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1.
J Clin Res Pediatr Endocrinol ; 11(2): 118-124, 2019 05 28.
Artigo em Inglês | MEDLINE | ID: mdl-30282617

RESUMO

Objective: While past research found family conflict, disordered eating, body image concerns and anxious self-doubts may affect adolescent diabetic glucose control, available measures of adherence mainly focus on management tasks. The current study aimed to combine measures of emotional distress and beliefs with decisions concerning management in a new measure of resistance to treatment adherence: the 12-item Glucose Control Resistance Scale (GCRS). Methods: Participants included 135 adolescents and their parents from a pediatric diabetes clinic. Family conflict, body image concerns, anxious self-doubts and glucose control resistance were assessed. Results: Factor analysis identified 12 items, with loadings of ≥0.40, which were used to form the GCRS. The scale had adequate reliability and there was a significant correlation between child and parent GCRS scores. One factor, family conflict, was significantly related to hemoglobin A1c (HbA1c) levels, but a set of four factors explained a total of 12% of the variance in HbA1c levels. Of the demographic variables considered (gender, number of parents at home, age, body mass index z-score), only gender was significantly associated with adolescent perceptions of family conflict. Conclusion: The GCRS may allow diabetic care teams to better understand the origin of family conflict perceptions and the motivational beliefs that modify behavior and contribute to independent self-management and glucose control. Each question was designed to be meaningful in interventions by addressing common items of resistance to adherence and impulsive management decisions. The GCRS may be used by providers as an initial short screening survey on an annual or semi-annual basis.


Assuntos
Automonitorização da Glicemia/psicologia , Conflito Psicológico , Diabetes Mellitus Tipo 1/tratamento farmacológico , Diabetes Mellitus Tipo 1/psicologia , Hipoglicemiantes/uso terapêutico , Relações Pais-Filho , Educação de Pacientes como Assunto , Adolescente , Adulto , Biomarcadores/análise , Glicemia/análise , Cuidadores , Criança , Diabetes Mellitus Tipo 1/sangue , Feminino , Seguimentos , Hemoglobinas Glicadas/análise , Humanos , Masculino , Pais/psicologia , Cooperação do Paciente , Prognóstico , Estresse Psicológico , Inquéritos e Questionários , Adulto Jovem
2.
Brain Res Bull ; 143: 27-35, 2018 10.
Artigo em Inglês | MEDLINE | ID: mdl-30278200

RESUMO

Depression is associated with uncontrolled diabetes, which indicates a lack of insulin effect, yet the role of the insulin receptor in mediating depression is not clearly established because insulin receptors are not required for glucose entry into the brain. However, insulin receptors are important for brain function since insulin receptor knockout mice have depressive-like activity. Depression and cognitive problems are also associated with low insulin-like growth factor-1 (IGF-1) in the elderly. Rodent studies showed chronic IGF-1 administration had antidepressant-like (AD) activity. We asked if insulin in the brain might act through the IGF-1 receptor, as it does in some tissues. We used acute insulin or IGF-1 infusions into the 3rd ventricle (icv) in rats and tested animals in a forced swim test. We found that antidepressive-like behavior is mediated by insulin and IGF-1. Further, administration of the IGF-1 receptor antagonist JB-1 blocked the antidepressive-like activity of the insulin and IGF-1, indicating a strong relationship between insulin, IGF-1 and depression. Insulin acts at least partially through the IGF-1 receptor and is responsive to receptor antagonism. The model offers promise for future studies of the mechanism of depression, and therapy to increase insulin sensitivity and IGF-1 action including exercise and nutrition.


Assuntos
Fator de Crescimento Insulin-Like I/farmacologia , Insulina/farmacologia , Receptor IGF Tipo 1/efeitos dos fármacos , Animais , Antidepressivos/metabolismo , Antidepressivos/farmacologia , Comportamento Animal/efeitos dos fármacos , Encéfalo/efeitos dos fármacos , Depressão/etiologia , Transtorno Depressivo/etiologia , Fluoxetina/metabolismo , Fluoxetina/farmacologia , Insulina/metabolismo , Fator de Crescimento Insulin-Like I/metabolismo , Masculino , Atividade Motora/efeitos dos fármacos , Oligopeptídeos/metabolismo , Oligopeptídeos/farmacologia , Ratos , Ratos Sprague-Dawley , Receptor IGF Tipo 1/metabolismo , Receptor IGF Tipo 1/farmacologia , Receptor de Insulina/efeitos dos fármacos , Receptor de Insulina/metabolismo , Natação/psicologia
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