Journal of Nuclear Medicine Vol. 44 No. 4 520-525
© 2003 by Society of Nuclear Medicine
Quantitative Measurement of Regional Cerebrovascular Reactivity to Acetazolamide Using 123I-N-Isopropyl-p-Iodoamphetamine Autoradiography with SPECT: Validation Study Using H215O with PET
Kuniaki Ogasawara, MD1,2,
Hiroshi Ito, MD3,
Masayuki Sasoh, MD1,2,
Taku Okuguchi, MD1,2,
Masakazu Kobayashi, MD1,2,
Hirotsugu Yukawa, MD1,2,
Kazunori Terasaki, PhD2 and
Akira Ogawa, MD1,2
1 Department of Neurosurgery, Iwate Medical University, Morioka, Japan
2 Cyclotron Research Center, Iwate Medical University, Morioka, Japan
3 Department of Radiology and Nuclear Medicine, Akita Research Institute of Brain and Blood Vessels, Akita, Japan
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ABSTRACT
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A simplified technique using 123I-N-isopropyl-p-iodoamphetamine (123I-IMP) autoradiography (ARG) with SPECT has been proposed recently for quantifying regional cerebral blood flow (rCBF). To validate the accuracy of 123I-IMP-ARG for quantifying regional cerebrovascular reactivity (rCVR) to acetazolamide, we compared rCVR determined using 123I-IMP-ARG with that determined using H215O PET. Methods: Thirty-nine patients with chronic stenoocclusive disease in a unilateral major cerebral artery underwent SPECT and PET studies before and after intravenous administration of acetazolamide. The rCBF images in the 4 conditions in each patient were calculated according to the ARG method. The same standard input function and the same distribution volume of 35 mL/mL were used in the calculation of rCBF images using the 123I-IMP-ARG method at resting state and with acetazolamide challenge. One large cortical region of interest (ROI) for a unilateral middle cerebral artery territory was bilaterally determined on each standardized summed rCBF image. On the basis of the rCBF values in each ROI, rCVR to acetazolamide was calculated as follows: rCVR (%) = ([acetazolamide challenge rCBF - resting rCBF]/resting rCBF) x 100. Results: Significant correlation was observed between rCVR values obtained using 123I-IMP-ARG and H215O PET methods in the 78 ROIs examined in the 39 patients (r = 0.820; P < 0.0001). When a rCVR lower than the mean - 2 SD of values obtained in healthy volunteers (18.4% for 123I-IMP-ARG and 18.2% for H215O PET) was defined as reduced, and when the H215O PET method was assumed to represent the true determinant of rCVR, 123I-IMP-ARG was 90% sensitive and 92% specific and displayed an 87% positive predictive value for detecting patients with reduced rCVR. Conclusion: These findings demonstrate that 123I-IMP-ARG methods accurately quantify rCVR and can adequately define subgroups of patients with reduced rCVR.
Key Words: cerebral blood flow quantitation cerebrovascular reactivity brain SPECT 123I-N-isopropyl-p-iodoamphetamine
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INTRODUCTION
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Evaluation of the regional cerebrovascular reactivity (rCVR) to a cerebral vasodilatory stimulus is important in the investigation of patients with ischemic cerebrovascular disease. Qualitative or quantitative measurement of regional cerebral blood flow (rCBF) using SPECT with 99mTc- hexamethylpropyleneamine oxime, 99mTc-ethylcysteinate dimer, 123I-N-isopropyl-p-iodoamphetamine (123I-IMP), or 133Xe has been widely used for assessing rCVR (16). Recent prospective studies have demonstrated that rCVR to acetazolamide determined quantitatively by 133Xe SPECT can predict the outcome of major cerebral arterial occlusive disease (7,8), whereas Yokota et al. (9) reported a prospective study using qualitative measurement of rCVR to acetazolamide with 123I-IMP SPECT that failed to find an association between hemodynamic failure and stroke risk. As Yonas et al. (10,11) indicated, qualitative assessment of acetazolamide reactivity is known to have low sensitivity and specificity for detecting patients with a compromised reserve. These authors reported that the positive predictive value of the qualitative methods was 50%. Therefore, the possibility arises that the acetazolamide reactivity of some patients has been incorrectly classified by qualitative analysis.
Recently, a simplified technique known as 123I-IMPautoradiography (ARG), which requires only 1-point arterial blood sampling and the acquisition of a single static scan, has been developed to quantify rCBF using 123I-IMP and SPECT (12,13). The 123I-IMP-ARG method is based on the 2-compartment model for tracer kinetics. The method uses a standard arterial input calibrated by the radioactivity of a single arterial whole-blood sample, a standard lipophilic fraction of 123I-IMP in whole blood, and a fixed distribution volume (Vd) of 123I-IMP. Previous studies have demonstrated a good correlation between rCBF at the resting state measured by PET with H215O and that measured by the 123I-IMP-ARG method (12,14).
The aim of this study was to validate the accuracy of the 123I-IMP-ARG method for quantifying rCVR to acetazolamide. We compared rCVR with acetazolamide determined quantitatively by the 123I-IMP-ARG method using SPECT with that determined quantitatively by the H215O autoradiographic method using PET in patients who had chronic stenoocclusive disease in a unilateral major cerebral artery.
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MATERIALS AND METHODS
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Subjects
Healthy Volunteers.
We studied 14 male and 6 female healthy volunteers between 30 and 68 y old (mean ± SD, 53 ± 11 y old) to measure the normal values of rCBF by SPECT or PET. Screening of the health status included a medical review of past history, a physical examination, and neurologic and mental tests. Subjects having a past history of hypertension, diabetes mellitus, atrial fibrillation, or pulmonary disease were excluded. Before the SPECT study or the PET study, brain CT was performed to rule out organic lesions of the brain. Subjects with leukoaraiosis or asymptomatic lacunar infarction were excluded from this study. These healthy volunteers were divided into 2 groups; the first group (7 men, 3 women; mean age, 52 ± 12 y; range, 3068 y) participated in the SPECT study and the second group (7 men, 3 women; mean age, 53 ± 11 y; range, 3566 y) participated in the PET study.
Stroke Patients.
From March 1997 to September 1998, 157 patients with unilateral chronic major cerebral artery stenoocclusive disease and a history of minor past strokes or transient ischemic attacks (TIAs) were admitted to our institute for evaluation of rCBF. Of the 157 patients, 39 (27 men, 12 women; mean age, 62 ± 12 y; range, 3576 y) who underwent both SPECT and PET studies were included in the study. All patients had their last cerebral ischemic event >2 mo before entry into the study. No patient had pulmonary disease. Brain CT or MRI and cerebral angiography were performed before PET and SPECT studies in all patients. No infarction or border zone infarction or lacunar infarction in the basal ganglia or deep white matter was observed in any of the patients. Twenty-two of the 39 patients examined had minor past strokes with definite cerebral infarctions on CT or MRI, and 10 had only TIAs with definite cerebral infarctions. The remaining 7 patients had TIAs without definite cerebral infarctions. Unilateral atherosclerotic vascular lesions were noted on the trunk of the middle cerebral artery (MCA) in 16 patients (10 occlusions, 6 stenoses) and the internal carotid artery (ICA) in 23 patients (13 occlusions, 10 stenoses).
Informed consent was obtained from all participants and the study was approved by our Ethics Committee.
123I-IMP SPECT Study
SPECT studies were performed using a ring-type SPECT scanner, a Headtome-SET080 (Shimadzu Corp., Kyoto, Japan), which provides 31 tomographic images simultaneously. The spatial resolution of the scanner with a low-energy, all-purpose collimator was 13-mm full width at half maximum at the center of the field of view, and the slice thickness was 25-mm full width at half maximum at the center of the field of view. Image slices were taken at 5-mm center-to-center spacing parallel to the orbitomeatal line. The images were reconstructed using the weighted-filtered backprojection technique, in which attenuation correction was made by detecting the edge of the object. An attenuation coefficient of 0.065 cm-1, a Butterworth filter (cutoff, 0.45 cycle/cm; order, 3), and a ramp filter were used for image reconstruction.
The 123I-IMP SPECT study was performed as described (12,13). After a 1-min intravenous infusion of 222 MBq of 123I-IMP (5-mL volume) at a constant rate of 5 mL/min and a 1-min infusion of physiologic saline at the same rate, data acquisition was performed at a midscan time of 30 min after the 123I-IMP administration for a scan duration of 20 min.
At 10 min after the beginning of the 123I-IMP infusion, arterial blood (2 mL) was taken from the brachial artery. The whole-blood radioactivity of 1 mL of each blood sample obtained was measured using a well counter that was cross-calibrated to the SPECT scanner. The arterial partial pressures of O2 (PaO2) and CO2 (PaCO2) and the blood pH were also measured in the remaining blood samples using a blood gas tension analyzer.
Two days after the measurement of the rCBF at the resting state, subjects underwent SPECT with acetazolamide challenge. Acetazolamide (1,000 mg; range, 1319 mg/kg body weight) was given intravenously 10 min before 123I-IMP administration, and the SPECT study was performed by the same procedure as for the resting state.
All reconstructed SPECT images were corrected for the radioactive decay of 123I back to the 123I-IMP injection start time, normalized by the data collection time and cross-calibrated to the well counter system. The rCBF images were calculated according to the 123I-IMP-ARG method (12). The whole-blood radioactivity counts of the single blood sample were refereed to the standard input function. The same standard input function at the resting state was used in the calculation of rCBF with acetazolamide challenge (15). The Vd value was assumed to be 35 mL/mL in the calculation of rCBF images both at resting state and with acetazolamide challenge (16,17).
H215O PET Study
All patients underwent PET 2 d before SPECT at the resting state. We used a 4-ring, 7-slice PET scanner (Headtome-IV; Shimadzu Corp.) with in-plane and axial resolutions of 8 and 10 mm, respectively (18). The PET scanner provides 14 tomographic images with 6.5-mm intervals by the continuous axial motion of the gantry. The image slices were parallel to the orbitomeatal line (same as for the SPECT studies).
Before emission scanning, a transmission scan using a 68Ga-68Ge line source was obtained to correct tissue attenuation. The rCBF was calculated using the ARG method with 90-s scanning after an intravenous bolus injection of 1,110 MBq H215O (19). Continuous arterial blood sampling and ß-ray monitoring with a scintillator were conducted throughout PET scanning using a catheter implanted in the radial artery to obtain the arterial input function. PaO2 and PaCO2 and the blood pH were also measured in the same blood samples.
The PET studies at the resting state and with acetazolamide challenge were performed on the same day. Ten minutes after the resting rCBF measurement, acetazolamide (1,000 mg; range, 1319 mg/kg body weight) was given intravenously. Fifteen minutes later, the rCBF was measured by the same procedure as for the resting state.
Blood pressure was measured by auscultation twice for each CBF measurement. The average values of mean blood pressure in each CBF measurement were used to assess the change in mean blood pressure.
Data Analysis
All SPECT and PET images obtained were analyzed as follows. Coregistration and anatomic standardization were performed on a 128 x 128 x 60 matrix (2.25 x 2.25 x 2.25 mm) for each rCBF image, using part of a program set within NEUROSTAT (2022). Slices between the anterior commissureposterior commissure level (ACPC level) - 11.25 mm and the AC-PC level + 9 mm of the standardized images, which had nearly identical cortical shapes, were summed for region-of-interest (ROI) analysis. The outer cortical border was automatically drawn on the section, and the inner cortical border was drawn 15.75 mm (7 pixels x 2.25 mm) further inward. The cortical ribbon was then divided into twelve 30° sectors in a clockwise fashion, and we defined 30° to 150° sectors as the left MCA territory and 210° to 330° sectors as the right MCA territory (Fig. 1). Thus, 1 large cortical ROI for each unilateral hemisphere was determined on each standardized summed rCBF image. Furthermore, the ROI was set bilaterally in all subjects.

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FIGURE 1. Regions of interest in image slice standardized and summed using 3-dimensional stereotactic surface projections.
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On the basis of the rCBF values in each ROI, rCVR to acetazolamide was calculated as follows: rCVR (%) = ([acetazolamide challenge rCBF - resting rCBF]/resting rCBF) x 100.
For statistical analysis, the data were expressed as the mean ± SD, and differences among the 4 groups were examined by repeated-measures ANOVA. Correlation between various parameters was determined by linear regression analysis. Statistical significance was set at the P < 0.05 level.
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RESULTS
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The values of rCBF at the resting state and with acetazolamide challenge and rCVR obtained by the 123I-IMP-ARG method in 20 ROIs of the first group (10 healthy volunteers) were 35.9 ± 4.4 mL/100 g/min, 48.7 ± 5.0 mL/100 g/min, and 36.8% ± 9.2%, respectively. The same values obtained by the H215O PET method in 20 ROIs of the second group (10 healthy volunteers) were 43.5 ± 3.1 mL/100 g/min, 58.7 ± 5.8 mL/100 g/min, and 34.8% ± 8.3%, respectively. For the 123I-IMP-ARG method and the H215O PET method, rCVR in the healthy volunteers was not age dependent.
Table 1 shows the average values of the physiologic variables measured in the 39 patients during SPECT and PET scanning at the resting state and after acetazolamide administration. No significant difference in PaO2, PaCO2, blood pH, or mean blood pressure was observed among the 4 conditions (repeated-measures ANOVA).
Figure 2 shows comparisons of rCBF values obtained by the 123I-IMP-ARG method and those by the H215O PET method (resting state and acetazolamide challenge, respectively) in 78 ROIs of 39 patients. In both conditions, the fits to the regression lines were significant (P < 0.0001), with the correlation coefficients being 0.808 and 0.872, respectively. In particular, rCBF values obtained by the 123I-IMP-ARG method were highly consistent with those obtained by the H215O PET method in the hypoperfusion areas. However, the rCBF values obtained by the 123I-IMP-ARG method were underestimated with increase in rCBF. Representative images are shown in Figure 3.

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FIGURE 2. Correlations of rCBF values calculated by 123I-IMP-ARG method with those calculated by H215O PET method. (A) Resting state. (B) Acetazolamide challenge. Significant correlation was observed in both conditions. Dashed straight line denotes line of identity.
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FIGURE 3. Functional rCBF images calculated by 123I-IMP-ARG method and those calculated by H215O PET method. Data were obtained from patient with left ICA occlusion. Same color scale is used to display these 2 quantitative rCBF images. rCBF images obtained by 123I-IMP-ARG method are reduced in high rCBF areas compared with PET images.
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Figure 4 shows comparisons of rCVR values obtained by the 123I-IMP-ARG method and those by the H215O PET method in 78 ROIs of 39 patients. Significant correlation was observed between the 2 methods (r = 0.820; P < 0.0001). When a rCVR lower than the mean - 2 SD of the values obtained in healthy volunteers (18.4% for the 123I-IMP-ARG method and 18.2% for the H215O PET method, respectively) was defined as reduced, and when the H215O PET method was assumed to be the true determinant (or gold standard) of rCVR, 4 of 31 ROIs (13%) in which the 123I-IMP-ARG method identified reduced rCVR were considered false-positives. The values of rCVR obtained by the 123I-IMP-ARG method in these 4 ROIs with false-positives were 13.1%17.8%. No ROIs with rCVR lower than the mean - 3 SD of the values obtained in healthy volunteers (9.2%) exhibited false-positives. Conversely, the H215O PET method detected reduced rCVR in 3 of the 47 ROIs (6%) identified as having no reduced rCVR using the 123I-IMP-ARG method (false-negatives). The values of rCVR obtained by the 123I-IMP-ARG method in these 3 ROIs with false-negatives were 20.9%25.5%. No ROIs with rCVR higher than the mean - 1 SD of the values obtained in healthy volunteers (27.6%) exhibited false-negative findings. Both analytic approaches obtained identical results in 91% of the ROIs; 35% (27/78 ROIs) were true-positives and 56% (44/78 ROIs) were true-negatives. Sensitivity, specificity, and predictive values were calculated for the 123I-IMP-ARG method of assessing rCVR. The 123I-IMP-ARG and H215O PET methods will identify the same patients as positive 90% of the time (sensitivity). The 2 methods will identify the same patients as negative 92% of the time (specificity). A patient that the 123I-IMP-ARG method identifies as positive will be positive according to the H215O PET method 87% of the time (positive predictive value). A patient that the 123I-IMP-ARG method identifies as negative will be negative according to the H215O PET method 94% of the time (negative predictive value).
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DISCUSSION
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Our findings indicated that the 123I-IMP-ARG method accurately quantifies rCVR to acetazolamide, with a high correlation (r = 0.820) between rCVR values obtained by the 123I-IMP-ARG method and those obtained by the H215O PET method. On the other hand, recent prospective studies have demonstrated that rCVR lower than the mean - 2 SD or the 95% confidence limit of the values quantitatively obtained in healthy volunteers using 133Xe SPECT is significantly associated with an increased risk of stroke recurrence in patients with symptomatic MCA or ICA occlusion (7,8). Therefore, we defined rCVR lower than the mean - 2 SD of the values obtained in healthy volunteers as reducedthat is, being at high risk of stroke recurrence. We also assumed the H215O PET method to be the true determinant (or gold standard) of rCVR. As a result, our study showed that the 123I-IMP-ARG method is 90% sensitive and 92% specific for detecting patients with reduced rCVR. The positive predictive value using the 123I-IMP-ARG method is 87%, and the negative predictive value is 94%. These findings suggest that the subgroup of patients at increased risk for stroke recurrence can be adequately defined by rCVR quantitatively measured using the 123I-IMP-ARG method.
This study also showed the high correlation of rCBF values obtained by the 123I-IMP-ARG method with those obtained by the H215O PET method. In particular, the 2 values coincided strongly in the hypoperfusion areas. These findings are noteworthy because correct quantification of rCBF values in the ischemic territories is the greatest clinical problem. On the other hand, the rCBF values obtained by the 123I-IMP-ARG method were underestimated as rCBF increased, which resulted in the slopes of the linear regression lines being significantly smaller than that of the identity line. This may be due to errors in the SPECT reconstruction, such as imperfect attenuation correction, scatter, and limited spatial resolution of the scanner (partial-volume effect). Another possible explanation for the systematic underestimation at high flow may be due to the limited first-pass extraction fraction of 123I-IMP in the brain (23). The use of a fixed Vd may also be one of the reasons why the rCBF values obtained by the 123I-IMP-ARG method were underestimated as rCBF increased. Because we performed coregistration and anatomic standardization for each rCBF image, and there was no significant difference in PaO2, PaCO2, blood pH, or mean blood pressure among each study, factors such as misalignment of ROIs and physiologic change in rCBF are unlikely to have contributed to the observed difference in rCBF values between the 123I-IMP-ARG method and the H215O PET method.
This study possesses several limitations regarding the 123I-IMP-ARG method. First, the method uses the same standard arterial input function both at the resting state and after acetazolamide administration instead of the measurement of arterial radioactivity. Hauge et al. (24) examined the pharmacologic effects on the cerebral and systemic conditions of acetazolamide and concluded that cardiac output and total peripheral resistance were unaltered during acetazolamide loading. Takeuchi et al. (25) also monitored cardiac output and systemic blood pressure during acetazolamide administration in healthy volunteers using an ultrasound Doppler system, with no significant changes observed. Furthermore, Ogura et al. (15) compared the percentage difference in the area under the curve of the estimated from the real arterial input functions between the resting and acetazolamide analyses of 19 cases. No significant difference in the area under the curve was observed between the 2 study groups. The integration period was 40 min, and the standardized input function was calibrated using a single sample at 10 min. Thus, arterial input after acetazolamide administration could be regarded as being the same as that at the resting state. Second, the Vd was assumed to be the same value (35 mL/mL) at the resting state and after acetazolamide administration. The mean Vd value of 123I-IMP for the normal cortex is 37.5 ± 3.6 mL/g and is independent of age and sex (16). In addition, Toyoda et al. (17) demonstrated that the optimal values for Vd at the resting state and after acetazolamide administration were both in the range of 3035 mL/mL and the difference between the values at the resting state and after acetazolamide administration was very small. Therefore, the Vd could be set as the constant value of 35 mL/mL both at the resting state and after acetazolamide administration.
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CONCLUSION
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The 123I-IMP-ARG method can be performed using conventional SPECT scanners (12,14) and does not require frequent arterial blood sampling. This allows the technique to be used much more readily in assessing patients with major cerebral artery occlusive disease in routine clinical practice, although 123I-IMP is now unavailable in the West because of the cost. Our study suggests that the ability of the 123I-IMP-ARG method to detect reduced rCVR is almost identical to that of the H215O PET method and that the subgroup of patients at increased risk for stroke recurrence can be adequately defined by rCVR quantitatively measured using the 123I-IMP-ARG method. Whether extracranialintracranial arterial bypass surgery, which improves impaired cerebral hemodynamics (26,27), reduces the risk of stroke in this subgroup remains unclear. Preoperative low rCVR quantitatively obtained using SPECT has been shown to be significantly associated with an increased risk of hyperperfusion syndrome after carotid endarterectomy (28,29). Standardization of hemodynamic compromise measurement and further investigation to assess the usefulness of extracranialintracranial arterial bypass surgery or the risk of hyperperfusion syndrome after carotid endarterectomy would be of great benefit.
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ACKNOWLEDGMENTS
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The authors thank Prof. Satoshi Minoshima, University of Washington Medical School, for the use of 3-dimensional stereotactic surface projections (NEUROSTAT) and his helpful suggestions. This work was supported in part by Grants-in-Aid for Advanced Medical Scientific Research by the Ministry of Science, Education, Sports and Culture, Japan.
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FOOTNOTES
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Received Jul. 25, 2002; revision accepted Oct. 31, 2002.
For correspondence or reprints contact: Kuniaki Ogasawara, MD, Department of Neurosurgery, Iwate Medical University, 19-1 Uchimaru, Morioka, 020-8505 Japan.
E-mail: kuogasa{at}iwate-med.ac.jp
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REFERENCES
|
|---|
- Burt RW, Witt RM, Cikrit DF, Reddy RV. Carotid artery disease: evaluation with acetazolamide-enhanced Tc-99m HMPAO SPECT. Radiology 1992;182:461466.[Abstract/Free Full Text]
- Hoshi H, Ohnishi T, Jinnouchi S, et al. Cerebral blood flow study in patients with moyamoya disease evaluated by IMP SPECT. J Nucl Med. 1994;35:4450.[Abstract/Free Full Text]
- Soricelli A, Postiglione A, Cuocolo A, et al. Effect of adenosine on cerebral blood flow as evaluated by single-photon emission computed tomography in normal subjects and in patients with occlusive carotid disease: a comparison with acetazolamide. Stroke. 1995;26:15721576.[Abstract/Free Full Text]
- Ohnishi T, Yano T, Nakano S, et al. Acetazolamide challenge and technetium-99m-ECD versus iodine-123-IMP SPECT in chronic occlusive cerebrovascular disease. J Nucl Med. 1997;38:14631467.[Abstract/Free Full Text]
- Kikuchi K, Murase K, Miki H, et al. Measurement of cerebral hemodynamics with perfusion-weighted MR imaging: comparison with pre- and post-acetazolamide 133Xe-SPECT in occlusive carotid disease. AJNR 2001;22:248254.[Abstract/Free Full Text]
- Ozgur HT, Kent Walsh T, Masaryk A, et al. Correlation of cerebrovascular reserve as measured by acetazolamide-challenged SPECT with angiographic flow patterns and intra- or extracranial arterial stenosis. AJNR 2001;22:928936.[Abstract/Free Full Text]
- Kuroda S, Houkin K, Kamiyama H, Mitsumori K, Iwasaki Y, Abe H. Long-term prognosis of medically treated patients with internal carotid or middle cerebral artery occlusion: can acetazolamide test predict it? Stroke. 2001;32:21102116.[Abstract/Free Full Text]
- Ogasawara K, Ogawa A, Yoshimoto T. Cerebrovascular reactivity to acetazolamide and outcome in patients with symptomatic internal carotid or middle cerebral artery occlusion: a xenon-133 single-photon emission computed tomography study. Stroke. 2002;33:18571862.[Abstract/Free Full Text]
- Yokota C, Hasegawa Y, Minematsu K, Yamaguchi T. Effect of acetazolamide reactivity and long-term outcome in patients with major cerebral artery occlusive diseases. Stroke. 1998;29:640644.[Abstract/Free Full Text]
- Yonas H, Pindzola RR, Meltzer CC, Sasser H. Qualitative versus quantitative assessment of cerebrovascular reserves. Neurosurgery. 1998;42:10051012.[Medline]
- Yonas H, Pindzola RR. Effect of acetazolamide reactivity and long-term outcome in patients with major cerebral artery occlusive diseases. Stroke. 1998;29:17421744.[Free Full Text]
- Iida H, Itoh H, Nakazawa M, et al. Quantitative mapping of regional cerebral blood flow using iodine-123-IMP and SPECT. J Nucl Med. 1994;35:20192030.[Abstract/Free Full Text]
- Iida H, Itoh H, Bloomfield PM, et al. A clinical method to quantitate cerebral blood flow using a rotating gamma camera and iodine-123 iodoamphetamine with one blood sampling. Eur J Nucl Med 1994;21:10721084.[Medline]
- Iida H, Akutsu T, Endo K, et al. A multicenter validation of regional cerebral blood flow quantitation using [123I]iodoamphetamine and single photon emission computed tomography. J Cereb Blood Flow Metab. 1996;16:781793.[Medline]
- Ogura T, Takikawa S, Saito H, Nakazawa M, Shidahara M, Iida H. Validation and optimization of the use of standardized arterial input function in N-isopropyl-p[123I]iodoamphetamine cerebral blood flow SPECT. Kaku Igaku 1999;36:879890.[Medline]
- Hatazawa J, Iida H, Shimosegawa E, Sato T, Murakami M, Miura Y. Regional cerebral blood flow measurement with iodine-123-IMP autoradiography: normal values, reproducibility and sensitivity to hypoperfusion. J Nucl Med. 1997;38:11021108.[Abstract/Free Full Text]
- Toyoda H, Nishizawa S, Shiozaki T, Ueno M, Konishi J. A simplified double-injection method to quantify cerebral blood flow and vascular reserve using iodine-123 IMP-SPECT. Ann Nucl Med. 2002;16:127135.[Medline]
- Iida H, Miura S, Kanno I, Murakami M, Takahashi K, Uemura K. Design and evaluation of Headtome-IV: a whole-body positron emission tomograph. IEEE Trans Nucl Sci. 1989;36:10061010.
- Kanno I, Iida H, Miura S, et al. A system for cerebral blood flow measurement using an H215O autoradiographic method and positron emission tomography. J Cereb Blood Flow Metab. 1987;7:143153.[Medline]
- Minoshima S, Frey KA, Koeppe RA, Foster NL, Kuhl DE. A diagnostic approach in Alzheimers disease using three-dimensional stereotactic surface projections of fluorine-18-FDG PET. J Nucl Med 1995;36:12381248.[Abstract/Free Full Text]
- Minoshima S, Koeppe RA, Fessler JA, et al. Integrated and automated data analysis method for neuronal activation studies using 15O-water PET. In: Uemura K, Lassen NA, Jones T, Kanno I, eds. Quantification of Brain Function: Tracer Kinetics and Image Analysis in Brain PET Amsterdam, The Netherlands: Excerpta Medica; 1993:409417.
- Maes F, Collignon A, Vandermeulen D, Marchal G, Suetens P. Multimodality image registration by maximization of mutual information. IEEE Trans Med Imaging. 1997;16:187198.[Medline]
- Murase K, Tanada S, Inoue T, et al. Measurement of the blood-brain-barrier permeability of I-123 IMP, Tc-99m HMPAO and Tc-99m ECD in the human brain using compartment model analysis and dynamic SPECT [abstract]. J Nucl Med. 1995;32.(suppl):911P.
- Hauge A, Nicolaysen G, Thoresen M. Acute effects of acetazolamide on cerebral blood flow in man. Acta Physiol Scand. 1983;117:233239.[Medline]
- Takeuchi R, Matsuda H, Yonekura Y, Sakahara H, Konishi J. Noninvasive quantitative measurements of regional cerebral blood flow using technetium-99m-L,L-ECD SPECT activated with acetazolamide: quantification analysis by equal-volume-split 99mTc-ECD consecutive SPECT method. J Cereb Blood Flow Metab. 1997;17:10201032.[Medline]
- Samson Y, Baron JC, Bousser MG, et al. Effects of extra-intracranial arterial bypass on cerebral blood flow and oxygen metabolism in humans. Stroke. 1985;16:609616.[Abstract/Free Full Text]
- Schmiedek P, Piepgras A, Leinsinger G, Kirsch CM, Einhupl K. Improvement of cerebrovascular reserve capacity by EC-IC arterial bypass surgery in patients with ICA occlusion and hemodynamic cerebral ischemia. J Neurosurg. 1994;81:236244.[Medline]
- Hosoda K, Kawaguchi T, Shibata Y, et al. Cerebral vasoreactivity and internal carotid artery flow help to identify patients at risk for hyperperfusion after carotid endarterectomy. Stroke. 2001;32:15671573.[Abstract/Free Full Text]
- Yoshimoto T, Houkin K, Kuroda S, Abe H, Kashiwaba T. Low cerebral blood flow and perfusion reserve induce hyperperfusion after surgical revascularization: case reports and analysis of cerebral hemodynamics. Surg Neurol. 1997;48:132139.[Medline]
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K. Chida, K. Ogasawara, Y. Suga, H. Saito, M. Kobayashi, K. Yoshida, Y. Otawara, and A. Ogawa
Postoperative Cortical Neural Loss Associated With Cerebral Hyperperfusion and Cognitive Impairment After Carotid Endarterectomy: 123I-iomazenil SPECT Study
Stroke,
February 1, 2009;
40(2):
448 - 453.
[Abstract]
[Full Text]
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M. Sasaki, K. Kudo, K. Ogasawara, and S. Fujiwara
Tracer Delay-Insensitive Algorithm Can Improve Reliability of CT Perfusion Imaging for Cerebrovascular Steno-Occlusive Disease: Comparison with Quantitative Single-Photon Emission CT
AJNR Am. J. Neuroradiol.,
January 1, 2009;
30(1):
188 - 193.
[Abstract]
[Full Text]
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Y. Suga, K. Ogasawara, H. Saito, N. Komoribayashi, M. Kobayashi, T. Inoue, Y. Otawara, and A. Ogawa
Preoperative Cerebral Hemodynamic Impairment and Reactive Oxygen Species Produced During Carotid Endarterectomy Correlate With Development of Postoperative Cerebral Hyperperfusion
Stroke,
October 1, 2007;
38(10):
2712 - 2717.
[Abstract]
[Full Text]
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T. Fukuda, K. Ogasawara, M. Kobayashi, N. Komoribayashi, H. Endo, T. Inoue, Y. Kuzu, H. Nishimoto, K. Terasaki, and A. Ogawa
Prediction of Cerebral Hyperperfusion after Carotid Endarterectomy Using Cerebral Blood Volume Measured by Perfusion-Weighted MR Imaging Compared with Single-Photon Emission CT
AJNR Am. J. Neuroradiol.,
April 1, 2007;
28(4):
737 - 742.
[Abstract]
[Full Text]
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H. Endo, T. Inoue, K. Ogasawara, T. Fukuda, Y. Kanbara, and A. Ogawa
Quantitative Assessment of Cerebral Hemodynamics Using Perfusion-Weighted MRI in Patients With Major Cerebral Artery Occlusive Disease: Comparison With Positron Emission Tomography
Stroke,
February 1, 2006;
37(2):
388 - 392.
[Abstract]
[Full Text]
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K. Ogasawara, T. Inoue, M. Kobayashi, H. Endo, K. Yoshida, T. Fukuda, K. Terasaki, and A. Ogawa
Cerebral Hyperperfusion Following Carotid Endarterectomy: Diagnostic Utility of Intraoperative Transcranial Doppler Ultrasonography Compared with Single-Photon Emission Computed Tomography Study
AJNR Am. J. Neuroradiol.,
February 1, 2005;
26(2):
252 - 257.
[Abstract]
[Full Text]
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S. Kuroda, T. Shiga, T. Ishikawa, K. Houkin, T. Narita, C. Katoh, N. Tamaki, and Y. Iwasaki
Reduced Blood Flow and Preserved Vasoreactivity Characterize Oxygen Hypometabolism Due to Incomplete Infarction in Occlusive Carotid Artery Diseases
J. Nucl. Med.,
June 1, 2004;
45(6):
943 - 949.
[Abstract]
[Full Text]
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H Yamauchi, H Okazawa, Y Kishibe, K Sugimoto, and M Takahashi
Oxygen extraction fraction and acetazolamide reactivity in symptomatic carotid artery disease
J. Neurol. Neurosurg. Psychiatry,
January 1, 2004;
75(1):
33 - 37.
[Abstract]
[Full Text]
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H. Okazawa, H. Yamauchi, K. Sugimoto, and M. Takahashi
Differences in Vasodilatory Capacity and Changes in Cerebral Blood Flow Induced by Acetazolamide in Patients with Cerebrovascular Disease
J. Nucl. Med.,
September 1, 2003;
44(9):
1371 - 1378.
[Abstract]
[Full Text]
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K. Ogasawara, T. Okuguchi, M. Sasoh, M. Kobayashi, H. Yukawa, K. Terasaki, T. Inoue, and A. Ogawa
Qualitative versus Quantitative Assessment of Cerebrovascular Reactivity to Acetazolamide Using iodine-123-N-Isopropyl-p-Iodoamphetamine SPECT in Patients with Unilateral Major Cerebral Artery Occlusive Disease
AJNR Am. J. Neuroradiol.,
June 1, 2003;
24(6):
1090 - 1095.
[Abstract]
[Full Text]
[PDF]
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