Vanderbilt Translational and Clinical Cardiovascular Research Center, Vanderbilt University School of Medicine, Nashville, TN, USA.
MRC Epidemiology Unit, University of Cambridge, Cambridge, UK.
Nat Med. 2024 Jun;30(6):1711-1721. doi: 10.1038/s41591-024-03039-x. Epub 2024 Jun 4.
Despite the wide effects of cardiorespiratory fitness (CRF) on metabolic, cardiovascular, pulmonary and neurological health, challenges in the feasibility and reproducibility of CRF measurements have impeded its use for clinical decision-making. Here we link proteomic profiles to CRF in 14,145 individuals across four international cohorts with diverse CRF ascertainment methods to establish, validate and characterize a proteomic CRF score. In a cohort of around 22,000 individuals in the UK Biobank, a proteomic CRF score was associated with a reduced risk of all-cause mortality (unadjusted hazard ratio 0.50 (95% confidence interval 0.48-0.52) per 1 s.d. increase). The proteomic CRF score was also associated with multisystem disease risk and provided risk reclassification and discrimination beyond clinical risk factors, as well as modulating high polygenic risk of certain diseases. Finally, we observed dynamicity of the proteomic CRF score in individuals who undertook a 20-week exercise training program and an association of the score with the degree of the effect of training on CRF, suggesting potential use of the score for personalization of exercise recommendations. These results indicate that population-based proteomics provides biologically relevant molecular readouts of CRF that are additive to genetic risk, potentially modifiable and clinically translatable.
尽管心肺适能 (CRF) 对代谢、心血管、肺部和神经系统健康有广泛影响,但 CRF 测量的可行性和可重复性方面的挑战阻碍了其在临床决策中的应用。在这里,我们将蛋白质组学特征与来自四个国际队列的 14145 个人的 CRF 联系起来,这些队列具有不同的 CRF 确定方法,以建立、验证和描述蛋白质组 CRF 评分。在英国生物库中约 22000 人的队列中,蛋白质组 CRF 评分与全因死亡率降低相关(未经调整的危险比为 0.50(95%置信区间为 0.48-0.52)每增加 1 个标准差)。蛋白质组 CRF 评分还与多系统疾病风险相关,并提供了超越临床危险因素的风险再分类和区分能力,以及调节某些疾病的高多基因风险。最后,我们观察到在进行 20 周运动训练计划的个体中蛋白质组 CRF 评分的动态性,以及该评分与训练对 CRF 的影响程度之间的关联,这表明该评分可能用于个性化运动建议。这些结果表明,基于人群的蛋白质组学提供了与遗传风险相加、潜在可调节和临床可转化的 CRF 的生物学相关分子读数。