Departments of Medicine and Neurology, University of California, Los Angeles, CA 90095, USA.
J Nutr. 2010 Apr;140(4):869-74. doi: 10.3945/jn.109.113910. Epub 2010 Feb 24.
The risk for dementia, a major contributor to incapacitation and institutionalization, rises rapidly as we age, doubling every 5 y after age 65. Tens of millions of new Alzheimer's disease (AD) and other dementia cases are projected as elderly populations increase around the world, creating a projected dementia epidemic for which most nations are not prepared. Thus, there is an urgent need for prevention approaches that are safe, effective, and affordable. This review addresses the potential of one promising candidate, the (n-3) fatty acid docosahexaenoic acid (DHA), which appears to slow pathogenesis of AD and possibly vascular dementia. DHA is pleiotropic, acting at multiple steps to reduce the production of the beta-amyloid peptide, widely believed to initiate AD. DHA moderates some of the kinases that hyperphosphorylate the tau-protein, a component of the neurofibrillary tangle. DHA may help suppress insulin/neurotrophic factor signaling deficits, neuroinflammation, and oxidative damage that contribute to synaptic loss and neuronal dysfunction in dementia. Finally, DHA increases brain levels of neuroprotective brain-derived neurotrophic factor and reduces the (n-6) fatty acid arachidonate and its prostaglandin metabolites that have been implicated in promoting AD. Clinical trials suggest that DHA or fish oil alone can slow early stages of progression, but these effects may be apolipoprotein E genotype specific, and larger trials with very early stages are required to prove efficacy. We advocate early intervention in a prodromal period with nutrigenomically defined subjects with an appropriately designed nutritional supplement, including DHA and antioxidants.
痴呆症是导致失能和住院的主要原因,随着年龄的增长,其风险迅速上升,65 岁以后每 5 年翻一番。随着全球老年人口的增加,预计会有数千万例新的阿尔茨海默病(AD)和其他痴呆病例,这将导致预计的痴呆症流行,而大多数国家对此都没有准备。因此,迫切需要安全、有效和负担得起的预防方法。本综述探讨了一种有前途的候选药物——(n-3)脂肪酸二十二碳六烯酸(DHA)的潜力,它似乎可以减缓 AD 和可能的血管性痴呆的发病机制。DHA 具有多效性,可通过多种途径减少β-淀粉样肽的产生,β-淀粉样肽被广泛认为是 AD 的起始因素。DHA 可以调节一些使tau 蛋白过度磷酸化的激酶,tau 蛋白是神经原纤维缠结的一个组成部分。DHA 可能有助于抑制胰岛素/神经营养因子信号转导缺陷、神经炎症和氧化损伤,这些损伤导致痴呆症中的突触丧失和神经元功能障碍。最后,DHA 可以增加大脑中神经保护因子脑源性神经营养因子的水平,并减少(n-6)脂肪酸花生四烯酸及其被认为会促进 AD 的前列腺素代谢物。临床试验表明,DHA 或鱼油单独使用可以减缓早期进展,但这些效果可能与载脂蛋白 E 基因型特异性有关,需要进行更大规模的早期临床试验来证明其疗效。我们提倡在有先兆期对具有适当设计的营养补充剂(包括 DHA 和抗氧化剂)进行营养基因组学定义的个体进行早期干预。