4.3 Article

Decreased occurrence of ketoacidosis and preservation of beta cell function in relatives screened and monitored for type 1 diabetes in Australia and New Zealand

期刊

PEDIATRIC DIABETES
卷 23, 期 8, 页码 1594-1601

出版社

WILEY-HINDAWI
DOI: 10.1111/pedi.13422

关键词

adolescent; Australasian diabetes data network; beta cell; child; diabetic ketoacidosis; HbA1c; IDAA1c; insulin dose; intranasal insulin trial; islet autoimmunity; screening; TrialNet; type 1 diabetes

资金

  1. Juvenile Diabetes Research Foundation International
  2. National Health and Medical Research Council
  3. National Institute of Diabetes and Digestive and Kidney Diseases
  4. JDRF Australia
  5. National Institute of Allergy and Infectious Diseases
  6. Eunice Kennedy Shriver National Institute of Child Health and Human Development [U01 DK 106693-02, UC4 DK11700901, UC4 DK106993, U01 DK107014, U01 DK107013, U01 DK106994, U01 DK106984, U01 DK103282, U01 DK103266, U01 DK103153, U01 DK103180]
  7. [U01 DK085509]
  8. [U01 DK085504]
  9. [U01 DK085499]
  10. [U01 DK085476]
  11. [U01 DK085466]
  12. [U01 DK085465]
  13. [U01 DK085461]
  14. [U01 DK085453]
  15. [U01 DK061058]
  16. [U01 DK061034]
  17. [U01 DK061010]

向作者/读者索取更多资源

T1D autoantibody screening and metabolic monitoring of older children and young adults in Australia and New Zealand can reduce the risk of DKA and improve glucose control. These clinical benefits support ongoing efforts to increase screening activity in the region.
Aims Islet autoantibody screening of infants and young children in the Northern Hemisphere, together with semi-annual metabolic monitoring, is associated with a lower risk of ketoacidosis (DKA) and improved glucose control after diagnosis of clinical (stage 3) type 1 diabetes (T1D). We aimed to determine if similar benefits applied to older Australians and New Zealanders monitored less rigorously. Methods DKA occurrence and metabolic control were compared between T1D relatives screened and monitored for T1D and unscreened individuals diagnosed in the general population, ascertained from the Australasian Diabetes Data Network. Results Between 2005 and 2019, 17,105 relatives (mean (SD) age 15.7 (10.8) years; 52% female) were screened for autoantibodies against insulin, glutamic acid decarboxylase, and insulinoma-associated protein 2. Of these, 652 screened positive to a single and 306 to multiple autoantibody specificities, of whom 201 and 215, respectively, underwent metabolic monitoring. Of 178 relatives diagnosed with stage 3 T1D, 9 (5%) had DKA, 7 of whom had not undertaken metabolic monitoring. The frequency of DKA in the general population was 31%. After correction for age, sex and T1D family history, the frequency of DKA in screened relatives was >80% lower than in the general population. HbA1c and insulin requirements following diagnosis were also lower in screened relatives, consistent with greater beta cell reserve. Conclusions T1D autoantibody screening and metabolic monitoring of older children and young adults in Australia and New Zealand, by enabling pre-clinical diagnosis when beta cell reserve is greater, confers protection from DKA. These clinical benefits support ongoing efforts to increase screening activity in the region and should facilitate the application of emerging immunotherapies.

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