Evaluation of left ventricular function in children and adolescents with type 1 diabetes

Sawsan Ali Hussein1, Basil Metti Hanoudi2

  • 1College of Medicine, Mustansiriyah University, Baghdad, Iraq.

Insights

Type 1 diabetes in children and adolescents can cause subclinical changes in heart function, even before symptoms appear. Poor blood sugar control and longer diabetes duration worsen these cardiac effects.

Area of Science:

  • Pediatric Cardiology
  • Endocrinology
  • Cardiovascular Research

Background:

  • Type 1 diabetes mellitus (T1DM) is a chronic condition affecting children and adolescents.
  • Cardiac function can be impacted by diabetes, but data in pediatric populations is limited.

Purpose of the Study:

  • To evaluate the effects of T1DM on cardiac systolic and diastolic functions in pediatric patients.
  • To identify potential early indicators of cardiac involvement in young T1DM patients.

Main Methods:

  • A case-control study involving 96 children and adolescents (5-18 years) with T1DM and healthy controls.
  • Utilized clinical evaluation, laboratory tests, conventional echocardiography, and Doppler assessment.
  • Analyzed data using SPSS 25.

Main Results:

  • Patients with T1DM showed significantly prolonged isovolumic relaxation time and reduced early diastolic filling velocity.
  • Uncontrolled diabetes and longer disease duration (≥7 years) were associated with more pronounced cardiac alterations, including changes in left atrial/ventricular dimensions and myocardial performance index.
  • Subclinical myocardial dysfunction was observed in T1DM patients.

Conclusions:

  • T1DM can induce subclinical myocardial functional changes in asymptomatic children and adolescents.
  • Glycemic control and diabetes duration are critical factors accelerating these cardiac alterations.
Abstract

Related Concept Videos

Diabetes Mellitus: Overview and Type I Subtype01:22

Diabetes Mellitus: Overview and Type I Subtype

Diabetes mellitus is a chronic metabolic disorder characterized by high blood glucose levels due to inadequate insulin production, insulin resistance, or both. The condition affects millions worldwide and can significantly impact their health and quality of life.
Type 1 diabetes is an autoimmune disease in which the immune system mistakenly attacks and destroys the insulin-producing beta cells in the pancreas. As a result, the body is unable to produce sufficient insulin, and individuals with...
3.4K
Cardiomyopathy II: Dilated Cardiomyopathy01:30

Cardiomyopathy II: Dilated Cardiomyopathy

Dilated cardiomyopathy, or DCM, is a progressive myocardial disorder characterized by ventricular chamber dilation and contractile dysfunction.EtiologyVarious factors can cause DCM, including hypertension and heavy alcohol intake, which contribute to the weakening and enlargement of the heart muscle. Viral infections, such as Coxsackievirus B, adenoviruses, and influenza, can lead to DCM by causing inflammation and damage to heart tissue. Certain chemotherapeutic agents, including daunorubicin,...
51
Heart Failure IV: Classification and Diagnostic Evaluation01:30

Heart Failure IV: Classification and Diagnostic Evaluation

Heart failure can be classified in various ways, with the most common classifications based on physical activity limitations, disease progression, severity, and treatment strategies.The Functional Classification of Heart Failure divides patients into four categories based on physical activity limitation due to symptom burden.Class I: Patients in this class have cardiac disease but no physical activity limitations. Ordinary activities like walking, climbing stairs, or routine tasks do not cause...
65
Cardiomyopathy III: Hypertrophic Cardiomyopathy01:29

Cardiomyopathy III: Hypertrophic Cardiomyopathy

Hypertrophic cardiomyopathy, or HCM, is an autosomal dominant genetic disorder characterized by asymmetric left ventricular hypertrophy without ventricular dilation. It is more common in men and is typically diagnosed in young, athletic adults.EtiologyHCM is primarily genetic and is caused by mutations in genes encoding sarcomeric proteins. Researchers have identified over 1400 mutations across at least 11 different genes. Among these, the most frequently occurring mutations are found in the...
79