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Identification of clinically relevant dysglycemia phenotypes based on continuous glucose monitoring data from youth with type 1 diabetes and elevated hemoglobin A1c.
Kahkoska, Anna R; Adair, Linda A; Aiello, Allison E; Burger, Kyle S; Buse, John B; Crandell, Jamie; Maahs, David M; Nguyen, Crystal T; Kosorok, Michael R; Mayer-Davis, Elizabeth J.
Afiliação
  • Kahkoska AR; Department of Nutrition, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
  • Adair LA; Department of Nutrition, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
  • Aiello AE; Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
  • Burger KS; Department of Nutrition, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
  • Buse JB; Department of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
  • Crandell J; School of Nursing, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
  • Maahs DM; Department of Pediatrics, School of Medicine, Stanford University, Stanford, California.
  • Nguyen CT; Stanford Diabetes Research Center, Stanford University, Stanford, California.
  • Kosorok MR; Department of Biostatistics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
  • Mayer-Davis EJ; Department of Biostatistics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
Pediatr Diabetes ; 20(5): 556-566, 2019 08.
Article em En | MEDLINE | ID: mdl-30972889
BACKGROUND/OBJECTIVE: To identify and characterize subgroups of adolescents with type 1 diabetes (T1D) and elevated hemoglobin A1c (HbA1c) who share patterns in their continuous glucose monitoring (CGM) data as "dysglycemia phenotypes." METHODS: Data were analyzed from the Flexible Lifestyles Empowering Change randomized trial. Adolescents with T1D (13-16 years, duration >1 year) and HbA1c 8% to 13% (64-119 mmol/mol) wore blinded CGM at baseline for 7 days. Participants were clustered based on eight CGM metrics measuring hypoglycemia, hyperglycemia, and glycemic variability. Clusters were characterized by their baseline features and 18 months changes in HbA1c using adjusted mixed effects models. For comparison, participants were stratified by baseline HbA1c (≤/>9.0% [75 mmol/mol]). RESULTS: The study sample included 234 adolescents (49.8% female, baseline age 14.8 ± 1.1 years, baseline T1D duration 6.4 ± 3.7 years, baseline HbA1c 9.6% ± 1.2%, [81 ± 13 mmol/mol]). Three Dysglycemia Clusters were identified with significant differences across all CGM metrics (P < .001). Dysglycemia Cluster 3 (n = 40, 17.1%) showed severe hypoglycemia and glycemic variability with moderate hyperglycemia and had a lower baseline HbA1c than Clusters 1 and 2 (P < .001). This cluster showed increases in HbA1c over 18 months (p-for-interaction = 0.006). No other baseline characteristics were associated with Dysglycemia Clusters. High HbA1c was associated with lower pump use, greater insulin doses, more frequent blood glucose monitoring, lower motivation, and lower adherence to diabetes self-management (all P < .05). CONCLUSIONS: There are subgroups of adolescents with T1D for which glycemic control is challenged by different aspects of dysglycemia. Enhanced understanding of demographic, behavioral, and clinical characteristics that contribute to CGM-derived dysglycemia phenotypes may reveal strategies to improve treatment.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hemoglobinas Glicadas / Diabetes Mellitus Tipo 1 Tipo de estudo: Clinical_trials / Diagnostic_studies / Prognostic_studies Limite: Adolescent / Female / Humans / Male Idioma: En Revista: Pediatr Diabetes Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hemoglobinas Glicadas / Diabetes Mellitus Tipo 1 Tipo de estudo: Clinical_trials / Diagnostic_studies / Prognostic_studies Limite: Adolescent / Female / Humans / Male Idioma: En Revista: Pediatr Diabetes Ano de publicação: 2019 Tipo de documento: Article