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脱盐盐角草乙醇提取物(PM-EE)对主诉记忆功能障碍但无痴呆的受试者的影响:一项 12 周、随机、双盲、安慰剂对照临床试验。

Effect of desalted Salicornia europaea L. ethanol extract (PM-EE) on the subjects complaining memory dysfunction without dementia: a 12 week, randomized, double-blind, placebo-controlled clinical trial.

机构信息

Department of Neurology, Seoul National University Hospital, 101 Daehak-ro, Jongno-gu, Seoul, 110-744, South Korea.

Center for Hospital Medicine, Department of Neurosurgery, Seoul, Republic of Korea.

出版信息

Sci Rep. 2020 Nov 16;10(1):19914. doi: 10.1038/s41598-020-76938-x.

Abstract

Desalted Salicornia europaea L. (SE) inhibits acetylcholine esterase, attenuates oxidative stress and inflammatory cytokines, and activates neurotrophic pathway. We performed 12-week, randomized, double-blind, placebo-controlled study to evaluate the efficacy of PhytoMeal(a desalted SE)-ethanol extract (PM-EE), in improving the cognitive performance in patients with subjective memory impairment. 63 participants complaining memory dysfunction without dementia (Korean Mini-Mental State Examination [K-MMSE] score ≥ 23) were assigned to PM-EE 600 mg/day or placebo. The cognitive domain of the Alzheimer's disease assessment scale-Korean version (ADAS-K) was set as the primary outcome. After 12 weeks, there was no differences in the changes in the primary outcome or the frequency of adverse events between the groups. In the subgroup analysis for the 30 subjects with mild cognitive impairment (MCI, baseline K-MMSE scores ≤ 28), PM-EE significantly improved the color-reading score of the Korean color-word stroop test (8.2 ± 25.0 vs. - 4.7 ± 13.2, P = 0.018). Our findings suggest that PM-EE is safe but might not be effective in this setting of this study. However, PM-EE may improve the frontal executive function in the patients with MCI. Further large-sized studies with longer follow-up period is warranted (trial registration number KCT0003418).

摘要

脱盐盐角草(SE)抑制乙酰胆碱酯酶,减轻氧化应激和炎症细胞因子,并激活神经营养途径。我们进行了为期 12 周的随机、双盲、安慰剂对照研究,以评估 PhytoMeal(一种脱盐 SE-乙醇提取物)(PM-EE)改善有主观记忆障碍的患者认知功能的疗效。63 名抱怨记忆障碍但无痴呆(韩国迷你精神状态检查[K-MMSE]评分≥23)的参与者被分配到 PM-EE 600mg/天或安慰剂。阿尔茨海默病评估量表-韩国版(ADAS-K)的认知域被设定为主要结局。12 周后,两组主要结局或不良事件的发生率均无差异。在 30 名轻度认知障碍(MCI,基线 K-MMSE 评分≤28)患者的亚组分析中,PM-EE 显著改善了韩国颜色词斯特鲁普测试的颜色阅读分数(8.2±25.0 与-4.7±13.2,P=0.018)。我们的研究结果表明,PM-EE 是安全的,但在本研究的这种情况下可能无效。然而,PM-EE 可能改善 MCI 患者的额叶执行功能。需要进一步进行更大规模、随访时间更长的研究(试验注册号 KCT0003418)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f39/7670404/a173064052fa/41598_2020_76938_Fig1_HTML.jpg

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