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本文引用的文献

1
Mechanisms underlying dorsolateral prefrontal cortex contributions to cognitive dysfunction in schizophrenia.背外侧前额叶皮层导致精神分裂症认知功能障碍的潜在机制。
Neuropsychopharmacology. 2022 Jan;47(1):292-308. doi: 10.1038/s41386-021-01089-0. Epub 2021 Jul 20.
2
Opportunities, barriers, and recommendations in down syndrome research.唐氏综合征研究中的机遇、障碍与建议
Transl Sci Rare Dis. 2021;5(3-4):99-129. doi: 10.3233/trd-200090. Epub 2021 Apr 15.
3
In vivo evidence of lower synaptic vesicle density in schizophrenia.精神分裂症中突触囊泡密度降低的体内证据。
Mol Psychiatry. 2021 Dec;26(12):7690-7698. doi: 10.1038/s41380-021-01184-0. Epub 2021 Jun 16.
4
White matter changes in psychosis risk relate to development and are not impacted by the transition to psychosis.精神病风险中的白质变化与发育有关,而与向精神病的转变无关。
Mol Psychiatry. 2021 Nov;26(11):6833-6844. doi: 10.1038/s41380-021-01128-8. Epub 2021 May 24.
5
Accelerated aging in the brain, epigenetic aging in blood, and polygenic risk for schizophrenia.大脑的加速衰老、血液中的表观遗传衰老和精神分裂症的多基因风险。
Schizophr Res. 2021 May;231:189-197. doi: 10.1016/j.schres.2021.04.005. Epub 2021 Apr 18.
6
Association of Age, Antipsychotic Medication, and Symptom Severity in Schizophrenia With Proton Magnetic Resonance Spectroscopy Brain Glutamate Level: A Mega-analysis of Individual Participant-Level Data.精神分裂症中年龄、抗精神病药物和症状严重程度与质子磁共振波谱脑谷氨酸水平的关联:个体参与者水平数据的荟萃分析。
JAMA Psychiatry. 2021 Jun 1;78(6):667-681. doi: 10.1001/jamapsychiatry.2021.0380.
7
Age-Specific Prevalence and Incidence of Dementia Diagnoses Among Older US Adults With Schizophrenia.年龄特异性患病率和发病率的老年美国成年人中精神分裂症的痴呆症诊断。
JAMA Psychiatry. 2021 Jun 1;78(6):632-641. doi: 10.1001/jamapsychiatry.2021.0042.
8
White matter brain aging in relationship to schizophrenia and its cognitive deficit.脑白质老化与精神分裂症及其认知缺陷的关系。
Schizophr Res. 2021 Apr;230:9-16. doi: 10.1016/j.schres.2021.02.003. Epub 2021 Mar 2.
9
Examining the independent and joint effects of genomic and exposomic liabilities for schizophrenia across the psychosis spectrum.探究精神分裂症基因组和外显子组负担在整个精神病谱中的独立和联合作用。
Epidemiol Psychiatr Sci. 2020 Nov 17;29:e182. doi: 10.1017/S2045796020000943.
10
Baseline Cortical Thickness Reductions in Clinical High Risk for Psychosis: Brain Regions Associated with Conversion to Psychosis Versus Non-Conversion as Assessed at One-Year Follow-Up in the Shanghai-At-Risk-for-Psychosis (SHARP) Study.首发精神病高危人群的皮层厚度基线降低:基于上海首发精神病高危人群研究(SHARP)一年随访的转换与非转换比较,探讨与转换至精神病相关的脑区。
Schizophr Bull. 2021 Mar 16;47(2):562-574. doi: 10.1093/schbul/sbaa127.

精神分裂症的神经退行性模型:越来越多的证据支持重新审视。

Neurodegenerative model of schizophrenia: Growing evidence to support a revisit.

机构信息

Harvard Medical School Department of Psychiatry at Beth Israel Deaconess Medical Center, Boston, MA, USA.

Shanghai Mental Health Center, School of Medicine, Shanghai Jiao Tong University, Shanghai, Shanghai, China; Department of Epidemiology, Columbia University Mailman School of Public Health, New York, NY, USA.

出版信息

Schizophr Res. 2022 May;243:154-162. doi: 10.1016/j.schres.2022.03.004. Epub 2022 Mar 25.

DOI:10.1016/j.schres.2022.03.004
PMID:35344853
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9189010/
Abstract

Multidimensional progressive declines in the absence of standard biomarkers for neurodegeneration are observed commonly in the development of schizophrenia, and are accepted as consistent with neurodevelopmental etiological hypotheses to explain the origins of the disorder. Far less accepted is the possibility that neurodegenerative processes are involved as well, or even that key dimensions of function, such as cognition and aspects of biological integrity, such as white matter function, decline in chronic schizophrenia beyond levels associated with normal aging. We propose that recent research germane to these issues warrants a current look at the question of neurodegeneration. We propose the view that a neurodegenerative hypothesis provides a better explanation of some features of chronic schizophrenia, including accelerated aging, than is provided by neurodevelopmental hypotheses. Moreover, we suggest that neurodevelopmental influences in early life, including those that may extend to later life, do not preclude the development of neurodegenerative processes in later life, including some declines in cognitive and biological integrity. We evaluate these views by integrating recent findings in representative domains such as cognition and white and gray matter integrity with results from studies on accelerated aging, together with functional implications of neurodegeneration for our understanding of chronic schizophrenia.

摘要

在精神分裂症的发展过程中,常观察到缺乏神经退行性变标准生物标志物的多维进行性下降,这被认为与解释该疾病起源的神经发育病因假说一致。但人们较少接受神经退行性过程也可能涉及,甚至在慢性精神分裂症中,认知等关键功能维度以及白质功能等生物学完整性方面的下降超出了与正常衰老相关的水平。我们提出,与这些问题相关的最新研究表明,目前有必要研究神经退行性变的问题。我们提出这样一种观点,即神经退行性假说比神经发育假说能更好地解释慢性精神分裂症的一些特征,包括加速衰老。此外,我们还认为,生命早期的神经发育影响,包括可能延伸到生命后期的影响,并不排除生命后期神经退行性过程的发展,包括认知和生物学完整性的某些下降。我们通过将认知和白质和灰质完整性等代表性领域的最近发现与加速衰老研究的结果,以及神经退行性变对我们理解慢性精神分裂症的功能意义相结合,来评估这些观点。