Diabetic Ketoacidosis at Onset of Type 1 Diabetes and Long-term HbA1c in 7,961 Children and Young Adults in the Australasian Diabetes Data Network

Author:

Clapin Helen F.12ORCID,Earnest Arul3,Colman Peter G.45,Davis Elizabeth A.12ORCID,Jefferies Craig6,Anderson Kym7,Chee Melissa8,Bergman Philip39,de Bock Martin1011ORCID,Kao Kung-Ting51213,Fegan P. Gerry14,Holmes-Walker D. Jane15ORCID,Johnson Stephanie16,King Bruce R.17,Mok Meng Tuck18,Narayan Kruthika1920,Peña Vargas Alexia S.21ORCID,Sinnott Richard5,Wheeler Benjamin J.22ORCID,Zimmermann Anthony23,Craig Maria E.1920ORCID,Couper Jenny J.21ORCID,Ambler Geoff,Andrikopoulos Sof,Barrett Helen,Batch Jenny,Cameron Fergus,Conwell Louise,Cotterill Andrew,Cooper Chris,Donaghue Kim,Fairchild Jan,Fourlanos Spiros,Glastras Sarah,Goss Peter,Gray Leonie,Hamblin Shane,Hofman Paul,Huynh Tony,James Steven,Jones Tim,Lafferty Antony,Martin Michelle,McCrossin Robert,Neville Kris,Pascoe Mark,Paul Ryan,Pawlak Dorota,Phillips Liza,Price Darrell,Rodda Christine,Simmons David,Smart Carmel,Stone Monique,Stranks Steve,Tham Elaine,Ward Glenn,Woodhead Helen,

Affiliation:

1. 1Perth Children’s Hospital, Nedlands, Western Australia, Australia

2. 2Telethon Kids Institute, Nedlands, Western Australia, Australia

3. 3Monash University, Clayton, Victoria, Australia

4. 4Royal Melbourne Hospital, Parkville, Victoria, Australia

5. 5The University of Melbourne, Parkville, Victoria, Australia

6. 6Starship Children’s Health, Grafton, Auckland, New Zealand

7. 7Barwon Health, Geelong, Victoria, Australia

8. 8JDRF Australia, St Leonards, New South Wales, Australia

9. 9Monash Children’s Hospital, Clayton, Victoria, Australia

10. 10Canterbury District Health Board, Christchurch, New Zealand

11. 11Christchurch School of Medicine, University of Otago, Otago, New Zealand

12. 12Royal Children’s Hospital, Parkville, Victoria, Australia

13. 13Murdoch Children’s Research Institute, Parkville, Victoria, Australia

14. 14Fiona Stanley Hospital, Murdoch, Western Australia, Australia

15. 15Westmead Hospital, Westmead, New South Wales, Australia

16. 16Queensland Children’s Hospital, South Brisbane, Queensland, Australia

17. 17John Hunter Children’s Hospital, New Lambton Heights, New South Wales, Australia

18. 18Australasian Diabetes Data Network, Australia

19. 19The Children’s Hospital at Westmead, Westmead, New South Wales, Australia

20. 20University of New South Wales, Sydney, New South Wales, Australia

21. 21Women’s and Children’s Hospital and Robinson Research Institute, University of Adelaide, North Adelaide, South Australia, Australia

22. 22Women’s and Children’s Health, Dunedin School of Medicine, University of Otago, Dunedin Central, Dunedin, New Zealand

23. 23Lyell McEwin & Modbury Hospitals, Elizabeth Vale, South Australia, Australia

Abstract

OBJECTIVE The relationship between diabetic ketoacidosis (DKA) at diagnosis of type 1 diabetes and long-term glycemic control varies between studies. We aimed, firstly, to characterize the association of DKA and its severity with long-term HbA1c in a large contemporary cohort, and secondly, to identify other independent determinants of long-term HbA1c. RESEARCH DESIGN AND METHODS Participants were 7,961 children and young adults diagnosed with type 1 diabetes by age 30 years from 2000 to 2019 and followed prospectively in the Australasian Diabetes Data Network (ADDN) until 31 December 2020. Linear mixed-effect models related variables to HbA1c. RESULTS DKA at diagnosis was present in 2,647 participants (33.2%). Over a median 5.6 (interquartile range 3.2, 9.4) years of follow-up, participants with severe, but not moderate or mild, DKA at diagnosis had a higher mean HbA1c (+0.23%, 95% CI 0.11,0.28; [+2.5 mmol/mol, 95% CI 1.4,3.6]; P < 0.001) compared with those without DKA. Use of continuous subcutaneous insulin infusion (CSII) was independently associated with a lower HbA1c (−0.28%, 95% CI −0.31, −0.25; [−3.1 mmol/mol, 95% CI −3.4, −2.8]; P < 0.001) than multiple daily injections, and CSII use interacted with severe DKA to lower predicted HbA1c. Indigenous status was associated with higher HbA1c (+1.37%, 95% CI 1.15, 1.59; [+15.0 mmol/mol, 95% CI 12.6, 17.4]; P < 0.001), as was residing in postcodes of lower socioeconomic status (most vs. least disadvantaged quintile +0.43%, 95% CI 0.34, 0.52; [+4.7 mmol/mol, 95% CI 3.4, 5.6]; P < 0.001). CONCLUSIONS Severe, but not mild or moderate, DKA at diagnosis was associated with a marginally higher HbA1c over time, an effect that was modified by use of CSII. Indigenous status and lower socioeconomic status were independently associated with higher long-term HbA1c.

Publisher

American Diabetes Association

Subject

Advanced and Specialized Nursing,Endocrinology, Diabetes and Metabolism,Internal Medicine

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