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临床试验/NCT06373913
NCT06373913招募中不适用

The Role of Proprotein-convertase-subtilisin/Kexin-type 9 in Kidney Damage in Nephrotic Syndrom

Kolding Sygehus1 个研究点 分布在 1 个国家目标入组 75 人开始时间: 2023年6月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
75
试验地点
1
主要终点
Plasma PCSK9 correlated to the degree of protein in the urine

研究概览

简要总结

Nephrotic syndrome (NS) is characterized by gross proteinuria (>3.5 g/day), hypoalbuminaemia, edema and often hyperlipidemia. Hyperlipidemia is correlated with increased morbidity and mortality.

The study aim is to investigate the role of the protein convertase subtilisin/kexin type 9 (PCSK9) in hyperlipidemia of NS, which has been suggested to play an important role. This is done by testing the following hypotheses:

  1. PCSK9 is increased in patients with NS and hyperlipidemia compared to kidney-healthy controls
  2. The level of PCSK9 in plasma correlates to the degree of proteinuria.
  3. PCSK9 i increased in the kidney tissue of patients with NS

The study will compare plasma levels of PCSK9 in correlation with degree of protein in the urine between test persons with NS and kidney healthy controls. Furthermore the investigators will study the the degree of PCSK9 in the kidney in biopsies obtained from test persons with nephrotic syndrome and test persons without proteinuria.

详细描述

Hyperlipidemia in kidney disease is associated with a substantially increase of risk in development of atherosclerotic cardiovascular disease (CVD) (European Atherosclerosis Society 2011). Furthermore animal studies have suggested that hyperlipidemia escalates progression of glomerular injury.

Nephrotic syndrome (NS) - the feature of many primary and secondary glomerulopathies - is characterized by gross proteinuria (>3.5 g/day), hypoalbuminaemia, edema and often hyperlipidemia. The protein Convertase subtilisin/kexin 9 (PCSK9) is over expressed in NS and has been suggested to play an important role in developing of hyperlipidemia. PCSK9 increases the LDL receptor degradation by preventing it from recycling to the cell membrane, resulting in increased plasma LDL cholesterol.

PCSK9 is produced primarily in the liver, but to a lesser extent in the brain, intestine and kidney. A recent study found that the expression of renal PCSK9 is increased in mice with experimental NS compared to controls. The investigators want to further explore this.

The overall aim is to decrease morbidity and mortality associated with NS and hyperlipidemia, by testing the following hypotheses:

  1. PCSK9 is increased in patients with NS and hyperlipidemia compared to kidney-healthy controls
  2. The level of PCSK9 in plasma correlates to the degree of proteinuria.
  3. PCSK9 i increased in the kidney tissue of patients with NS

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 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 18 years old
  • Patients admitted to the Medical Department and/or the Medical Emergency Department, Kolding Sygehus.

排除标准

  • Refusal to give informed consent
  • Treatment with PCSK9 inhibitors
  • Any acute or chronic condition that would limit the ability of the patient to participate in the study
  • Control group: proteinuria

结局指标

主要结局

Plasma PCSK9 correlated to the degree of protein in the urine

时间窗: Measured at inclusion and for the nephrotic group after remission, if this is accomplished within a year

PCSK9 in plasma measured by ELISA, correlated to protein in 24hour urine

Degree of PCSK9 in kidney tissue

时间窗: Measured at inclusion in test person group, if this is performed within in the study period (before august 2028).

Immunohistochemistry; degree of staining a in test persons, who are subjected to kidney biopsy.

次要结局

  • Localization of PCSK9 in kidney tissue(Measured at inclusion in test person group, if this is performed within in the study period (before august 2028).)

研究者

发起方
Kolding Sygehus
申办方类型
Other
责任方
Sponsor

研究点 (1)

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