Department of Anthropology, Emory University, Atlanta, GA, USA.
Neurobiol Aging. 2013 Oct;34(10):2248-60. doi: 10.1016/j.neurobiolaging.2013.03.028. Epub 2013 Apr 24.
Among primates, humans are uniquely vulnerable to many age-related neurodegenerative disorders. We used structural and diffusion magnetic resonance imaging (MRI) to examine the brains of chimpanzees and rhesus monkeys across each species' adult lifespan, and compared these results with published findings in humans. As in humans, gray matter volume decreased with age in chimpanzees and rhesus monkeys. Also like humans, chimpanzees showed a trend for decreased white matter volume with age, but this decrease occurred proportionally later in the chimpanzee lifespan than in humans. Diffusion MRI revealed widespread age-related decreases in fractional anisotropy and increases in radial diffusivity in chimpanzees and macaques. However, both the fractional anisotropy decline and the radial diffusivity increase started at a proportionally earlier age in humans than in chimpanzees. Thus, even though overall patterns of gray and white matter aging are similar in humans and chimpanzees, the longer lifespan of humans provides more time for white matter to deteriorate before death, with the result that some neurological effects of aging may be exacerbated in our species.
在灵长类动物中,人类特别容易受到许多与年龄相关的神经退行性疾病的影响。我们使用结构和扩散磁共振成像(MRI)技术来研究黑猩猩和恒河猴在每个物种成年后的大脑,并将这些结果与已发表的人类研究结果进行比较。与人类一样,黑猩猩和恒河猴的灰质体积随年龄增长而减少。与人类一样,黑猩猩也表现出白质体积随年龄增长而减少的趋势,但这种减少在黑猩猩的寿命中出现的时间比人类晚。扩散 MRI 显示,黑猩猩和猕猴的各向异性分数和径向扩散率随年龄增长而普遍下降。然而,人类的各向异性分数下降和径向扩散率增加开始的年龄比例早于黑猩猩。因此,尽管人类和黑猩猩的灰质和白质老化的总体模式相似,但人类的寿命更长,为白质在死亡前恶化提供了更多时间,结果是我们物种的一些衰老的神经影响可能会加剧。