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Tittel Artificial intelligence in drug development for delirium and Alzheimer’s disease
Medansvarlig Xiao, Xianglu Deng, Shenglong Yang, Nan Xing, Xiaodan Watne, Leiv Otto Selbæk, Geir Wedatilake, Yehani Xie, Chenglong Rubinsztein, David C. Palmer, Jennifer E. Neerland, Bjørn Erik Chen, Hongming Niu, Zhangming Yang, Guang Fang, Evandro Fei
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Noter Abstract: Delirium is a common cause and complication of hospitalization in the elderly and is associated with higher risk of future dementia and progression of existing dementia, of which 70% is Alzheimer’s disease (AD). AD and delirium, which are known to be aggravated by one another, represent significant societal challenges, especially in light of the absence of effective treatments capable. The intricate biological mechanisms have led to numerous clinical trial setbacks and likely contribute to the limited efficacy of existing therapeutics. Artificial intelligence (AI) presents a promising avenue for overcoming these hurdles by deploying algorithms to uncover hidden patterns across diverse data types. This review explores the pivotal role of AI in revolutionizing drug discovery for AD and delirium from target identification to the development of small molecule and protein-based therapies. Recent advances in deep learning, particularly in accurate protein structure prediction, are facilitating novel approaches to drug design and expediting the discovery pipeline for biological and small molecule therapeutics. This review concludes with an appraisal of current achievements and limitations, and touches on prospects for the use of AI in advancing drug discovery in AD and delirium, emphasizing its transformative potential in addressing these two and possibly other neurodegenerative conditions.
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L�nere p� venteliste
*000 ap
*00142395
*100 $aAi, Ruixue
*245 $aArtificial intelligence in drug development for delirium and Alzheimer’s disease$cRuixue Ai, Xianglu Xiao, Shenglong Deng, Nan Yang, Xiaodan Xing, Leiv Otto Watne, Geir Selbæk, Yehani Wedatilake, Chenglong Xie, David C. Rubinsztein, Jennifer E. Palmer, Bjørn Erik Neerland, Hongming Chen, Zhangming Niu, Guang Yang, Evandro Fei Fang
*260 $c2025
*300 $ahttps://doi.org/10.1016/j.apsb.2025.04.026
*440 $aActa Pharmaceutica Sinica B
*505 $aAbstract: Delirium is a common cause and complication of hospitalization in the elderly and is associated with higher risk of future dementia and progression of existing dementia, of which 70% is Alzheimer’s disease (AD). AD and delirium, which are known to be aggravated by one another, represent significant societal challenges, especially in light of the absence of effective treatments capable. The intricate biological mechanisms have led to numerous clinical trial setbacks and likely contribute to the limited efficacy of existing therapeutics. Artificial intelligence (AI) presents a promising avenue for overcoming these hurdles by deploying algorithms to uncover hidden patterns across diverse data types. This review explores the pivotal role of AI in revolutionizing drug discovery for AD and delirium from target identification to the development of small molecule and protein-based therapies. Recent advances in deep learning, particularly in accurate protein structure prediction, are facilitating novel approaches to drug design and expediting the discovery pipeline for biological and small molecule therapeutics. This review concludes with an appraisal of current achievements and limitations, and touches on prospects for the use of AI in advancing drug discovery in AD and delirium, emphasizing its transformative potential in addressing these two and possibly other neurodegenerative conditions.
*650 $aKunstig intelligens
*700 $aXiao, Xianglu
*700 $aDeng, Shenglong
*700 $aYang, Nan
*700 $aXing, Xiaodan
*700 $aWatne, Leiv Otto
*700 $aSelbæk, Geir
*700 $aWedatilake, Yehani
*700 $aXie, Chenglong
*700 $aRubinsztein, David C.
*700 $aPalmer, Jennifer E.
*700 $aNeerland, Bjørn Erik
*700 $aChen, Hongming
*700 $aNiu, Zhangming
*700 $aYang, Guang
*700 $aFang, Evandro Fei
*856 $uhttps://doi.org/10.1016/j.apsb.2025.04.026
^
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