Correlates of axonal content in healthy adult span: Age, sex, myelin, and metabolic health

IF 1.9 Q3 CLINICAL NEUROLOGY
Agnieszka Z Burzynska , Charles Anderson , David B. Arciniegas , Vince Calhoun , In-Young Choi , Andrea Mendez Colmenares , Arthur F Kramer , Kaigang Li , Jongho Lee , Phil Lee , Michael L Thomas
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Abstract

As the emerging treatments that target grey matter pathology in Alzheimer's Disease have limited effectiveness, there is a critical need to identify new neural targets for treatments. White matter's (WM) metabolic vulnerability makes it a promising candidate for new interventions. This study examined the age and sex differences in estimates of axonal content, as well the associations of with highly prevalent modifiable health risk factors such as metabolic syndrome and adiposity. We estimated intra-axonal volume fraction (ICVF) using the Neurite Orientation Dispersion and Density Imaging (NODDI) in a sample of 89 cognitively and neurologically healthy adults (20–79 years). We showed that ICVF correlated positively with age and estimates of myelin content. The ICVF was also lower in women than men, across all ages, which difference was accounted for by intracranial volume. Finally, we found no association of metabolic risk or adiposity scores with the current estimates of ICVF. In addition, the previously observed adiposity-myelin associations (Burzynska et al., 2023) were independent of ICVF. Although our findings confirm the vulnerability of axons to aging, they suggest that metabolic dysfunction may selectively affect myelin content, at least in cognitively and neurologically healthy adults with low metabolic risk, and when using the specific MRI techniques. Future studies need to revisit our findings using larger samples and different MRI approaches, and identify modifiable factors that accelerate axonal deterioration as well as mechanisms linking peripheral metabolism with the health of myelin.

健康成人跨度中轴突含量的相关性:年龄、性别、髓鞘和代谢健康
由于针对阿尔茨海默病灰质病变的新兴治疗方法效果有限,因此亟需确定新的神经治疗靶点。白质(WM)在新陈代谢方面的脆弱性使其有希望成为新干预措施的候选对象。本研究考察了轴突含量估计值的年龄和性别差异,以及与代谢综合征和脂肪过多等高发可调节健康风险因素的关联。我们使用神经元定向分散和密度成像(NODDI)估算了89名认知和神经健康成年人(20-79岁)的轴突内体积分数(ICVF)。我们的研究表明,ICVF 与年龄和髓鞘含量估计值呈正相关。在所有年龄段中,女性的 ICVF 也低于男性,颅内容积可以解释这种差异。最后,我们发现代谢风险或脂肪评分与目前估计的 ICVF 没有关联。此外,之前观察到的肥胖与髓鞘的关联(Burzynska 等人,2023 年)与 ICVF 无关。尽管我们的研究结果证实了轴突对衰老的脆弱性,但它们表明,代谢功能障碍可能会选择性地影响髓鞘含量,至少在代谢风险较低的认知和神经系统健康的成年人中,以及在使用特定的磁共振成像技术时是如此。未来的研究需要使用更大的样本和不同的磁共振成像方法重新审视我们的发现,并找出加速轴突退化的可改变因素以及外周代谢与髓鞘健康的关联机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cerebral circulation - cognition and behavior
Cerebral circulation - cognition and behavior Neurology, Clinical Neurology
CiteScore
2.00
自引率
0.00%
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审稿时长
14 weeks
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