Hostname: page-component-7479d7b7d-fwgfc Total loading time: 0 Render date: 2024-07-10T20:47:49.957Z Has data issue: false hasContentIssue false

Relationship between Glycated Hemoglobin in Adolescents with Type 1 Diabetes Mellitus (T1DM) and Parental Anxiety and Depression

Published online by Cambridge University Press:  19 July 2023

E. Silina*
Affiliation:
Doctoral studies, Riga Stradins University, Riga The Seaside Hospital, Liepaja
M. Taube
Affiliation:
Department of Psychiatry and Narcology
M. Zolovs
Affiliation:
Statistics Unit, Riga Stradins University, Riga Institute of Life Sciences and Technology, Daugavpils University, Daugavpils, Latvia
*
*Corresponding author.

Abstract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.
Introduction

T1D is the most common chronic endocrine pathology in children. The management of type 1 diabetes requires strong diet, physical activity, lifelong insulin therapy, and proper self-monitoring of blood glucose and is usually complicated and, therefore may result in a psychosocial problems for the whole family. Metabolic control of the disease is determined by glycated haemoglobin (HbA1c), the main criterion for diabetes compensation. It is assumed that anxiety and depression symptoms negatively affect glycaemic control. Parental psychological distress was associated with higher child self-report of stress and depressive symptoms, and it had negative effects on diabetes management.

Type 1 diabetes mellitus (T1D) is the most common chronic endocrine pathology in children. The management of type 1 diabetes requires strong diet, physical activity, lifelong insulin therapy, and proper self-monitoring of blood glucose and is usually complicated and, therefore may result in a variety of psychosocial problems for children, adolescents, and their families. Metabolic control of the disease is determined by glycated haemoglobin (HbA1c), the main criterion for diabetes compensation. A correlation is observed between anxiety and depression level and glycaemic control in many previous studies. It is assumed that anxiety and depression symptoms negatively affect glycaemic control. Parental psychological distress was associated with higher child self-report of stress and depressive symptoms, and it had negative effects on diabetes management.

Objectives

To evaluate the relationship between parental depression and anxiety and metabolic control of their adolescents with T1DM.

Methods

Cross-sectional study recruited adolescents with T1D (N=251) and their parents (N=251). Anxiety level was measured by 7-item Generalized Anxiety Disorder (GAD-7) scale. Depressive symptms wasdetected using The Patient Health Questionnaire – 9 (PHQ-9). Glycaemic control of patients was assessed using the last HbA1c values. GLM mediation analysis was performed to determine the potential mediating effect of parental depression and anxiety on the relationship between depression and anxiety of the child on the level of glycated hemoglobin.

Results

502 respondents were eligible for screening. Mediation analysis was performed to assess the mediating role of parent GAD-7 on the linkage between HbA1c, child GAD-7 and child PHQ-9. The total effect of child GAD-7 on HbA1c was significant but the total effect of child PHQ-9 was not. With the inclusion of the mediating variable (parent GAD-7) (Figure 1), the indirect effect of child GAD-7 and the child PHQ-9 on HbA1c though parent GAD-7 was found significant (Table 1).

Image:

Image 2:

Conclusions

Parental anxiety is a significant risk factor for child depression and anxiety, which determines poorer T1D metabolic compensation ard worse HbA1C scores.

Disclosure of Interest

None Declared

Type
Abstract
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
Copyright
© The Author(s), 2023. Published by Cambridge University Press on behalf of the European Psychiatric Association
Submit a response

Comments

No Comments have been published for this article.