• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

联合代谢激活剂可改善阿尔茨海默病患者的认知功能:一项随机、双盲、安慰剂对照的 II 期试验。

Combined metabolic activators improve cognitive functions in Alzheimer's disease patients: a randomised, double-blinded, placebo-controlled phase-II trial.

机构信息

Department of Neurology and Neuroscience, Faculty of Medicine, Alanya Alaaddin Keykubat University, Antalya, Turkey.

Science for Life Laboratory, KTH - Royal Institute of Technology, Stockholm, Sweden.

出版信息

Transl Neurodegener. 2023 Jan 26;12(1):4. doi: 10.1186/s40035-023-00336-2.

DOI:10.1186/s40035-023-00336-2
PMID:36703196
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9879258/
Abstract

BACKGROUND

Alzheimer's disease (AD) is associated with metabolic abnormalities linked to critical elements of neurodegeneration. We recently administered combined metabolic activators (CMA) to the AD rat model and observed that CMA improves the AD-associated histological parameters in the animals. CMA promotes mitochondrial fatty acid uptake from the cytosol, facilitates fatty acid oxidation in the mitochondria, and alleviates oxidative stress.

METHODS

Here, we designed a randomised, double-blinded, placebo-controlled phase-II clinical trial and studied the effect of CMA administration on the global metabolism of AD patients. One-dose CMA included 12.35 g L-serine (61.75%), 1 g nicotinamide riboside (5%), 2.55 g N-acetyl-L-cysteine (12.75%), and 3.73 g L-carnitine tartrate (18.65%). AD patients received one dose of CMA or placebo daily during the first 28 days and twice daily between day 28 and day 84. The primary endpoint was the difference in the cognitive function and daily living activity scores between the placebo and the treatment arms. The secondary aim of this study was to evaluate the safety and tolerability of CMA. A comprehensive plasma metabolome and proteome analysis was also performed to evaluate the efficacy of the CMA in AD patients.

RESULTS

We showed a significant decrease of AD Assessment Scale-cognitive subscale (ADAS-Cog) score on day 84 vs day 0 (P = 0.00001, 29% improvement) in the CMA group. Moreover, there was a significant decline (P = 0.0073) in ADAS-Cog scores (improvement of cognitive functions) in the CMA compared to the placebo group in patients with higher ADAS-Cog scores. Improved cognitive functions in AD patients were supported by the relevant alterations in the hippocampal volumes and cortical thickness based on imaging analysis. Moreover, the plasma levels of proteins and metabolites associated with NAD + and glutathione metabolism were significantly improved after CMA treatment.

CONCLUSION

Our results indicate that treatment of AD patients with CMA can lead to enhanced cognitive functions and improved clinical parameters associated with phenomics, metabolomics, proteomics and imaging analysis. Trial registration ClinicalTrials.gov NCT04044131 Registered 17 July 2019, https://clinicaltrials.gov/ct2/show/NCT04044131.

摘要

背景

阿尔茨海默病(AD)与与神经退行性变的关键因素有关的代谢异常有关。我们最近给 AD 大鼠模型施用了联合代谢激活剂(CMA),并观察到 CMA 改善了动物的 AD 相关组织学参数。CMA 促进细胞质中脂肪酸向线粒体的摄取,促进线粒体中脂肪酸的氧化,并减轻氧化应激。

方法

在这里,我们设计了一项随机、双盲、安慰剂对照的 II 期临床试验,研究 CMA 给药对 AD 患者整体代谢的影响。一剂 CMA 包括 12.35g L-丝氨酸(61.75%)、1g 烟酰胺核苷(5%)、2.55g N-乙酰-L-半胱氨酸(12.75%)和 3.73g 酒石酸左旋肉碱(18.65%)。AD 患者在第 1 至 28 天每天接受一剂 CMA 或安慰剂,在第 28 至 84 天每天接受两剂。主要终点是安慰剂和治疗组之间认知功能和日常生活活动评分的差异。本研究的次要目的是评估 CMA 的安全性和耐受性。还进行了全面的血浆代谢组和蛋白质组分析,以评估 CMA 在 AD 患者中的疗效。

结果

我们发现 CMA 组在第 84 天与第 0 天相比,AD 评估量表认知子量表(ADAS-Cog)评分显著下降(P = 0.00001,改善 29%)。此外,在 ADAS-Cog 评分较高的患者中,与安慰剂组相比,CMA 组的 ADAS-Cog 评分(认知功能改善)显著下降(P = 0.0073)。AD 患者认知功能的改善得到了基于影像学分析的海马体积和皮质厚度相关的相关变化的支持。此外,CMA 治疗后,与 NAD+和谷胱甘肽代谢相关的蛋白质和代谢物的血浆水平显著改善。

结论

我们的结果表明,用 CMA 治疗 AD 患者可导致认知功能增强,并改善与表型、代谢组学、蛋白质组学和影像学分析相关的临床参数。

试验注册

ClinicalTrials.gov NCT04044131 于 2019 年 7 月 17 日注册,https://clinicaltrials.gov/ct2/show/NCT04044131。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9698/9881384/cf9e705653b8/40035_2023_336_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9698/9881384/1d9f73eed08f/40035_2023_336_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9698/9881384/a6d8e81f122a/40035_2023_336_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9698/9881384/a6c263763276/40035_2023_336_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9698/9881384/6dfee83b21f6/40035_2023_336_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9698/9881384/cf9e705653b8/40035_2023_336_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9698/9881384/1d9f73eed08f/40035_2023_336_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9698/9881384/a6d8e81f122a/40035_2023_336_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9698/9881384/a6c263763276/40035_2023_336_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9698/9881384/6dfee83b21f6/40035_2023_336_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9698/9881384/cf9e705653b8/40035_2023_336_Fig5_HTML.jpg

相似文献

1
Combined metabolic activators improve cognitive functions in Alzheimer's disease patients: a randomised, double-blinded, placebo-controlled phase-II trial.联合代谢激活剂可改善阿尔茨海默病患者的认知功能:一项随机、双盲、安慰剂对照的 II 期试验。
Transl Neurodegener. 2023 Jan 26;12(1):4. doi: 10.1186/s40035-023-00336-2.
2
Multi-omics characterization of improved cognitive functions in Parkinson's disease patients after the combined metabolic activator treatment: a randomized, double-blinded, placebo-controlled phase II trial.帕金森病患者联合代谢激活剂治疗后认知功能改善的多组学特征:一项随机、双盲、安慰剂对照的II期试验。
Brain Commun. 2025 Jan 6;7(1):fcae478. doi: 10.1093/braincomms/fcae478. eCollection 2025.
3
Medium-chain triglycerides improved cognition and lipid metabolomics in mild to moderate Alzheimer's disease patients with APOE4: A double-blind, randomized, placebo-controlled crossover trial.中链甘油三酯改善了携带APOE4的轻度至中度阿尔茨海默病患者的认知功能和脂质代谢组学:一项双盲、随机、安慰剂对照交叉试验。
Clin Nutr. 2020 Jul;39(7):2092-2105. doi: 10.1016/j.clnu.2019.10.017. Epub 2019 Oct 22.
4
Cognitive improvement in mild to moderate Alzheimer's dementia after treatment with the acetylcholine precursor choline alfoscerate: a multicenter, double-blind, randomized, placebo-controlled trial.乙酰胆碱前体阿福特罗胆碱治疗轻至中度阿尔茨海默病痴呆后的认知改善:一项多中心、双盲、随机、安慰剂对照试验。
Clin Ther. 2003 Jan;25(1):178-93. doi: 10.1016/s0149-2918(03)90023-3.
5
ABT-126 monotherapy in mild-to-moderate Alzheimer's dementia: randomized double-blind, placebo and active controlled adaptive trial and open-label extension.ABT-126单药治疗轻至中度阿尔茨海默病性痴呆:随机双盲、安慰剂和活性对照适应性试验及开放标签扩展研究
Alzheimers Res Ther. 2016 Oct 18;8(1):44. doi: 10.1186/s13195-016-0210-1.
6
Efficacy and safety of tarenflurbil in mild to moderate Alzheimer's disease: a randomised phase II trial.他仑氟比(tarenflurbil)治疗轻至中度阿尔茨海默病的疗效与安全性:一项随机II期试验。
Lancet Neurol. 2008 Jun;7(6):483-93. doi: 10.1016/S1474-4422(08)70090-5. Epub 2008 Apr 29.
7
Effect of dimebon on cognition, activities of daily living, behaviour, and global function in patients with mild-to-moderate Alzheimer's disease: a randomised, double-blind, placebo-controlled study.二甲金刚胺对轻至中度阿尔茨海默病患者认知、日常生活活动能力、行为及整体功能的影响:一项随机、双盲、安慰剂对照研究
Lancet. 2008 Jul 19;372(9634):207-15. doi: 10.1016/S0140-6736(08)61074-0.
8
Evaluation of the efficacy, safety and tolerability of orally administered BI 409306, a novel phosphodiesterase type 9 inhibitor, in two randomised controlled phase II studies in patients with prodromal and mild Alzheimer's disease.评价新型磷酸二酯酶 9 抑制剂 BI 409306 口服制剂在伴有前驱期和轻度阿尔茨海默病的患者中进行的两项随机对照 2 期研究中的疗效、安全性和耐受性。
Alzheimers Res Ther. 2019 Feb 12;11(1):18. doi: 10.1186/s13195-019-0467-2.
9
Safety, efficacy, and biomarker findings of PBT2 in targeting Abeta as a modifying therapy for Alzheimer's disease: a phase IIa, double-blind, randomised, placebo-controlled trial.PBT2靶向β淀粉样蛋白作为阿尔茨海默病修饰疗法的安全性、有效性及生物标志物研究结果:一项IIa期、双盲、随机、安慰剂对照试验
Lancet Neurol. 2008 Sep;7(9):779-86. doi: 10.1016/S1474-4422(08)70167-4. Epub 2008 Jul 30.
10
Optimal dosing of galantamine in patients with mild or moderate Alzheimer's disease: post Hoc analysis of a randomized, double-blind, placebo-controlled trial.轻度或中度阿尔茨海默病患者加兰他敏的最佳剂量:一项随机、双盲、安慰剂对照试验的事后分析
Drugs Aging. 2009;26(3):231-9. doi: 10.2165/00002512-200926030-00004.

引用本文的文献

1
Emerging strategies, applications and challenges of targeting NAD in the clinic.临床中靶向烟酰胺腺嘌呤二核苷酸(NAD)的新兴策略、应用及挑战
Nat Aging. 2025 Sep 9. doi: 10.1038/s43587-025-00947-6.
2
Investigating the Correlation Between Gray Matter Volume Changes and Cognitive Function Among Alzheimer's Disease Patients: An MRI-Based Analysis.阿尔茨海默病患者灰质体积变化与认知功能的相关性研究:基于磁共振成像的分析
Actas Esp Psiquiatr. 2025 Aug;53(4):756-765. doi: 10.62641/aep.v53i4.1914.
3
Diagnostic and inclusion criteria in Alzheimer's disease clinical trials: A systematic review of the past decade.

本文引用的文献

1
Compromised autophagy and mitophagy in brain ageing and Alzheimer's diseases.大脑衰老和阿尔茨海默病中自噬和线粒体自噬受损。
Aging Brain. 2022 Nov 24;2:100056. doi: 10.1016/j.nbas.2022.100056. eCollection 2022.
2
Combined metabolic activators improve metabolic functions in the animal models of neurodegenerative diseases.联合代谢激活剂可改善神经退行性疾病动物模型的代谢功能。
Life Sci. 2023 Feb 1;314:121325. doi: 10.1016/j.lfs.2022.121325. Epub 2022 Dec 26.
3
The niacin receptor HCAR2 modulates microglial response and limits disease progression in a mouse model of Alzheimer's disease.
阿尔茨海默病临床试验的诊断与纳入标准:对过去十年的系统评价
J Alzheimers Dis Rep. 2025 Jul 30;9:25424823251362444. doi: 10.1177/25424823251362444. eCollection 2025 Jan-Dec.
4
Pathological mechanisms and treatment progression of Alzheimer's disease.阿尔茨海默病的病理机制与治疗进展
Eur J Med Res. 2025 Jul 14;30(1):625. doi: 10.1186/s40001-025-02886-9.
5
Beneficial Effects of Traditional Fermented Soybean Sauce (Kanjang) on Memory Function, Body Water, and Glucose Metabolism: Roles of Gut Microbiota and Neuroinflammation.传统发酵酱油(甘酱)对记忆功能、身体水分及葡萄糖代谢的有益作用:肠道微生物群与神经炎症的作用
Nutrients. 2025 May 8;17(10):1617. doi: 10.3390/nu17101617.
6
Presence of chronic morbidities alters skeletal muscle health and amino acid kinetics in mild cognitive impairment.慢性疾病的存在会改变轻度认知障碍患者的骨骼肌健康和氨基酸动力学。
J Alzheimers Dis. 2025 Jun;105(4):1413-1431. doi: 10.1177/13872877251336618. Epub 2025 May 4.
7
Advances in research on mitochondrial dysfunction in neurodegenerative diseases.神经退行性疾病中线粒体功能障碍的研究进展
J Neurol. 2025 Apr 28;272(5):364. doi: 10.1007/s00415-025-13101-4.
8
Extracellular vesicles as therapeutic modulators of neuroinflammation in Alzheimer's disease: a focus on signaling mechanisms.细胞外囊泡作为阿尔茨海默病神经炎症的治疗调节剂:聚焦信号传导机制
J Neuroinflammation. 2025 Apr 25;22(1):120. doi: 10.1186/s12974-025-03443-1.
9
Modeling for understanding and engineering metabolism.用于理解和设计新陈代谢的建模。
QRB Discov. 2025 Feb 18;6:e11. doi: 10.1017/qrd.2025.1. eCollection 2025.
10
Antiageing strategy for neurodegenerative diseases: from mechanisms to clinical advances.神经退行性疾病的抗衰老策略:从机制到临床进展
Signal Transduct Target Ther. 2025 Mar 10;10(1):76. doi: 10.1038/s41392-025-02145-7.
烟酸受体HCAR2调节小胶质细胞反应并限制阿尔茨海默病小鼠模型中的疾病进展。
Sci Transl Med. 2022 Mar 23;14(637):eabl7634. doi: 10.1126/scitranslmed.abl7634.
4
Amelioration of Alzheimer's disease pathology by mitophagy inducers identified via machine learning and a cross-species workflow.通过机器学习和跨物种工作流程鉴定的诱导细胞自噬改善阿尔茨海默病病理学。
Nat Biomed Eng. 2022 Jan;6(1):76-93. doi: 10.1038/s41551-021-00819-5. Epub 2022 Jan 6.
5
Combined metabolic activators therapy ameliorates liver fat in nonalcoholic fatty liver disease patients.联合代谢激活剂治疗可改善非酒精性脂肪性肝病患者的肝脂肪。
Mol Syst Biol. 2021 Oct;17(10):e10459. doi: 10.15252/msb.202110459.
6
NAD supplementation reduces neuroinflammation and cell senescence in a transgenic mouse model of Alzheimer's disease via cGAS-STING.NAD 补充通过 cGAS-STING 减少阿尔茨海默病转基因小鼠模型中的神经炎症和细胞衰老。
Proc Natl Acad Sci U S A. 2021 Sep 14;118(37). doi: 10.1073/pnas.2011226118.
7
Combined Metabolic Activators Accelerates Recovery in Mild-to-Moderate COVID-19.联合代谢激活剂可加速轻度至中度 COVID-19 的康复。
Adv Sci (Weinh). 2021 Sep;8(17):e2101222. doi: 10.1002/advs.202101222. Epub 2021 Jun 28.
8
The significance of sialylation on the pathogenesis of Alzheimer's disease.唾液酸化在阿尔茨海默病发病机制中的意义。
Brain Res Bull. 2021 Aug;173:116-123. doi: 10.1016/j.brainresbull.2021.05.009. Epub 2021 May 12.
9
iNetModels 2.0: an interactive visualization and database of multi-omics data.iNetModels 2.0:一个多组学数据的交互式可视化和数据库。
Nucleic Acids Res. 2021 Jul 2;49(W1):W271-W276. doi: 10.1093/nar/gkab254.
10
Metabolic Profiling of Female Tg2576 Mouse Brains Provides Novel Evidence Supporting Intranasal Low-Dose Pioglitazone for Long-Term Treatment at an Early Stage of Alzheimer's Disease.雌性Tg2576小鼠大脑的代谢谱分析提供了新证据,支持在阿尔茨海默病早期阶段使用鼻内低剂量吡格列酮进行长期治疗。
Biomedicines. 2020 Dec 9;8(12):589. doi: 10.3390/biomedicines8120589.