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精神分裂症是一种神经退行性疾病吗?来自精神分裂症患者及匹配的非精神疾病对照者大脑中脑源性神经营养因子随年龄下降的证据。

Is schizophrenia a neurodegenerative disease? Evidence from age-related decline of brain-derived neurotrophic factor in the brains of schizophrenia patients and matched nonpsychiatric controls.

作者信息

Rao Jagadeesh, Chiappelli Joshua, Kochunov Peter, Regenold William T, Rapoport Stanley I, Hong L Elliot

机构信息

Brain Physiology and Metabolism Section, Laboratory of Neurosciences, National Institute on Aging, National Institutes of Health, Bethesda, Md., USA.

出版信息

Neurodegener Dis. 2015;15(1):38-44. doi: 10.1159/000369214. Epub 2014 Dec 17.

Abstract

BACKGROUND

Brain-derived neurotrophic factor (BDNF) protein levels decline in the brain during senescence and are also shown to be reduced in schizophrenia patients. BDNF is present in both the gray and white matters of the brain. It is unclear whether BDNF abnormalities in schizophrenia are specific to gray and/or white matter.

OBJECTIVE

We hypothesized that the age-related BDNF decline is abnormal and contributes to the reduced BDNF in schizophrenia.

METHODS

We tested this hypothesis by measuring BDNF protein levels in postmortem gray and white matter, using the prefrontal cortex (PFC) and the genu of the corpus callosum as regions of interests, from 20 schizophrenia patients and 20 matched nonpsychiatric controls. Samples were selected across the adult lifespan--from 20 to 80 years of age.

RESULTS

PFC gray matter BDNF protein levels were significantly lower in older age in both nonpsychiatric comparisons and patients, while BDNF in white matter did not decrease significantly with age in either group. PFC BDNF was linearly lower from 20 to 80 years of age in nonpsychiatric comparisons. In schizophrenia, the age effect was similarly linear in younger patients but a decline did not occur in older patients.

CONCLUSION

PFC BDNF does not follow a normative linear age effect in schizophrenia patients as they grow older, which may represent a 'floor effect' due to earlier decline or a survivor cohort of older patient donors who are less susceptible to a schizophrenia-related pathological aging process.

摘要

背景

脑源性神经营养因子(BDNF)蛋白水平在衰老过程中会在大脑中下降,并且在精神分裂症患者中也显示降低。BDNF存在于大脑的灰质和白质中。目前尚不清楚精神分裂症中BDNF异常是否特定于灰质和/或白质。

目的

我们假设与年龄相关的BDNF下降是异常的,并且导致了精神分裂症患者BDNF的降低。

方法

我们通过测量20例精神分裂症患者和20例匹配的非精神科对照的死后灰质和白质中的BDNF蛋白水平来检验这一假设,使用前额叶皮质(PFC)和胼胝体膝部作为感兴趣区域。样本选取了20至80岁的整个成年寿命阶段。

结果

在非精神科对照和患者中,年龄较大时PFC灰质BDNF蛋白水平均显著降低,而两组中白质BDNF水平均未随年龄显著下降。在非精神科对照中,20至80岁期间PFC BDNF呈线性降低。在精神分裂症中,年龄效应在年轻患者中同样呈线性,但老年患者中未出现下降。

结论

随着年龄增长,精神分裂症患者的PFC BDNF不遵循正常的线性年龄效应,这可能代表由于早期下降导致的“下限效应”,或者是对精神分裂症相关病理衰老过程不太敏感的老年患者供体的幸存者队列。

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