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Volume 16, Issue 4, Pages 226-236 (December 2009)


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A History of Our Understanding of Cerebral Vascular Development and Pathogenesis of Perinatal Brain Damage Over the Past 30 Years

Sachio Takashima, MDCorresponding Author Informationemail address, Masayuki Itoh, MD, Akira Oka, MD

This article reviews our studies focusing on cerebral vascular development, the pathogenesis of subependymal/intraventricular hemorrhage (SEH/IVH), periventricular leukomalacia (PVL), and pontosubicular neuron necrosis (PSN). Their pathogenesis consists of predisposing developmental and causal factors. SEH/IVH may be caused by reperfusion or overperfusion following ischemia in the subependymal germinal matrix with characteristic vasculature. The cause of PVL is multifactorial (ie, ischemia and inflammation), predisposed by the maturational status of the vasculature and oligodendroglia in the white matter. Focal PVL is ischemic necrosis, and diffuse PVL or white matter injury may include cytotoxic damage. PSN has an apoptotic character, and may be induced by ischemic and oxidative stress on specific immature neurons. Further studies on preventive and therapeutic measures are necessary in clinical, pathologic, and experimental fields. The monitoring and control methods of brain hemodynamics and cellular stability should be more developed to prevent brain damages.

 Yanagawa Institute for Developmental Disabilities, International University of Health and Welfare, Fukuoka, Japan

 Division of Mental Retardation and Birth Defect Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Kodaira, Tokyo, Japan

 Department of Pediatrics, Kyorin University Faculty of Medicine, Tokyo, Japan

Corresponding Author InformationAddress reprint requests to Sachio Takashima, Yanagawa Institute for Developmental Disabilities, 284-2 Kamimiyanaga-machi, Yanagawa, Fukuoka 832-0059, Japan

PII: S1071-9091(09)00062-X

doi:10.1016/j.spen.2009.09.004


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