重新利用乙酰布洛尔治疗骨质疏松症:来自多组学和多模式数据分析的见解。

IF 6.3 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Dan-Yang Liu, Hui Shen, Jonathan Greenbaum, Qiao-Rong Yi, Shuang Liang, Yue Zhang, Jia-Chen Liu, Chuan Qiu, Lan-Juan Zhao, Qing Tian, Kuan-Jui Su, Zhe Luo, Li Wu, Xiang-He Meng, Hong-Mei Xiao, Yun Deng, Yang Li, Dragana Lovre, Vivian Fonseca, Fernando L Sanchez, Li-Jun Tan, Hong-Wen Deng
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引用次数: 0

摘要

骨质疏松症是一种常见的随年龄增长而发生的代谢性骨病,其特点是骨密度低,脆性骨折风险高。虽然目前的药物干预提供了治疗益处,但长期使用受到副作用和合并症的限制。在这项研究中,我们采用驱动信号网络识别(DSNI)和药物功能网络(DFN)从基于集成网络的蜂窝签名库中识别可重复使用的药物。我们利用多组学数据构建骨质疏松驱动信号网络(ODSN),并基于药物相似度构建了骨质疏松驱动信号网络(DFN)。通过整合ODSN和DFN与药物诱导的转录反应,我们筛选了10,158个化合物,并确定了几种对ODSN具有强靶向作用的药物。孟德尔随机化利用全基因组关联研究数据评估药物靶点的顺式等效qtl与BMD之间的潜在因果关系。我们的研究结果表明,四种药物,包括鲁索利替尼,阿法骨化醇和多铁钙化醇,可能具有抗骨质疏松的作用。值得注意的是,乙酰布洛尔,一种用于高血压的β受体阻滞剂,以前没有涉及骨质疏松症治疗。为了验证,采用地塞米松诱导骨质流失的方法建立斑马鱼骨质疏松模型,然后用盐酸乙酰布洛尔和阿法骨化醇治疗。这两种化合物对骨质疏松相关的骨质退化都有显著的保护作用。此外,利用倾向评分匹配和广义线性模型分析的基于人群的数据集显示,服用β受体阻滞剂药物的个体的骨密度明显高于其他心血管药物的使用者。总之,本研究整合了多组学方法、实验验证和现实世界人口数据,提出乙酰布洛尔作为骨质疏松症治疗的新候选药物。这些发现需要进一步的机制研究和临床试验来评估其在骨质疏松症治疗中的疗效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Repurposing Acebutolol for Osteoporosis Treatment: Insights From Multi-Omics and Multi-Modal Data Analysis.

Osteoporosis is a common metabolic bone disease with aging, characterized by low bone mineral density (BMD) and higher fragility fracture risk. Although current pharmacological interventions provide therapeutic benefits, long-term use is limited by side effects and comorbidities. In this study, we employed driver signaling network identification (DSNI) and drug functional networks (DFN) to identify repurposable drugs from the Library of Integrated Network-Based Cellular Signatures. We constructed osteoporosis driver signaling networks (ODSN) using multi-omics data and developed DFN based on drug similarity. By integrating ODSN and DFN with drug-induced transcriptional responses, we screened 10,158 compounds and identified several drugs with strong targeting effects on ODSN. Mendelian randomization assessed potential causal links between cis-eQTLs of drug targets and BMD using genome-wide association study data. Our findings indicate four drugs, including Ruxolitinib, Alfacalcidol, and Doxercalciferol, may exert anti-osteoporosis effects. Notably, Acebutolol, a β-blocker for hypertension, has not previously been implicated in osteoporosis therapy. For validation, zebrafish osteoporosis models were established using Dexamethasone-induced bone loss, followed by treatment with Acebutolol hydrochloride and Alfacalcidol. Both compounds demonstrated significant protective effects against osteoporosis-related bone deterioration. Furthermore, a population-based data set, utilizing propensity score matching and analyzed via a generalized linear model, revealed that individuals taking β-blocker drugs exhibited significantly higher BMD than users of other cardiovascular medications. In summary, this study integrates multi-omics approaches, experimental validation, and real-world population data to propose acebutolol as a novel candidate for osteoporosis treatment. These findings warrant further mechanistic studies and clinical trials to evaluate its efficacy in osteoporosis management.

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来源期刊
CiteScore
12.70
自引率
7.50%
发文量
290
审稿时长
2 months
期刊介绍: Clinical Pharmacology & Therapeutics (CPT) is the authoritative cross-disciplinary journal in experimental and clinical medicine devoted to publishing advances in the nature, action, efficacy, and evaluation of therapeutics. CPT welcomes original Articles in the emerging areas of translational, predictive and personalized medicine; new therapeutic modalities including gene and cell therapies; pharmacogenomics, proteomics and metabolomics; bioinformation and applied systems biology complementing areas of pharmacokinetics and pharmacodynamics, human investigation and clinical trials, pharmacovigilence, pharmacoepidemiology, pharmacometrics, and population pharmacology.
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