High prevalence of low bone mineral density in young adults with phenylketonuria

Kısmet Çıkı1, Ayça Burcu Kahraman1, Halil Tuna Akar1

  • 1Division of Pediatric Metabolism, Department of Pediatrics, Faculty of Medicine, Hacettepe University, Ankara, Turkey.

Postgraduate Medicine
|December 18, 2024
PubMed

Insights

Low bone mineral density (BMD) affects 25% of adults with classical phenylketonuria (cPKU). Male sex and low body mass index (BMI) are identified as key risk factors for reduced BMD in this population.

Area of Science:

  • Metabolic Disorders
  • Bone Health
  • Nutritional Science

Background:

  • Phenylalanine (Phe)-restricted diets in classical phenylketonuria (cPKU) may negatively impact bone health.
  • Limited data exist on bone mineral density (BMD) in adults with cPKU, with conflicting reports.
  • This study evaluates BMD and associated risk factors in a cohort of adult cPKU patients.

Purpose of the Study:

  • To assess bone mineral density (BMD) in adults diagnosed with classical phenylketonuria (cPKU).
  • To identify specific risk factors contributing to low BMD within this patient group.
  • To inform clinical monitoring and management strategies for bone health in cPKU.

Main Methods:

  • Eighty adult patients with cPKU (18.3-39.4 years) were studied.
  • Bone mineral density (BMD) at the femur and lumbar spine was measured using dual-energy X-ray absorptiometry.
  • Patients were categorized into low BMD (Z-score ≤-2) and normal BMD (Z-score > -2) groups for analysis.

Main Results:

  • Low BMD was observed in 25% of the adult cPKU cohort.
  • The low BMD group exhibited a higher prevalence of males (75% vs. 40%) and lower mean body mass index (BMI).
  • Elevated, though marginal, levels of calcium and vitamin D were noted in the low BMD group; age and Phe levels were not significant factors.

Conclusions:

  • This study confirms that male sex and low BMI are significant risk factors for low BMD in adults with cPKU.
  • Low BMD is prevalent even in young adults with cPKU, irrespective of age, Phe levels, or supplementation.
  • Regular bone health evaluation is crucial for young adult cPKU patients, particularly males and those with low BMI.
Abstract

Related Concept Videos

Inborn Errors of Metabolism01:20

Inborn Errors of Metabolism

Phenylketonuria (PKU) is a protein metabolism disorder characterized by high blood levels of the amino acid phenylalanine. This results from a mutation in the gene responsible for phenylalanine hydroxylase, an enzyme that converts phenylalanine into tyrosine. When this enzyme is deficient, phenylalanine builds up in the blood, leading to symptoms such as vomiting, rashes, seizures, growth deficiency, and severe mental retardation. An early diagnosis and a diet restricting phenylalanine intake...
127
Overview of Protein Metabolism01:21

Overview of Protein Metabolism

Proteins are broken down into amino acids during digestion. Unlike fats and carbohydrates, which are stored for later use, proteins are not. Instead, amino acids are either used to produce ATP through oxidation or contribute to the creation of new proteins for the growth and repair of the body. Any surplus amino acids from the diet are converted into glucose or triglycerides rather than excreted.
Amino acids play various roles in the body once they are absorbed into cells. They are restructured...
723
Bone Disorders01:29

Bone Disorders

Aging and its effect on bone remodeling is the most common cause of bone disorders. In young and healthy people, bone deposition and resorption happen at an equal rate to maintain optimal bone health.
Bone deposition is also affected by the levels of sex hormones like estrogen and testosterone that promote osteoblast activity and bone matrix synthesis. When the level of these hormones decreases due to aging, it causes a reduction in bone deposition. As a result, bone resorption by osteoclasts...
3.4K
Pedigree Analysis01:35

Pedigree Analysis

Overview
83.9K