TY - JOUR
T1 - Linear vs volume measures of ventricle size
T2 - Relation to present and future gait and cognition
AU - Crook, Julia E.
AU - Gunter, Jeffrey L.
AU - Ball, Colleen T.
AU - Jones, David T.
AU - Graff-Radford, Jonathan
AU - Knopman, David S.
AU - Boeve, Bradley F.
AU - Petersen, Ronald C.
AU - Jack, Clifford R.
AU - Graff-Radford, Neill R.
N1 - Funding Information:
Supported by the NIH (U01 AG006786, R01 AG011378, R01 AG041851, P50 AG44170, RF1 AG55151, and R01 AG049704) and the Robert H. and Clarice Smith and Abigail van Buren Alzheimer’s Disease Research Program. This study was made possible by the Rochester Epidemiology Project (R01 AG034676). It also was partially funded by the David Eisenberg Endowed Chair at Mayo Clinic. The content is solely the responsibility of the authors and does not necessarily represent the official views of NIH.
Publisher Copyright:
© American Academy of Neurology.
PY - 2020/2/4
Y1 - 2020/2/4
N2 - ObjectiveTo compare the clinical utility of volume-based ratios with the standard linear ratio of Evans index (EI) by examining their associations with gait, cognition, and other patient and imaging variables.MethodsFrom MRI scans of 1,774 participants in the Mayo Clinic Study of Aging, we calculated 3 ventricle size measures: Evan index (frontal horn width divided by widest width of skull inner table), total ventricular volume, and frontal horn volume as ratios of total intracranial volume. Gait was measured by a timed 25-foot walk and cognition by a composite of psychometric tests. We also evaluated variables associated with the measures of ventricular size. Further, we evaluated gait and cognition associations with MRI of extraventricular findings seen in normal-pressure hydrocephalus: disproportionate enlargement of subarachnoid space (DESH) and focal sulcal dilations (FSD).ResultsVentricular volume measures had stronger association with gait and cognition measures than EI. In decreasing order of strength of association with ventricle size were DESH, FSD, white matter hyperintensity volume ratio, age, male sex, cortical thickness, and education. Modest evidence was observed that FSD was associated with future decline in gait and cognition.ConclusionVentricular volume measures are clinically more useful than EI in indicating current and future gait and cognition. Multiple factors are associated with ventricle volume size, including FSD and DESH, suggesting that changes in CSF dynamics may go beyond simple ventriculomegaly.
AB - ObjectiveTo compare the clinical utility of volume-based ratios with the standard linear ratio of Evans index (EI) by examining their associations with gait, cognition, and other patient and imaging variables.MethodsFrom MRI scans of 1,774 participants in the Mayo Clinic Study of Aging, we calculated 3 ventricle size measures: Evan index (frontal horn width divided by widest width of skull inner table), total ventricular volume, and frontal horn volume as ratios of total intracranial volume. Gait was measured by a timed 25-foot walk and cognition by a composite of psychometric tests. We also evaluated variables associated with the measures of ventricular size. Further, we evaluated gait and cognition associations with MRI of extraventricular findings seen in normal-pressure hydrocephalus: disproportionate enlargement of subarachnoid space (DESH) and focal sulcal dilations (FSD).ResultsVentricular volume measures had stronger association with gait and cognition measures than EI. In decreasing order of strength of association with ventricle size were DESH, FSD, white matter hyperintensity volume ratio, age, male sex, cortical thickness, and education. Modest evidence was observed that FSD was associated with future decline in gait and cognition.ConclusionVentricular volume measures are clinically more useful than EI in indicating current and future gait and cognition. Multiple factors are associated with ventricle volume size, including FSD and DESH, suggesting that changes in CSF dynamics may go beyond simple ventriculomegaly.
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U2 - 10.1212/WNL.0000000000008673
DO - 10.1212/WNL.0000000000008673
M3 - Article
C2 - 31748251
AN - SCOPUS:85079018202
SN - 0028-3878
VL - 94
SP - E549-E556
JO - Neurology
JF - Neurology
IS - 5
ER -