Reduced blood flow response to acetazolamide reflects pre-existing vasodilation and decreased oxygen metabolism in major cerebral arterial occlusive disease
被引:0
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作者:
Hiroshi Yamauchi
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机构:Research Institute,
Hiroshi Yamauchi
Hidehiko Okazawa
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h-index: 0
机构:Research Institute,
Hidehiko Okazawa
Yoshihiko Kishibe
论文数: 0引用数: 0
h-index: 0
机构:Research Institute,
Yoshihiko Kishibe
Kanji Sugimoto
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机构:Research Institute,
Kanji Sugimoto
Masaaki Takahashi
论文数: 0引用数: 0
h-index: 0
机构:Research Institute,
Masaaki Takahashi
机构:
[1] Research Institute,
[2] Shiga Medical Center,undefined
[3] 5–4-30 Moriyama,undefined
[4] Moriyama-city,undefined
[5] Shiga 524–8524,undefined
来源:
European Journal of Nuclear Medicine and Molecular Imaging
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2002年
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29卷
A decrease in the cerebral blood flow (CBF) response to acetazolamide may indicate an increase in cerebral blood volume (CBV) caused by reduced perfusion pressure in patients with major cerebral artery steno-occlusive lesions. However, a decrease in cerebral metabolic rate of oxygen (CMRO2) caused by ischemic changes may also decrease the CBF response to acetazolamide by decreasing the production of carbon dioxide. The purpose of this study was to determine whether the values of CBV and CMRO2 are independent predictors of the CBF response to acetazolamide in major cerebral arterial occlusive disease. We used positron emission tomography to study 30 patients with major cerebral artery steno-occlusive lesions. The CBF response to acetazolamide was assessed by measuring baseline CBF and CBF 10 min after an intravenous injection of 1 g of acetazolamide. Multivariate analysis was used to test the independent predictive value of the CBV and CMRO2 at baseline with respect to the percent change in CBF during acetazolamide administration. Both increased CBV and decreased CMRO2 were significant and independent predictors of the reduced CBF response to acetazolamide. CBV accounted for 25% of the variance in the absolute change in CBF during acetazolamide administration and 42% of the variance in the percent change in CBF, whereas CMRO2 accounted for 19% and 4% of the variance, respectively. In patients with major cerebral arterial occlusive disease, a decrease in CMRO2 may contribute to the reduced CBF response to acetazolamide, although an increase in CBV appears to be the major contributing factor.