Growth Assessment and Nutritional Status in Children with Congenital Adrenal Hyperplasia-A Cross-Sectional Study from

Thi Thuy Hong Nguyen1, Khanh Minh Le1, Thi Anh Thuong Tran1,2

  • 1Department of Paediatrics, Hanoi Medical University, Hanoi 11521, Vietnam.

Insights

Children with congenital adrenal hyperplasia (CAH) experience significant growth and nutritional issues, including stunting and vitamin D deficiency. Early intervention is key to managing these complex health challenges in pediatric patients.

Area of Science:

  • Pediatric Endocrinology
  • Metabolic Disorders
  • Nutritional Science

Background:

  • Congenital adrenal hyperplasia (CAH) poses risks for impaired growth and metabolic disturbances in children.
  • Standard glucocorticoid therapy may not fully address these complications.
  • Vietnamese children with CAH require focused evaluation for growth and nutritional status.

Purpose of the Study:

  • To assess growth outcomes, nutritional status, and associated factors in children with CAH.
  • To identify clinical, biochemical, and treatment-related factors influencing health in pediatric CAH patients.
  • To provide data for optimizing management strategies in a Vietnamese tertiary pediatric center.

Main Methods:

  • Cross-sectional study of 201 children (1.1-16.5 years) with CAH.
  • Evaluation of anthropometric parameters, WHO growth standards, and bone age (radiographic assessment).
  • Assessment of biochemical markers (calcium, phosphate, 25-hydroxyvitamin D) and clinical features.

Main Results:

  • Stunting affected 16.4%, while 53.3% were overweight/obese.
  • Bone age advancement occurred in 51.7%; 85.6% had vitamin D insufficiency/deficiency; 85.1% had hypocalcemia.
  • Risk factors for adverse outcomes included older age, prolonged corticosteroid use, high androgens, and treatment imbalance.

Conclusions:

  • Growth impairment, nutritional deficiencies, and skeletal maturation issues are common in Vietnamese children with CAH.
  • Identifying risk factors and implementing tailored endocrine and nutritional management are vital.
  • Optimizing long-term outcomes requires a comprehensive approach to pediatric CAH care.

Related Concept Videos

Nature and Nurture01:10

Nature and Nurture

Many human characteristics, like height, are shaped by both nature—in other words, by our genes—and by nurture, or our environment. For example, chronic stress during childhood inhibits the production of growth hormones and consequently reduces bone growth and height. Scientists estimate that 70-90% of variation in height is due to genetic differences among individuals, and 10-30% of variation in height is due to differences in the environments that individuals experience,...
19.4K
Adrenal Gland Disorders01:27

Adrenal Gland Disorders

Adrenal gland disorders manifest when the production of adrenal hormones deviates from the norm, resulting in either excessive or insufficient concentrations.
Adrenal insufficiency, characterized by insufficient cortisol and aldosterone production, leads to conditions like Addison's disease. This disorder, affecting the adrenal cortex, exhibits symptoms such as skin bronzing, dehydration, low blood pressure, fatigue, and weight loss. Congenital adrenal hyperplasia, a genetic ailment causing...
3.7K
Pharmacokinetics in Pediatric Patients: Overview and Drug Absorption01:23

Pharmacokinetics in Pediatric Patients: Overview and Drug Absorption

Understanding the physiological differences in the pediatric population is crucial for effective pharmacotherapy. Neonates, infants, and children exhibit significant variations in gastric pH, gastric emptying time, intestinal transit time, and biliary function. These variations profoundly affect oral drug absorption, necessitating a nuanced approach to pediatric dosing.Neonates present with a unique physiological profile, having a gastric pH greater than 4 and faster and more irregular gastric...
967
Pharmacokinetics in Pediatric Patients: Drug Metabolism01:24

Pharmacokinetics in Pediatric Patients: Drug Metabolism

In pediatric care, understanding the nuances of hepatic drug metabolism is crucial, as it significantly differs from that of adults. This divergence is primarily due to the developmental stage of drug-metabolizing enzymes, which affects how medications are processed in the body. In neonates, for instance, the activity of Phase I enzymes—critical for the initial breakdown of drugs—is markedly reduced, functioning at just 20–40% of the levels seen in adults. This reduction poses...
410
Pharmacokinetics in Pediatric Patients: Drug Excretion01:26

Pharmacokinetics in Pediatric Patients: Drug Excretion

In pediatric medicine, understanding the renal function and drug elimination nuances is crucial for administering safe and effective treatments. Newborns, in particular, display markedly slower renal functions than adults, profoundly affecting how drugs are cleared from their bodies. This slower drug clearance requires clinicians to extend the dosing intervals for many medications to prevent drug accumulation and toxicity while ensuring therapeutic efficacy.One key area where these adjustments...
408
Cushing Syndrome II: Pathophysiology01:19

Cushing Syndrome II: Pathophysiology

Cortisol production is normally governed by the hypothalamic–pituitary–adrenal (HPA) axis, which maintains hormonal balance through tightly regulated feedback mechanisms. Disruption of this regulatory system is central to the development of Cushing syndrome, whether the excess cortisol originates from external medications or internal pathology. Persistent cortisol elevation alters metabolism, immune function, and endocrine signaling, producing the characteristic clinical features...
24