4.6 Article

Stability of mild cognitive impairment in newly diagnosed Parkinson's disease

Journal

JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
Volume 88, Issue 8, Pages 648-652

Publisher

BMJ PUBLISHING GROUP
DOI: 10.1136/jnnp-2016-315099

Keywords

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Funding

  1. Parkinson's UK [J-0802]
  2. Lockhart Parkinson's Disease Research Fund
  3. National Institute for Health Research (NIHR) Newcastle Biomedical Research Unit based at Newcastle upon Tyne Hospitals NHS Foundation Trust
  4. Newcastle University
  5. NIHR Biomedical Research Centre
  6. MRC [MC_U105597119, MC_UU_00005/12] Funding Source: UKRI
  7. Medical Research Council [MC_U105597119, MC_UU_00005/12] Funding Source: researchfish
  8. National Institute for Health Research [NF-SI-0616-10011] Funding Source: researchfish
  9. Parkinson's UK [J-0802, G-1301] Funding Source: researchfish
  10. Wellcome Trust [103838/Z/14/Z] Funding Source: researchfish

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Background Mild cognitive impairment (MCI) is common in early Parkinson's disease (PD). We evaluated the stability of PD-MCI over time to determine its clinical utility as a marker of disease. Methods 212 newly diagnosed participants with PD were recruited into a longitudinal study and reassessed after 18 and 36 months. Participants completed a range of clinical and neuropsychological assessments. PD-MCI was classified using Movement Disorders Society Task Force level I (Montreal Cognitive Assessment <26) and level II (using cut-offs of 1, 1.5 and 2SD) criteria. Results After 36 months, 75% of participants returned; 8% of patients had developed a dementia all of which were previously PD-MCI. Applying level I criteria, 70% were cognitively stable, 19% cognitively declined and 11% improved over 36 months. Applying level II criteria (1, 1.5 and 2SD), 25% were cognitively stable, 41% cognitively declined, 15% improved and 19% fluctuated over 36 months. 18% of participants reverted to normal cognition from PD-MCI. Discussion Cognitive impairment in PD is complex, with some individuals' function fluctuating over time and some reverting to normal cognition. PD-MCI level I criteria may have greater clinical convenience, but more comprehensive level II criteria with 2SD cut-offs may offer greater diagnostic certainty.

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