Cardiac remodeling and exercise tolerance in small for gestational age: a follow-up cohort study from preadolescence

Rommy H Novoa1,2, Dora Fabijanovic3,4, Kilian Vellvé1,2

  • 1BCNatal-Barcelona Center for Maternal-Fetal and Neonatal Medicine (Hospital Clínic and Hospital Sant Joan de Déu), Centre for Biomedical Research on Rare Diseases (CIBER-ER), Barcelona, Spain.

PubMed

Insights

Small for gestational age (SGA) adolescents show normalized cardiac structure but reduced exercise capacity. Compensatory growth may improve cardiac shape, but exercise tolerance remains impaired in these individuals.

Area of Science:

  • Cardiology
  • Pediatrics
  • Developmental Biology

Background:

  • Small for gestational age (SGA) affects 7%-10% of newborns.
  • SGA is linked to increased cardiovascular risk and reduced exercise capacity in adulthood.
  • Cardiac changes in SGA fetuses and children may persist into adolescence.

Purpose of the Study:

  • To assess resting cardiovascular morphology and function in adolescents born SGA.
  • To evaluate exercise tolerance in adolescents born SGA.
  • To understand the long-term cardiovascular impact of being born SGA.

Main Methods:

  • A cohort of 30 SGA adolescents and 28 controls were followed from preadolescence to adolescence.
  • Echocardiography was used to assess cardiac morphology and function.
  • Incremental cardiopulmonary exercise testing (CPET) evaluated exercise tolerance.

Main Results:

  • SGA adolescents exhibited a greater increase in left ventricular base-to-apex length and altered LV sphericity compared to controls.
  • No significant differences in left ventricular dimensions or deformation were found in SGA adolescents at follow-up.
  • SGA adolescents showed reduced oxygen uptake, expired carbon dioxide, and peak expiratory flow rate during exercise.

Conclusions:

  • Cardiac remodeling and dysfunction observed in SGA children appear to ameliorate in adolescence due to compensatory growth.
  • Despite improved cardiac structure, SGA adolescents demonstrate significantly reduced exercise tolerance.
  • These findings highlight the persistent impact of being born SGA on cardiovascular health and exercise capacity.
Abstract

Related Concept Videos

Exercise and Cardiac Output01:17

Exercise and Cardiac Output

Regular physical activity is essential for maintaining cardiovascular health, with aerobic exercises being particularly effective. According to the American Heart Association, 150 minutes of moderate to intense aerobic exercise per week is recommended for a healthy heart. Aerobic activities may include brisk walking, running, bicycling, cross-country skiing, and swimming, ideally performed three to five times per week.
Sustained exercise increases the muscles' oxygen demand, which can be...
1.8K
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...
374
Exercise and Cardiovascular Response01:20

Exercise and Cardiovascular Response

Exercise significantly impacts cardiovascular response, which is crucial for understanding patient health and designing effective treatment plans.
Light to moderate physical activity initiates a series of interconnected responses in the body. The heart rate modestly increases in anticipation of the workout, followed by widespread vasodilation as oxygen consumption by skeletal muscles increases. This results in decreased peripheral resistance, increased capillary blood flow, and accelerated...
3.8K
Cardiomyopathy IV: Restrictive Cardiomyopathy01:29

Cardiomyopathy IV: Restrictive Cardiomyopathy

Restrictive cardiomyopathy (RCM) is a rare heart muscle disease characterized by impaired ventricular filling due to stiffened ventricular walls, leading to significant diastolic dysfunction.EtiologyRestrictive cardiomyopathy can arise from both inherited and acquired diseases, many of which are systemic. It is categorized into four main types: infiltrative, storage, non-infiltrative, and endomyocardial diseases.Infiltrative diseases, such as amyloidosis, lead to RCM by depositing amyloid...
431