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Makale detayı · 2025

Feeding Models in Classical Phenylketonuria: Do They Make a Difference in Infant Sleep?

Nutrients

YÖKSİS OpenAlex Açık erişim · gold SJR Q1 JCR Q1 Atıf 0 Yüzdelik 23.0% FWCI 0.0
Yıl
2025
ISSN
2072-6643
Tür
article

Veri kaynağı ayrımı

  • YÖKSİS YÖKSİS makale kaydı
  • OpenAlex OpenAlex zenginleştirmesi (özet, atıf, konular)

Özet

İngilizce (OpenAlex)

BACKGROUND: Phenylketonuria (PKU) is an inherited metabolic disorder that requires early diagnosis and strict phenylalanine (Phe)-restricted diet to prevent neurocognitive impairment. Various infant feeding models have been used to achieve optimal metabolic control during early life. The aim of this study was to compare two different feeding models for infants with classical PKU in terms of metabolic control, growth parameters, micronutrient status, the process of introducing complementary foods, and with a particular focus on sleep quality. METHODS: In this prospective observational study, 26 infants with classical PKU were followed for 12 months. Patients were assigned to one of two feeding groups: Group-1 received breast milk and Phe-free formula in alternating feeds, while Group-2 received Phe-free formula followed by breastfeeding until satiety. Blood Phe, micronutrient levels and anthropometric measurements were recorded. Sleep quality was evaluated using the Brief Infant Sleep Questionnaire-Revised (BISQ-R). A structured set of parental questions was used to evaluate their experiences during the complementary feeding period. RESULTS: No statistically significant differences were observed between the groups in terms of blood Phe levels, anthropometric measurements, serum levels of iron, ferritin, vitamin-B12, vitamin-D, and zinc. Complementary feeding tolerance were similar across the groups. The BISQ-R analysis revealed no significant differences between the groups. CONCLUSIONS: Both feeding models were equally effective in maintaining metabolic control, supporting normal growth, complementary feeding processes, and preserving sleep quality during infancy. These findings suggest that either approach can be adopted based on the preference of the caregiver and the practicality of the clinical setting.

Konular

  • Metabolism and Genetic Disorders
  • Folate and B Vitamins Research
  • Diet and metabolism studies

Birincil konu Metabolism and Genetic Disorders

Yazarlar

  1. EZGİ BURGAÇ
  2. ebru çiçek türköz
  3. ADNAN BARUTÇU
  4. FATMA DERYA BULUT
  5. DENİZ KOR ÇUKUROVA ÜNİVERSİTESİ
  6. TUĞÇE KARTAL
  7. sema uzunoğlu
  8. esra kara
  9. BURCU KÖŞECİ
  10. İREM KAPLAN
  11. NAZLI TOTİK DOĞAN HATAY MUSTAFA KEMAL ÜNİVERSİTESİ
  12. HALİSE NESLİHAN ÖNENLİ MUNGAN ÇUKUROVA ÜNİVERSİTESİ