Evolution of the Human Brain Can Help Determine Pathophysiology of Neurodevelopmental Disorders

The evolution of humans brought about a co-occurring evolution of the human brain, which is far larger and more complex than that of many other organisms. The brain has evolved characteristically in humans in many respects, including macro-and micro-anatomical changes in the brain structure, changes...

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Published in:Frontiers in neuroscience Vol. 16; p. 871979
Main Authors: Irie, Koichiro, Doi, Miyuki, Usui, Noriyoshi, Shimada, Shoichi
Format: Journal Article
Language:English
Published: Switzerland Frontiers Research Foundation 01-04-2022
Frontiers Media S.A
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Summary:The evolution of humans brought about a co-occurring evolution of the human brain, which is far larger and more complex than that of many other organisms. The brain has evolved characteristically in humans in many respects, including macro-and micro-anatomical changes in the brain structure, changes in gene expression, and cell populations and ratios. These characteristics are essential for the execution of higher functions, such as sociality, language, and cognition, which express humanity, and are thought to have been acquired over evolutionary time. However, with the acquisition of higher functions also comes the risk of the disease in which they fail. This review focuses on human brain evolution and neurodevelopmental disorders (NDDs) and discusses brain development, molecular evolution, and human brain evolution. Discussing the potential for the development and pathophysiology of NDDs acquired by human brain evolution will provide insights into the acquisition and breakdown of higher functions from a new perspective.
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This article was submitted to Neurodevelopment, a section of the journal Frontiers in Neuroscience
Reviewed by: Kei Hori, National Center of Neurology and Psychiatry, Japan
These authors have contributed equally to this work and share first authorship
Edited by: Toru Takumi, RIKEN Brain Science Institute (BSI), Japan
ISSN:1662-4548
1662-453X
1662-453X
DOI:10.3389/fnins.2022.871979