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Family structure and HbA1c in children with type 1 diabetes, a cohort study
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Women's and Children's Health, Paediatric Inflammation, Metabolism and Child Health Research.ORCID iD: 0000-0002-8502-8568
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Medical Sciences, Clinical diabetology and metabolism. Dalarna University, Falun.ORCID iD: 0000-0001-8682-2045
(English)Manuscript (preprint) (Other academic)
Abstract [en]

Objective: To study the impact of family structure on glycemic control in children and adolescents during the first two years following the diagnosis of type 1 diabetes. 

Research Design and Methods: 215 children and adolescents (<18 years) lived in four different family structures: 158 (74%) whole family, seven (3%) stepfamily, 26 (12%) shared custody and 24 (11%) single-parent family at diagnosis of type 1 diabetes. A questionnaire on the family’s social situation was completed at diagnosis and at one-year follow-up. HbA1c was analyzed at every follow-up during the first two years of treatment. Univariate and multivariate linear regression analyses were carried out with average Hb1Ac for the first and second years as dependent variables, family structure adjusted for age, body mass index standard deviation score, daily insulin dose and C-peptide.

Results: HbA1c at diagnosis was higher in participants in the single-parent family 12.0± 4.5 %(108±26 mmol/mol) vs whole family 10.9±4.3 %(96±23 mmol/mol; p=0.024). In the whole family, first and second year average HbA1c was 6.4± 2.8 %(46±7 mmol/mol) and 6.7±2.9% (50±8 mmol/mol) vs 6.7±3.1% (50±10 mmol/mol) (p=0.011) and 7.1± 3.1%(54±10 mmol/mol (p=0.004) in the single-parent family. The average HbA1c in the first year was a predictor of HbA1c in the second year (p=0.024; R2 = 0.44) and when added to the multivariate model for HbA1c in the second year, no differences were found between the family groups. 

Conclusions: Family structure at type 1 diabetes diagnosis affects the glycemic control of children and adolescents during the first two years following diagnosis. 

Keywords [en]
family structure, HbA1c, type 1 diabetes, children and adolescent
National Category
Pediatrics Endocrinology and Diabetes
Research subject
Pediatrics; Medical Science; Endocrinology and Diabetology
Identifiers
URN: urn:nbn:se:uu:diva-498955OAI: oai:DiVA.org:uu-498955DiVA, id: diva2:1745087
Funder
Swedish Child Diabetes FoundationGillbergska stiftelsenSven Jerring FoundationSamariten foundation for paediatric researchSwedish Research CouncilUppsala UniversityAvailable from: 2023-03-22 Created: 2023-03-22 Last updated: 2023-03-22Bibliographically approved
In thesis
1. Predictors of long-term glycemic control, pancreatic function and BMI trajectory in children with type 1 diabetes
Open this publication in new window or tab >>Predictors of long-term glycemic control, pancreatic function and BMI trajectory in children with type 1 diabetes
2023 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

Background: The maintenance of normal metabolic control underpins all management of insulin dependent diabetes whether in terms of preserved beta-cell function, body composition, or family support. The hypothesis of this work was that preserved C-peptide predicts better glycemic control and lowers risk of severe hypoglycemia. It was additionally investigated whether Body Mass Index (BMI) and family structure contributes to the prediction of long-term glycemic control. 

Objectives: This thesis aimed to 1) identify the factors associated with residual C peptide production at least 10 years after diagnosis, 2) evaluate the association of BMI trajectory and long-term glycemic control, 3) identify early characteristics associated with rapid or slow decline of beta-cell function and how it affects the clinical course, and 4) investigate the relations of family structure at diagnosis and long-term glycemic control. 

Methods: Data from four cohorts were used: In the Uppsala cohort, measurement of long-term residual C-peptide was undertaken using ultrasensitive C-peptide ELISA in 73 children and adolescents <25 years, BMI trajectory prior diagnosis was evaluated in 295 children, while family structure at diagnosis was evaluated in 215 children in relation to glycemic control. In the Linköping cohort, stimulated C-peptide was assessed by mixed meal tolerance test in 50 children. 

Results: The cohort studies showed that better early glycemic control predicted long term residual C-peptide and that long term residual C-peptide, in turn, was protective against severe hypoglycemia. Additionally, BMI trajectory was predicted by BMI prior to the presentation of type 1 diabetes. There was no association with glycemic outcome. Children living in a whole family had a lower probability of long-term dysglycemia. 

Conclusions: Residual C-peptide is important for better glycemic control and to reduce complications in children with type 1 diabetes. Family structure, but not BMI trajectory, contributes to the prediction of long-term glycemic control. However, more research is needed to understand how to preserve the beta-cell function in children and to target and support families in those children with early deteriorating glycemic control to reduce future complications. 

 

Place, publisher, year, edition, pages
Uppsala: Uppsala universitet, 2023. p. 77
Series
Digital Comprehensive Summaries of Uppsala Dissertations from the Faculty of Medicine, ISSN 1651-6206 ; 1926
National Category
Clinical Medicine Pediatrics Endocrinology and Diabetes
Research subject
Endocrinology and Diabetology; Pediatrics
Identifiers
urn:nbn:se:uu:diva-498959 (URN)978-91-513-1764-9 (ISBN)
Public defence
2023-05-11, Rudbecksalen, Rudbeck entréplan C11, Uppsala, 09:15 (Swedish)
Opponent
Supervisors
Funder
Swedish Child Diabetes FoundationDiabetesfondenEXODIAB - Excellence of Diabetes Research in SwedenSven Jerring FoundationGillbergska stiftelsenSamariten foundation for paediatric researchUppsala University
Available from: 2023-04-19 Created: 2023-03-22 Last updated: 2023-04-19

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Grönberg, AnnikaLeksell, Janeth

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