Kim Shin Gyeom, Keum Musung, Choe Young Min, Suh Guk-Hee, Lee Boung Chul, Kim Hyun Soo, Lee Jun Hyung, Hwang Jaeuk, Yi Dahyun, Kim Jee Wook
Department of Neuropsychiatry, Soonchunhyang University Bucheon Hospital, Bucheon 14584, Republic of Korea.
Department of Neuropsychiatry, Hallym University Dongtan Sacred Heart Hospital, Hwaseong 18450, Gyeonggi, Republic of Korea.
Nutrients. 2025 Feb 6;17(3):595. doi: 10.3390/nu17030595.
Selenium (Se), a vital trace element, plays a neuroprotective role by mitigating oxidative stress through selenoproteins and regulating metal balance. The apolipoprotein E ε4 allele (APOE4), a significant genetic risk factor for Alzheimer's disease (AD), has been linked to reduced Se levels and weakened antioxidant capacity. This research explores the association between serum Se concentrations and cognitive performance, with an emphasis on how APOE4 status influences this relationship. This study included 196 older adults from community and memory clinic settings, who underwent assessments for episodic memory, global cognition, and non-memory functions using the Consortium to Establish a Registry for Alzheimer's Disease (CERAD) neuropsychological battery, with serum selenium levels analyzed via inductively coupled plasma-mass spectrometry (ICP-MS) and APOE genotyping conducted to determine allele status. Higher serum Se levels were associated with better episodic memory score (EMS) (B = 0.065, 95% CI = 0.020-0.110, = 0.005) and CERAD total score (TS) (B = 0.119, 95% CI = 0.046-0.193, = 0.002). However, the interaction between Se and APOE4 status significantly affected EMS (B = -0.074, 95% CI = -0.109 to -0.039, < 0.001), with significant benefits observed in APOE4-negative participants. This study highlights the genotype-specific impact of Se on cognitive health, emphasizing the need for personalized nutritional interventions targeting Se levels, particularly for APOE4-negative individuals. Future research should further elucidate the mechanisms of Se's effects and assess its therapeutic potential in aging populations.
硒(Se)是一种重要的微量元素,通过硒蛋白减轻氧化应激并调节金属平衡,从而发挥神经保护作用。载脂蛋白Eε4等位基因(APOE4)是阿尔茨海默病(AD)的一个重要遗传风险因素,与硒水平降低和抗氧化能力减弱有关。本研究探讨血清硒浓度与认知表现之间的关联,重点关注APOE4状态如何影响这种关系。本研究纳入了196名来自社区和记忆诊所的老年人,他们使用阿尔茨海默病注册协会(CERAD)神经心理成套测验进行了情景记忆、整体认知和非记忆功能评估,通过电感耦合等离子体质谱法(ICP-MS)分析血清硒水平,并进行APOE基因分型以确定等位基因状态。较高的血清硒水平与更好的情景记忆分数(EMS)(B = 0.065,95%CI = 0.020 - 0.110,P = 0.005)和CERAD总分(TS)(B = 0.119,95%CI = 0.046 - 0.193,P = 0.002)相关。然而,硒与APOE4状态之间的相互作用显著影响EMS(B = -0.074,95%CI = -0.109至-0.039,P < 0.001),在APOE4阴性参与者中观察到显著益处。本研究强调了硒对认知健康的基因型特异性影响,强调需要针对硒水平进行个性化营养干预,特别是对于APOE4阴性个体。未来的研究应进一步阐明硒作用的机制,并评估其在老年人群中的治疗潜力。