Magalhães Thamires N C, Hicks Tracey H, Jackson T Bryan, Ballard Hannah K, Herrejon Ivan A, Bernard Jessica A
Department of Psychological and Brain Sciences, Texas A&M University, College Station, Texas, USA.
Vanderbilt, Memory & Alzheimer's Center, Nashville, Tennessee, USA.
Hum Brain Mapp. 2025 Oct 1;46(14):e70356. doi: 10.1002/hbm.70356.
Aging involves complex biological changes that affect disease susceptibility and aging trajectories. Although females typically live longer than males, they have a higher susceptibility to diseases like Alzheimer's, speculated to be influenced by menopause, and reduced ovarian hormone production. Understanding sex-specific differences is crucial for personalized medical interventions and sex equality in health. Our study aims to elucidate sex differences in regional cerebellar structure and connectivity during normal aging by investigating both structural and functional connectivity variations in the context of sex-steroid hormones. The study included 138 participants (mean age = 57 (13.3) years, age range = 35-86 years, 54% women). The cohort was divided into three groups: 38 early middle-aged (EMA) individuals (mean age = 41 (4.7) years), 48 late middle-aged (LMA) individuals (mean age = 58 (4) years), and 42 older adults (OAs) (mean age = 72 (6.3) years). All participants underwent MRI scans, and saliva samples were collected for sex-steroid hormone quantification (17β-estradiol (E), progesterone (P), and testosterone (T)). We found less connectivity in females between Lobules I and IV and the cuneus, and greater connectivity in females between Crus I, Crus II, and the precuneus with increased age. Higher 17β-estradiol levels were linked to greater connectivity in Crus I and Crus II cerebellar subregions. Analyzing all participants together, testosterone was associated with both higher and lower connectivity in Lobules I-IV and Crus I, respectively, while higher progesterone levels were linked to lower connectivity in females. Structural differences were observed, with EMA males having larger volumes compared to LMA and OA groups, particularly in the Right I-IV, Right Crus I, Right V, and Right VI. EMA females showed higher volumes in the Right Lobules V and VI. These results highlight the significant role of sex steroid hormones in modulating cerebellar connectivity and structure across adulthood, emphasizing the need to consider sex and hormonal status in neuroimaging studies to better understand age-related cognitive decline and neurological disorders.
衰老涉及复杂的生物学变化,这些变化会影响疾病易感性和衰老轨迹。尽管女性通常比男性寿命更长,但她们对阿尔茨海默病等疾病的易感性更高,据推测这受到更年期以及卵巢激素分泌减少的影响。了解性别差异对于个性化医疗干预和健康领域的性别平等至关重要。我们的研究旨在通过研究在性类固醇激素背景下的结构和功能连接变化,阐明正常衰老过程中小脑区域结构和连接的性别差异。该研究包括138名参与者(平均年龄 = 57(13.3)岁,年龄范围 = 35 - 86岁,54%为女性)。该队列分为三组:38名早中年(EMA)个体(平均年龄 = 41(4.7)岁),48名中年晚期(LMA)个体(平均年龄 = 58(4)岁),以及42名老年人(OA)(平均年龄 = 72(6.3)岁)。所有参与者均接受了MRI扫描,并收集唾液样本进行性类固醇激素定量分析(17β - 雌二醇(E)、孕酮(P)和睾酮(T))。我们发现,女性小叶I和IV与楔叶之间的连接较少,而随着年龄增长,女性 Crus I、Crus II与楔前叶之间的连接更多。较高的17β - 雌二醇水平与小脑Crus I和Crus II亚区域更强的连接有关。综合分析所有参与者,睾酮分别与小叶I - IV和Crus I中较高和较低的连接有关,而较高的孕酮水平与女性较低的连接有关。观察到了结构差异,EMA男性与LMA组和OA组相比,脑容量更大,特别是在右侧I - IV、右侧Crus I、右侧V和右侧VI。EMA女性右侧小叶V和VI的脑容量更高。这些结果凸显了性类固醇激素在调节成年期小脑连接和结构方面的重要作用,强调在神经影像学研究中需要考虑性别和激素状态,以更好地理解与年龄相关的认知衰退和神经系统疾病。