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临床试验/NCT03205865
NCT03205865Enrolling By Invitation不适用

Natural History of Pre-Diabetic Autoimmunity

University of Colorado, Denver0 个研究点目标入组 2,700 人开始时间: 1993年12月6日最近更新:
适应症

试验速览

阶段
不适用
状态
Enrolling By Invitation
入组人数
2,700
主要终点
Diagnosis of Type 1 Diabetes

研究概览

简要总结

Type 1 diabetes (T1D) affects 1.4 million people in the U.S. and its incidence has doubled over the past 20 years. The Diabetes Autoimmunity in the Young Study (DAISY) will estimate overall burden of T1D and other autoimmune diseases in the general population by age 30. The study will evaluate environmental risk factors for development of islet autoimmunity and progression to T1D.

详细描述

Children determined to be at an increased risk for development of type 1 diabetes, either due to known genetic markers or due to family history of T1D, are followed from birth and monitored for development of T1D-related autoimmunity, on an annual basis. At annual clinic visits, participants are tested for development of these autoantibodies and data is collected related to environmental exposures. In addition to blood collection for determination of autoantibodies, serum and plasma are frozen, and stored for future analyses. Other biological samples collected for further future analysis include: throat swabs, rectal swabs, saliva, and urine. If T1D-related autoantibodies are detected, the participant is asked to increase the frequency of clinic visits to 2-4 visits per year in order to more closely monitor for onset of disease. The endpoint of the study is diagnosis of T1D per the American Diabetes Association (ADA) criteria.

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
1 Month 至 30 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • General Population Genetic Screening to determine Enrollment Eligibility for the Follow-Up Study Criteria
  • Child born at St. Joseph Hospital between 1/1/1993 and 6/30/2006
  • Informed consent for genetic screening obtained
  • Cord blood sample available
  • No other severe co-existent condition
  • At least one parent/guardian speaks English
  • General Population Follow Up Study Criteria
  • Informed consent for Follow Up obtained
  • Initial telephone interview at 3 months of age, initial blood draw at 9 months of age
  • High or moderate risk of T1D, as determined from genetic screening (300 low risk children also enrolled as a control group)
  • Sibling/offspring Follow Up Criteria
  • Informed consent for follow up obtained
  • Age < 4 yrs (< 7 yrs prior to 1997)
  • No other severe co-existent condition
  • At least one parent/guardian speaks English
  • Family Members Follow Up Criteria
  • Informed consent obtained
  • First degree relative of either a sibling/offspring participant or general population newborn participant
  • No other severe co-existent condition
  • Ages 12 months to 65 years
  • One clinic visit to obtain blood for genetic marker determination and islet autoantibody screening
  • TEDDY Grad participants
  • Completed the TEDDY protocol
  • TEDDY home center is Colorado, Washington, Georgia
  • Upon completion of the TEDDY protocol, persistently positive for islet autoantibodies at 13.5 yrs of age or older
  • Not diagnosed with T1D
  • Informed Consent obtained

排除标准

  • Cord blood was not available for genetic screening,
  • Other severe co-morbidities were indicated,
  • Parents refused consent to screening or follow-up,
  • At least one parent or legal guardian did not speak English, or
  • If T1D had been diagnosed.
  • Individuals were not eligible to be enrolled into the DAISY study under the Sibling/offspring criteria if:
  • They did not have a first degree relative with T1D,
  • Other severe co-morbidities were indicated,
  • They were older than 4 years of age (older than 7 years of age, before 1997),
  • Parents refused consent to follow-up,
  • At least one parent or legal guardian did not speak English, or
  • T1D had been diagnosed.
  • Individuals do not agree to the long-term storage of data and specimen samples.

结局指标

主要结局

Diagnosis of Type 1 Diabetes

时间窗: From date of birth until the date of first documentation of type 1 diabetes up to 30 years of age.

Children determined to be at an increased risk for development of type 1 diabetes (T1D), either due to known genetic markers or due to family history of T1D, are followed from birth and monitored for development of T1D-related autoimmunity, on an annual basis. The endpoint of the study is diagnosis of T1D per the American Diabetes Association (ADA) criteria.

次要结局

  • Detection of Islet Autoantibodies(From date of birth until the date of first documentation of Islet auto-antibodies up to 20years of age.)

研究者

申办方类型
Other
责任方
Sponsor

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