Jeon Keun Hye, Han Kyungdo, Jeong Su-Min, Park Junhee, Yoo Jung Eun, Yoo Juhwan, Lee Jinkook, Kim SangYun, Shin Dong Wook
Department of Family Medicine, Cha Gumi Medical Center, Cha University, Gumi, Republic of Korea.
Department of Statistics and Actuarial Science, Soongsil University, Seoul, Republic of Korea.
JAMA Netw Open. 2023 Feb 1;6(2):e2254771. doi: 10.1001/jamanetworkopen.2022.54771.
The impact of serial changes in alcohol consumption on dementia risk has rarely been investigated to date.
To investigate the association of comprehensive patterns of changes in alcohol consumption with the incidence of all-cause dementia, Alzheimer disease (AD), and vascular dementia (VaD).
DESIGN, SETTING, AND PARTICIPANTS: This is a retrospective cohort study. Data were obtained from the Korean National Health Insurance Service database. Adults aged 40 years and older underwent 2 health examinations in 2009 and 2011. The cohort was assessed until December 31, 2018, and statistical analysis was performed in December 2021.
Alcohol consumption level was categorized into none (0 g per day), mild (<15 g per day), moderate (15-29.9 g per day), and heavy (≥30 g per day) drinking. On the basis of changes in alcohol consumption level from 2009 to 2011, participants were categorized into the following groups: nondrinker, quitter, reducer, sustainer, and increaser.
The primary outcome was newly diagnosed AD, VaD, or other dementia.
Among 3 933 382 participants (mean [SD] age, 55.0 [9.6] years; 2 037 948 men [51.8%]), during a mean (SD) follow-up of 6.3 (0.7) years, there were 100 282 cases of all-cause dementia, 79 982 cases of AD, and 11 085 cases of VaD. Compared with sustained nondrinking, sustained mild (adjusted hazard ratio [aHR], 0.79; 95% CI, 0.77-0.81) and moderate (aHR, 0.83; 95% CI, 0.79-0.88) drinking were associated with a decreased risk of all-cause dementia, whereas sustained heavy drinking was associated with an increased risk of all-cause dementia (aHR, 1.08; 95% CI, 1.03-1.12). Compared with sustained levels of drinking, reducing alcohol consumption from a heavy to a moderate level (aHR, 0.92; 95% CI, 0.86-0.99) and the initiation of mild alcohol consumption (aHR, 0.93; 95% CI, 0.90-0.96) were associated with a decreased risk of all-cause dementia. Increasers and quitters exhibited an increased risk of all-cause dementia compared with sustainers. The trends in AD and VaD remained consistent.
In this cohort study of a Korean population, decreased risk of dementia was associated with maintaining mild to moderate alcohol consumption, reducing alcohol consumption from a heavy to a moderate level, and the initiation of mild alcohol consumption, suggesting that the threshold of alcohol consumption for dementia risk reduction is low.
迄今为止,很少有人研究饮酒量的连续变化对痴呆症风险的影响。
研究饮酒量综合变化模式与全因性痴呆、阿尔茨海默病(AD)和血管性痴呆(VaD)发病率之间的关联。
设计、设置和参与者:这是一项回顾性队列研究。数据来自韩国国民健康保险服务数据库。40岁及以上的成年人在2009年和2011年接受了两次健康检查。对该队列进行评估直至2018年12月31日,并于2021年12月进行统计分析。
饮酒量分为不饮酒(每天0克)、轻度饮酒(每天<15克)、中度饮酒(每天15 - 29.9克)和重度饮酒(每天≥30克)。根据2009年至2011年饮酒量的变化,参与者被分为以下几组:从不饮酒者、戒酒者、饮酒量减少者、持续饮酒者和饮酒量增加者。
主要结局是新诊断出的AD、VaD或其他痴呆症。
在3933382名参与者中(平均[标准差]年龄为55.0[9.6]岁;2037948名男性[51.8%]),在平均(标准差)6.3(0.7)年的随访期间,有100282例全因性痴呆病例、79982例AD病例和11085例VaD病例。与持续不饮酒相比,持续轻度饮酒(调整后风险比[aHR],0.79;95%置信区间,0.77 - 0.81)和中度饮酒(aHR,0.83;95%置信区间,0.79 - 0.88)与全因性痴呆风险降低相关,而持续重度饮酒与全因性痴呆风险增加相关(aHR,1.08;95%置信区间,1.03 - 1.12)。与持续饮酒水平相比,将饮酒量从重度降至中度(aHR,0.92;95%置信区间,0.86 - 0.99)以及开始轻度饮酒(aHR,0.93;95%置信区间,0.90 - 0.96)与全因性痴呆风险降低相关。与持续饮酒者相比,饮酒量增加者和戒酒者患全因性痴呆的风险更高。AD和VaD的趋势保持一致。
在这项针对韩国人群的队列研究中,痴呆症风险降低与维持轻度至中度饮酒、将饮酒量从重度降至中度以及开始轻度饮酒有关,这表明降低痴呆症风险的饮酒量阈值较低。