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临床试验/NCT03664908
NCT03664908已完成不适用

Detection of Anti-glomerular Basement Membrane Antibodies (Anti-GBM): a Promising Biomarker for Lupus Nephritis (LN) Screening in Systemic Lupus Erythematosus (SLE) Patients?

CHU de Reims1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2018年9月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
CHU de Reims
入组人数
100
试验地点
1
主要终点
Percentage of serum with anti GBM positivity

研究概览

简要总结

Introduction and background :

Glomerulonephritis and auto-immune diseases are often associated. Lupus nephritis (LN) is one of the major clinical manifestations of systemic lupus erythematosus (SLE) which have a severe impact on prognosis. This complication is a real challenge for clinicians because of insidious-onset and no predictable relapses. Biomarker use is therefore essential, but conventional biomarkers such as proteinuria have poor sensivity and low specificity to predict LN occurrence, and new more reliable biomarkers (genetic, epigenetic or protein biomarkers) are difficult to use for daily medical practice.

Anti-glomerular membrane basement disease (anti-GBM disease) is a rare (0.5 to 1/millions of inhabitants) and severe illness, characterised by rapidly progressive glomerulonephritis, pulmonary haemorrhage and the presence of anti-GBM antibodies, which are highly sensible (100%) and specific (92-100%) of this condition

. Our experience and literature review

In our department of internal medicine, we report one case of anti-GBM glomerulonephritis associated to an active SLE. After literature review, we note the following studies:

  • some similar association cases had been reported.
  • In 2006, a Chinese cohort study highlighted important rates of anti-GBM antibodies, in serum samples from patients with SLE (14 positives/157patients (8.9%) using ELISA method). Moreover, every SLE patient with positive circulating anti-GMB antibodies LN and a severer SLE (with significantly more anemias, pulmonary hemorrhage). According to histological data's, they also had more important kidney damages (10/14 had necrotizing crescentic glomerulonephritis lesions and 5/14 fulfil criteria's for anti-GBM disease diagnosis).
  • We also note that some authors published experimental studies showing that immunological and genetic links exist between LN and anti-GBM disease, which could explain this association.

3. Main Hypothesis: Based on these findings, we suspect that detection of significant levels of circulating anti-GBM antibodies may be more frequent in SLE followed patients than in general population, and that it could be an interesting biomarker of LN in patient with SLE.

4. Objectives First objective: based on 2 SLE patient groups (one having lupus nephritis and the other without it) we would like to compare the ratio of positive anti-GBM antibodies in each group, expecting a higher rate in SLE patients with LN.

Second objective: will be to study the positive anti-GBM group patients in their clinical aspects, serological features and renal characteristics, in this SLE population.

5. Materials and methods We suggest a retrospective analytic transversal controlled study, based on serum samples from the Lupus Biobank of Upper Rhine (LBBR project), and based on serum samples from healthy voluntary blood donors (control group). We will then perform tests in each serum sample group in our immunology laboratory and compare the ratio of positive anti-GBM in each arm.

详细描述

Introduction and context :

Glomerulonephritis and auto-immune diseases are often associated. Lupus nephritis (LN) is one of the major clinical manifestations of systemic lupus erythematosus (SLE) which have a severe impact on prognosis. This complication is a real challenge for clinicians because of insidious-onset and no predictable relapses. Biomarker use is therefore essential, but conventional biomarkers such as proteinuria, glomerular filtration rate, urine sediments, anti-dsDNA antibodies and complement levels, have poor sensivity and low specificity to predict LN occurrence, and new more reliable biomarkers (such as genetic, epigenetic or protein biomarkers) are difficult to use for daily medical practice , .

Anti-glomerular membrane basement disease (anti-GBM disease) is a rare (0.5 to 1/millions of inhabitants , ) and severe illness , , characterised by rapidly progressive glomerulonephritis, pulmonary haemorrhage and the presence of anti-GBM antibodies, which are highly sensible (100%) and specific (92-100%) of this condition .

In our department of internal medicine, one case of Goodpasture glomerulonephritis associated to an active SLE has been reported , and after searching data in literature, we note the following studies:

  • some similar cases were reported such as a case of pulmonary hemorrhage and positive anti-GBM in SLE , or a case of anti-GBM disease and LN presenting as pulmonary-renal syndrome .
  • In 2006, a Chinese cohort study highlighted an elevated prevalence of anti-GBM antibodies, in serum samples from patients with SLE (14 positives/157patients (8.9%) with ELISA method). Moreover, every patient with positive anti-GMB antibodies had LN and a severer SLE (with more anemias, pulmonary hemorrhage). They also suffered from more important kidney disease. In fact, in histological criteria's, 10/14 had necrotizing crescentic glomerulonephritis lesions and 5/14 had a real diagnosis of Goodpasture disease.
  • We also note that some authors have already studied pathogenesis of this association (whether immunological explanations , genetics links , ).

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Screening
盲法
None

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

  • serum samples coming from LBBR lupus biobank (diagnosis of lupus according ACR criteria or diagnosis of lupus nephritis according to ISN/RPS2003) or serum sample coming from healthy bload donor volunters
  • having signed the informed consent

排除标准

  • diagnosis of lupus nephritis and having a beginning kidney disease (every class I and II of WHO classification and class I or II of ISN/RPS classification)
  • lack of data regarding kidney histology on clinical LBBR file
  • minor healthy blood donor
  • healthy blood donor volunters with auto immune disease, or kidney disease, or chronic renal failure or taking immunosuppressive or immunomodulatory therapy or with history of cutaneous lupus or SLE

结局指标

主要结局

Percentage of serum with anti GBM positivity

时间窗: Day 0

circulating antibody rates higher than 20 cu/mi using chemiluminescence

次要结局

  • Description of clinical features of patients(Day 0)
  • Description of SLE characteristics(Day 0)
  • Description of immunological characteristics of patients with anti GBM positivity(Day 0)
  • Description of renal characteristics of patient with anti GBM positivity(Day 0)

研究者

发起方
CHU de Reims
申办方类型
Other
责任方
Sponsor

研究点 (1)

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