Department of Nutrition and Food Science, School of Public Health, Tianjin Medical University, Tianjin, China.
Tianjin Key Laboratory of Environment, Nutrition and Public Health, Tianjin, China.
JAMA Netw Open. 2023 Jul 3;6(7):e2324031. doi: 10.1001/jamanetworkopen.2023.24031.
IMPORTANCE: Apolipoprotein E polymorphism ε4 (APOE ε4) and methylenetetrahydrofolate reductase (MTHFR) TT genotype are genetic risk factors of mild cognitive impairment (MCI), but whether this risk can be changed by modifiable lifestyle factors is unknown. OBJECTIVE: To explore whether unhealthy lifestyle (unhealthy dietary intake, current smoking, nonlimited alcohol consumption, and irregular physical activities) is associated with a higher risk of age-related MCI considering genetic risk. DESIGN, SETTING, AND PARTICIPANTS: This population-based cohort study used data from Tianjin Elderly Nutrition and Cognition (TENC) study participants, recruited from March 1, 2018, through June 30, 2021, and followed up until November 30, 2022. Participants were Chinese adults aged 60 years or older who completed the neuropsychological assessments, general physical examinations, and a personal interview. EXPOSURES: Healthy lifestyle was defined according to the Chinese Dietary Guidelines 2022, including healthy diet, regular physical activity, limited alcohol consumption, and no current smoking, categorized into healthy and unhealthy lifestyles according to weighted standardized lifestyle score. Genetic risk was defined by MTHFR TT genotype and APOE ε4, categorized into low and high genetic risk according to weighted standardized genetic risk score. MAIN OUTCOMES AND MEASURES: The main outcome was newly diagnosed MCI as identified using a modified version of Petersen criteria. Hazard ratios (HRs) and 95% CIs were estimated using Cox proportional hazard regression models. RESULTS: A total of 4665 participants were included (mean [SD] age, 67.9 [4.9] years; 2546 female [54.6%] and 2119 male [45.4%]); 653 participants with new-onset MCI (mean [SD] age, 68.4 [5.4] years; 267 female [40.9%] and 386 male [59.1%]) were identified after a median follow-up of 3.11 years (range, 0.82-4.61 years). Individuals with a low genetic risk and an unhealthy lifestyle (HR, 3.01; 95% CI, 2.38-3.79), a high genetic risk and a healthy lifestyle (HR, 2.65; 95% CI, 2.03-3.44), and a high genetic risk and an unhealthy lifestyle (HR, 3.58; 95% CI, 2.73-4.69) had a higher risk of MCI compared with participants with a low genetic risk and a healthy lifestyle. There was a synergistic interaction between lifestyle categories and genetic risk (β = 3.58; 95% CI, 2.73-4.69). CONCLUSIONS AND RELEVANCE: In this cohort study of TENC participants, the findings show that unhealthy lifestyle and high genetic risk were significantly associated with a higher risk of MCI among Chinese older adults. Unhealthy lifestyle factors were associated with a higher risk of MCI regardless of genetic risk, and lifestyle and genetic risk had synergistic interactions. These findings could contribute to the development of dietary guidelines and the prevention of early-stage dementia.
重要性:载脂蛋白 E 多态性 ε4(APOE ε4)和亚甲基四氢叶酸还原酶(MTHFR)TT 基因型是轻度认知障碍(MCI)的遗传风险因素,但这种风险是否可以通过可改变的生活方式因素改变尚不清楚。 目的:探讨在考虑遗传风险的情况下,不健康的生活方式(不健康的饮食摄入、当前吸烟、非限制饮酒和不规律的体育活动)是否与与年龄相关的 MCI 风险增加有关。 设计、设置和参与者:本基于人群的队列研究使用了来自天津老年人营养与认知(TENC)研究参与者的数据,参与者于 2018 年 3 月 1 日至 2021 年 6 月 30 日招募,并随访至 2022 年 11 月 30 日。参与者为年龄在 60 岁及以上的中国成年人,他们完成了神经心理评估、一般体检和个人访谈。 暴露因素:健康的生活方式是根据 2022 年中国膳食指南定义的,包括健康饮食、规律的体育活动、限制饮酒和不当前吸烟,根据加权标准化生活方式评分分为健康和不健康的生活方式。遗传风险由 MTHFR TT 基因型和 APOE ε4 定义,根据加权标准化遗传风险评分分为低和高遗传风险。 主要结果和测量:主要结局是使用彼得森标准的改良版本确定新诊断的 MCI。使用 Cox 比例风险回归模型估计危险比(HR)和 95%置信区间(CI)。 结果:共纳入 4665 名参与者(平均[标准差]年龄,67.9[4.9]岁;2546 名女性[54.6%]和 2119 名男性[45.4%]);在中位随访 3.11 年后(范围,0.82-4.61 年),确定了 653 名新发 MCI 患者(平均[标准差]年龄,68.4[5.4]岁;267 名女性[40.9%]和 386 名男性[59.1%])。与具有低遗传风险和不健康生活方式的参与者相比(HR,3.01;95%CI,2.38-3.79)、具有高遗传风险和健康生活方式的参与者(HR,2.65;95%CI,2.03-3.44)以及具有高遗传风险和不健康生活方式的参与者(HR,3.58;95%CI,2.73-4.69),MCI 的风险更高。生活方式类别和遗传风险之间存在协同交互作用(β=3.58;95%CI,2.73-4.69)。 结论和相关性:在 TENC 参与者的这项队列研究中,研究结果表明,在中国老年人中,不健康的生活方式和高遗传风险与 MCI 风险增加显著相关。无论遗传风险如何,不健康的生活方式因素都与 MCI 风险增加有关,并且生活方式和遗传风险之间存在协同作用。这些发现可能有助于制定饮食指南和预防早期痴呆症。
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