血清 GLYcomics 预测肝移植后移植物丢失和死亡率 (GLYGALT)
血清糖组学预测肝移植后移植物丢失和死亡率的验证
The first 12 months after liver transplantation (LT) are decisive in posttransplant outcome, as almost half of deaths and two thirds of graft loss requiring retransplant occur in the first year after LT. Since delaying retransplantation in those patients that experience an unfavorable posttransplant course directly impacts their outcome, timely decision making is of paramount importance in these individuals. However, balancing the need and right timing for retransplantation in individual patients with a complicated posttransplant course is currently a difficult challenge that relies on imperfect clinical variables and biomarkers, as well as the experienced judgment of the transplant team.
Building on the findings of a pilot study in liver transplant recipients (n = 131) led by the Ghent University Hospital, we want to validate the prognostic performance of the GlycoTransplantTest on a multicentric scale. In this pilot study, a single glycomic signature at day 7 after LT allowed accurate prediction of graft loss at 3 months after LT. The serum glycome of those patients experiencing graft loss was characterized by increased undergalactosylation and an increased presence of fucosylated and triantennary glycans. After statistical modeling, use of an optimized cutoff based on the relative abundance of 13 serum glycans showed a strong association with graft loss at 3 months (odds ratio 70.211; P<0.001; 95% CI: 10.876-453.23).
Using sequential measurements of serum glycomics in liver transplant recipients, we want to prospectively study and validate the predictive value of the serum glycomic signature for graft survival and overall survival at 3-months (primary end point) and 12-months after liver transplantation (secondary end point).
Determination of the serum glycomic profile is a high-throughput technique that allows to study and quantify the relative abundance of sugar chains (glycans) anchored at specific sites of serum proteins. This technique has shown a very strong prognostic value for graft loss at 3-months after liver transplantation in a pilot study at the Ghent University Hospital.
In this large-scale multicentric prognostic study, we will collect serum samples of liver transplant recipients at fixed time points.
Apart from the serum glycomic profile, we will collect data from the patients electronic record: demographic data (gender, age), data directly relevant to the indication of transplant (eg. imaging for primary liver cancer, lab values for diagnosis of end-stage liver disease), and outcome data (graft survival, overall survival, follow-up time). This list is non-exhaustive.
Using this approach, we will demonstrate the predictive validity of serum glycomics in liver transplant recipients for graft survival and overall survival at 3- and 12-months post-LT. Building on these data, the use of a simple blood test could differentiate patients at risk of graft loss and thus represent a paradigm shift directing these patients to timely treatment adaptations.
研究概览
研究类型
注册 (估计的)
联系人和位置
学习联系方式
- 姓名:Xavier Verhelst, MD, PhD
- 电话号码:0032 9 332 23 71
- 邮箱:xavier.verhelst@uzgent.be
研究联系人备份
- 姓名:Lorenz Grossar, MD
- 电话号码:0032 494 088 789
- 邮箱:lorenz.grossar@uzgent.be
学习地点
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Flanders
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Ghent、Flanders、比利时、9000
- 招聘中
- Xavier Verhelst
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接触:
- Xavier Verhelst, MD, PhD
- 电话号码:+3293322371
- 邮箱:xavier.verhelst@uzgent.be
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接触:
- Lorenz Grossar, MD
- 电话号码:+32494088789
- 邮箱:lorenz.grossar@uzgent.be
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参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
取样方法
研究人群
Adult patients active on the waiting list or undergoing a liver transplantation. All indications for liver transplantations are eligible.
描述
Inclusion Criteria:
- Signed and dated patient informed consent document
- Age ≥ 18 years
- Ability to comply with protocol-specified evaluations and scheduled visits
- Diagnosis of end-stage liver disease, primary hepatic malignancy meeting the Milan criteria for liver transplantation, or acute hepatic failure
- Eligible for liver transplantation and/or active on the waiting list for liver transplantation. Individuals eligible and/or active on the waiting list for multiple organ transplantation including the liver (eg. Combined liver and kidney transplantation, or intestinal transplantation) are also eligible for inclusion.
- Consulted the department of Gastroenterology and Hepatology at Ghent University Hospital
Exclusion Criteria:
- Transplantation of one or more organs not including the liver
学习计划
研究是如何设计的?
设计细节
- 观测模型:COHORT
- 时间观点:PROSPECTIVE
队列和干预
团体/队列 |
干预/治疗 |
|---|---|
|
No graft loss
Patients receiving liver transplantation that do NOT experience graft loss within 3-months or 12-months after liver transplantation. |
Determination of serum glycomics in the early posttransplant stage, using an optimal cutoff based on statistic modeling. |
|
Graft loss
Patients receiving liver transplantation that experience graft loss within 3-months or 12-months after liver transplantation. Graft loss is defined as either death of the liver transplant recipient (all-cause), or need for retransplantation of the liver. |
Determination of serum glycomics in the early posttransplant stage, using an optimal cutoff based on statistic modeling. |
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Graft loss
大体时间:3 months after liver transplantation
|
Death or need for retransplantation |
3 months after liver transplantation
|
|
Mortality
大体时间:3 months after liver transplantation
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All-cause mortality |
3 months after liver transplantation
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Graft loss
大体时间:12 months after liver transplantation
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Death or need for retransplantation |
12 months after liver transplantation
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Mortality
大体时间:12 months after liver transplantation
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All-cause mortality |
12 months after liver transplantation
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合作者和调查者
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
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