Effect of screening for type 1 diabetes on early metabolic control: the DiPiS study

Aims/hypothesis It has been shown that children previously enrolled in follow-up studies have better glycaemic control during the early period after diabetes diagnosis. The aim of this study was to analyse glycaemic control over a longer period, past the period of partial remission, after diagnosis...

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Veröffentlicht in:Diabetologia Jg. 62; H. 1; S. 53 - 57
Hauptverfasser: Lundgren, Markus, Jonsdottir, Berglind, Elding Larsson, Helena
Format: Journal Article
Sprache:Englisch
Veröffentlicht: Berlin/Heidelberg Springer Berlin Heidelberg 01.01.2019
Springer Nature B.V
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ISSN:0012-186X, 1432-0428, 1432-0428
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Abstract Aims/hypothesis It has been shown that children previously enrolled in follow-up studies have better glycaemic control during the early period after diabetes diagnosis. The aim of this study was to analyse glycaemic control over a longer period, past the period of partial remission, after diagnosis in children followed before diagnosis in the Swedish Diabetes Prediction in Skåne (DiPiS) study compared with children of equal age not enrolled in pre-diabetes follow-up, receiving equivalent diabetes care. Methods HbA 1c from diagnosis and for the following 5 years, as well as differences in insulin dosage, BMI, pump use, partial remission according to insulin dose-adjusted HbA 1c and baseline demographics were compared between children who were enrolled in follow-up and had received information on diabetes risk ( n  = 51) and children not enrolled in follow-up ( n  = 78). Results The group followed before diagnosis had a higher proportion of first-degree relatives (FDRs) with diabetes (28% vs 5.6%; p  = 0.001) and a higher proportion of participants with mothers born in Sweden (100% vs 89%; p  = 0.02). No significant differences in total daily insulin dose, pump use or other baseline sociodemographic factors were detected between the groups. Median HbA 1c at diagnosis and at 1, 2, 3, 4 and 5 years after diabetes diagnosis was significantly lower in children followed before diagnosis (all p  < 0.05), and was not related to FDR status. Conclusions/interpretation Compared with controls not previously enrolled in follow-up, our study shows that children enrolled in longitudinal follow-up before the diagnosis of diabetes have better glycaemic control, measured by HbA 1c , up to 5 years after diagnosis and during the initial period of partial remission. Improved glycaemic control in the initial years of living with type 1 diabetes could affect long-term outcome and complications and might also improve study enrolment in future longitudinal studies.
AbstractList Aims/hypothesisIt has been shown that children previously enrolled in follow-up studies have better glycaemic control during the early period after diabetes diagnosis. The aim of this study was to analyse glycaemic control over a longer period, past the period of partial remission, after diagnosis in children followed before diagnosis in the Swedish Diabetes Prediction in Skåne (DiPiS) study compared with children of equal age not enrolled in pre-diabetes follow-up, receiving equivalent diabetes care.MethodsHbA1c from diagnosis and for the following 5 years, as well as differences in insulin dosage, BMI, pump use, partial remission according to insulin dose-adjusted HbA1c and baseline demographics were compared between children who were enrolled in follow-up and had received information on diabetes risk (n = 51) and children not enrolled in follow-up (n = 78).ResultsThe group followed before diagnosis had a higher proportion of first-degree relatives (FDRs) with diabetes (28% vs 5.6%; p = 0.001) and a higher proportion of participants with mothers born in Sweden (100% vs 89%; p = 0.02). No significant differences in total daily insulin dose, pump use or other baseline sociodemographic factors were detected between the groups. Median HbA1c at diagnosis and at 1, 2, 3, 4 and 5 years after diabetes diagnosis was significantly lower in children followed before diagnosis (all p < 0.05), and was not related to FDR status.Conclusions/interpretationCompared with controls not previously enrolled in follow-up, our study shows that children enrolled in longitudinal follow-up before the diagnosis of diabetes have better glycaemic control, measured by HbA1c, up to 5 years after diagnosis and during the initial period of partial remission. Improved glycaemic control in the initial years of living with type 1 diabetes could affect long-term outcome and complications and might also improve study enrolment in future longitudinal studies.
It has been shown that children previously enrolled in follow-up studies have better glycaemic control during the early period after diabetes diagnosis. The aim of this study was to analyse glycaemic control over a longer period, past the period of partial remission, after diagnosis in children followed before diagnosis in the Swedish Diabetes Prediction in Skåne (DiPiS) study compared with children of equal age not enrolled in pre-diabetes follow-up, receiving equivalent diabetes care. HbA from diagnosis and for the following 5 years, as well as differences in insulin dosage, BMI, pump use, partial remission according to insulin dose-adjusted HbA and baseline demographics were compared between children who were enrolled in follow-up and had received information on diabetes risk (n = 51) and children not enrolled in follow-up (n = 78). The group followed before diagnosis had a higher proportion of first-degree relatives (FDRs) with diabetes (28% vs 5.6%; p = 0.001) and a higher proportion of participants with mothers born in Sweden (100% vs 89%; p = 0.02). No significant differences in total daily insulin dose, pump use or other baseline sociodemographic factors were detected between the groups. Median HbA at diagnosis and at 1, 2, 3, 4 and 5 years after diabetes diagnosis was significantly lower in children followed before diagnosis (all p < 0.05), and was not related to FDR status. Compared with controls not previously enrolled in follow-up, our study shows that children enrolled in longitudinal follow-up before the diagnosis of diabetes have better glycaemic control, measured by HbA , up to 5 years after diagnosis and during the initial period of partial remission. Improved glycaemic control in the initial years of living with type 1 diabetes could affect long-term outcome and complications and might also improve study enrolment in future longitudinal studies.
It has been shown that children previously enrolled in follow-up studies have better glycaemic control during the early period after diabetes diagnosis. The aim of this study was to analyse glycaemic control over a longer period, past the period of partial remission, after diagnosis in children followed before diagnosis in the Swedish Diabetes Prediction in Skåne (DiPiS) study compared with children of equal age not enrolled in pre-diabetes follow-up, receiving equivalent diabetes care.AIMS/HYPOTHESISIt has been shown that children previously enrolled in follow-up studies have better glycaemic control during the early period after diabetes diagnosis. The aim of this study was to analyse glycaemic control over a longer period, past the period of partial remission, after diagnosis in children followed before diagnosis in the Swedish Diabetes Prediction in Skåne (DiPiS) study compared with children of equal age not enrolled in pre-diabetes follow-up, receiving equivalent diabetes care.HbA1c from diagnosis and for the following 5 years, as well as differences in insulin dosage, BMI, pump use, partial remission according to insulin dose-adjusted HbA1c and baseline demographics were compared between children who were enrolled in follow-up and had received information on diabetes risk (n = 51) and children not enrolled in follow-up (n = 78).METHODSHbA1c from diagnosis and for the following 5 years, as well as differences in insulin dosage, BMI, pump use, partial remission according to insulin dose-adjusted HbA1c and baseline demographics were compared between children who were enrolled in follow-up and had received information on diabetes risk (n = 51) and children not enrolled in follow-up (n = 78).The group followed before diagnosis had a higher proportion of first-degree relatives (FDRs) with diabetes (28% vs 5.6%; p = 0.001) and a higher proportion of participants with mothers born in Sweden (100% vs 89%; p = 0.02). No significant differences in total daily insulin dose, pump use or other baseline sociodemographic factors were detected between the groups. Median HbA1c at diagnosis and at 1, 2, 3, 4 and 5 years after diabetes diagnosis was significantly lower in children followed before diagnosis (all p < 0.05), and was not related to FDR status.RESULTSThe group followed before diagnosis had a higher proportion of first-degree relatives (FDRs) with diabetes (28% vs 5.6%; p = 0.001) and a higher proportion of participants with mothers born in Sweden (100% vs 89%; p = 0.02). No significant differences in total daily insulin dose, pump use or other baseline sociodemographic factors were detected between the groups. Median HbA1c at diagnosis and at 1, 2, 3, 4 and 5 years after diabetes diagnosis was significantly lower in children followed before diagnosis (all p < 0.05), and was not related to FDR status.Compared with controls not previously enrolled in follow-up, our study shows that children enrolled in longitudinal follow-up before the diagnosis of diabetes have better glycaemic control, measured by HbA1c, up to 5 years after diagnosis and during the initial period of partial remission. Improved glycaemic control in the initial years of living with type 1 diabetes could affect long-term outcome and complications and might also improve study enrolment in future longitudinal studies.CONCLUSIONS/INTERPRETATIONCompared with controls not previously enrolled in follow-up, our study shows that children enrolled in longitudinal follow-up before the diagnosis of diabetes have better glycaemic control, measured by HbA1c, up to 5 years after diagnosis and during the initial period of partial remission. Improved glycaemic control in the initial years of living with type 1 diabetes could affect long-term outcome and complications and might also improve study enrolment in future longitudinal studies.
Aims/hypothesis It has been shown that children previously enrolled in follow-up studies have better glycaemic control during the early period after diabetes diagnosis. The aim of this study was to analyse glycaemic control over a longer period, past the period of partial remission, after diagnosis in children followed before diagnosis in the Swedish Diabetes Prediction in Skåne (DiPiS) study compared with children of equal age not enrolled in pre-diabetes follow-up, receiving equivalent diabetes care. Methods HbA 1c from diagnosis and for the following 5 years, as well as differences in insulin dosage, BMI, pump use, partial remission according to insulin dose-adjusted HbA 1c and baseline demographics were compared between children who were enrolled in follow-up and had received information on diabetes risk ( n  = 51) and children not enrolled in follow-up ( n  = 78). Results The group followed before diagnosis had a higher proportion of first-degree relatives (FDRs) with diabetes (28% vs 5.6%; p  = 0.001) and a higher proportion of participants with mothers born in Sweden (100% vs 89%; p  = 0.02). No significant differences in total daily insulin dose, pump use or other baseline sociodemographic factors were detected between the groups. Median HbA 1c at diagnosis and at 1, 2, 3, 4 and 5 years after diabetes diagnosis was significantly lower in children followed before diagnosis (all p  < 0.05), and was not related to FDR status. Conclusions/interpretation Compared with controls not previously enrolled in follow-up, our study shows that children enrolled in longitudinal follow-up before the diagnosis of diabetes have better glycaemic control, measured by HbA 1c , up to 5 years after diagnosis and during the initial period of partial remission. Improved glycaemic control in the initial years of living with type 1 diabetes could affect long-term outcome and complications and might also improve study enrolment in future longitudinal studies.
Aims/hypothesis: It has been shown that children previously enrolled in follow-up studies have better glycaemic control during the early period after diabetes diagnosis. The aim of this study was to analyse glycaemic control over a longer period, past the period of partial remission, after diagnosis in children followed before diagnosis in the Swedish Diabetes Prediction in Skåne (DiPiS) study compared with children of equal age not enrolled in pre-diabetes follow-up, receiving equivalent diabetes care. Methods: HbA1c from diagnosis and for the following 5 years, as well as differences in insulin dosage, BMI, pump use, partial remission according to insulin dose-adjusted HbA1c and baseline demographics were compared between children who were enrolled in follow-up and had received information on diabetes risk (n = 51) and children not enrolled in follow-up (n = 78). Results: The group followed before diagnosis had a higher proportion of first-degree relatives (FDRs) with diabetes (28% vs 5.6%; p = 0.001) and ahigher proportion of participants with mothers born in Sweden (100% vs 89%; p = 0.02). No significant differences in total daily insulin dose, pump use or other baseline sociodemographic factors were detected between the groups. Median HbA1c at diagnosis and at 1, 2, 3, 4 and 5 years after diabetes diagnosis was significantly lower in children followed before diagnosis (all p < 0.05), and was not related to FDR status. Conclusions/interpretation: Compared with controls not previously enrolled in follow-up, our study shows that children enrolled in longitudinal follow-up before the diagnosis of diabetes have better glycaemic control, measured by HbA1c, up to 5 years after diagnosis and during the initial period of partial remission. Improved glycaemic control in the initial years of living with type 1 diabetes could affect long-term outcome and complications and might also improve study enrolment in future longitudinal studies.
Author Jonsdottir, Berglind
Lundgren, Markus
Elding Larsson, Helena
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  surname: Elding Larsson
  fullname: Elding Larsson, Helena
  organization: Unit for Pediatric Endocrinology, Department of Clinical Sciences Malmö, Lund University, Pediatric Endocrinology and Gastroenterology, Skåne University hospital
BackLink https://www.ncbi.nlm.nih.gov/pubmed/30109365$$D View this record in MEDLINE/PubMed
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Cites_doi 10.1111/pedi.12208
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ContentType Journal Article
Copyright The Author(s) 2018
Diabetologia is a copyright of Springer, (2018). All Rights Reserved. © 2018. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
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– notice: Diabetologia is a copyright of Springer, (2018). All Rights Reserved. © 2018. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
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Issue 1
Keywords Screening
Longitudinal studies
Type 1 diabetes
Metabolic control
Language English
License Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
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PublicationSubtitle Clinical, Translational and Experimental Diabetes and Metabolism
PublicationTitle Diabetologia
PublicationTitleAbbrev Diabetologia
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PublicationYear 2019
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References LundgrenMSahlinÅSvenssonCReduced morbidity at diagnosis and improved glycemic control in children previously enrolled in DiPiS follow-upPediatr Diabetes2014154945011:CAS:528:DC%2BC2cXhs1yis7fM10.1111/pedi.12151248238164190091
Winkler C, Schober E, Ziegler A-G, Holl RW (2012) Markedly reduced rate of diabetic ketoacidosis at onset of type 1 diabetes in relatives screened for islet autoantibodies. 13:308–313
Max AndersenMLCHougaardPPörksenSPartial Remission Definition: validation based on the insulin dose-adjusted HbA1c (IDAA1C) in 129 Danish Children with New-Onset Type 1 DiabetesPediatr Diabetes2014154694761:CAS:528:DC%2BC2cXhs1yis7bF10.1111/pedi.1220825287319
Steck AK, Larsson HE, Liu X, et al (2017) Residual beta-cell function in diabetes children followed and diagnosed in the TEDDY study compared to community controls
Larsson HE, Vehik KK, Gesualdo P et al (2013) Children followed in the TEDDY study are diagnosed with type 1 diabetes at an early stage of disease. 15:118–126
Smith LB, Liu X, Johnson SB et al (2018) Family adjustment to diabetes diagnosis in children: can participation in a study on type 1 diabetes genetic risk be helpful? Pediatr Diabetes 19:1025–1033
DucaLMWangBRewersMRewersADiabetic ketoacidosis at diagnosis of type 1 diabetes predicts poor long-term glycemic controlDiabetes Care201740124912551:CAS:528:DC%2BC1cXitVShsbbE10.2337/dc17-055828667128
Elding LarssonHVehikKVehikKKReduced prevalence of diabetic ketoacidosis at diagnosis of type 1 diabetes in young children participating in longitudinal follow-upDiabetes Care2011342347235210.2337/dc11-1026219724093198296
KellerRJEisenbarthGSJacksonRAInsulin prophylaxis in individuals at high risk of type I diabetesLancet19933419279281:STN:280:DyaK3s3htFajtg%3D%3D10.1016/0140-6736(93)91215-88096268
PerssonMBeckerCElding LarssonHThe Better Diabetes Diagnosis (BDD) study - a review of a nationwide prospective cohort study in SwedenDiabetes Res Clin Pract20181402362441:STN:280:DC%2BC1MnpvVCgtw%3D%3D10.1016/j.diabres.2018.03.05729626585
BarkerJMGoehrigSHBarrigaKClinical characteristics of children diagnosed with type 1 diabetes through intensive screening and follow-upDiabetes Care2004271399140410.2337/diacare.27.6.139915161795
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– reference: Winkler C, Schober E, Ziegler A-G, Holl RW (2012) Markedly reduced rate of diabetic ketoacidosis at onset of type 1 diabetes in relatives screened for islet autoantibodies. 13:308–313
– reference: Steck AK, Larsson HE, Liu X, et al (2017) Residual beta-cell function in diabetes children followed and diagnosed in the TEDDY study compared to community controls
– reference: DucaLMWangBRewersMRewersADiabetic ketoacidosis at diagnosis of type 1 diabetes predicts poor long-term glycemic controlDiabetes Care201740124912551:CAS:528:DC%2BC1cXitVShsbbE10.2337/dc17-055828667128
– reference: PerssonMBeckerCElding LarssonHThe Better Diabetes Diagnosis (BDD) study - a review of a nationwide prospective cohort study in SwedenDiabetes Res Clin Pract20181402362441:STN:280:DC%2BC1MnpvVCgtw%3D%3D10.1016/j.diabres.2018.03.05729626585
– reference: Max AndersenMLCHougaardPPörksenSPartial Remission Definition: validation based on the insulin dose-adjusted HbA1c (IDAA1C) in 129 Danish Children with New-Onset Type 1 DiabetesPediatr Diabetes2014154694761:CAS:528:DC%2BC2cXhs1yis7bF10.1111/pedi.1220825287319
– reference: LundgrenMSahlinÅSvenssonCReduced morbidity at diagnosis and improved glycemic control in children previously enrolled in DiPiS follow-upPediatr Diabetes2014154945011:CAS:528:DC%2BC2cXhs1yis7fM10.1111/pedi.12151248238164190091
– reference: Larsson HE, Vehik KK, Gesualdo P et al (2013) Children followed in the TEDDY study are diagnosed with type 1 diabetes at an early stage of disease. 15:118–126
– reference: Elding LarssonHVehikKVehikKKReduced prevalence of diabetic ketoacidosis at diagnosis of type 1 diabetes in young children participating in longitudinal follow-upDiabetes Care2011342347235210.2337/dc11-1026219724093198296
– reference: BarkerJMGoehrigSHBarrigaKClinical characteristics of children diagnosed with type 1 diabetes through intensive screening and follow-upDiabetes Care2004271399140410.2337/diacare.27.6.139915161795
– reference: Smith LB, Liu X, Johnson SB et al (2018) Family adjustment to diabetes diagnosis in children: can participation in a study on type 1 diabetes genetic risk be helpful? Pediatr Diabetes 19:1025–1033
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  publication-title: Diabetes Care
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  publication-title: Pediatr Diabetes
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  publication-title: Lancet
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Snippet Aims/hypothesis It has been shown that children previously enrolled in follow-up studies have better glycaemic control during the early period after diabetes...
It has been shown that children previously enrolled in follow-up studies have better glycaemic control during the early period after diabetes diagnosis. The...
Aims/hypothesisIt has been shown that children previously enrolled in follow-up studies have better glycaemic control during the early period after diabetes...
Aims/hypothesis: It has been shown that children previously enrolled in follow-up studies have better glycaemic control during the early period after diabetes...
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StartPage 53
SubjectTerms Blood Glucose - metabolism
Child
Child, Preschool
Children
Clinical Medicine
Demography
Diabetes
Diabetes mellitus
Diabetes mellitus (insulin dependent)
Diabetes Mellitus, Type 1 - blood
Diabetes Mellitus, Type 1 - diagnosis
Diabetes Mellitus, Type 1 - drug therapy
Diagnosis
Endocrinology and Diabetes
Endokrinologi och diabetes
Female
Glycated Hemoglobin A - metabolism
Human Physiology
Humans
Hypoglycemic Agents - therapeutic use
Insulin
Insulin - therapeutic use
Internal Medicine
Klinisk medicin
Longitudinal Studies
Male
Medical and Health Sciences
Medicin och hälsovetenskap
Medicine
Medicine & Public Health
Metabolic Diseases
Pediatrics
Pediatrik
Prospective Studies
Remission
Short Communication
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Title Effect of screening for type 1 diabetes on early metabolic control: the DiPiS study
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