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ω-3 脂肪酸与阿尔茨海默病和轻度认知障碍的血液生物标志物:一项随机安慰剂对照试验。

Omega-3 fatty acids and blood-based biomarkers in Alzheimer's disease and mild cognitive impairment: A randomized placebo-controlled trial.

机构信息

Department of Psychiatry & Mind-Body Interface Laboratory (MBI-Lab), China Medical University Hospital, Taichung, Taiwan; College of Medicine, China Medical University, Taichung, Taiwan; Department of Psychiatry, Wei Gong Memorial Hospital, Miaoli, Taiwan.

Department of Psychiatry & Mind-Body Interface Laboratory (MBI-Lab), China Medical University Hospital, Taichung, Taiwan; Good Day Psychiatric Clinic, Taichung, Taiwan.

出版信息

Brain Behav Immun. 2022 Jan;99:289-298. doi: 10.1016/j.bbi.2021.10.014. Epub 2021 Oct 29.

Abstract

BACKGROUND

Increased serum levels of pro-inflammatory biomarkers are consistently associated with cognitive decline. The omega-3 unsaturated fatty acids (n-3 PUFAs) had been linked to slowing cognitive decline due to their potential anti-inflammatory effects. To our knowledge, the different regiments of pure DHA, pure EPA, and their combination on various associated symptoms of dementia, including a mild form of cognitive impairment (MCI) and Alzheimer's disease (AD), have never been studied.

METHODS

This multisite, randomized, double-blind, placebo-controlled trial was conducted at two veteran's retirement centers and one medical center in central Taiwan between 2013 and 2015. 163 MCI or AD patients were randomly assigned to placebo (n = 40), docosahexaenoic acid (DHA, 0.7 g/day, n = 41), eicosapentaenoic acid (EPA, 1.6 g/day, n = 40), or EPA (0.8 g/day) + DHA (0.35 g/day) (n = 42) group for 24 months. The results were measured as the cognitive and functional abilities, biochemical, and inflammatory cytokines profiles. Chi-square tests, two-sample t-test, ANOVA, and linear mixedeffects models were conducted with p < 0.05.

RESULTS

131 (80%) participants had completed the trial with all cognitive, functional, and mood status assessments. The statistically significant difference between the placebo and treatment groups was not determined, concerning the changes in cognitive, functional, and mood status scores, the biochemical profiles, and inflammatory cytokines levels. However, EPA was found to reduce the C-C motif ligands 4 (CCL4) level (p < 0.001). Additionally, EPA could reduce the constructional praxis (p < 0.05) and spoken language ability scores (p < 0.01), and DHA also reduced the spoken language ability score (p < 0.05).

CONCLUSION

Overall, n-3 PUFAs supplements did not reduce cognitive, functional, and depressive symptom outcomes, but spoken language ability and constructional praxis subitems of ADAS-cog. These findings show that attention to clinical heterogeneity in dementia is crucial when studying nutrients interventions, such as n-3 PUFAs. In addition, with small effect size CCL4 is a better indicator than other inflammatory cytokines for EPA treatment response.

摘要

背景

血清中促炎生物标志物水平升高与认知能力下降密切相关。由于具有潜在的抗炎作用,ω-3 不饱和脂肪酸(n-3PUFAs)已被证明可以减缓认知能力下降。据我们所知,DHA 纯品、EPA 纯品及其组合的不同方案对痴呆相关的各种症状(包括轻度认知障碍(MCI)和阿尔茨海默病(AD))的影响从未被研究过。

方法

本研究是一项多中心、随机、双盲、安慰剂对照试验,于 2013 年至 2015 年在台湾中部的两个退伍军人退休中心和一家医疗中心进行。共有 163 名 MCI 或 AD 患者被随机分配至安慰剂(n=40)、二十二碳六烯酸(DHA,0.7g/天,n=41)、二十碳五烯酸(EPA,1.6g/天,n=40)或 EPA(0.8g/天)+DHA(0.35g/天)(n=42)组,治疗 24 个月。以认知和功能能力、生化和炎症细胞因子谱为观察指标。采用卡方检验、两样本 t 检验、方差分析和线性混合效应模型,p<0.05 为差异有统计学意义。

结果

共有 131 名(80%)参与者完成了所有认知、功能和情绪状态评估的试验。在认知、功能和情绪状态评分、生化谱和炎症细胞因子水平方面,安慰剂组和治疗组之间的统计学差异无显著性。然而,EPA 可降低 C 型凝集素 4(CCL4)水平(p<0.001)。此外,EPA 可降低结构练习(p<0.05)和口语语言能力评分(p<0.01),DHA 也可降低口语语言能力评分(p<0.05)。

结论

总的来说,n-3PUFAs 补充剂并不能降低认知、功能和抑郁症状的结局,但可降低 ADAS-cog 的口语语言能力和结构练习亚项。这些发现表明,在研究营养干预(如 n-3PUFAs)时,应注意痴呆症的临床异质性。此外,与其他炎症细胞因子相比,小效应量的 CCL4 是 EPA 治疗反应的更好指标。

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