4.7 Article

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

期刊

NEUROLOGY
卷 80, 期 20, 页码 1856-1861

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1212/WNL.0b013e318292a2d2

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资金

  1. PSP (Europe) Association
  2. Medical Research Council
  3. Alzheimer Research UK
  4. National Institute for Health Research
  5. UK Department of Health's National Institute for Health Research Biomedical Research Centres funding scheme (UCLH/UCL Comprehensive Biomedical Research Trust)
  6. Medical Research Council [MR/K000608/1, G0601846] Funding Source: researchfish
  7. National Institute for Health Research [NF-SI-0508-10123] Funding Source: researchfish
  8. MRC [MR/K000608/1, G0601846] Funding Source: UKRI

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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.

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