Dynamic Contrast-Enhanced MRI Evaluation of Cerebral Cavernous Malformations

被引:28
|
作者
Hart, Blaine L. [1 ]
Taheri, Saeid [2 ]
Rosenberg, Gary A. [3 ]
Morrison, Leslie A. [3 ]
机构
[1] Univ New Mexico, Dept Radiol, Albuquerque, NM 87131 USA
[2] Med Univ S Carolina, Dept Radiol, Charleston, SC 29425 USA
[3] Univ New Mexico, Dept Neurol, Albuquerque, NM 87131 USA
基金
美国国家卫生研究院;
关键词
MRI dynamic contrast enhanced; Brain/brain stem; Genetic defects; BLOOD-BRAIN-BARRIER; TRANSFER CONSTANTS; NATURAL-HISTORY; PERMEABILITY; INTEGRITY;
D O I
10.1007/s12975-013-0285-y
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The aim of this study is to quantitatively evaluate the behavior of CNS cavernous malformations (CCMs) using a dynamic contrast-enhanced MRI (DCEMRI) technique sensitive for slow transfer rates of gadolinium. The prospective study was approved by the institutional review board and was HIPPA compliant. Written informed consent was obtained from 14 subjects with familial CCMs (4 men and 10 women, ages 22-76 years, mean 48.1 years). Following routine anatomic MRI of the brain, DCEMRI was performed for six slices, using T1 mapping with partial inversion recovery (TAPIR) to calculate T1 values, following administration of 0.025 mmol/kg gadolinium DTPA. The transfer rate (Ki) was calculated using the Patlak model, and Ki within CCMs was compared to normal-appearing white matter as well as to 17 normal control subjects previously studied. All subjects had typical MRI appearance of CCMs. Thirty-nine CCMs were studied using DCEMRI. Ki was low or normal in 12 lesions and elevated from 1.4 to 12 times higher than background in the remaining 27 lesions. Ki ranged from 2.1E-6 to 9.63E-4 min(-1), mean 3.55E-4. Normal-appearing white matter in the CCM patients had a mean Ki of 1.57E-4, not statistically different from mean WM Ki of 1.47E-4 in controls. TAPIR-based DCEMRI technique permits quantifiable assessment of CCMs in vivo and reveals considerable differences not seen with conventional MRI. Potential applications include correlation with biologic behavior such as lesion growth or hemorrage, and measurement of drug effects.
引用
收藏
页码:500 / 506
页数:7
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