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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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