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Prevalence of DSM-5 mild neurocognitive disorder in dementia-free older adults: Results of the population-based LIFE-adult-study

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Schroeter,  Matthias L.
Department Neurology, MPI for Human Cognitive and Brain Sciences, Max Planck Society;
Clinic for Cognitive Neurology, University of Leipzig, Germany;

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Witte,  Veronica
Collaborative Research Center Obesity Mechanisms, Institute of Biochemistry, University of Leipzig, Germany;
Department Neurology, MPI for Human Cognitive and Brain Sciences, Max Planck Society;

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Villringer,  Arno
Department Neurology, MPI for Human Cognitive and Brain Sciences, Max Planck Society;
Clinic for Cognitive Neurology, University of Leipzig, Germany;

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Citation

Luck, T., Then, F. S., Schroeter, M. L., Witte, V., Engel, C., Loeffler, M., et al. (2017). Prevalence of DSM-5 mild neurocognitive disorder in dementia-free older adults: Results of the population-based LIFE-adult-study. The American Journal of Geriatric Psychiatry, 25(4), 328-339. doi:10.1016/j.jagp.2016.07.001.


Cite as: https://hdl.handle.net/11858/00-001M-0000-002B-8506-E
Abstract
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.