Walker Ryan G, Kato Tomohiro, Ben Driss Laura, Williams Stephen A, Hinterberg Michael A, Janjic Nebojsa, Gelinas Amy D, Carpenter Meredith A, Kattamuri Chandramohan, Walter Joan E, Mueller Christian, Mendello Kourtney R, Gordon Justis V, Walker Keenan A, Coresh Josef, Bhasin Shalender, Rubin Lee L, Wagers Amy J, Thompson Thomas B, Ganz Peter, Lee Richard T
Department of Stem Cell and Regenerative Biology and the Harvard Stem Cell Institute, Harvard University, Cambridge, MA, USA.
SomaLogic Inc, Boulder, CO, USA.
Nat Commun. 2025 Jul 15;16(1):6534. doi: 10.1038/s41467-025-61815-w.
Circulating Growth Differentiation Factors 11 and 8 (GDF11/8) exist in both latent and active forms, and it is unclear if specific forms can predict disease outcomes. Our data suggest that a dual-specific aptamer selectively binds GDF11/8 after prodomain activation. In 11,609 patients at risk for future cardiovascular events, low dual-specific aptamer-detected GDF11/8 levels strongly predicted adverse outcomes, including cardiovascular events (HR = 0.43, p = 9.1 × 10⁻⁶³) and all-cause mortality (HR = 0.33, p = 4.8 × 10⁻⁴⁰). Use of selective aptamers suggested that results observed with the dual-specific aptamer for cardiovascular and mortality risk replicated with a GDF8 aptamer although with a smaller effect size. In a second cohort of 4110 individuals (ARIC), low dual-specific aptamer-detected GDF11/8 levels also predicted increased 8 year dementia risk (HR = 0.66, p = 0.00148). Our findings reveal that activation of GDF11/8 may be a factor in future aging-related cardiovascular and cognitive decline.
循环生长分化因子11和8(GDF11/8)以潜伏和活性两种形式存在,目前尚不清楚特定形式是否能预测疾病预后。我们的数据表明,一种双特异性适体在原结构域激活后能选择性结合GDF11/8。在11609名有未来心血管事件风险的患者中,双特异性适体检测到的低GDF11/8水平强烈预示着不良预后,包括心血管事件(HR = 0.43,p = 9.1×10⁻⁶³)和全因死亡率(HR = 0.33,p = 4.8×10⁻⁴⁰)。使用选择性适体表明,双特异性适体对心血管和死亡风险的观察结果在使用GDF8适体时得到了重复,尽管效应大小较小。在第二个包含4110名个体的队列(ARIC)中,双特异性适体检测到的低GDF11/8水平也预示着8年痴呆风险增加(HR = 0.66,p = 0.00148)。我们的研究结果表明,GDF11/8的激活可能是未来与衰老相关的心血管和认知衰退的一个因素。