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Stroke. 2005;36:193-195
Published online before print December 29, 2004, doi: 10.1161/01.STR.0000153064.41332.f6
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(Stroke. 2005;36:193.)
© 2005 American Heart Association, Inc.


Advances in Stroke 2004

Adult or Perinatal Brain Injury

Does Sex Matter?

Patricia D. Hurn, PhD; Susan J. Vannucci, PhD Henrik Hagberg, MD, PhD

From Anesthesiology and Perioperative Medicine (P.D.H.), Oregon Health Sciences University, Portland, Ore; the Department of Pediatrics (S.J.V.), Columbia Presbyterian University, New York, NY; and the Perinatal Center (H.H.), Sahlgrenska University Hospital, Goteborg, Sweden.

Correspondence to Dr Patricia D. Hurn, Professor and Vice Chairman for Research, Anesthesiology and Perioperative Medicine, Oregon Health Sciences University, 3181 SW Sam Jackson Pk Rd, UHS-2, Portland OR 97239-3098. E-mail hurnp@ohsu.edu


Key Words: Advances in Stroke • hypoxia-ischemia, brain • ischemia • poly (ADP-ribose) polymerase • sex


An extract of the first 250 words of the full text is provided, because this article has no abstract.
 


*    Introduction
 
Biological sex and sex-defining steroids are strikingly under-rated as modulators of cerebral ischemic cell death. In adults, male sex has been long identified as a risk factor for clinical stroke, yet the biology behind this fact remains veiled. We know that overall stroke incidence is lower in women than in men, across widely varying ethnic and cultural backgrounds.1 Newer glimpses into this sexual dimorphism indicate that women continue to sustain lower stroke rates until beyond the menopausal years, suggesting that hormonal factors are not solely responsible. For example, stroke rates in female subjects of the Northern Manhattan Stroke Study did not exceed those of men until aged ≥85 years.2 Importantly, data from sex-stratified preclinical studies indicate that stroke sensitivity (the damage resulting when an ischemic insult occurs) is also sexually dimorphic in adults. It is less clear if ischemic injury in the developing brain develops differently in males and females. However, provocative new evidence from cells cultured directly from fetal or newborn brain suggests that mechanisms of cell death are not identical in cells that are genetically male (XY) versus female (XX). This article evaluates linkages between sex, sex steroids, and neuroprotection throughout life.


*    Adult Brain Injury Is Sexually Dimorphic
 
The presence of a male "ischemia-sensitive" phenotype has been suggested in a wide variety of animal studies. One of the most impressive early studies included >2000 animals.3 Yamori et al showed that life expectancy was longer in female spontaneously hypertensive stroke-prone rats, and the development of cerebral hemorrhage and vascular lesions was attenuated relative to male . . . [Full Text of this Article]




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