Emotional and behavioural functioning in children with tyrosinaemia type 1.

Monika Pohorecka, Marcin Biernacki, Anna Jakubowska-Winecka, Kinga Leszczynska-Iwanicka, Dariusz Rokicki, Paulina Pokora, Barbara Perkowska, Magdalena Pajdowska, Marta Biernacka
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Abstract

Introduction: Tyrosinaemia type I is a rare hereditary metabolic disease caused by deficiency of the enzyme involved in the breakdown of tyrosine. Since the use of nitisinone in addition to diet in 1992, survival rates have increased significantly, but more and more socio-emotional problems have become apparent. The aim of the study was the assessment the relationship between variations in serum tyrosine and phenylalanine levels and measurements of socio-emotional functioning and determination of patients' IQs.

The aim of the study: was the assessment the relationship between variations in serum tyrosine and phenylalanine levels and measurements of socio-emotional functioning and determination of patients' IQs.

Material and methods: Twelve children were studied, from a single centre, born between 1994 and 2012, treated with nitisinone and a low-phenylalanine and -tyrosine diet. The psychological evaluation was conducted using the parent form of the Child Behaviour Checklist (CBCL)/4-18. Additionally, the patients' IQs were measured using the Stanford-Binet 5 (SB5) Intelligence Scale. Statistical analyses were performed using PAWS software suite version 26. We found that phenylalanine variability over time correlated with measures of emotional and behavioural functioning. This relationship holds true for externalising behaviour, associated with the experience of maladjustment and aggression. Total score intellectual and cognitive function was within the norm for all patients.

Conclusions: To maintain better quality of life for patients and their families in terms of emotional and behavioural functioning, it may be important to avoid spikes (significant fluctuations) in phenylalanine levels. Regular, detailed psychological evaluations are recommended to detect potential problems and implement interventions aimed at achieving the best possible individual development and realise the intellectual and behavioural potential, thereby improving the patient's and her family's quality of life.

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1 型酪氨酸血症患儿的情绪和行为功能。
导言酪氨酸血症 I 型是一种罕见的遗传性代谢疾病,由参与酪氨酸分解的酶缺乏引起。自 1992 年在饮食之外使用尼替西酮以来,存活率显著提高,但社会情感问题也越来越多。该研究的目的是评估血清中酪氨酸和苯丙氨酸水平的变化与社会情感功能测量和患者智商测定之间的关系:研究对象为来自一个中心的12名儿童,他们出生于1994年至2012年,接受了尼替西酮和低苯丙氨酸及酪氨酸饮食治疗。心理评估采用儿童行为检查表(CBCL)/4-18的家长表进行。此外,还使用斯坦福-比奈5(SB5)智力量表测量了患者的智商。统计分析使用 PAWS 软件套件 26 版进行。我们发现,苯丙氨酸随时间的变化与情绪和行为功能的测量结果相关。这种关系适用于与适应不良和攻击行为相关的外化行为。所有患者的智力和认知功能总分均符合标准:为了让患者及其家人在情绪和行为功能方面保持更好的生活质量,避免苯丙氨酸水平出现峰值(大幅波动)可能很重要。建议定期进行详细的心理评估,以发现潜在问题并采取干预措施,尽可能实现最佳的个体发展,发挥智力和行为潜能,从而提高患者及其家人的生活质量。
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来源期刊
Pediatric Endocrinology, Diabetes and Metabolism
Pediatric Endocrinology, Diabetes and Metabolism Medicine-Pediatrics, Perinatology and Child Health
CiteScore
2.00
自引率
0.00%
发文量
36
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