Screening for Type 1 Diabetes in the General Population: A Status Report and Perspective
Most screening programs to identify individuals at risk for type 1 diabetes have targeted relatives of people living with the disease to improve yield and feasibility. However, ∼90% of those who develop type 1 diabetes do not have a family history. Recent successes in disease-modifying therapies to...
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| Veröffentlicht in: | Diabetes (New York, N.Y.) Jg. 71; H. 4; S. 610 |
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| Format: | Journal Article |
| Sprache: | Englisch |
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01.04.2022
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| ISSN: | 1939-327X, 1939-327X |
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| Abstract | Most screening programs to identify individuals at risk for type 1 diabetes have targeted relatives of people living with the disease to improve yield and feasibility. However, ∼90% of those who develop type 1 diabetes do not have a family history. Recent successes in disease-modifying therapies to impact the course of early-stage disease have ignited the consideration of the need for and feasibility of population screening to identify those at increased risk. Existing population screening programs rely on genetic or autoantibody screening, and these have yielded significant information about disease progression and approaches for timing for screening in clinical practice. At the March 2021 Type 1 Diabetes TrialNet Steering Committee meeting, a session was held in which ongoing efforts for screening in the general population were discussed. This report reviews the background of these efforts and the details of those programs. Additionally, we present hurdles that need to be addressed for successful implementation of population screening and provide initial recommendations for individuals with positive screens so that standardized guidelines for monitoring and follow-up can be established. |
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| AbstractList | Most screening programs to identify individuals at risk for type 1 diabetes have targeted relatives of people living with the disease to improve yield and feasibility. However, ∼90% of those who develop type 1 diabetes do not have a family history. Recent successes in disease-modifying therapies to impact the course of early-stage disease have ignited the consideration of the need for and feasibility of population screening to identify those at increased risk. Existing population screening programs rely on genetic or autoantibody screening, and these have yielded significant information about disease progression and approaches for timing for screening in clinical practice. At the March 2021 Type 1 Diabetes TrialNet Steering Committee meeting, a session was held in which ongoing efforts for screening in the general population were discussed. This report reviews the background of these efforts and the details of those programs. Additionally, we present hurdles that need to be addressed for successful implementation of population screening and provide initial recommendations for individuals with positive screens so that standardized guidelines for monitoring and follow-up can be established.Most screening programs to identify individuals at risk for type 1 diabetes have targeted relatives of people living with the disease to improve yield and feasibility. However, ∼90% of those who develop type 1 diabetes do not have a family history. Recent successes in disease-modifying therapies to impact the course of early-stage disease have ignited the consideration of the need for and feasibility of population screening to identify those at increased risk. Existing population screening programs rely on genetic or autoantibody screening, and these have yielded significant information about disease progression and approaches for timing for screening in clinical practice. At the March 2021 Type 1 Diabetes TrialNet Steering Committee meeting, a session was held in which ongoing efforts for screening in the general population were discussed. This report reviews the background of these efforts and the details of those programs. Additionally, we present hurdles that need to be addressed for successful implementation of population screening and provide initial recommendations for individuals with positive screens so that standardized guidelines for monitoring and follow-up can be established. Most screening programs to identify individuals at risk for type 1 diabetes have targeted relatives of people living with the disease to improve yield and feasibility. However, ∼90% of those who develop type 1 diabetes do not have a family history. Recent successes in disease-modifying therapies to impact the course of early-stage disease have ignited the consideration of the need for and feasibility of population screening to identify those at increased risk. Existing population screening programs rely on genetic or autoantibody screening, and these have yielded significant information about disease progression and approaches for timing for screening in clinical practice. At the March 2021 Type 1 Diabetes TrialNet Steering Committee meeting, a session was held in which ongoing efforts for screening in the general population were discussed. This report reviews the background of these efforts and the details of those programs. Additionally, we present hurdles that need to be addressed for successful implementation of population screening and provide initial recommendations for individuals with positive screens so that standardized guidelines for monitoring and follow-up can be established. |
| Author | Rich, Stephen S Martin, Frank Herold, Kevan C Dayan, Colin Rewers, Marian Griffin, Kurt J Knip, Mikael Sims, Emily K Ziegler, Anette-Gabriele Long, Anna E Kordonouri, Olga Wentworth, John M Besser, Rachel E J Hagopian, William Greenbaum, Carla Mathieu, Chantal Steck, Andrea K Geno Rasmussen, Cristy |
| Author_xml | – sequence: 1 givenname: Emily K orcidid: 0000-0002-4393-954X surname: Sims fullname: Sims, Emily K organization: Department of Pediatrics, Indiana University School of Medicine, Indianapolis, IN – sequence: 2 givenname: Rachel E J surname: Besser fullname: Besser, Rachel E J organization: Wellcome Centre for Human Genetics, University of Oxford, Oxford, U.K – sequence: 3 givenname: Colin surname: Dayan fullname: Dayan, Colin organization: Cardiff University School of Medicine, Cardiff, U.K – sequence: 4 givenname: Cristy surname: Geno Rasmussen fullname: Geno Rasmussen, Cristy organization: Barbara Davis Center for Diabetes, School of Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO – sequence: 5 givenname: Carla orcidid: 0000-0003-4451-9800 surname: Greenbaum fullname: Greenbaum, Carla organization: Benaroya Research Institute, Seattle, WA – sequence: 6 givenname: Kurt J surname: Griffin fullname: Griffin, Kurt J organization: Sanford Health, Sioux Falls, SD – sequence: 7 givenname: William orcidid: 0000-0003-2979-0475 surname: Hagopian fullname: Hagopian, William organization: Pacific Northwest Research Institute, Seattle, WA – sequence: 8 givenname: Mikael orcidid: 0000-0003-0474-0033 surname: Knip fullname: Knip, Mikael organization: Tampere Center for Child Health Research, Tampere University Hospital, Tampere, Finland – sequence: 9 givenname: Anna E surname: Long fullname: Long, Anna E organization: Bristol Medical School, University of Bristol, Bristol, U.K – sequence: 10 givenname: Frank surname: Martin fullname: Martin, Frank organization: JDRF, New York, NY – sequence: 11 givenname: Chantal orcidid: 0000-0002-6099-2406 surname: Mathieu fullname: Mathieu, Chantal organization: Department of Endocrinology, UZ Gasthuisberg, KU Leuven, Leuven, Belgium – sequence: 12 givenname: Marian surname: Rewers fullname: Rewers, Marian organization: Barbara Davis Center for Diabetes, School of Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO – sequence: 13 givenname: Andrea K orcidid: 0000-0002-5931-9484 surname: Steck fullname: Steck, Andrea K organization: Barbara Davis Center for Diabetes, School of Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO – sequence: 14 givenname: John M orcidid: 0000-0002-5197-3529 surname: Wentworth fullname: Wentworth, John M organization: Departments of Diabetes and Endocrinology and Population Health and Immunity, Royal Melbourne Hospital and Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia – sequence: 15 givenname: Stephen S orcidid: 0000-0003-3872-7793 surname: Rich fullname: Rich, Stephen S organization: Center for Public Health Genomics, University of Virginia, Charlottesville, VA – sequence: 16 givenname: Olga orcidid: 0000-0001-9563-3537 surname: Kordonouri fullname: Kordonouri, Olga organization: Kinder und Jugendkrankenhaus Auf der Bult, Hannover, Germany – sequence: 17 givenname: Anette-Gabriele orcidid: 0000-0002-6290-5548 surname: Ziegler fullname: Ziegler, Anette-Gabriele organization: School of Medicine, Technical University of Munich, Munich, Germany – sequence: 18 givenname: Kevan C orcidid: 0000-0003-1534-6613 surname: Herold fullname: Herold, Kevan C organization: Department of Immunobiology and Department of Internal Medicine, Yale University, New Haven, CT |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/35316839$$D View this record in MEDLINE/PubMed |
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| Title | Screening for Type 1 Diabetes in the General Population: A Status Report and Perspective |
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