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The role of the Montreal Cognitive Assessment (MoCA) and its memory tasks for detecting mild cognitive impairment

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Abstract

To investigate the role of the Montreal Cognitive Assessment (MoCA) (Beijing version) and its memory tasks on detecting different mild cognitive impairment (MCI) subtypes including amnestic MCI (aMCI) and nonamnestic MCI (naMCI) in memory clinics. A total of 121 patients with MCI and 53 healthy controls were included. Fifty-six aMCI-multiple domains (amMCI), 32 aMCI-single domain (asMCI), and 33 naMCI patients were diagnosed according to extensive cognitive tests. All participants were administered by the Mini Mental State Examination (MMSE) and the MoCA. Patients with amMCI performed worse than patients with asMCI, naMCI, and healthy controls on the MMSE and the MoCA (p < 0.001). The area under the curve (AUC) value for the MoCA when comparing the amMCI and control groups was 0.884 (p < 0.001), which was superior to that of the MMSE. The AUC value decreased to 0.687 when applied to the naMCI and control groups (p = 0.007), which was still higher than that of the Rey Auditory Verbal Learning Test (RAVLT) or the Rey-Osterrieth complex figure (ROCF). Delayed free recall or category prompted recall in the MoCA had roles in differentiating asMCI and controls groups with AUC value of 0.717 (p = 0.002) and 0.691 (p = 0.005), respectively. The MoCA is a good screening tool for detecting different types of MCI and is suitable for patients in outpatient clinics.

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Acknowledgements

The authors thank all participating investigators.

Funding

The study was supported by the China-Japan Friendship Hospital (2014-4-QN-32).

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Correspondence to Xudong Li.

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The objectives of the research were explained to participants and their families and written informed consent was obtained. The research was approved by the Ethics Committee of the China-Japan Friendship Hospital.

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Li, X., Jia, S., Zhou, Z. et al. The role of the Montreal Cognitive Assessment (MoCA) and its memory tasks for detecting mild cognitive impairment. Neurol Sci 39, 1029–1034 (2018). https://doi.org/10.1007/s10072-018-3319-0

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  • DOI: https://doi.org/10.1007/s10072-018-3319-0

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