为什么Omega-3多不饱和脂肪酸在阿尔茨海默病预防研究中产生不同结果的原因

A. Fonteh
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引用次数: 3

摘要

阿尔茨海默病(AD)的典型异常衰老伴随着记忆和认知缺陷,干扰日常活动。随着科学家们寻找治疗AD的原因和方法,ω-3(n-3)多不饱和脂肪酸(PUFA)因其在大脑功能中的重要性和在AD中的消耗而变得越来越重要[1]。一个直接的补救措施是饮食补充剂研究,不幸的是,这些研究结果喜忧参半。令人困惑的问题是,为什么一些研究取得了有益的结果,而另一些研究对AD相关的认知或记忆问题没有影响。造成这些差异的因素包括对PUFA代谢途径的不完全理解和研究设计不足。大多数发现是基于流行病学观察,而不是安慰剂对照干预研究。通过检查这些研究,很明显,结果的任何改善都必须包括更好地了解ω-3脂肪酸代谢、初步临床观察的标准化、确保ω-3补充剂的药物质量,以及基于遗传学的研究参与者选择,并结合可量化的结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Reasons Why Omega-3 Polyunsaturated Fatty Acids Produce Mixed Results in Alzheimer's Disease Prevention Studies
Abnormal aging that epitomizes Alzheimer’s disease (AD) is accompanied by memory and cognitive deficits that interfere with daily activities. As scientists look for causes and means of treating AD, omega-3 (n-3) polyunsaturated fatty acids (PUFA) are gaining significance because of their importance in brain function and their depletion in AD [1]. A direct remedy is dietary supplementation studies that have unfortunately yielded mixed results. The perplexing question is why some studies have beneficial outcomes while others report no effects on AD-associated cognitive or memory problems. Factors that may account for these discrepancies include an incomplete understanding of PUFA metabolic pathways and inadequate study design. Most findings are based on epidemiological observations rather than placebo-controlled intervention studies. From examining these studies, it is evident that any improvement in the outcome must include a better understanding of omega-3 fatty acid metabolism, standardization of initial clinical observations, assurance of pharmaceutical quality of omega-3 supplements, and genetics based selection of study participants combined with quantifiable outcomes.
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