Felix Cynthia, Chahine Lana M, Hengenius James, Chen Honglei, Rosso Andrea L, Zhu Xiaonan, Cao Zichun, Rosano Caterina
Department of Epidemiology, University of Pittsburgh, Pittsburgh, PA, United States.
Department of Neurology, University of Pittsburgh, Pittsburgh, PA, United States.
Front Aging Neurosci. 2021 Oct 22;13:648598. doi: 10.3389/fnagi.2021.648598. eCollection 2021.
To compare gray matter microstructural characteristics of higher-order olfactory regions among older adults with and without hyposmia. Data from the Brief Smell Identification Test (BSIT) were obtained in 1998-99 for 265 dementia-free adults from the Health, Aging, and Body Composition study (age at BSIT: 74.9 ± 2.7; 62% White; 43% male) who received 3T diffusion tensor imaging in 2006-08 [Interval of time: mean (SD): 8.01 years (0.50)], Apolipoprotein (ApoEε4) genotypes, and repeated 3MS assessments until 2011-12. Cognitive status (mild cognitive impairment, dementia, normal cognition) was adjudicated in 2011-12. Hyposmia was defined as BSIT ≤ 8. Microstructural integrity was quantified by mean diffusivity (MD) in regions of the primary olfactory cortex amygdala, orbitofrontal cortex (including olfactory cortex, gyrus rectus, the orbital parts of the superior, middle, and inferior frontal gyri, medial orbital part of the superior frontal gyrus), and hippocampus. Multivariable regression models were adjusted for total brain atrophy, demographics, cognitive status, and ApoEε4 genotype. Hyposmia in 1998-99 ( = 57, 21.59%) was significantly associated with greater MD in 2006-08, specifically in the orbital part of the middle frontal gyrus, and amygdala, on the right [adjusted beta (p value): 0.414 (); 0.527 (); respectively]. Older adults with higher mean diffusivity in regions important for olfaction are more likely to have hyposmia up to ten years prior. Future studies should address whether hyposmia can serve as an early biomarker of brain microstructural abnormalities for older adults with a range of cognitive functions, including those with normal cognition.
比较有嗅觉减退和无嗅觉减退的老年人高阶嗅觉区域的灰质微观结构特征。1998 - 1999年从健康、衰老和身体成分研究中获取了265名无痴呆症成年人的简易嗅觉识别测试(BSIT)数据(BSIT时年龄:74.9±2.7;62%为白人;43%为男性),这些人在2006 - 2008年接受了3T扩散张量成像[时间间隔:平均(标准差):8.01年(0.50)],载脂蛋白(ApoEε4)基因型,并在2011 - 2012年进行了多次3MS评估。2011 - 2012年判定认知状态(轻度认知障碍、痴呆、正常认知)。嗅觉减退定义为BSIT≤8。通过初级嗅觉皮质杏仁核、眶额皮质(包括嗅觉皮质、直回、额上回、额中回和额下回的眶部、额上回内侧眶部)和海马区域的平均扩散率(MD)来量化微观结构完整性。多变量回归模型针对全脑萎缩情况、人口统计学特征、认知状态和ApoEε4基因型进行了调整。1998 - 1999年的嗅觉减退(n = 57,21.59%)与2006 - 2008年更大的MD显著相关,特别是在右侧额中回眶部和杏仁核[调整后β(p值):分别为0.414();0.527()]。嗅觉重要区域平均扩散率较高的老年人在十年前更有可能出现嗅觉减退。未来的研究应探讨嗅觉减退是否可作为具有一系列认知功能的老年人脑微观结构异常的早期生物标志物,包括认知正常的老年人。