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Vitamin D deficiency may accelerate cognitive decline in female apolipoprotein E ε4 non-carriers

Authors
Kim, JiwonJi, EunjeongBae, Jong BinHan, Ji WonKim, Tae HuiKwak, Kyung PhilKim, Bong JoKim, Shin GyeomKim, Jeong LanMoon, Seok WooPark, Joon HyukRyu, Seung-HoYoun, Jong ChulLee, Dong YoungLee, Dong WooLee, Seok BumLee, Jung JaeJhoo, Jin HyeongSong, JunghanLee, KyunghoonKim, Ki Woong
Issue Date
Feb-2025
Publisher
Churchill Livingstone
Keywords
Apolipoprotein E4; Cognition; Cohort studies; Gender; Old; Vitamin D deficiency
Citation
Clinical Nutrition, v.45, pp 167 - 173
Pages
7
Indexed
SCIE
SCOPUS
Journal Title
Clinical Nutrition
Volume
45
Start Page
167
End Page
173
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/75827
DOI
10.1016/j.clnu.2024.12.029
ISSN
0261-5614
1532-1983
Abstract
Background & aims: The impact of vitamin D deficiency (VDD) on cognition remains controversial. Evidences suggest that variability based on apolipoprotein E (APOE) ε4 status and gender, given APOE ε4's influence on vitamin D metabolism and women's heightened vitamin D sensitivity. We investigated the interplay between APOE ε4, gender, and VDD in cognitive decline among older adults. Methods: In a population-based cohort of 1547 cognitively normal Koreans aged ≥60 years, Mini Mental State Examination (MMSE) changes were tracked biennially (2010–2020). VDD was defined as serum 25-hydroxyvitamin D < 10 ng/mL. Linear mixed models analyzed VDD effects, with subgroup analyses for APOE ε4 status and gender. Results: VDD was present in 21.3 % at baseline and was linked to faster MMSE decline (estimate = −0.054, 95 % CI [-0.091, −0.017], p = 0.004), particularly in APOE ε4 non-carriers (estimate = −0.070, 95 % CI [-0.112, −0.029], p = 0.001). A gender-based analysis revealed that this effect was significant only in female non-carriers (estimate = −0.097, 95 % CI [-0.156, −0.038], p = 0.001). Conversely, male non-carriers demonstrated an absence of a statistically significant association (estimate = −0.017, 95 % CI [-0.076, 0.041], p = 0.562). Conclusions: VDD accelerates cognitive decline in cognitively normal APOE ε4 non-carriers, particularly women, underscoring the importance of tailored prevention strategies. © 2024 Elsevier Ltd and European Society for Clinical Nutrition and Metabolism
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