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Validation of a Predictive Risk Equation for Type 2 Diabetes in Families With Risk (DESCENDANCE)

Validation of a Predictive Risk Equation for Type 2 Diabetes in Children With Diabetes to Achieve a Predictive Diagnostic Biochip for the Early Detection of Individuals at Risk in Families.

Considering its epidemic-like development worldwide, associated with modifications in lifestyle, as well as its enormous social and economic weight, the prevention of type II diabetes is certain to be a central concern of health systems within the developed countries in the decades to come. However, while simple obesity concerns the entire population, type 2 diabetes affects only one sub-population at high genetic risk. To be effective and realistic in economic terms, efforts at prevention must be thus targeted towards these subjects at high risk. The key issue involves identifying such subjects early enough so that a strategy of effective prevention can be organized in good time.

Until now, efforts have been concentrated on individuals at risk for diabetes readily identifiable within the general population, typically subjects in the second half of adulthood, presenting abdominal obesity and mild abnormalities of blood sugar. Preventive lifestyle and dietary measures are proposed but are constrictive and difficult to maintain over time, and the results, although they may be significant, remain disappointing, with mere postponement of an outcome which at this stage appears inevitable. The reason is ascribable to excessively tardy intervention, when the pathogenic process has already been ongoing for some ten years and the endocrine function of the pancreas is probably already irreparably impaired.

The alternative thus is earlier intervention, in childhood, adolescence or early adulthood. The problem is to identify individuals at high risk of becoming diabetic at a time when they are presenting no simple clinical or laboratory abnormalities allowing easy diagnosis. The familial character of type 2 diabetes is now well established, and future diabetic subjects are themselves above all the children of diabetic subjects. However, the prevalence of the disease among the descendants of type 2 diabetic subjects is around 20-30% and predictive tools are needed to combat diabetes in these high-risk families.

We propose to create a risk equation using an algorithm to reliably predict children most likely to develop diabetes later in life.

The algorithm will include 3 classes of data:

  • The genotype stemming from the genetic characterization of individuals and those their parents;
  • Environmental data concerning childhood, especially eating habits and physical activity;
  • Data of the mother who was eventually diabetic during pregnancy.

From a methodological standpoint, it would be rather difficult to take blood samples from children and wait some 50 years to determine whether or not they develop diabetes. To circumvent this difficulty, we will recruit subjects in families with a history of type II diabetes:

  • Parents alive, including at least one type 2 diabetic subject
  • Adult children (aged over 35 years), some of whom are already presenting type II diabetes, and healthy brothers and sisters, who form the control population. Test will be done to determine whether healthy subjects are really safe from the risk of diabetes (HbA1c measurement and glucose load test).

The Descendence study will include 500 families at risk involving about 3000 subjects (1000 subjects with diabetes and 2000 healthy subjects). It is expected to answer the following question: for a child born in such families at risk, what is the probability of developing diabetes later in life, so that early preventive action may be taken

研究概览

研究类型

介入性

注册 (实际的)

1035

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

      • Liege、比利时、4000
        • CHU Sart Tilman Liege
      • Besancon、法国、25030
        • Chu Jean Minjoz
      • Bobigny、法国、93000
        • CHU Avicenne
      • Bondy、法国
        • CHU de Bondy
      • Brest、法国
        • CHU de Brest
      • Caen、法国、14000
        • CHU de Caen
      • Evry、法国、91000
        • Ch Sud Francilien
      • Grenoble、法国、38043
        • University Hospital Grenoble
      • Le Kremlin-Bicêtre、法国、94270
        • CHU de Bicêtre
      • Lille、法国、59037
        • CHRU Lille
      • Marseille、法国、13274
        • CHU Marseille Hôpitaux Sud
      • Nancy、法国、54500
        • CHU de Nancy
      • Nantes、法国、44000
        • CHU de Nantes
      • Paris、法国、75877
        • CHU Bichat
      • Reims、法国
        • CHU de Reims
      • Strasbourg、法国、67000
        • Centre Hospitalier Strasbourg
      • Toulouse、法国、31403
        • CHU Toulouse

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

25年 及以上 (成人、年长者)

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Families at risk for diabetes defined by the existence of the disease in two successive generations and consists with healthy subject in the two generations.
  • Subjects must be aged over 25 years

Exclusion Criteria:

  • subject refusing to participate
  • pregnant women

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:预防
  • 分配:非随机化
  • 介入模型:并行分配
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
其他:Type 2 diabetic subject
Subject with type 2 diabetes
其他:healthy subject
Healthy subjet from family where there is the existence of the disease (type 2 diabetes) in two successive generations
Oral Glucoce Tolerance Test

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
Measure of risk of developing type 2 diabetes in at-risk families
大体时间:participants will be followed from the moment where they sign consent form and until they have sent back questionnary and done the blood test, an expected average of 4 weeks
Oral Glucose Tolerance Test (only for health volunteers) HbA1c assay (for type 2 diabetic subject)
participants will be followed from the moment where they sign consent form and until they have sent back questionnary and done the blood test, an expected average of 4 weeks

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2011年12月14日

初级完成 (实际的)

2020年11月24日

研究完成 (实际的)

2020年11月24日

研究注册日期

首次提交

2012年11月8日

首先提交符合 QC 标准的

2012年11月12日

首次发布 (估计)

2012年11月16日

研究记录更新

最后更新发布 (实际的)

2021年5月11日

上次提交的符合 QC 标准的更新

2021年5月7日

最后验证

2020年8月1日

更多信息

与本研究相关的术语

其他研究编号

  • 2011-A00686-35

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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