与年龄有关的血浆蛋白水平的多基因代理揭示了 TIMP2 在认知能力中的作用

Federica Anastasi, Patricia Genius, Blanca Rodríguez-Fernández, Chengran Yang, Priyanka Gorijala, Jigyasha Timsina, Felipe Hernández-Villamizar, Luigi Lorenzini, Marta del Campo, Gonzalo Sánchez-Benavides, Carolina Minguillón, Arcadi Navarro, Carlos Cruchaga, Marc Suárez-Calvet, Natalia Vilor-Tejedor
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引用次数: 0

摘要

有几项研究发现了影响小鼠大脑衰老表现的血液蛋白质,但将这些发现转化到人类身上仍具有挑战性。在这里,我们发现较高的组织金属蛋白酶抑制剂 2 TIMP2 预测血浆水平与人类整体认知和记忆能力的改善有显著关联。我们首先通过系统综述确定了 12 种对小鼠大脑具有衰老或恢复活力作用的蛋白质。利用这些蛋白质的蛋白质定量性状位点数据,我们计算了多基因分数作为血浆蛋白质水平的代用指标,并在两个独立队列中验证了其预测准确性。基因代用指标与认知能力之间的关联模型凸显了 TIMP2 的重要性,在根据性别、APOE-e4 和 Abeta-42 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再生作用相吻合,表明它是人类大脑衰老和老年相关脑疾病的一个很有希望的治疗靶点。
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Polygenic proxies of age-related plasma protein levels reveal TIMP2 role in cognitive performance
Several studies have identified blood proteins that influence brain aging performance in mice, yet translating these findings to humans remains challenging. Here we found that higher predicted plasma levels of Tissue Inhibitor of Metalloproteinases 2 TIMP2 were significantly associated with improved global cognition and memory performance in humans. We first identified 12 proteins with aging or rejuvenating effects on murine brains through a systematic review. Using protein quantitative trait loci data for these proteins, we computed polygenic scores as proxies for plasma protein levels and validated their prediction accuracy in two independent cohorts. Association models between genetic proxies and cognitive performance highlighted the significance of TIMP2, also when the models were stratified by sex, APOE-e4, and Abeta-42 status. This finding aligns with TIMP2s brain rejuvenating role in murine models, suggesting it as a promising therapeutic target for brain aging and age-related brain diseases in humans.
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