Germinal matrix hemorrhage (GMH) occurs in approximately 45% of very low birth weight neonates. Slightly more than 1% of live births in the U.S. weigh less that 1.5_kg, thus it can be estimated that GMH affects 10,000 neonates annually. These babies will account for 30% of patients who will later exhibit cerebral palsy. GMH will continue to be a perplexing medical problem due to technological advances allowing survival of very premature babies, and socioeconomic conditions associated with their births. Little is known concerning specific factors and mechanisms involved in the development of GMH. Recent discussion of the physiologic factors predisposing to GMH concern unstable arterial blood pressure, ischemic brain injury, and wide swings in venous pressure. Certain large, fragile germinal matrix (GM) periventricular vascular """"""""channels"""""""" from which bleeding often occurs have been characterized as """"""""veins,"""""""" """"""""capillary sinusoids,"""""""" or """"""""a vascular rete."""""""" Previous investigations of the vascular anatomy of the GM are flawed. In ordinary neuropathological techniques, the sections are too thin to trace vessels; furthermore, veins cannot be discriminated from arteries because these immature vessels do not have mural smooth muscle or collagen. Studies employing intravascular injection into cadaveric vasculature produce an unintelligible mass of vessels and artifacts. Errors in this basic concept may have adversely influenced strategies for the salvage of these babies. Clearly, innovative techniques are required to investigate the nature of vascular morphology and pathology in the neonate with GMH. The native alkaline phosphatase (AP) ectoenzyme, present in the endothelial plasma cell membrane of small arteries, arterioles, and capillaries, but not of venule/veins, can be exploited to differentially stain the GM vasculature in thick celloidin sections. This histochemical technique is superior to injection methods of outlining vasculature because it avoids artifacts of injection and the background tissue can be examined with counterstains. The broad objective of this study is to characterize the GM angioarchitecture, identify the precise site(s) of bleeding, and determine the ultimate fate of the immature GM sinusoids with AP staining and thick celloidin sections in the brains from 40 pediatric subjects ranging from 22- to 40-weeks' post-conception age.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS036780-05
Application #
6539942
Study Section
Neurology A Study Section (NEUA)
Program Officer
Hicks, Ramona R
Project Start
1998-07-03
Project End
2005-06-30
Budget Start
2002-07-01
Budget End
2005-06-30
Support Year
5
Fiscal Year
2002
Total Cost
$288,356
Indirect Cost
Name
Wake Forest University Health Sciences
Department
Radiation-Diagnostic/Oncology
Type
Schools of Medicine
DUNS #
937727907
City
Winston-Salem
State
NC
Country
United States
Zip Code
27157
Brown, W R; Thore, C R (2011) Review: cerebral microvascular pathology in ageing and neurodegeneration. Neuropathol Appl Neurobiol 37:56-74
Brown, William R (2010) A review of string vessels or collapsed, empty basement membrane tubes. J Alzheimers Dis 21:725-39
Brown, William R; Moody, Dixon M; Thore, Clara R et al. (2009) Microvascular changes in the white mater in dementia. J Neurol Sci 283:28-31
Brown, William R (2009) Association of preterm birth with brain malformations. Pediatr Res 65:642-6
Anstrom, John A; Thore, Clara R; Moody, Dixon M et al. (2007) Immunolocalization of tight junction proteins in blood vessels in human germinal matrix and cortex. Histochem Cell Biol 127:205-13
Thore, Clara R; Anstrom, John A; Moody, Dixon M et al. (2007) Morphometric analysis of arteriolar tortuosity in human cerebral white matter of preterm, young, and aged subjects. J Neuropathol Exp Neurol 66:337-45
Moody, Dixon M (2006) The blood-brain barrier and blood-cerebral spinal fluid barrier. Semin Cardiothorac Vasc Anesth 10:128-31
Anstrom, John A; Thore, Clara R; Moody, Dixon M et al. (2005) Germinal matrix cells associate with veins and a glial scaffold in the human fetal brain. Brain Res Dev Brain Res 160:96-100
Anstrom, John A; Thore, Clara R; Moody, Dixon M et al. (2005) Morphometric assessment of collagen accumulation in germinal matrix vessels of premature human neonates. Neuropathol Appl Neurobiol 31:181-90
Anstrom, John A; Brown, William R; Moody, Dixon M et al. (2004) Subependymal veins in premature neonates: implications for hemorrhage. Pediatr Neurol 30:46-53

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