Looking back at the TEDDY study: lessons and future directions
Lernmark, Åke; Agardh, Daniel; Akolkar, Beena; Gesualdo, Patricia; Hagopian, William A.; Haller, Michael J.; Hyöty, Heikki; Johnson, Suzanne Bennett; Larsson, Helena Elding; Liu, Edwin; Lynch, Kristian F.; McKinney, Eoin F.; McIndoe, Richard; Melin, Jessica; Norris, Jill M.; Rewers, Marian; Rich, Stephen S.; Toppari, Jorma; Triplett, Eric; Vehik, Kendra; Virtanen, Suvi M.; Ziegler, Anette G.; Schatz, Desmond A.; Krischer, Jeffrey (2024)
Lernmark, Åke
Agardh, Daniel
Akolkar, Beena
Gesualdo, Patricia
Hagopian, William A.
Haller, Michael J.
Hyöty, Heikki
Johnson, Suzanne Bennett
Larsson, Helena Elding
Liu, Edwin
Lynch, Kristian F.
McKinney, Eoin F.
McIndoe, Richard
Melin, Jessica
Norris, Jill M.
Rewers, Marian
Rich, Stephen S.
Toppari, Jorma
Triplett, Eric
Vehik, Kendra
Virtanen, Suvi M.
Ziegler, Anette G.
Schatz, Desmond A.
Krischer, Jeffrey
2024
Nature Reviews Endocrinology
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Julkaisun pysyvä osoite on
https://urn.fi/URN:NBN:fi:tuni-202602122464
https://urn.fi/URN:NBN:fi:tuni-202602122464
Kuvaus
Peer reviewed
Tiivistelmä
The goal of the TEDDY (The Environmental Determinants of Diabetes in the Young) study is to elucidate factors leading to the initiation of islet autoimmunity (first primary outcome) and those related to progression to type 1 diabetes mellitus (T1DM; second primary outcome). This Review outlines the key findings so far, particularly related to the first primary outcome. The background, history and organization of the study are discussed. Recruitment and follow-up (from age 4 months to 15 years) of 8,667 children showed high retention and compliance. End points of the presence of autoantibodies against insulin, GAD65, IA-2 and ZnT8 revealed the HLA-associated early appearance of insulin autoantibodies (1–3 years of age) and the later appearance of GAD65 autoantibodies. Competing autoantibodies against tissue transglutaminase (marking coeliac disease autoimmunity) also appeared early (2–4 years). Genetic and environmental factors, including enterovirus infection and gastroenteritis, support mechanistic differences underlying one phenotype of autoimmunity against insulin and another against GAD65. Infant growth and both probiotics and high protein intake affect the two phenotypes differently, as do serious life events during pregnancy. As the end of the TEDDY sampling phase is approaching, major omics approaches are in progress to further dissect the mechanisms that might explain the two possible endotypes of T1DM.
Kokoelmat
- TUNICRIS-julkaisut [24353]
