DAISY: Diabetes Autoimmunity Study in the Young
Study Details
Study Description
Brief Summary
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.
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Detailed Description
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.
Study Design
Outcome Measures
Primary Outcome Measures
- Diagnosis of Type 1 Diabetes [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.
Secondary Outcome Measures
- Detection of Islet Autoantibodies [From date of birth until the date of first documentation of Islet auto-antibodies up to 20years of age.]
At annual clinic visits, participants are tested for development of these auto-antibodies and data is collected related to environmental exposures. In addition to blood collection for determination of auto-antibodies, serum and plasma are frozen, and stored for future analyses.
Other Outcome Measures
- Detection of Transglutaminase Antibodies [From date of birth until the date of first documentation of Transglutaminase auto-antibodies up to 18 years of age.]
At annual clinic visits, using a validated assay, detection of a Celiac Disease related antibody, transglutaminase indicates seroconversion and isolates a period of time in which a change in the immune response, targeting the small intestine.
Eligibility Criteria
Criteria
Inclusion Criteria:
General Population Genetic Screening to determine Enrollment Eligibility for the Follow-Up Study Criteria
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Child born at St. Joseph Hospital between 1/1/1993 and 6/30/2006
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Informed consent for genetic screening obtained
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Cord blood sample available
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No other severe co-existent condition
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At least one parent/guardian speaks English
General Population Follow Up Study Criteria
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Informed consent for Follow Up obtained
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Initial telephone interview at 3 months of age, initial blood draw at 9 months of age
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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
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Informed consent for follow up obtained
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Age < 4 yrs (< 7 yrs prior to 1997)
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No other severe co-existent condition
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At least one parent/guardian speaks English
Family Members Follow Up Criteria
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Informed consent obtained
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First degree relative of either a sibling/offspring participant or general population newborn participant
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No other severe co-existent condition
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Ages 12 months to 65 years
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One clinic visit to obtain blood for genetic marker determination and islet autoantibody screening
Exclusion Criteria:
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Cord blood was not available for genetic screening,
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Other severe co-morbidities were indicated,
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Parents refused consent to screening or follow-up,
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At least one parent or legal guardian did not speak English, or
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If T1D had been diagnosed.
Individuals were not eligible to be enrolled into the DAISY study under the
Sibling/offspring criteria if:
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They did not have a first degree relative with T1D,
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Other severe co-morbidities were indicated,
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They were older than 4 years of age (older than 7 years of age, before 1997),
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Parents refused consent to follow-up,
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At least one parent or legal guardian did not speak English, or
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T1D had been diagnosed.
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Individuals do not agree to the long-term storage of data and specimen samples.
Contacts and Locations
Locations
No locations specified.Sponsors and Collaborators
- University of Colorado, Denver
Investigators
- Principal Investigator: Marian J Rewers, MD, PhD, MPH, Executive Director-Barbara Davis Center for Diabetes, Professor
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 92-080