Phenylketonuria in adulthood: A collaborative study

被引:158
作者
Koch, R
Burton, B
Hoganson, G
Peterson, R
Rhead, W
Rouse, B
Scott, R
Wolff, J
Stern, AM
Guttler, F
Nelson, M
de la Cruz, F
Coldwell, J
Erbe, R
Geraghty, MT
Shear, C
Thomas, J
Azen, C
机构
[1] Univ So Calif, Childrens Hosp Los Angeles, Keck Sch Med, Dept Pediat,Div Med Genet,PKU Program 73, Los Angeles, CA 90027 USA
[2] Dept Radiol, Los Angeles, CA USA
[3] Childrens Mem Med Ctr, Chicago, IL USA
[4] Univ Illinois, Dept Pediat, Chicago, IL USA
[5] San Diego Reg Ctr, San Diego, CA USA
[6] Univ Iowa, Div Med Genet, Iowa City, IA USA
[7] Univ Texas, Med Branch, Childrens Hosp, Galveston, TX 77550 USA
[8] Univ Washington, Sch Med, Dept Pediat, Seattle, WA 98195 USA
[9] Univ Wisconsin, Waisman Ctr Mental Retardat & Human Dev, Madison, WI 53706 USA
[10] Univ Copenhagen, John F Kennedy Inst, Dept Inherited Metab Dis, Glostrup, Denmark
[11] NICHHD, Bethesda, MD 20892 USA
[12] Childrens Med Ctr, Tulsa, OK USA
[13] Childrens Hosp, Div Genet, Buffalo, NY 14222 USA
[14] Johns Hopkins Univ Hosp, Inst Genet, Baltimore, MD 21287 USA
[15] Childrens Hosp, Denver, CO 80218 USA
关键词
D O I
10.1023/A:1020158631102
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
During 1967-1983, the Maternal and Child Health Division of the Public Health Services funded a collaborative study of 211 newborn infants identified on newborn screening as having phenylketonuria (PKU). Subsequently, financial support was provided by the National Institute of Child Health and Human Development (NICHD). The infants were treated with a phenylalanine (Phe)-restricted diet to age 6 years and then randomized either to continue the diet or to discontinue dietary treatment altogether. One hundred and twenty-five of the 211 children were then followed until 10 years of age. In 1998, NICHD scheduled a Consensus Development Conference on Phenylketonuria and initiated a study to follow up the participants from the original Collaborative Study to evaluate their present medical, nutritional, psychological, and socioeconomic status. Fourteen of the original clinics (1967-1983) participated in the Follow-up Study effort. Each clinic director was provided with a list of PKU subjects who had completed the original study (1967-1983), and was asked to evaluate as many as possible using a uniform protocol and data collection forms. In a subset of cases, magnetic resonance imaging and spectroscopy (MRI/MRS) were performed to study brain Phe concentrations. The medical evaluations revealed that the subjects who maintained a phenylalanine-restricted diet reported fewer problems than the diet discontinuers, who had an increased rate of eczema, asthma, mental disorders, headache, hyperactivity and hypoactivity. Psychological data showed that lower intellectual and achievement test scores were associated with dietary discontinuation and with higher childhood and adult blood Phe concentrations. Abnormal MRI results were associated with higher brain Phe concentrations. Early dietary discontinuation for subjects with PKU is associated with poorer outcomes not only in intellectual ability, but also in achievement test scores and increased rates of medical and behavioural problems.
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收藏
页码:333 / 346
页数:14
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