Division of Child and Adolescent Psychiatry, Department of Psychiatry, University of Utah School of Medicine, Salt Lake City, UT, USA.
Mol Genet Metab. 2010;99 Suppl 1:S18-21. doi: 10.1016/j.ymgme.2009.10.015.
Phenylketonuria (PKU) results in profound intellectual disability in untreated individuals and more subtle cognitive deficits in individuals treated early and continuously. The assessment of intellectual functioning has been an important outcome variable and the focus of extensive research. Since the implementation of neonatal PKU screening programs in the 1960s, research on intellectual functioning in individuals with PKU has played a significant and positive role in guiding therapy and improving results. This is a literature review examining the relationship between intellectual outcome and treatment parameters including initiation of treatment, duration of treatment, and blood phenylalanine (Phe) levels from infancy through adulthood. While current PKU treatment practices have eliminated severe neurological and cognitive impairment, evidence suggests that intellectual functioning, although typically within the average range when PKU is treated early and continuously, may not be maximized under the current definition of well-controlled PKU, which is based on blood Phe levels. Future research assessing intellectual and neurocognitive outcome in PKU will enhance the development of new treatment strategies.
苯丙酮尿症(PKU)可导致未经治疗的患者出现严重的智力障碍,而早期和持续治疗的患者则存在更微妙的认知缺陷。智力功能评估一直是一个重要的结果变量,也是广泛研究的重点。自 20 世纪 60 年代新生儿 PKU 筛查项目实施以来,PKU 患者的智力功能研究在指导治疗和改善结果方面发挥了重要而积极的作用。这是一篇文献综述,探讨了智力结果与治疗参数之间的关系,包括治疗的开始时间、治疗的持续时间以及婴儿期到成年期的血液苯丙氨酸(Phe)水平。虽然目前的 PKU 治疗方法已经消除了严重的神经和认知障碍,但有证据表明,智力功能虽然在早期和持续治疗时通常处于平均范围内,但在当前基于血液 Phe 水平的良好控制 PKU 的定义下,可能无法达到最佳状态。未来评估 PKU 患者智力和神经认知结果的研究将有助于开发新的治疗策略。