DoliClock: a lipid-based aging clock reveals accelerated aging in neurological disorders.

IF 3.9 3区 医学 Q2 CELL BIOLOGY
Aging-Us Pub Date : 2025-06-04 DOI:10.18632/aging.206266
Djakim Latumalea, Maximilian Unfried, Diogo Barardo, Jan Gruber, Brian K Kennedy
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引用次数: 0

Abstract

Aging is a multifaceted process influenced by intrinsic and extrinsic factors, with lipid alterations playing a critical role in brain aging and neurological disorders. This study introduces DoliClock, a lipid-based biological aging clock designed to predict the age of the prefrontal cortex using post-mortem lipidomic data. Significant age acceleration was observed in autism, schizophrenia, and Down syndrome. Additionally, an increase in entropy around age 40 suggests dysregulation of the mevalonate pathway and dolichol accumulation. Dolichol, a lipid integral to N-glycosylation and intracellular transport, emerged as a potential aging biomarker, with specific variants such as dolichol-19 and dolichol-20 showing unique age-related associations. These findings suggest that lipidomics can provide valuable insights into the molecular mechanisms of brain aging and neurological disorders. By linking dolichol levels and entropy changes to accelerated aging, this study highlights the potential of lipid-based biomarkers for understanding and predicting biological age, especially in conditions associated with premature aging.

DoliClock:一种基于脂质的衰老时钟,揭示了神经系统疾病的加速衰老。
衰老是一个受内在和外在因素影响的多方面过程,脂质改变在脑老化和神经系统疾病中起着关键作用。本研究介绍了DoliClock,一种基于脂质的生物衰老时钟,旨在利用死后脂质组学数据预测前额皮质的年龄。在自闭症、精神分裂症和唐氏综合症中观察到明显的年龄加速。此外,40岁左右的熵增加表明甲羟戊酸途径和酒精积累的失调。Dolichol是一种对n -糖基化和细胞内运输不可或缺的脂质,是一种潜在的衰老生物标志物,其特定变体如Dolichol -19和Dolichol -20显示出独特的年龄相关关联。这些发现表明,脂质组学可以为大脑衰老和神经系统疾病的分子机制提供有价值的见解。通过将酒精水平和熵变化与加速衰老联系起来,本研究强调了基于脂质的生物标志物在理解和预测生物年龄方面的潜力,特别是在与早衰相关的情况下。
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
Aging-Us
Aging-Us CELL BIOLOGY-
CiteScore
10.00
自引率
0.00%
发文量
595
审稿时长
6-12 weeks
期刊介绍: Information not localized
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