Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/10840
Title: Serum vitamin D in patients with mild cognitive impairment and Alzheimer's disease
Authors: Ouma, S.
Suenaga, M.
Bölükbaşı Hatip, Funda Fatma
Hatip-Al-Khatib, I.
Tsuboi, Y.
Matsunaga, Y.
Keywords: 1,25(OH) 2 D 3
25(OH)D 3
Alzheimer's disease
mild cognitive impairment
mini-mental state examination
25 hydroxyvitamin D
calcifediol
vitamin D
25-hydroxyvitamin D
biological marker
calcitriol
age
Alzheimer disease
Article
cognition
controlled study
diagnostic accuracy
diagnostic test accuracy study
disease severity
female
gender
human
major clinical study
male
Mini Mental State Examination
priority journal
radioimmunoassay
receiver operating characteristic
sensitivity and specificity
aged
analogs and derivatives
blood
classification
cognitive defect
mental health
sex factor
very elderly
Age Factors
Aged
Aged, 80 and over
Alzheimer Disease
Biomarkers
Calcitriol
Cognitive Dysfunction
Correlation of Data
Female
Humans
Male
Mental Status Schedule
ROC Curve
Sensitivity and Specificity
Sex Factors
Vitamin D
Publisher: John Wiley and Sons Ltd
Abstract: Objectives: To determine the relevance of Mini-Mental State Examination (MMSE), serum 25-hydroxyvitamin D (25(OH)D3), and 1,25(OH)2D3 concentrations to mild cognitive impairment (MCI) and various stages of Alzheimer's disease (AD). Materials and Methods: The study included 230 participants (>74 years) allocated to three main groups: 1-healthy subjects (HS, n = 61), 2-patients with MCI (n = 61), and 3- patients with Alzheimer's disease (AD) subdivided into three stages: mild (n = 41), moderate (n = 35), and severe AD (n = 32). The cognitive status was evaluated using MMSE. Serum 25 (OH)D3 (ng/ml) and 1,25(OH)2D3 concentrations (pg/ml) were determined by competitive radioimmunoassay. Results: MMSE scores and 25(OH)D3 were decreased in MCI and all stages of the AD in both genders. MMSE variability was due to gender in HS (11%) and to 25(OH)D3 in MCI (15%) and AD (26%). ROC analysis revealed an outstanding property of MMSE in diagnosis of MCI (AUC, 0.906; CI 95%, 0.847–0.965; sensitivity 82%; specificity, 98%) and AD (AUC, 0.997; CI 95%, 0.992–1; sensitivity, 100%; specificity, 98%). 25(OH)D3 exhibited good property in MCI (AUC, 0.765; CI 95%, 0.681–0.849; sensitivity, 90%; specificity, 54%) and an excellent property in diagnosis of AD (AUC, 0.843; CI 95%, 0.782–0.904; sensitivity, 97%; specificity, 79%). Logistic analyses revealed that, in MCI, MMSE could predict (or classify correctly) with 97.6% accuracy (Wald, 15.22, ß, -0.162; SE, 0.554; OR = 0.115:0.039–0.341; p =.0001), whereas 25(OH)D3 with 80% accuracy (Wald, 41,013; ß, -0.213; SE, 0.033; OR = 0.808: 0.757–863; p =.0001). 25(OH)D3 was the only significant predictor for the severe AD and contributed to MMSE variability. Age and gender were significant predictors only in the moderate AD. In patients with MCI, 25(OH)D3 and 1,25(OH)2D3 were correlated men, but in case of the AD, they were correlated in women. Conclusions: MMSE and serum 25(OH)D3 concentrations could be useful biomarkers for prediction and diagnosis of MCI and various stages of the AD. The results support the utility of vitamin D supplementation in AD therapy regimen. © 2018 The Authors. Brain and Behavior published by Wiley Periodicals, Inc.
URI: https://hdl.handle.net/11499/10840
https://doi.org/10.1002/brb3.936
ISSN: 2162-3279
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

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