Alexithymia in people with subjective cognitive decline, mild cognitive impairment, and mild Alzheimer’s disease View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2017-01-21

AUTHORS

Mehmet Yuruyen, Fundan Engin Akcan, Gizem Cetiner Batun, Gozde Gultekin, Mesut Toprak, Hakan Yavuzer, Murat Emul

ABSTRACT

BackgroundBehavioral and psychological symptoms are widely accepted as accelerator factors in progression to dementia. Although alexithymia is closely related to normal aging process and poor neurocognitive performance, alexithymia has not been included in these symptoms yet.AimsHere, we aimed to investigate alexithymia features in people with prominent clinical memory complaints.MethodsThe participants (n = 82) were classified into three groups as: subjective cognitive decline (n = 30), mild cognitive impairment (n = 27), and mild Alzheimer’s disease (n = 25) after Mini-Mental State Examination, Clinical Dementia Rating Scale, neuropsychological test battery, Geriatric Depression Scale, and Hachinski Ischemic Scale. All participants were assessed with 20-item Toronto Alexithymia Scale.ResultsThe patients with mild Alzheimer’s disease and mild cognitive impairment have significantly greater alexithymia features than individuals with subjective cognitive decline in Toronto Alexithymia Scale (p < 0.05 for all). The alexithymia features in patients with mild Alzheimer’s disease and mild cognitive impairment did not significantly differ (p > 0.05, for all).DiscussionPeople who have objective cognitive decline seem to have more alexithymia features than people with subjective cognitive decline. Moreover, alexithymia features seem to be similar in people mild Alzheimer’s disease and in mild cognitive impairment.ConclusionAlexithymia might be an important searching domain of behavioral–psychological symptoms in people with cognitive problems beyond aging. More... »

PAGES

1105-1111

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s40520-017-0725-8

DOI

http://dx.doi.org/10.1007/s40520-017-0725-8

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1054065155

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/28110464


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