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Examination of quality of life and psychiatric symptoms in childhood Graves’ disease

  • Gözde Yazkan Akgül ORCID logo and Özge Köprülü ORCID logo EMAIL logo
Published/Copyright: April 22, 2024

Abstract

Objectives

The aim of our study is to examine the emotional, behavioral problems, and psychiatric symptoms of children diagnosed with Graves’ disease (GD), to assess their quality of life, and to compare with control group.

Methods

The research was planned as a cross-sectional study and included 16 patients with GD (13 female and three male) and 29 healthy children for control group (19 female and 10 male). Sociodemographic form, Pediatric Quality of Life Inventory, Revised Child Anxiety and Depression Scale-Child Version (RCADS-CV), Strengths and Difficulties Questionnaire (SDQ), Turgay DSM-IV-Based Child and Adolescent Behavior Disorders Screening and Rating Scale (T-DSM-IV-S), and Affective Reactivity Index scale were applied to the children and their families.

Results

Eighty one percent of GD group (GG) (n=13, mean age 15.1 ± 2.2) and 66 % of control group (CG) (n=19, 14.6 ± 2.2) were girls. No significant difference was found between GG and CG in terms of quality of life, anxiety, and depression scores. GG had higher scores in affective reactivity index, SDQ-P total score, and T-DSM-IV-S total scores (p values 0.039; 0.009; 0.023, respectively). While no significant difference was detected in the T-DSM-IV-S-inattention and hyperactivity scores, significantly higher scores were detected in oppositional defiance and conduct disorder scores (p values 0.172; 0.294; 0.019; 0.027, respectively).

Conclusions

In children with GD, irritability, oppositional defiant, and conduct disorder symptoms have been detected. Children with these mental health symptoms experience behavioral and emotional difficulties in their daily lives. It is important to follow up children with GD for possible comorbid psychiatric disorders.


Corresponding author: Özge Köprülü, MD, Division of Pediatric Endocrinology, Tekirdağ IFC City Hospital, Tekirdağ, Türkiye, Fax: +90 0232 489 23 15, E-mail:

  1. Research ethics: The study protocol was approved by the Tekirdağ Namık Kemal University Medical Faculty Ethics Committee (2022.94.05.21).

  2. Informed consent: Informed consent was obtained from all individuals included in this study.

  3. Author contributions: All authors have accepted responsibility for the entire content of this manuscript and approved its submission.

  4. Competing interests: Authors state no conflict of interest.

  5. Research funding: None declared.

  6. Data availability: The raw data can be obtained on request from the corresponding author.

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Received: 2023-12-14
Accepted: 2024-03-13
Published Online: 2024-04-22
Published in Print: 2024-05-27

© 2024 Walter de Gruyter GmbH, Berlin/Boston

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