Biopsy-proven Diabetic Nephropathy in People With Type 2 Diabetes. Prevalence and Predictive Factors
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 300
- 试验地点
- 13
- 主要终点
- Prevalence
研究概览
简要总结
a prospective, observational, multi-center study with a cohort of 300 patients with Type 2 diabetes and macroalbuminuria. Prospectively we will collect kidney biopsies and analyse the transciptome of the kidney tissue and other biomarkers from blood, faeces, urine, proteomic- and metabolomic profiles and DNA-variants. Thereby we hope to be able to discover molecular and clinical profiles, that can help us in the diagnosis of DKD, and to identify different risks of progression that can benefit from different forms of personalized treatment.
详细描述
The PRIMETIME project is made to bring together molecular, translational and clinical scientists to create collaborations and build a scientific bridge between diabetology, nephrology, clinical biochemistry, and pathology. The ultimately goal is to bring forward an improved understanding of the most frequent cause of end stage renal disease: DKD. We aim to improve the diagnostic accuracy as well as the treatment precision by investigating in detail the features of histology and protein expression in both retrospective(WP1) and prospective(WP2) kidney biopsy material.
PRIMETIME WP2 is a prospective, observational, multi-center study with a cohort of 300 patients. We plan to create a systematically unselected cohort of patients with Type2 diabetes and macroalbuminuria as a sign of kidney injury. Prospectively we will collect research kidney biopsies and other biomarkers from blood, faeces, urine, proteomic- and metabolomic profiles and DNA-variants. The biopsies will be thoroughly investigated with cutting-edge molecular technologies and associated to the biomarkers, disease course and clinical outcome. The participants will afterward be followed in 20 years.Thereby we hope to be able to discover molecular and clinical profiles, that can help us in the diagnosis of DKD, and to identify different risks of progression that can benefit from different forms of personalized treatment.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 120 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Age ≥ 18 years
- •Written informed consent
- •Diagnosis with T2DM according to the American diabetes Association (20)
- •eGFR >30 mL/min/1.73 m2 (maximum six months old)
- •urine-albumin/creatinine-ratio (uACR) > 700 mg/g or 24 hours urine albumin >700 mg on more than one measurement
排除标准
- •Signs of acute kidney failure according to the KDIGO classification (21) at the time for kidney biopsy or the last 6 months before kidney biopsy
- •Factors that increases the risk of complications due to kidney biopsy:
- •Hemoglobin < 6 mmol/L
- •INR >1,4 at the time for biopsy
- •Platelet count < 100 x 109/l
- •Uncontrolled high blood pressure (defined as systolic blood pressure > 160 mmHg and/or diastolic blood pressure > 100 mmHg)
- •Only one functioning kidney
- •Evidence of urinary tract obstruction or hydronephrosis at the time of biopsy
- •Multiple bilateral kidney cysts
- •Kidney infection, peri-renal infection, or cutaneous infection that overlies the kidney at time for biopsy
- •Unwilling to receive blood transfusion
- •Unable to lie flat in bed six hours after biopsy
- •Any other contra-indications for percutaneous kidney biopsy according to local clinical guidelines
- •Unable to understand written and oral information
- •Kidney transplant recipient
- •Previous medical kidney biopsy
- •Women who are pregnant or planning to become pregnant before the kidney biopsy is performed
- •Treatment with Marcoumar (all other anticoagulants are accepted)
- •High thromboembolic risk combined with held in anticoagulation therapy according to the report "Perioperative regulation of antithrombotic treatment" (PRAB) (22)
- •mechanical heart valve
- •atrial fibrillation AND CHA2DS2-VASc> 5 and/or stroke within the last three months
- •recurrent venous thromboembolism OR venous thromboembolism within the last three months
- •less than 6 weeks after uncomplicated Acute Coronary Syndrome (ACS) with or without revascularization (Percutaneous Coronary Intervention (PCI)) with Bare Metal Stents (BMS) or Coronary Artery Bypass Grafting (CABG))
- •less than 3 months after uncomplicated ACS with revascularization (PCI with Drug Eluting Stent (DES))
- •less than 9-12 months after complicated ACS (e.g. reinfarction or stent thrombosis)
- •less than 1 month after revascularization in individuals with stable Coronary Artery Disease (CAD) (PCI with BMS or CABG)
- •less than 3 months after revascularization in individuals with stable CAD (PCI with DES)
- •less than 3 months after stroke, or Transient Ischemic Attack (TIA)
- •Inability to withdraw nonsteroidal anti-inflammatory drugs (NSAID) 7 days before biopsy
- •If a participant meets one or more exclusion criteria, that are reversible, the participant can be rescreened later on, to evaluate whether or not the participant now is qualified for participation.
结局指标
主要结局
Prevalence
时间窗: From baseline to end inclusion (3 years)
To investigate the prevalence of biopsy-proven diabetic nephropathy in individuals with T2DM with severe albuminuria; urine albumin/creatinine ratio (UACR) \>700 mg/g.
次要结局
- diabetic retinopathy(From baseline to end inclusion (3 years))
- non-diabetic nephropathy vs. biopsy-proven diabetic nephropathy(From baseline to end of followup (20 years))
- proteomic and metabolomic(From baseline to end of followup (20 years))
- Microbiome(From baseline to end of followup (20 years))
- Kidney Biopsy(From baseline to end of followup (20 years))
- Improved clinical diagnosis(From baseline to end inclusion (3 years))
- Annual changes in kidney status(From baseline to end of followup (20 years))
- Annual decline in eGRF(From baseline to end of followup (20 years))
- genetic variants(From baseline to end of followup (20 years))
- Death(From baseline to end of followup (20 years))
- Annual changes in albuminuria.(From baseline to end of followup (20 years))
- Annual events of cardiovascular disease(From baseline to end of followup (20 years))
研究者
Marie Møller
MD, PhD-student
Herlev Hospital