Jennifer M Rohan1, Joseph R Rausch1, Jennifer Shroff Pendley2, Alan M Delamater3, Lawrence Dolan4, Grafton Reeves5, Dennis Drotar1. 1. Department of Pediatrics, Cincinnati Children's Hospital Medical Center. 2. Division of Behavioral Health, Alfred I. DuPont Hospital for Children. 3. Department of Pediatrics, University of Miami. 4. Department of Endocrinology, Cincinnati Children's Hospital Medical Center. 5. Division of Pediatric Endocrinology, Alfred I. DuPont Hospital for Children.
Abstract
OBJECTIVE: To identify trajectories of glycemic control over a period of 3 years in a pediatric sample of youth diagnosed with Type 1 diabetes transitioning to adolescence. A second aim was to examine a set of modifiable individual and family level baseline predictors of glycemic control group membership. METHODS: This multisite, prospective study included 239 children and adolescents (ages 9-11 years at baseline) diagnosed with Type 1 diabetes and their caregivers. Glycemic control was based on hemoglobin A1c (HbA1c) collected at 6-month intervals over a period of 3 years. Predictors of glycemic control membership included baseline global executive functioning, diabetes self-management, diabetes-specific family conflict, blood glucose monitoring frequency, and relevant individual and family level covariates. RESULTS: Group-based trajectory analyses were used to describe patterns of glycemic control from baseline to 36 months and 3 trajectories were identified: low risk (42.9%), elevated risk (44.6%), and high risk (12.1%) subgroups. Baseline maternal-reported family conflict, blood glucose monitoring frequency, and gender were significant predictors of glycemic control group membership. Higher levels of baseline family conflict, lower frequency of blood glucose monitoring, and female gender were associated with elevated and high-risk group membership. CONCLUSIONS: These findings underscore the importance of examining trajectories of HbA1c across time. These results suggest that problematic trajectories of glycemic control are evident during the transition to adolescence. Furthermore, there are modifiable individual and family level characteristics that predict group membership and hence could be targeted in interventions to ensure adequate glycemic control is maintained over time and that risks for diabetes-related complications are reduced.
OBJECTIVE: To identify trajectories of glycemic control over a period of 3 years in a pediatric sample of youth diagnosed with Type 1 diabetes transitioning to adolescence. A second aim was to examine a set of modifiable individual and family level baseline predictors of glycemic control group membership. METHODS: This multisite, prospective study included 239 children and adolescents (ages 9-11 years at baseline) diagnosed with Type 1 diabetes and their caregivers. Glycemic control was based on hemoglobin A1c (HbA1c) collected at 6-month intervals over a period of 3 years. Predictors of glycemic control membership included baseline global executive functioning, diabetes self-management, diabetes-specific family conflict, blood glucose monitoring frequency, and relevant individual and family level covariates. RESULTS: Group-based trajectory analyses were used to describe patterns of glycemic control from baseline to 36 months and 3 trajectories were identified: low risk (42.9%), elevated risk (44.6%), and high risk (12.1%) subgroups. Baseline maternal-reported family conflict, blood glucose monitoring frequency, and gender were significant predictors of glycemic control group membership. Higher levels of baseline family conflict, lower frequency of blood glucose monitoring, and female gender were associated with elevated and high-risk group membership. CONCLUSIONS: These findings underscore the importance of examining trajectories of HbA1c across time. These results suggest that problematic trajectories of glycemic control are evident during the transition to adolescence. Furthermore, there are modifiable individual and family level characteristics that predict group membership and hence could be targeted in interventions to ensure adequate glycemic control is maintained over time and that risks for diabetes-related complications are reduced.
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Authors: Deborah A Butler; Jessica B Zuehlke; Alison Tovar; Lisa K Volkening; Barbara J Anderson; Lori M B Laffel Journal: Pediatr Diabetes Date: 2008-08 Impact factor: 4.866
Authors: Megan M Miller; Jennifer M Rohan; Alan Delamater; Jennifer Shroff-Pendley; Lawrence M Dolan; Grafton Reeves; Dennis Drotar Journal: J Pediatr Psychol Date: 2012-09-30
Authors: Joseph R Rausch; Korey K Hood; Alan Delamater; Jennifer Shroff Pendley; Jennifer M Rohan; Grafton Reeves; Lawrence Dolan; Dennis Drotar Journal: Diabetes Care Date: 2012-04-03 Impact factor: 19.112
Authors: Meg C Nicholl; Jessica M Valenzuela; Keith Lit; Christian DeLucia; Amanda M Shoulberg; Jennifer M Rohan; Jennifer Shroff Pendley; Lawrence Dolan; Alan M Delamater Journal: J Pediatr Psychol Date: 2019-07-01
Authors: Jennifer M Rohan; Bin Huang; Jennifer Shroff Pendley; Alan Delamater; Lawrence Dolan; Grafton Reeves; Dennis Drotar Journal: J Pediatr Psychol Date: 2015-07-07