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      MoCA, ACE-R and MMSE versus the NINDS-CSN VCI Harmonisation Standards Neuropsychological Battery after TIA and stroke

      research-article
      , MRCP DPhil 1 , 2 , , MD 1 , , RGN 1 , , DPhil 1 , , FRCP FMedSci 1
      Stroke
      MoCA, ACE-R, vascular cognitive impairment, MCI, MMSE

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          Abstract

          Background

          The Montreal Cognitive Assessment (MoCA) and Addenbrooke’s cognitive examination-revised (ACE-R) are proposed as short cognitive tests for use after stroke but there are few published validations against neuropsychological battery. We studied MoCA, ACE-R and mini-mental-state-examination(MMSE) in patients with cerebrovascular disease and mild cognitive impairment (MCI)

          Methods

          100 consecutive patients had the MMSE, MoCA, ACE-R and NINDS-CSN VCI Harmonisation Standards Neuropsychological Battery ≥1 year after TIA or stroke in a population-based study. MCI was diagnosed using modified Petersen criteria in which subjective cognitive complaint is not required (equivalent to cognitive- impairment-no-dementia (CIND)) and sub-typed by number and type of cognitive domains affected.

          Results

          Among 91 non-demented subjects completing neuropsychological testing (mean/sd age 73.4/11.6 years, 44% female, 56% stroke), 39 (42%) had MCI (amnestic multiple domain=10, non-amnestic multiple domain=9, non-amnestic single domain=19, amnestic single domain=1). Sensitivity and specificity for MCI were optimal with MoCA<25 (sensitivity=77%, specificity=83%) and ACE-R<94 (sensitivity=83%, specificity=73%). Both tests detected amnestic MCI better than non-amnestic single domain impairment. MMSE only achieved sensitivity>70% at a cut-off of<29, mainly due to relative insensitivity to single domain impairment.

          Conclusion

          The MoCA and ACE-R had good sensitivity and specificity for MCI defined using the NINDS-CSN VCI Battery ≥1 year after TIA and stroke whereas the MMSE showed a ceiling effect. However, optimal cut-offs will depend on use for screening (high sensitivity) or diagnosis (high specificity). Lack of timed measures of processing speed may explain the relative insensitivity of the MoCA and ACE-R to single non-memory domain impairment.

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          Author and article information

          Journal
          0235266
          7613
          Stroke
          Stroke
          Stroke
          0039-2499
          1524-4628
          11 April 2017
          08 December 2011
          February 2012
          13 April 2017
          : 43
          : 2
          : 464-469
          Affiliations
          [1 ]Stroke Prevention Research Unit, University Department of Clinical Neurology, John Radcliffe Hospital, and the University of Oxford
          [2 ]NIHR Biomedical Research Centre, John Radcliffe Hospital, Oxford
          Author notes
          Correspondence to: Dr Sarah Pendlebury, Consultant Physician, Stroke Prevention Research Unit, Level 6 West Wing, John Radcliffe Hospital, Oxford OX3 9DU, Tel: +44 1865 231603, Fax: +44 1865 234639, sarah.pendlebury@ 123456clneuro.ox.ac.uk
          Article
          PMC5390857 PMC5390857 5390857 ems54348
          10.1161/STROKEAHA.111.633586
          5390857
          22156700
          b5dcb516-59e7-4e35-b1b8-2f3d2f3e7681
          History
          Categories
          Article

          vascular cognitive impairment,MCI,MMSE,MoCA,ACE-R
          vascular cognitive impairment, MCI, MMSE, MoCA, ACE-R

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