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晚发性苯丙酮尿症患者的生化、临床及神经放射学(MRI)相关性研究

Biochemical, clinical and neuroradiological (MRI) correlations in late-detected PKU patients.

作者信息

Leuzzi V, Trasimeni G, Gualdi G F, Antonozzi I

机构信息

Dipartimento di Scienze Neurologiche e Psichiatriche dell'Età Evolutiva, Università, La Sapienza, Roma, Italy.

出版信息

J Inherit Metab Dis. 1995;18(5):624-34. doi: 10.1007/BF02436009.

Abstract

Brain magnetic resonance imaging (MRI) was performed in 17 late-detected PKU patients (aged 2.8-25 years). Twelve subjects had been treated late (0.7-4.5 years), and 5 not at all. Four were still on diet when the study was performed. Mental development was normal in 4 subjects, mildly retarded in 6, and moderately or severely retarded in 7. None had exhibited mental or neurological deterioration. On MRI examination a symmetrical increase of T2-weighted signal in the periventricular white matter was found in all patients, although to different degrees. Concomitant signal decrease on the T1-weighted sequences was detected in 9 patients. Ten subjects showed focal white-matter abnormalities. A variable degree of cortical and subcortical atrophy was found in 12 subjects, and asymmetry of lateral ventricles in 4. White-matter involvement correlated with phenylalanine concentrations during the year preceding (rs = 0.5706; p < 0.02) and at the time of (rs = 0.6182, p < 0.01) the investigation. Cortical and subcortical atrophy correlated with the patient's age (rs = 0.5889, p < 0.02, and rs = 0.5929, p < 0.02, respectively). We conclude that late-detected PKU patients showed the same MRI abnormalities reported in early-treated subjects and in subjects who underwent neurological deterioration; white-matter abnormalities possibly result from the recent exposure to high phenylalanine concentrations; in late-detected PKU subjects cerebral atrophy could be the late result of chronic exposure to high phenylalanine concentrations.

摘要

对17例晚发性苯丙酮尿症患者(年龄2.8 - 25岁)进行了脑磁共振成像(MRI)检查。其中12例患者治疗较晚(0.7 - 4.5岁),5例未接受任何治疗。研究进行时,4例仍在进行饮食治疗。4例患者智力发育正常,6例轻度发育迟缓,7例中度或重度发育迟缓。所有患者均未出现智力或神经功能恶化。MRI检查发现,所有患者脑室周围白质T2加权信号均有对称性增强,只是程度不同。9例患者在T1加权序列上伴有信号降低。10例患者出现局灶性白质异常。12例患者发现不同程度的皮质和皮质下萎缩,4例患者侧脑室不对称。白质受累情况与检查前一年(rs = 0.5706;p < 0.02)及检查时(rs = 0.6182,p < 0.01)的苯丙氨酸浓度相关。皮质和皮质下萎缩与患者年龄相关(分别为rs = 0.5889,p < 0.02和rs = 0.5929,p < 0.02)。我们得出结论,晚发性苯丙酮尿症患者表现出与早期治疗患者以及出现神经功能恶化患者相同的MRI异常;白质异常可能是近期暴露于高苯丙氨酸浓度所致;在晚发性苯丙酮尿症患者中,脑萎缩可能是长期暴露于高苯丙氨酸浓度的晚期结果。

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