The midbrain to pons ratio A simple and specific MRI sign of progressive supranuclear palsy

被引:137
作者
Massey, Luke A. [1 ]
Jaeger, Hans R. [2 ,3 ]
Paviour, Dominic C. [1 ]
O'Sullivan, Sean S. [1 ]
Ling, Helen [1 ]
Williams, David R. [5 ]
Kallis, Constantinos [6 ]
Holton, Janice [1 ]
Revesz, Tamas [1 ]
Burn, David J. [7 ]
Yousry, Tarek [2 ,3 ]
Lees, Andrew J. [1 ]
Fox, Nick C. [4 ]
Micallef, Caroline [2 ,3 ]
机构
[1] UCL Inst Neurol, Sara Koe PSP Res Ctr, Rita Lila Weston Inst Neurol Studies & Queen Sq B, Dept Mol Neurosci, London, England
[2] UCL Inst Neurol, Dept Brain Repair & Rehabil, London, England
[3] Natl Hosp Neurol & Neurosurg, Lysholm Dept Neuroradiol, London WC1N 3BG, England
[4] UCL Inst Neurol, Dementia Res Ctr, London, England
[5] Monash Univ, Van Cleef Roet Ctr Nervous Dis, Melbourne, Vic 3004, Australia
[6] Univ London, Forens Psychiat Res Unit, London WC1E 7HU, England
[7] Newcastle Univ, Inst Ageing & Hlth, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
基金
英国医学研究理事会;
关键词
MULTIPLE SYSTEM ATROPHY; PARKINSON-DISEASE; DIAGNOSIS; DIFFERENTIATION; SCALE;
D O I
10.1212/WNL.0b013e318292a2d2
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objectives: MRI-based measurements used to diagnose progressive supranuclear palsy (PSP) typically lack pathologic verification and are not easy to use routinely. We aimed to develop in histologically proven disease a simple measure of the midbrain and pons on sagittal MRI to identify PSP. Methods: Measurements of the midbrain and pontine base on midsagittal T1-weighted MRI were performed in confirmed PSP (n = 12), Parkinson disease (n = 2), and multiple system atrophy (MSA) (n = 7), and in controls (n = 8). Using receiver operating characteristic curve analysis, cutoff values were applied to a clinically diagnosed cohort of 62 subjects that included PSP (n = 21), Parkinson disease (n = 10), MSA (n = 10), and controls (n = 21). Results: The mean midbrain measurement of 8.1 mm was reduced in PSP (p < 0.001) with reduction in the midbrain to pons ratio (PSP smaller than MSA; p < 0.001). In controls, the mean midbrain ratio was approximately two-thirds of the pontine base, in PSP it was <52%, and in MSA the ratio was greater than two-thirds. A midbrain measurement of <9.35 mm and ratio of 0.52 had 100% specificity for PSP. In the clinically defined group, 19 of 21 PSP cases (90.5%) had a midbrain measurement of <9.35 mm. Conclusions: We have developed a simple and reliable measurement in pathologically confirmed disease based on the topography of atrophy in PSP with high sensitivity and specificity that may be a useful tool in the clinic.
引用
收藏
页码:1856 / 1861
页数:6
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