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Circulating Biomarkers in the Development of Type 1 Diabetes

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City of Hope

Status

Enrolling

Conditions

Diabetes

Treatments

Other: One-time blood (up to 100 ml) will be drawn and the amount of blood drawn is based on weight. Saliva and urine will be collected during the blood draw visit.

Study type

Observational

Funder types

Other
NIH

Identifiers

NCT05505669
R01DK125856 (U.S. NIH Grant/Contract)
20477

Details and patient eligibility

About

More than 100 million U.S. adults are now living with diabetes or prediabetes. Investigators still do not fully understand how diabetes develops and how the disease worsens. Insulin is a hormone that helps the body use sugar as a fuel and control blood-sugar levels. People with diabetes have problems making insulin. This is because their insulin-producing beta cells -in the pancreas-are damaged or destroyed. A biomarker is a biological molecule (such as DNA, RNA (the genetic material of cells) or protein) that is a sign of a normal or abnormal process, or of a condition or disease. A biomarker can be measured and found in blood and/or other body fluids (such as saliva and urine). Understanding the biology of beta cells could help find diabetes-related biomarkers. The discoveries from this research could help with early diagnosis of diabetes and lead to the creation of therapies for treating diabetes.

Enrollment

165 estimated patients

Sex

All

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Documented informed consent/ assent from the subject

  • ONE of the following:

    • Type 1 diabetes patients (including pediatric patients) -OR-
    • Adult type 2 diabetes patients -OR-
    • Volunteers who are islet auto-antibody positive (i.e. insulin, GAA, IA-2, IAA and ZnT8 antibodies) with HbA1c ≤ 5.6% (including pediatric patients)-OR-
    • Adult participants with clinical diagnosis of high blood sugar (i.e. HbA1c of 5.7% to 6.4%)-OR-
    • Adult control subjects with HbA1cc ≤ 5.6%
  • Weight ≥ 30 kg

  • Willingness to: Provide blood sample(s) and if applicable: permit medical record/ clinical laboratory result review

Exclusion criteria

  • Control subjects must not have any chronic conditions or have undergone cellular, tissue or organ transplant
  • Sickle cell disease or anemia (exception: anemia that is corrected with treatment and source documents confirm corrected blood parameters current within 6 months of blood draw)
  • Active infection
  • Active malignancy (i.e., currently undergoing treatment)
  • Immunomodulatory therapy within 1 year of planned blood draw (may include immune checkpoint inhibitors, thalidomide, lenalidomide, pomalidomide, imiquimod, Bacillus Calmette-Guérin, and cytokines/ growth factors (e.g. interferons, interleukins)
  • Type 1 diabetes only: polyclonal regulatory T cell and/or dendritic cell therapy
  • Bleeding disorder
  • Women of childbearing potential: Pregnant/ nursing (Note: Eligibility may be deferred per blood donation timelines for pregnancy/nursing)
  • Diabetic patients only: Any clinical condition that might be adversely affected by the removal of up to 100 mL of blood
  • An employee who is under the direct/ indirect supervision of the PI/ a co-investigator/ the study manager
  • A direct study team member

Trial design

165 participants in 6 patient groups

Adults with type 1 diabetes
Description:
Adults with type 1 diabetes
Treatment:
Other: One-time blood (up to 100 ml) will be drawn and the amount of blood drawn is based on weight. Saliva and urine will be collected during the blood draw visit.
Adult healthy volunteers
Description:
Adult healthy volunteers
Treatment:
Other: One-time blood (up to 100 ml) will be drawn and the amount of blood drawn is based on weight. Saliva and urine will be collected during the blood draw visit.
Children with type 1 diabetes
Description:
Children with type 1 diabetes
Treatment:
Other: One-time blood (up to 100 ml) will be drawn and the amount of blood drawn is based on weight. Saliva and urine will be collected during the blood draw visit.
Adults with type 2 diabetes
Description:
Adults with type 2 diabetes
Treatment:
Other: One-time blood (up to 100 ml) will be drawn and the amount of blood drawn is based on weight. Saliva and urine will be collected during the blood draw visit.
Adults with high blood sugar
Description:
Adults with high blood sugar
Treatment:
Other: One-time blood (up to 100 ml) will be drawn and the amount of blood drawn is based on weight. Saliva and urine will be collected during the blood draw visit.
Those at risk of developing type 1 diabetes
Description:
Those at risk of developing type 1 diabetes
Treatment:
Other: One-time blood (up to 100 ml) will be drawn and the amount of blood drawn is based on weight. Saliva and urine will be collected during the blood draw visit.

Trial contacts and locations

1

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Central trial contact

Study Coordinator

Data sourced from clinicaltrials.gov

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