Dietary intake of tocopherols and risk of incident disabling dementia

• Published in: Scientific reports Vol. 11; no. 1; p. 16429
• Main Authors: Aoki, Shoko, Yamagishi, Kazumasa, Maruyama, Koutatsu, Kishida, Rie, Ikeda, Ai, Umesawa, Mitsumasa, Renzhe, Cui, Kubota, Yasuhiko, Hayama-Terada, Mina, Shimizu, Yuji, Muraki, Isao, Imano, Hironori, Sankai, Tomoko, Okada, Takeo, Kitamura, Akihiko, Kiyama, Masahiko, Iso, Hiroyasu
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 12.08.2021; Nature Publishing Group; Nature Portfolio
• Subjects: 692/499; 692/617; Antioxidants; Community involvement; Dementia; Dementia disorders; Diet; Dietary intake; Epidemiology; Humanities and Social Sciences; Linoleic acid; Linolenic acid; multidisciplinary; Science; Science (multidisciplinary); Tocopherols; Vitamin E
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-021-95671-7

Tocopherols, strong antioxidants, may be useful in preventing dementia, but the epidemiological evidence is insufficient. We performed a community-based follow-up study of Japanese, the Circulatory Risk in Community Study, involving 3739 people aged 40–64 years at baseline (1985–1999). Incident disabling dementia was followed up from 1999 through 2020. For subtype analysis, we classified disabling dementia into that with and that without a history of stroke. Dietary intake of tocopherols (total, α, β, γ, and δ) were estimated using 24-h recall surveys. During a median follow-up of 19.7 years, 670 cases of disabling dementia developed. Total tocopherol intake was inversely associated with risk of disabling dementia with multivariable hazard ratios (95% confidence intervals) of 0.79 (0.63–1.00) for the highest versus lowest quartiles of total tocopherol intake (P for trend = 0.05). However, the association was strengthened when further adjusted for α-linolenic acid intake (Spearman correlation with total tocopherol intake = 0.93), with multivariable hazard ratios of 0.50 (0.34–0.74) (P for trend = 0.001) but was weakened and nonsignificant when further adjusted for linoleic acid intake (Spearman correlation with total tocopherol intake = 0.92), with multivariable hazard ratios of 0.69 (0.47–1.01) (P for trend = 0.05). Similar but nonsignificant inverse associations were observed for α-, γ-, and δ-tocopherols but not for β-tocopherol. These results were similar regardless of the presence of a history of stroke. Dietary tocopherol intake was inversely associated with risk of disabling dementia, but its independent effect was uncertain owing to a high intercorrelation of α-linolenic linoleic acids with total tocopherol intake. Even with such confounding, a diet high in tocopherols may help prevent the onset of dementia.