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弥散张量成像检测到部分鸟氨酸转氨甲酰酶缺乏症患者的白质微观结构异常区域。

Diffusion tensor imaging detects areas of abnormal white matter microstructure in patients with partial ornithine transcarbamylase deficiency.

机构信息

Department of Neurology, Children's National Medical Center, 111 Michigan Avenue NW, Washington, DC 20010, USA.

出版信息

AJNR Am J Neuroradiol. 2010 Oct;31(9):1719-23. doi: 10.3174/ajnr.A2122. Epub 2010 May 20.

Abstract

BACKGROUND AND PURPOSE

OTCD, an X-linked disorder, is the most common of the UCDs. Neonatal onset is associated with uniformly poor outcome. Males with late-onset OTCD show deficits in executive function, motor planning, and working memory. A broad phenotype is observed in heterozygous females. A specific neurobehavioral phenotype with white matter dysfunction and impaired attention and working memory has been described. The extent to which the deficits involve specific pathways in the brain is unknown. We hypothesized that DTI would disclose white matter microstructure in OTCD correlating with cognitive deficits.

MATERIALS AND METHODS

Nineteen adults with partial OTCD and 18 adult control subjects ages 19-59 years participated. MR imaging was performed by using a 3T whole-body scanner. Anisotropy was calculated from the eigenvalues of the diffusion tensor by using the FA metric and was compared between the study and control groups.

RESULTS

FA of the frontal white matter was significantly decreased in subjects, indicating changes in white matter microstructure. There was an inverse relationship between FA and disease severity, but not with age.

CONCLUSIONS

Findings of MR imaging in OTCD are often normal in patients with late-onset disease, heterozygotes, or in those not in hyperammonemic crisis. DTI was more sensitive than FSE T2-weighted imaging for detecting abnormalities in normal-appearing white matter. The extent of abnormality correlated with cognitive deficits. The location of the deficits in the frontal white matter is important because this area connects fibers that are vital to executive function, attention, and working memory.

摘要

背景与目的

OTCD 是一种 X 连锁疾病,是 UCD 中最常见的一种。新生儿发病与预后不良相关。晚发型 OTCD 男性表现出执行功能、运动规划和工作记忆缺陷。杂合子女性表现出广泛的表型。已经描述了一种具有白质功能障碍、注意力和工作记忆受损的特定神经行为表型。在多大程度上这些缺陷涉及大脑中的特定通路尚不清楚。我们假设 DTI 可以揭示与认知缺陷相关的 OTCD 中的白质微观结构。

材料与方法

19 名部分 OTCD 成年患者和 18 名年龄在 19-59 岁的成年对照组参与了本研究。使用 3T 全身扫描仪进行 MRI 检查。通过使用 FA 指标从扩散张量的特征值中计算各向异性,并比较研究组和对照组之间的差异。

结果

额叶白质的 FA 值显著降低,表明白质微观结构发生了变化。FA 值与疾病严重程度呈负相关,但与年龄无关。

结论

在晚发型疾病、杂合子或非高氨血症危象患者中,OTCD 的 MRI 检查结果通常正常。DTI 比 FSE T2 加权成像更敏感,能够检测正常表现的白质异常。异常程度与认知缺陷相关。额叶白质缺陷的位置很重要,因为这个区域连接着对执行功能、注意力和工作记忆至关重要的纤维。

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