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Partial clinical remission of type 1 diabetes in Swedish children: a longitudinal study from the Swedish national quality register (SWEDIABKIDS) and the better diabetes diagnosis (BDD) study
Umeå University, Faculty of Medicine, Department of Clinical Sciences, Paediatrics.ORCID iD: 0000-0002-3390-778x
Department of Biomedical and Clinical Sciences, Division of Children’s and Women’s Health, Linköping University, Linköping, Sweden.
Department of Clinical Sciences, Lund, Lund University, Skånes University Hospital, Lund, Sweden.
Queen Silvia Children’s Hospital, Sahlgrenska University Hospital, Institute of Clinical Sciences, University of Gothenburg, Gothenburg, Sweden.
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2024 (English)In: Diabetes Technology & Therapeutics, ISSN 1520-9156, E-ISSN 1557-8593, Vol. 26, no 11, p. 851-861Article in journal (Refereed) Published
Abstract [en]

Aims/Hypotheses: To investigate the frequency and characteristics of partial remission in Swedish children with type 1 diabetes and whether the insulin delivery method, that is, continuous subcutaneous insulin infusion (CSII) or multiple daily injections (MDIs), affects incidence and duration of this period, 2007-2011. Factors that increase the proportion of subjects who enter partial remission and extend this period can improve long-term metabolic control and reduce the risk of severe hypoglycemia, improve quality of life, and, in the long run, reduce late complications.

Methods: Longitudinal data from 2007 to 2020 were extracted from the Swedish National Quality Register (SWEDIABKIDS) with all reported newly diagnosed children. Data on C-peptide from the participants in the Better Diabetes Diagnosis study from 2007 to 2010 were used. The definition of partial remission was insulin dose-adjusted HbA1c: HbA1c (%) + [4 × total daily insulin dose (U/kg/day)] ≤9.

Results: Of the 3887 patients, 56% were boys. More boys than girls were in partial remission throughout the follow-up period until 24 months after diabetes onset. Fewer children 0-6 years old had partial remission at 3 and 12 months but not at 24 months compared with older age-groups. A larger proportion of patients using CSII at 12 and 24 months remained in partial remission compared with those with MDI (37% vs. 33%, P = 0.02 and 31% vs. 27%, P = 0.01, respectively). The level of C-peptide was higher in the group with partial remission and mean HbA1c was lower (both P < 0.001). Partial remission at 12 months after diabetes onset was associated with CSII (odds ratio [OR]: 1.39, confidence interval [CI]:1.13, 1.71), shorter diabetes duration (OR: 0.80, CI: 0.76, 0.84), and male sex (OR: 1.23, CI: 1.04, 1.46).

Conclusions/Interpretation: Insulin through MDI, longer duration of diabetes, and female sex were associated with lower frequency of partial remission. Use of CSII seems to contribute to longer partial remission among Swedish children with type 1 diabetes.

Place, publisher, year, edition, pages
Mary Ann Liebert, 2024. Vol. 26, no 11, p. 851-861
Keywords [en]
C-peptide, continuous subcutaneous insulin infusion, HbA1c, multiple daily injection, partial clinical remission
National Category
Pediatrics
Identifiers
URN: urn:nbn:se:umu:diva-227863DOI: 10.1089/dia.2024.0112ISI: 001254878300001PubMedID: 38842902Scopus ID: 2-s2.0-85197500148OAI: oai:DiVA.org:umu-227863DiVA, id: diva2:1884922
Available from: 2024-07-19 Created: 2024-07-19 Last updated: 2025-09-16Bibliographically approved
In thesis
1. Teknik och glukoskontroll hos barn och ungdomar med typ 1 diabetes
Open this publication in new window or tab >>Teknik och glukoskontroll hos barn och ungdomar med typ 1 diabetes
2025 (Swedish)Doctoral thesis, comprehensive summary (Other academic)
Alternative title[en]
Technology and Glucose Metabolic Control in Children and Adolescents with Type 1 Diabetes
Abstract [en]

Background: There has been a rapid technological development during the last decade concerning insulin pumps andcontinuous glucose monitoring (CGM) for children and adolescents with type 1 diabetes. Few studies have been performedon real-life data from children with type 1 diabetes to investigate the effects of such technological devices on glucosemetabolic control and partial clinical remission.

Aim: The aim of this thesis was to expand the understanding of what methods of insulin administration and glucosemonitoring give the best opportunity to achieve good glucose metabolic control in children and adolescents with type 1diabetes, and to explore the experiences of youths and parents using technological devices such as insulin pumps and CGM, the glucose target and the support from healthcare.

Methods: Three of the studies were prospective, longitudinal, observational research with quantitative data from the Swedish National Diabetes Register (NDR-Swediabkids), and the Better Diabetes Diagnosis Study (BDD), where two include cross-sectional comparisons or cohort analysis (Papers I and II), and one is cross-linked with the BDD-register (Paper III). Papers I-III covered different time periods, i.e., Paper I 2011-2016, Paper II 2016-2023 and paper III2007-2020. The fourth paper was an interview study with qualitative content analysis (Paper IV).

Results: Overall, the use of insulin pumps and CGM-meters became increasingly common, where practically all children and adolescents with type 1 diabetes used CGM, most often in combination with an insulin pump by the end of the studyperiod. In Paper I, we showed a small decrease of mean HbA1c (0.7-1.5 mmol/mol) without effects on the prevalence of reported hypoglycaemic events with insulin pump treatment compared to multiple daily injections. Insulin pump treatment was associated with female sex (OR: 1.30, 95% CI 1.16-1.45), higher BMI-SDS (OR: 1.13, 95% CI 1.07-1.19) and longer diabetes duration (OR: 1.16, 95% CI 1.14-1.18). In Paper II, the group with CGM and insulin pump had lower mean HbA1c compared with MDI treatment, 59.4 mmol/mol vs. 61.0 mmol/mol, p<0.001, but patients with rtCGM and MDI had the relatively largest reduction in HbA1c over time. There were associations between higher BMI and insulin pump use. InPaper III, we found that partial clinical remission was associated with insulin pump treatment (OR: 1.39, 95% CI 1.13-1.71), shorter diabetes duration (OR: 0.80, 95% CI 0.76- 0.84), and male sex (OR: 1.23, 95% CI 1.04-1.46). In Paper IV, the youths described increased satisfaction, security, freedom, and strengthened independence. The parents described improved sleep at night leading to increased quality of life. The opportunity for parents to follow their youth’s glucose values from a distance does not seem to be a problem for neither youths nor parents, and the lowering of the glucose target was not anything they had considered a problem. Both youths and parents had positive experiences of the diabetes teams, and parents emphasized the need of technical support and to stay connected during the transition period from childhood into adult life.

Conclusions: New technologies facilitate life with type 1 diabetes for both youths and their parents, and CGM and insulinpump treatment improve glycaemic control, without substantial side-effects and seem to contribute to a longer period of partial remission. There are concerns regarding BMI-trajectories tied to the use of insulin pumps, particularly among teenagers, but from a user perspective, these devices confer improvements in quality of life, both for the adolescents using them and their parents. With the devices now being almost ubiquitous among paediatric patients, the diabetes teams will have to keep up with the rapid technological development to support the patients and their families as well as being vigilant to possible negative consequences of their use.

Place, publisher, year, edition, pages
Umeå: Umeå University, 2025. p. 68
Series
Umeå University medical dissertations, ISSN 0346-6612 ; 2378
Keywords
Children and adolescents, type 1 diabetes, continuous subcutaneous insulin infusion, multiple daily injections, continuous glucose monitoring, glycaemic control, partial clinical remission, C-peptide
National Category
Pediatrics Endocrinology and Diabetes
Research subject
Pediatrics
Identifiers
urn:nbn:se:umu:diva-244221 (URN)978-91-8070-765-7 (ISBN)978-91-8070-766-4 (ISBN)
Public defence
2025-10-10, Hörsalen Snäckan, Östersunds sjukhus, Kyrkgatan 16, 831 27, Östersund, 13:00 (Swedish)
Opponent
Supervisors
Available from: 2025-09-19 Created: 2025-09-16 Last updated: 2025-09-18Bibliographically approved

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Fureman, Anna-LenaLilja, MikaelLind, Torbjörn

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