Anastasi Federica, Genius Patricia, Rodriguez-Fernandez Blanca, Yang Chengran, Gorijala Priyanka, Timsina Jigyasha, Hernández-Villamizar Felipe, Lorenzini Luigi, Del Campo Marta, Sanchez-Benavides Gonzalo, Minguillon Carolina, Navarro Arcadi, Cruchaga Carlos, Suárez-Calvet Marc, Vilor-Tejedor Natalia
Barcelonaβeta Brain Research Center (BBRC), Pasqual Maragall Foundation.
Department of Psychiatry, Washington University, St. Louis.
Res Sq. 2024 Oct 18:rs.3.rs-5267673. doi: 10.21203/rs.3.rs-5267673/v1.
While numerous studies have identified blood proteins that modulate brain aging in mice, the direct translation of these findings to human health remains a substantial challenge. Bridging this gap is critical for developing interventions that can effectively target human brain aging and associated diseases.
We first identified 12 proteins with aging or rejuvenating properties in murine brains through a systematic review. Using protein quantitative trait loci data for these proteins, we developed polygenic scores to predict plasma protein levels, which we then validated in two independent human cohorts. We employed association models to explore the association between these genetically predicted protein levels and cognitive performance, focusing specifically on their interaction with key genetic markers such as sex, ε4 and Aβ42 status.
Predicted plasma levels of Tissue Inhibitor of Metalloproteinases 2 (TIMP2) were significantly associated with improved global cognition and memory performance in humans, also when the models were stratified by sex, ε4, and Aβ42 status.
This finding aligns with TIMP2's brain-rejuvenating role in murine models, suggesting it as a promising therapeutic target for brain aging and age-related brain diseases in humans.
虽然众多研究已在小鼠中鉴定出可调节大脑衰老的血液蛋白质,但将这些发现直接转化应用于人类健康仍面临重大挑战。弥合这一差距对于开发能够有效针对人类大脑衰老及相关疾病的干预措施至关重要。
我们首先通过系统综述在小鼠大脑中鉴定出12种具有衰老或年轻化特性的蛋白质。利用这些蛋白质的蛋白质数量性状位点数据,我们开发了多基因评分来预测血浆蛋白水平,随后在两个独立的人类队列中进行了验证。我们采用关联模型来探索这些基因预测的蛋白水平与认知表现之间的关联,特别关注它们与性别、ε4和Aβ42状态等关键遗传标记的相互作用。
金属蛋白酶组织抑制剂2(TIMP2)的预测血浆水平与人类整体认知和记忆表现的改善显著相关,在按性别、ε4和Aβ42状态对模型进行分层时也是如此。
这一发现与TIMP2在小鼠模型中的大脑年轻化作用相符,表明它有望成为人类大脑衰老及与年龄相关的脑部疾病的治疗靶点。