Neurobiological correlates of depressive symptoms in people with subjective and mild cognitive impairment

التفاصيل البيبلوغرافية
العنوان: Neurobiological correlates of depressive symptoms in people with subjective and mild cognitive impairment
المؤلفون: Ramune Grambaite, Per Kristian Hol, Atle Bjørnerud, Per Selnes, Tormod Fladby, Astrid Haram, Erik Hessen, A. Muftuler Londalen, J. Šaltytė Benth, Dag Aarsland, Eirik Auning, A. Løvli Stav
المصدر: Acta Psychiatrica Scandinavica. 131:139-147
بيانات النشر: Wiley, 2014.
سنة النشر: 2014
مصطلحات موضوعية: Adult, Male, Oncology, medicine.medical_specialty, Disease, Hippocampus, Alzheimer Disease, Fluorodeoxyglucose F18, Internal medicine, medicine, Humans, Cognitive Dysfunction, Psychiatry, Pathological, Depression (differential diagnoses), Aged, Cerebral Cortex, medicine.diagnostic_test, Depression, Middle Aged, Hyperintensity, Functional imaging, Psychiatry and Mental health, Diffusion Tensor Imaging, Positron emission tomography, Positron-Emission Tomography, Female, Geriatric Depression Scale, Radiopharmaceuticals, Cognition Disorders, Psychology, Biomarkers, Diffusion MRI
الوصف: Objective To test the hypothesis that depressive symptoms correlate with Alzheimer's disease (AD) type changes in CSF and structural and functional imaging including hippocampus volume, cortical thickness, white matter lesions, Diffusion tensor imaging (DTI), and fluoro-deoxy-glucose positron emission tomography (FDG-PET) in patient with subjective (SCI) and mild (MCI) cognitive impairment. Method In 60 patients, depressive symptoms were assessed using the Geriatric Depression Scale. The subjects underwent MRI, 18F-FDG PET imaging, and lumbar CSF extraction. Results Subjects with depressive symptoms (n = 24) did not have more pathological AD biomarkers than non-depressed. Uncorrected there were trends towards larger hippocampal volumes (P = 0.06), less orbital WM damage measured by DTI (P = 0.10), and higher orbital glucose metabolism (P = 0.02) in the depressed group. The findings were similar when SCI and MCI were analyzed separately. Similarly, in patients with pathological CSF biomarkers (i.e., predementia AD, n = 24), we found that correlations between scores on GDS and CSF As42 and P-tau indicated less severe AD-specific CSF changes with increasing depression. Conclusion Depressive symptoms are common in SCI/MCI, but are not associated with pathological imaging or CSF biomarkers of AD. Depression can explain cognitive impairment in SCI/MCI or add to cognitive impairment leading to an earlier clinical investigation in predementia AD.
تدمد: 0001-690X
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8faf223fcf1a1162e103fc92403768f7
https://doi.org/10.1111/acps.12352
حقوق: CLOSED
رقم الأكسشن: edsair.doi.dedup.....8faf223fcf1a1162e103fc92403768f7
قاعدة البيانات: OpenAIRE