTN, and chronic kidney disease. Recent data suggest that AA living kidney donors are more likely to have a pre-donation IMA. It remains unclear what impact, if any, living donation will have on development of these comorbidities, and whether racial disparities in risk attributable to donation exist. Current methods for assessing living donor long-term health risks are imprecise, relying heavily on traditional factors such as family and social histories. Morphometric measures (e.g. vascular calcifications; fat distribution), using radiologic imaging, have emerged as strong predictors of cardiovascular risk. Pre-donation imaging, routinely acquired during donor evaluations to assess renal anatomy, can be leveraged to identify novel morphometric risk predictors for post-donation comorbidities. I hypothesize that morphometric measures will greatly improve prediction of post-donation comorbidities, including risk directly attributable to donation. Given significant knowledge gaps in risk prediction and stratification of donors with IMAs, I propose an ancillary study that will leverage data from an ongoing R01-funded cohort study of live donors to create the largest cohort of IMA donors studied and will address unique aims: (1) explore the association of novel morphometric measures and traditional risk factors with post-donation comorbidity stratified by race; (2) develop a risk tool for predicting post-donation comorbidities; and (3) estimate risk attributable to living kidney donation. Utilization o novel morphometric measures obtained from routine pre- donation imaging is innovative, highly practical, and will create a level of risk prediction of living donor outcomes that currently does not exist. Precise risk prediction will improve informed consent, donor autonomy in medical decision making, and will change the practice of live kidney donor selection in the US. Resources and infrastructure at the University of Alabama at Birmingham, including the most AA living kidney donors in the US, are keenly in-line with the proposed aims, and will provide the necessary foundation to see the proposed project to its successful completion. The mentored award will foster my growth as an independent investigator by affording me opportunities to focus on building an expertise in novel risk prediction research and enhancing my exposure to health disparities and chronic disease epidemiology in minority populations. This additional training will inform my path toward long-term career goals of research independence as a surgeon-scientist and R01 funding.

 描述（由申请人提供）：肾移植的需求继续超过供应。增加活体肾脏捐赠者的数量是一个主要优先事项。从历史上看， 活体捐赠者在捐赠时是健康的并且没有孤立的医学异常（IMA）。最近，一般美国人口统计学发生了变化，作为回应，移植中心现在包括患有IMA的供体，如高血压前期（pre-HTN），肥胖和代谢综合征。在一般人群水平，患有IMA的个体，特别是非洲裔美国人（AA），更有可能患上合并症，如糖尿病，HTN和慢性肾脏疾病。最近的数据表明，AA活体肾脏捐赠者更有可能有捐赠前IMA。目前尚不清楚活体捐赠对这些合并症的发展有何影响（如果有的话），以及捐赠造成的风险是否存在种族差异。目前评估活体捐献者长期健康风险的方法不准确，严重依赖于家庭和社会历史等传统因素。使用放射成像的形态测量（例如血管钙化;脂肪分布）已成为心血管风险的强有力预测因素。捐赠前成像，在捐赠者评估肾脏解剖结构的过程中常规采集，可用于识别捐赠后合并症的新形态学风险预测因子。我假设形态测量将大大提高捐献后合并症的预测，包括直接归因于捐献的风险。鉴于IMA供体的风险预测和分层方面存在显著的知识缺口，我提出了一项辅助研究，该研究将利用来自R 01资助的活体供体队列研究的数据，以创建最大的IMA供体队列研究，并将解决独特的目标：（1）探索新的形态测量指标和传统风险因素与按种族分层的捐赠后合并症的关联;（2）开发一种预测捐献后合并症的风险工具;（3）估计活体肾脏捐献的风险。利用从常规捐献前成像获得的新的形态测量是创新的、高度实用的，并且将创建目前不存在的活体供体结果的风险预测水平。准确的风险预测将改善知情同意，捐赠者在医疗决策中的自主权，并将改变美国活体肾脏捐赠者选择的实践。亚拉巴马大学伯明翰分校的资源和基础设施，包括美国最多的AA活体肾脏捐赠者，与拟议的目标非常一致，并将为拟议的项目成功完成提供必要的基础。指导奖将促进我作为一个独立的研究者的成长，让我有机会专注于建立一个新的风险预测研究的专业知识，并提高我对少数民族人群的健康差异和慢性病流行病学的了解。这一额外的培训将告知我的研究独立的长期职业目标的道路作为一个外科医生，科学家和R 01资金。