4.5 Article

Prevalence of DSM-5 Mild Neurocognitive Disorder in Dementia-Free Older Adults: Results of the Population-Based LIFE-Adult-Study

Journal

AMERICAN JOURNAL OF GERIATRIC PSYCHIATRY
Volume 25, Issue 4, Pages 328-339

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jagp.2016.07.001

Keywords

mild neurocognitive disorder; prevalence; mild cognitive impairment; dementia; diagnostic and statistical manual of mental disorders (DSM-5)

Funding

  1. LIFE - Leipzig Research Center for Civilization Diseases, Universitat Leipzig
  2. European Union
  3. European Regional Development Fund (ERDF)
  4. European Social Fund
  5. Free State of Saxony
  6. German Federal Ministry of Education and Research (German Consortium for Frontotemporal Lobar Degeneration)
  7. Parkinson's Disease Foundation [PDF-IRG-1307]

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Objective: The DSM-5 introduces mild neurocognitive disorder (miNCD) as a syndrome that recognizes the potential clinical importance of acquired cognitive deficits being too mild to qualify for diagnosis of dementia. We provide new empirical data on miNCD including total, age-, and sex-specific prevalence rates; number and types of neurocognitive domains being impaired; and diagnostic overlap with the well-established mild cognitive impairment (MCI) concept. Design: Cross-sectional results of an observational cohort study (LIFE-Adult-Study). Setting: General population. Participants: A total of 1,080 dementia-free individuals, aged 60-79 years. Measurements: We calculated weighted point prevalence rates with confidence intervals (95% CI) for miNCD and analyzed diagnostic overlap between miNCD and MCI by calculating overall percentage agreement and Cohen's kappa coefficient. Results: Weighted total prevalence of miNCD was 20.3% (95% CI: 17.8-23.0). Prevalence was similar in both sexes, but significantly higher in older age. Two-thirds (66.2%) of the individuals with miNCD showed impairment restricted to only one out of six possible neurocognitive domains. Learning and memory was the most frequently (38.3%) impaired domain in all miNCD-cases, followed by social cognition (26.1%). Analysis of diagnostic overlap with MCI yielded an overall agreement of 98.6% and a kappa of 0.959. Conclusions: By considering all six predefined neurocognitive domains, our study observed a substantial proportion of dementia-free older adults having miNCD. Provision of information on the underlying etiology/ies may be of prime importance in future studies aiming at evaluating the clinical relevance of the miNCD syndrome.

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