Healthy Longevity Translational Research Programme, Yong Loo Lin School of Medicine, National University of Singapore, Singapore; Centre for Healthy Longevity, @AgeSingapore, National University Health System, Singapore.
School of Anesthesiology, Weifang Medical University, Weifang, China.
Ageing Res Rev. 2023 Sep;90:102029. doi: 10.1016/j.arr.2023.102029. Epub 2023 Aug 6.
Dementia is prevalent in aged populations and is associated with disability and distress for those affected. Therapeutic benefits of drugs targeting dementia are small. Impaired nutrient sensing pathways have been implicated in the pathogenesis of dementia and may offer a novel treatment target.
This systematic review collated evidence for novel therapeutic compounds that modify nutrient sensing pathways, particularly the sirtuin pathway, in preventing cognitive decline or improving cognition in normal ageing, mild cognitive impairment (MCI), and dementia.
PubMed, Embase and Web of Science databases were searched using key search terms. Articles were screened using Covidence systematic review software. The risk of bias was assessed using the Systematic Review Center for Laboratory animal Experimentation (SYRCLE)'s risk of bias tool for animal studies and Cochrane Risk of Bias tool v 2.0 for human studies.
Out of 3841 articles, 68 were included describing 38 different novel therapeutic compounds that modulate the nutrient sensing pathway via the sirtuin pathway. In animal models (58 studies), all investigated novel therapeutic compounds showed cognitive benefits. Ten studies were human intervention trials targeting normal ageing (1 study) and dementia populations (9 studies). Direct sirtuin (silent mating type information regulation 2 homolog) 1 (SIRT1) activators Resveratrol and Nicotinamide derivatives improved cognitive outcomes among human subjects with normal cognition and MCI.
Animal studies support that modulation of the sirtuin pathway has the potential to improve cognitive outcomes. Overall, there is a clear lack of translation from animal models to human populations.
痴呆在老年人群中很常见,会给患者及其家属带来残疾和痛苦。针对痴呆的药物治疗效果甚微。有研究表明,营养感应通路的损伤与痴呆的发病机制有关,可能成为新的治疗靶点。
本系统评价汇总了可调节营养感应通路(尤其是沉默信息调节因子 2 相关酶 1 通路)的新型治疗化合物的证据,这些化合物可预防认知能力下降或改善正常衰老、轻度认知障碍和痴呆患者的认知功能。
使用关键搜索词检索 PubMed、Embase 和 Web of Science 数据库。使用 Covidence 系统评价软件筛选文章。采用系统评价实验室动物实验中心(SYRCLE)的动物研究偏倚风险工具和 Cochrane 偏倚风险工具 v 2.0 评估人类研究的偏倚风险。
在 3841 篇文章中,有 68 篇符合描述通过 Sirtuin 通路调节营养感应通路的 38 种不同新型治疗化合物的纳入标准。在动物模型(58 项研究)中,所有研究的新型治疗化合物均显示出认知益处。有 10 项研究是针对正常衰老(1 项研究)和痴呆人群(9 项研究)的人类干预试验。直接激活沉默信息调节因子 2 同源物 1(SIRT1)的白藜芦醇和烟酰胺衍生物可改善认知能力正常和轻度认知障碍的人类受试者的认知结果。
动物研究表明,调节 Sirtuin 通路具有改善认知结果的潜力。总的来说,从动物模型到人类群体的转化明显不足。