Machine Learning in Hyperlipidaemia Research: Screening and Experimental Insights into Lipid Metabolism Modulators.

IF 3.2 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Ashish Srivastava, Mohit Prajapati, Parul Srivastava, Anil Kumar Yadav, Ankita Wal, Manshi Singh, Ritik Yadav
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引用次数: 0

Abstract

Hyperlipidemia, characterized by elevated blood lipid levels, represents a major global health concern due to its strong association with cardiovascular disease, diabetes, and metabolic syndrome. While current therapies - such as statins, fibrates, bile acid sequestrants, and PCSK9 inhibitors - are effective in controlling hyperlipidemia, they are often associated with adverse effects, potential drug resistance, and suboptimal efficacy in certain patient populations. All of the above underscore the urgent need for safer and more effective therapeutic alternatives. Among the major molecular targets involved in the regulation of lipid metabolism are HMG-CoA reductase, PCSK9, peroxisome proliferator-activated receptors (PPARs), cholesteryl ester transfer protein (CETP), and nuclear receptors, including the liver X receptor (LXR) and farnesoid X receptor (FXR), which are also targets for future antihyperlipidemic drug development. Recent advancements in artificial intelligence (AI) and machine learning (ML) have significantly transformed and accelerated drug discovery by enabling the processing of vast amounts of genomic, proteomic, and chemical data. Furthermore, ML tools such as quantitative structure-activity relationship (QSAR) modelling, deep learning, random forest, and support vector machines (SVM) have proven predictive and effective in identifying novel lipid metabolism modulators, thereby enhancing the efficacy and accuracy of virtual screening. Meanwhile, molecular docking has become an integral part of structure-based drug design (SBDD), and software such as AutoDock, Glide, and GOLD have proven effective in generating accurate ligand-target docking models. Molecular docking, together with ML-based approaches, enables the identification of potent and selective drug candidates. Overall, the combination of ML and molecular docking offers an efficient and accurate platform for antihyperlipidemic drug discovery, helping to overcome the limitations of currently available therapeutic strategies.

高脂血症研究中的机器学习:脂质代谢调节剂的筛选和实验见解。
以血脂水平升高为特征的高脂血症,由于与心血管疾病、糖尿病和代谢综合征密切相关,是一个主要的全球健康问题。虽然目前的治疗方法,如他汀类药物、贝特类药物、胆汁酸隔离剂和PCSK9抑制剂,在控制高脂血症方面是有效的,但在某些患者群体中,它们往往与不良反应、潜在的耐药性和次优疗效有关。所有这些都强调了迫切需要更安全、更有效的治疗方案。参与脂质代谢调节的主要分子靶点包括HMG-CoA还原酶、PCSK9、过氧化物酶体增殖物激活受体(PPARs)、胆固醇酯转移蛋白(CETP)和核受体,包括肝X受体(LXR)和法内酯X受体(FXR),它们也是未来抗高脂血症药物开发的靶点。人工智能(AI)和机器学习(ML)的最新进展通过处理大量基因组、蛋白质组学和化学数据,显着改变和加速了药物发现。此外,定量构效关系(QSAR)建模、深度学习、随机森林和支持向量机(SVM)等机器学习工具已被证明在识别新型脂质代谢调节剂方面具有预测性和有效性,从而提高了虚拟筛选的有效性和准确性。同时,分子对接已成为基于结构的药物设计(SBDD)的重要组成部分,AutoDock、Glide、GOLD等软件已被证明在生成精确的配体-靶标对接模型方面是有效的。分子对接,再加上基于ml的方法,使有效和选择性候选药物的鉴定成为可能。总的来说,ML和分子对接的结合为抗高脂血症药物的发现提供了一个高效、准确的平台,有助于克服目前可用治疗策略的局限性。
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来源期刊
CiteScore
6.30
自引率
0.00%
发文量
302
审稿时长
2 months
期刊介绍: Current Pharmaceutical Design publishes timely in-depth reviews and research articles from leading pharmaceutical researchers in the field, covering all aspects of current research in rational drug design. Each issue is devoted to a single major therapeutic area guest edited by an acknowledged authority in the field. Each thematic issue of Current Pharmaceutical Design covers all subject areas of major importance to modern drug design including: medicinal chemistry, pharmacology, drug targets and disease mechanism.
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