Mccafferty Kieran, Caplin Ben, Knight Sinead, Hockings Paul, Wheeler David, Fan Stanley L, Hulthe Johannes, Kleta Robert, Ashman Neil, Papastefanou Vasilios, Mehta Hemal, Salama Alan, Hadzovic Sinela, Chowdhury Tahseen Ahmad, Jarl Lisa, Unwin Robert, Challis Benjamin, Sundgren Anna K, Yaqoob Muhammad Magdi
Department of Nephrology, Barts Health NHS Trust, London, UK.
Centre for Nephrology, University College London Medical School, London, UK.
BMJ Open. 2020 Sep 9;10(9):e033923. doi: 10.1136/bmjopen-2019-033923.
Diabetic kidney disease (DKD) is the leading cause of end-stage kidney disease worldwide and a major cause of premature mortality in diabetes mellitus (DM). While improvements in care have reduced the incidence of kidney disease among those with DM, the increasing prevalence of DM means that the number of patients worldwide with DKD is increasing. Improved understanding of the biology of DKD and identification of novel therapeutic targets may lead to new treatments. A major challenge to progress has been the heterogeneity of the DKD phenotype and renal progression. To investigate the heterogeneity of DKD we have set up The East and North London Diabetes Cohort (HEROIC) Study, a secondary care-based, multiethnic observational study of patients with biopsy-proven DKD. Our primary objective is to identify histological features of DKD associated with kidney endpoints in a cohort of patients diagnosed with type 1 and type 2 DM, proteinuria and kidney impairment.
HEROIC is a longitudinal observational study that aims to recruit 500 patients with DKD at high-risk of renal and cardiovascular events. Demographic, clinical and laboratory data will be collected and assessed annually for 5 years. Renal biopsy tissue will be collected and archived at recruitment. Blood and urine samples will be collected at baseline and during annual follow-up visits. Measured glomerular filtration rate (GFR), echocardiography, retinal optical coherence tomography angiography and kidney and cardiac MRI will be performed at baseline and twice more during follow-up. The study is 90% powered to detect an association between key histological and imaging parameters and a composite of death, renal replacement therapy or a 30% decline in estimated GFR.
Ethical approval has been obtained from the Bloomsbury Research Ethics Committee (REC 18-LO-1921). Any patient identifiable data will be stored on a password-protected National Health Services N3 network with full audit trail. Anonymised imaging data will be stored in a ISO27001-certificated data warehouse.Results will be reported through peer-reviewed manuscripts and conferences and disseminated to participants, patients and the public using web-based and social media engagement tools as well as through public events.
糖尿病肾病(DKD)是全球终末期肾病的主要病因,也是糖尿病(DM)患者过早死亡的主要原因。尽管医疗护理的改善降低了糖尿病患者中肾病的发病率,但糖尿病患病率的上升意味着全球DKD患者数量正在增加。对DKD生物学的深入了解以及新治疗靶点的识别可能会带来新的治疗方法。进展面临的一个主要挑战是DKD表型和肾脏进展的异质性。为了研究DKD的异质性,我们开展了东伦敦和北伦敦糖尿病队列(HEROIC)研究,这是一项基于二级医疗的多民族观察性研究,研究对象为经活检证实患有DKD的患者。我们的主要目标是在一组诊断为1型和2型糖尿病、蛋白尿和肾功能损害的患者中,确定与肾脏终点相关的DKD组织学特征。
HEROIC是一项纵向观察性研究,旨在招募500名有肾脏和心血管事件高风险的DKD患者。将收集人口统计学、临床和实验室数据,并在5年内每年进行评估。在招募时收集肾活检组织并存档。在基线和年度随访期间收集血液和尿液样本。在基线时以及随访期间再进行两次测量肾小球滤过率(GFR)、超声心动图、视网膜光学相干断层扫描血管造影以及肾脏和心脏MRI检查。该研究有90%的把握度检测关键组织学和影像学参数与死亡、肾脏替代治疗或估计GFR下降30%的综合指标之间的关联。
已获得布卢姆斯伯里研究伦理委员会(REC 18 - LO - 1921)的伦理批准。任何可识别患者的数据将存储在受密码保护的国家医疗服务体系N3网络上,并具有完整的审计跟踪。匿名的影像数据将存储在获得ISO27001认证的数据仓库中。研究结果将通过同行评审的手稿和会议报告,并使用基于网络和社交媒体的参与工具以及通过公共活动传播给参与者、患者和公众。