丙酮酸和相关的能量代谢产物调节对青光眼高遗传风险的恢复能力。

Keva Li, Nicholas Tolman, Ayellet V Segrè, Kelsey V Stuart, Oana A Zeleznik, Neeru A Vallabh, Kuang Hu, Nazlee Zebardast, Akiko Hanyuda, Yoshihiko Raita, Christa Montgomery, Chi Zhang, Pirro G Hysi, Ron Do, Anthony P Khawaja, Janey L Wiggs, Jae H Kang, Simon Wm John, Louis R Pasquale
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引用次数: 0

摘要

青光眼多基因风险评分(PRS)能有效识别青光眼的患病风险,但一些PRS高的个体并不会发生青光眼。促成这种韧性的因素仍不清楚。在英国生物银行(UK Biobank)的一项横断面研究中,我们使用4658例青光眼病例和113040例对照,研究血浆代谢物是否能增强青光眼的预测能力,以及是否存在高遗传风险个体恢复能力的代谢组学特征。将168种基于核磁共振的代谢物纳入基于prs的青光眼评估中,建立了逻辑回归模型,并进行了多次比较校正。虽然代谢物对青光眼的预测较弱(曲线下面积=0.579),但在仅基于prs的模型中,代谢物对青光眼的预测有适度改善(P=0.004)。我们在PRS的前十分位数中发现了与恢复力相关的代谢组学特征,糖酵解相关代谢物——乳酸(P=8.8E-12)、丙酮酸(P=1.9E-10)和柠檬酸(P=0.02)的升高与青光眼患病率的降低有关。这些代谢物联合使用显著改变了prs与青光眼的关系(P互作=0.011)。最高PRS四分位数内较高的总弹性代谢物水平对应着较低的青光眼患病率(优势比最高与最低总弹性代谢物四分位数=0.71,95%可信区间[CI]=0.64-0.80)。由于丙酮酸是连接糖酵解与三羧酸循环代谢和ATP生成的基础代谢物,我们在与人类相关的小鼠青光眼模型中对这种假定的弹性生物标志物进行了实验验证。膳食丙酮酸可减轻眼压升高(P=0.002)和视神经损伤(PLmx1b V265D)小鼠。这些发现强调了丙酮酸相关代谢对青光眼的保护作用,并提出了治疗干预的潜在途径。
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Pyruvate and Related Energetic Metabolites Modulate Resilience Against High Genetic Risk for Glaucoma.

A glaucoma polygenic risk score (PRS) can effectively identify disease risk, but some individuals with high PRS do not develop glaucoma. Factors contributing to this resilience remain unclear. Using 4,658 glaucoma cases and 113,040 controls in a cross-sectional study of the UK Biobank, we investigated whether plasma metabolites enhanced glaucoma prediction and if a metabolomic signature of resilience in high-genetic-risk individuals existed. Logistic regression models incorporating 168 NMR-based metabolites into PRS-based glaucoma assessments were developed, with multiple comparison corrections applied. While metabolites weakly predicted glaucoma (Area Under the Curve=0.579), they offered marginal prediction improvement in PRS-only-based models (P=0.004). We identified a metabolomic signature associated with resilience in the top glaucoma PRS decile, with elevated glycolysis-related metabolites-lactate (P=8.8E-12), pyruvate (P=1.9E-10), and citrate (P=0.02)-linked to reduced glaucoma prevalence. These metabolites combined significantly modified the PRS-glaucoma relationship (Pinteraction=0.011). Higher total resilience metabolite levels within the highest PRS quartile corresponded to lower glaucoma prevalence (Odds Ratiohighest vs. lowest total resilience metabolite quartile=0.71, 95% Confidence Interval=0.64-0.80). As pyruvate is a foundational metabolite linking glycolysis to tricarboxylic acid cycle metabolism and ATP generation, we pursued experimental validation for this putative resilience biomarker in a human-relevant Mus musculus glaucoma model. Dietary pyruvate mitigated elevated intraocular pressure (P=0.002) and optic nerve damage (P<0.0003) in Lmx1b V265D mice. These findings highlight the protective role of pyruvate-related metabolism against glaucoma and suggest potential avenues for therapeutic intervention.

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