Department of Neurology, Jinan University First Affiliated Hospital, Guangzhou, Guangdong, China.
School of Nursing, Jinan University, Guangzhou, Guangdong, China.
Transl Psychiatry. 2024 Oct 1;14(1):398. doi: 10.1038/s41398-024-03131-3.
The role of alcohol consumption as a mediator in the risk between sarcopenia and dementia remains inadequately studied. There is currently limited research on whether the association between sarcopenia and the risk of Alzheimer's disease (AD) is influenced by genetic susceptibility. Our study incorporated a total of 483,637 baseline non-dementia participants, who were classified into groups of individuals with no sarcopenia and those with probable sarcopenia based on the definition. We employed Cox proportional hazards models to evaluate the association between probable sarcopenia and the risk of all cause dementia (ACD), AD, and vascular dementia (VD). We conducted mediation analysis to explore the role of alcohol consumption in the association between probable sarcopenia and the risk of ACD, AD, and VD. During the median follow-up period of 13.6 years, we documented 9000 new cases of ACD (including 4061 AD and 2025 VD). Fully adjusted multivariate model revealed a significant correlation between probable sarcopenia and elevated risk for ACD (HR = 1.54, 95% CI: 1.46-1.62, p < 0.001), AD (HR = 1.32, 95% CI: 1.21-1.43, p < 0.001), and VD (HR = 1.69, 95% CI: 1.52-1.89, p < 0.001). Mediation analysis elucidates that alcohol consumption explained 12.8%, 15.2%, and 11.1% of the associations of probable sarcopenia with the risk of ACD, AD, and VD, respectively. An interactive relationship prevails between probable sarcopenia and genetic factors (p for interaction <0.001), and regardless of the degree of genetic risk, probable sarcopenia correlates with an elevated AD risk. Our study reveals a significant association between probable sarcopenia and an increased risk of dementia, with alcohol consumption playing a mediating role in this association. There is an interaction between probable sarcopenia and genetic susceptibility related to the risk of AD.
酒精摄入在肌少症和痴呆风险之间的中介作用研究不足。目前关于肌少症与阿尔茨海默病(AD)风险之间的关联是否受到遗传易感性影响的研究有限。我们的研究共纳入了 483637 名基线无痴呆的参与者,根据定义将他们分为无肌少症组和可能有肌少症组。我们采用 Cox 比例风险模型评估可能有肌少症与所有原因痴呆(ACD)、AD 和血管性痴呆(VD)风险之间的关系。我们进行了中介分析,以探讨酒精摄入在可能有肌少症与 ACD、AD 和 VD 风险之间的关系中的作用。在中位随访 13.6 年期间,我们记录了 9000 例新的 ACD 病例(包括 4061 例 AD 和 2025 例 VD)。完全调整后的多变量模型显示,可能有肌少症与 ACD 风险升高显著相关(HR=1.54,95%CI:1.46-1.62,p<0.001)、AD(HR=1.32,95%CI:1.21-1.43,p<0.001)和 VD(HR=1.69,95%CI:1.52-1.89,p<0.001)。中介分析表明,酒精摄入分别解释了可能有肌少症与 ACD、AD 和 VD 风险关联的 12.8%、15.2%和 11.1%。可能有肌少症和遗传因素之间存在交互关系(p 交互<0.001),无论遗传风险程度如何,可能有肌少症都与 AD 风险升高相关。我们的研究表明,可能有肌少症与痴呆风险增加之间存在显著关联,酒精摄入在这种关联中起中介作用。可能有肌少症与与 AD 风险相关的遗传易感性之间存在相互作用。