Your browser doesn't support javascript.
loading
Islet autoantibody frequency in relatives of children with type 1 diabetes who have a type 2 diabetes diagnosis.
Lewis, Shanice J; Williams, Claire L; Mortimer, Georgina L; Oram, Richard A; Hagopian, William A; Gillespie, Kathleen M; Long, Anna E.
Afiliação
  • Lewis SJ; Translational Health Sciences, Diabetes and Metabolism, Bristol Medical School, University of Bristol, Bristol, UK.
  • Williams CL; Translational Health Sciences, Diabetes and Metabolism, Bristol Medical School, University of Bristol, Bristol, UK.
  • Mortimer GL; Translational Health Sciences, Diabetes and Metabolism, Bristol Medical School, University of Bristol, Bristol, UK.
  • Oram RA; Institute of Biomedical and Clinical Science, Faculty of Health and Life Sciences, University of Exeter, Exeter, United Kingdom.
  • Hagopian WA; Pacific Northwest Diabetes Research Institute, University of Washington, Seattle, Washington, USA.
  • Gillespie KM; Translational Health Sciences, Diabetes and Metabolism, Bristol Medical School, University of Bristol, Bristol, UK.
  • Long AE; Translational Health Sciences, Diabetes and Metabolism, Bristol Medical School, University of Bristol, Bristol, UK.
Diabet Med ; : e15394, 2024 Jun 27.
Article em En | MEDLINE | ID: mdl-38937948
ABSTRACT

AIM:

This study aimed to evaluate characteristics of autoimmunity in individuals who have a type 2 diagnosis and are relatives of children with type 1 diabetes.

METHODS:

Pre-diagnosis samples (median 17 months before onset) from relatives who were later diagnosed with type 2 diabetes were measured for autoantibodies to glutamate decarboxylase 65 (GADA), islet antigen-2 (IA-2A), zinc transporter 8 (ZnT8A) and insulin (IAA) as well as the type 1 diabetes genetic risk score (GRS2). Associations between islet autoantibodies, insulin treatment and GRS2 were analysed using Fisher's exact and t-tests.

RESULTS:

Among 226 relatives (64% men; mean age at sampling 41 years; mean age 54 years at diagnosis), 32 (14%) were islet autoantibody-positive for at least one autoantibody more than a decade before diagnosis. Approximately half of these (n = 15) were treated with insulin. GADA-positivity was higher in insulin-treated relatives than in non-insulin-treated relatives (12/18 [67%] vs. 6/18 [33%], p < 0.001). IAA-positivity was observed in 13/32 (41%) of relatives with autoantibodies. GRS2 scores were increased in autoantibody-positive relatives (p = 0.032), but there was no clear evidence for a difference according to treatment (p = 0.072).

CONCLUSION:

This study highlights the importance of measuring islet autoantibodies, including IAA, in relatives of people with type 1 diabetes to avoid misdiagnosis.
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Diabet Med Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Diabet Med Ano de publicação: 2024 Tipo de documento: Article