Vitamin D deficiency may accelerate cognitive decline in female apolipoprotein E ε4 non-carriers
- Authors
- Kim, Jiwon; Ji, Eunjeong; Bae, Jong Bin; Han, Ji Won; Kim, Tae Hui; Kwak, Kyung Phil; Kim, Bong Jo; Kim, Shin Gyeom; Kim, Jeong Lan; Moon, Seok Woo; Park, Joon Hyuk; Ryu, Seung-Ho; Youn, Jong Chul; Lee, Dong Young; Lee, Dong Woo; Lee, Seok Bum; Lee, Jung Jae; Jhoo, Jin Hyeong; Song, Junghan; Lee, Kyunghoon; Kim, 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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