Arterial Spin-Labeling Evaluation of Cerebrovascular Reactivity to Acetazolamide in Healthy Subjects

Y. Inoue; Y. Tanaka; H. Hata; T. Hara

doi:10.3174/ajnr.A3815

Abstract

BACKGROUND AND PURPOSE: Arterial spin-labeling MR imaging permits safe, repeated CBF measurement. We investigated the potential and technical factors of arterial spin-labeling imaging in assessing cerebrovascular reactivity to acetazolamide.

MATERIALS AND METHODS: The regional CBF was measured in 8 healthy volunteers by use of a 3D pseudocontinuous arterial spin-labeling sequence. Arterial spin labeling imaging was performed at rest and every 2 minutes after intravenous acetazolamide injection. To evaluate repeatability, regional CBF measurements were repeated without acetazolamide within an imaging session and on a separate day. Additionally, arterial spin-labeling imaging was performed at rest and after acetazolamide injection with different postlabeling delays, and regional cerebrovascular reactivity was calculated.

RESULTS: The regional CBF started to increase immediately after acetazolamide injection and peaked at approximately 10 minutes, followed by a slow decrease. Favorable intrasession repeatability was demonstrated, especially when scanner tuning was omitted between scans. Rest regional CBF was slightly lower with a postlabeling delay of 2525 ms than with a postlabeling delay of 1525 ms, and the postlabeling delay–dependent difference was more evident for regional CBF after acetazolamide injection and regional cerebrovascular reactivity.

CONCLUSIONS: Arterial spin-labeling imaging allows evaluation of the distribution, magnitude, and time course of cerebrovascular response to acetazolamide. The influence of the postlabeling delay on the estimated cerebrovascular reactivity should be noted.

ABBREVIATIONS:

ACZ: acetazolamide
ant-MCA: anterior part of the territory of the MCA
ASL: arterial spin-labeling
CVR: cerebrovascular reactivity
PLD: postlabeling delay
post-MCA: posterior part of the territory of the MCA
rCBF: regional CBF
rCVR: regional cerebrovascular reactivity

MR imaging with an arterial spin-labeling (ASL) technique permits evaluation of cerebral perfusion with neither radiation exposure nor the administration of an exogenous contrast agent.^1,2 Arterial water in the neck is labeled with a radiofrequency pulse, and the brain is imaged after a fixed time interval, termed postlabeling delay (PLD). Cerebral perfusion is estimated on the basis of signal changes caused by an influx of magnetically labeled water into brain tissues, and absolute values of CBF are calculated. The 3D ASL MR imaging by use of a pseudocontinuous arterial spin-labeling technique for magnetic labeling offers contiguous CBF images covering the whole brain with a favorable signal-to-noise ratio³ and is expected to enhance the utility of ASL imaging.

In occlusive cerebrovascular diseases, the cerebral vessels dilate to compensate for decreased cerebral perfusion pressure and to maintain CBF in areas with compromised cerebral hemodynamics.⁴ Such areas are presumably vulnerable to ischemic brain injury after further reduction in perfusion pressure and are considered to have decreased cerebral perfusion reserve. CBF measurements at rest and after acetazolamide (ACZ) injection allow evaluation of compensatory vasodilation and reveal impaired cerebral hemodynamics even when rest CBF is preserved.^5,6 ACZ is a potent dilator of cerebral vessels and increases CBF after intravenous injection. In brain regions in which decreased cerebral perfusion pressure has already caused compensatory vasodilation, cerebrovascular response to ACZ diminishes. Comparison of rest and post-ACZ CBFs demonstrates compromised cerebral hemodynamics as decreased cerebrovascular reactivity (CVR) to ACZ.

CVR is commonly assessed with the use of SPECT measurements of CBF at rest and after ACZ injection.^5,6 This method is well established but requires radiation exposure and long examination times. CBF and CVR can be assessed by ASL MR imaging with ACZ.^{7⇓⇓⇓⇓–12} The ASL technique allows estimation of rest and post-ACZ CBFs, in addition to morphologic assessments by conventional MR imaging, in one imaging session. In the present study, we used 3D pseudocontinuous ASL imaging to evaluate CVR to ACZ in healthy volunteers. We acquired ASL images after ACZ injection repeatedly with high temporal resolution and investigated the time course of CBF changes for each vascular territory. Intrasession and interday repeatabilities were assessed to evaluate the capability of ASL imaging to detect changes in CBF. The magnitude and distribution of ASL signals depends on the time after labeling, and thus the PLD is the key parameter of ASL imaging.^2,13 ASL signals may originate from labeled water in blood vessels in addition to that in brain tissues. Prolongation of the PLD facilitates labeled water entering brain tissues and appears to be beneficial for evaluation of tissue perfusion. However, magnetic labeling decays rapidly with T1 relaxation, and a longer PLD may result in weaker signals. In the present study, we examined the effect of the PLD on rest CBF, post-ACZ CBF, and CVR. The aim of this study was to investigate the potential and technical factors of the ASL assessment of CVR.

MATERIALS AND METHODS

Subjects

This study included 8 healthy adult volunteers (7 men and 1 woman), ages 30.1 ± 4.6 (mean ± SD) years. The volunteers had no history of chronic diseases and no contraindications to MR imaging. No abnormalities were found in the brain on T2-weighted FSE images. The study protocol was approved by the institutional review board of the host institute, and written informed consent was obtained from all subjects before participation.

3D ASL Imaging

All imaging studies were performed in the evening on a 1.5T clinical scanner (Signa HDxt; GE Healthcare, Milwaukee, Wisconsin) with the 12-channel head component of the head-neck-spine coil. ASL imaging of the whole brain was performed by use of a 3D pseudocontinuous ASL sequence, which consisted of a pseudocontinuous ASL labeling sequence and a 3D spiral FSE acquisition sequence,³ with background suppression and no vascular suppression. Each spiral arm contained 512 sampling points in the k-space, and 4 arms (interleaves) were acquired. The PLD was set at 1525 or 2525 ms. Other imaging parameters were as follows: TR = 4608 ms, TE = 10.5 ms, flip angle = 155°, bandwidth = ±62.5 kHz, FOV = 24 × 24 cm², section numbers = 36, section thickness = 4 mm, NEX = 2 or 6. A pair of label and control image sets covering the whole brain was acquired for 40 seconds, and the acquisition was repeated as indicated by NEX. ASL perfusion images were generated by subtraction of the label and control image sets and averaging. Immediately after the completion of acquisition of the label and control image sets, a reference proton attenuation image set was obtained by means of a fluid saturation pulse to determine the spatial distribution of signal sensitivity. In total, acquisition times were 1 minute, 42 seconds for a NEX of 2 and a PLD of 1525 ms; 4 minutes, 10 seconds for a NEX of 6 and a PLD of 1525 ms; and 4 minutes, 48 seconds for a NEX of 6 and a PLD of 2525 ms. Quantitative CBF images were created from the ASL perfusion images and proton attenuation images by use of the software on the MR scanner.¹⁴

Calculation of Regional CBF Values

ROIs were determined by means of automated software (3D stereotactic region of interest template, 3D-SRT; Fujifilm RI Pharama, Tokyo, Japan)¹⁵ to calculate regional CBF (rCBF) values. The quantitative CBF images obtained in the study subject were registered anatomically to the standard brain atlas. Parameters for anatomic standardization were determined with the use of proton attenuation images but not CBF images because the margin was clearer in the proton attenuation images. The 3D-SRT software has ROIs predefined on the standard brain atlas and provides rCBF values for each of the right and left sides of the following 12 regions: callosomarginal, precentral, central, parietal, angular, temporal, posterior cerebral, pericallosal, basal ganglia, thalamus, hippocampus, and cerebellum. In the present study, we determined rCBF in the territory of the anterior cerebral artery through the use of callosomarginal and pericallosal ROIs; rCBF in the anterior part of the territory of the middle cerebral artery (ant-MCA) through the use of precentral and central ROIs; rCBF in the posterior part of the territory of the middle cerebral artery (post-MCA) through the use of parietal, angular, and temporal ROIs; and rCBF in the territory of the posterior cerebral artery through the use of a posterior cerebral ROI.

Time Course after ACZ Injection

The time course of cerebrovascular response to ACZ was evaluated by means of serial ASL imaging. The subjects underwent ASL imaging with a NEX of 2 and a PLD of 1525 ms twice at rest. Thereafter, 1000 mg of ACZ in 20 mL of saline was injected intravenously for 30 seconds by use of an autoinjector, followed by a 20-mL saline flush for 30 seconds. ASL imaging was started at the beginning of ACZ injection and repeated every 2 minutes for 32 minutes, yielding 16 post-ACZ image sets. Although scanner tuning consisting of shimming and auto prescan is commonly performed before each imaging to adjust scanner settings, it was performed before the first rest imaging and omitted thereafter. Such omission was made only in this time course study. The rCBF value for each brain region, that is, the anterior cerebral artery, ant-MCA, post-MCA, or posterior cerebral artery region, was calculated as the average of the right and left values obtained by ROI analysis. The normalized rCBF at each time point was determined as a percentage of the average of the 2 rest values, and its temporal change was evaluated.

Repeatability of Rest rCBF Measurement

The repeatability of rest rCBF measurement by ASL imaging was assessed by use of 4 measurements in each subject. Two rest measurements performed for the evaluation of the time course after ACZ injection without intervening scanner tuning were also used for the assessment of repeatability. On another day, with an interval of approximately 3 months, ASL imaging was performed twice in 1 imaging session. Unlike the time course study, scanner tuning was performed between the 2 data acquisitions. The NEX was 2 and the PLD was 1525 ms in all 4 measurements.

The rCBF values were obtained by the automated ROI method, and data for the right and left sides were analyzed separately for this repeatability study, yielding 8 brain regions for analysis. The coefficient of variance was calculated from 2 corresponding rCBF values in each subject and was regarded as an indicator of variation of rest measurement. The coefficient of variance between the 2 serial measurements of the time course study was calculated to assess intrasession variation without tuning. The coefficient of variance between the 2 serial measurements performed on the other day was used to assess intrasession variation with tuning. The coefficient of variance was also calculated between the preceding measurements on separate days and was used as an indicator of interday variation.

rCBF and Regional Cerebrovascular Reactivity with Different PLDs

ASL imaging before and after ACZ injection was performed with different PLDs, and the effects of the PLD on rCBF and regional cerebrovascular reactivity (rCVR) were investigated. The PLDs studied were 1525 and 2525 ms, and the NEX was set at 6. ASL imaging was performed twice at rest: initially with a PLD of 1525 ms and then with a PLD of 2525 ms. After the completion of imaging at rest, 1000 mg of ACZ was injected intravenously, similarly to the time course study. ASL imaging with a PLD of 1525 ms was started 8 minutes after the start of ACZ injection, followed by imaging with a PLD of 2525 ms. This order of imaging with different PLDs was applied to 4 subjects, and imaging with a PLD of 2525 ms was performed before that with a PLD of 1525 ms in the remaining 4 subjects for both rest and post-ACZ imaging. Scanner tuning preceded each ASL acquisition.

The rCVR was defined as percent increase in rCBF and was calculated by the equation rCVR = (post-ACZ rCBF/rest rCBF − 1) × 100 for each of the 8 brain regions. The rCBF and rCVR were compared between regions and between PLDs. The CVR image was created by pixel-by-pixel calculation of the percent increase in CBF after noise reduction by use of a 3D Gaussian filter of 8-mm full width at half maximum.

Statistical Analysis

Values are expressed as mean ± SD. Paired comparisons between PLDs were performed by Wilcoxon signed rank tests, and brain regions were compared by use of the Kruskal-Wallis test followed by the Steel-Dwass test. A value of P < .05 was deemed to indicate statistical significance.

RESULTS

Time Course after ACZ Injection

CBF images with acceptable qualities were obtained serially after ACZ injection, and augmentation of CBF was noted visually (Fig 1). ROIs were successfully placed by use of the 3D-SRT software, providing an absolute rCBF value for each brain region. The mean rest rCBF calculated from the first scan was 51.9 ± 4.5, 52.4 ± 5.0, 51.6 ± 5.3, and 50.1 ± 8.0 mL/min per 100 g in the anterior cerebral artery, ant-MCA, post-MCA, and posterior cerebral artery regions, respectively. The rCBF started to increase just after ACZ injection, peaked at approximately 10 minutes, and then decreased slowly (Fig 2). The temporal patterns of cerebrovascular response were similar among the brain regions.

Fig 1.

CBF images at the level of the basal ganglia in a 28-year-old woman. Data were acquired with a NEX of 2 and a postlabeling delay of 1525 ms at rest (A) and 3 minutes (B), 9 minutes (C), 15 minutes (D), and 31 minutes (E) after acetazolamide injection. The time indicates the mid time of data acquisition. The upper and lower limits of the color scale are set at 110 and 0 mL/min per 100 g, respectively. F, ROIs placed automatically by the 3D-SRT software.

Fig 2.

Time courses of normalized regional CBF after acetazolamide injection in the anterior cerebral artery (A), anterior MCA (B), posterior MCA (C), and posterior cerebral artery (D) regions. Error bars indicate SDs. ACZ was injected at time 0, and plots with negative x values represent data of rest imaging.

Repeatability of Rest rCBF Measurement

Mean coefficients of variance of rCBF measurements representing intrasession variation without tuning were generally small, ranging from 1.7–2.7%, depending on the brain regions (Table 1). Insertion of tuning, consisting of shimming and auto prescan, between 2 measurements increased variation in rCBF definitely. The mean coefficients of variance representing intrasession variation with tuning ranged from 3.3–5.7%. Interday variation was still larger, with mean coefficients of variance ranging from 6.2–9.4%. There were no significant differences in coefficients of variance among the brain regions.

View this table:

Table 1:

Coefficients of variance for repeated measurements

rCBF and rCVR with Different PLDs

The rest and post-ACZ CBF images as well as the CVR images are illustrated in Fig 3, and numeric values obtained by automated ROI analysis are presented in Table 2. Significant differences were not found in rest rCBF, post-ACZ rCBF, or rCVR among the brain regions, irrespective of the PLD. With a PLD of 1525 ms, mean rest rCBF and mean post-ACZ rCBF ranged, depending on the brain regions, from 45.9–50.1 mL/min per 100 g and from 67.3–72.7 mL/min per 100 g, respectively, resulting in mean rCVR values ranging from 42.5–46.4%. Despite negligible differences in mean values, the standard deviations of rCVR among subjects were obviously different among the brain regions and were the smallest in the anterior cerebral artery region, followed by the ant-MCA, post-MCA, and posterior cerebral artery regions.

Fig 3.

CBF and cerebrovascular reactivity images with different postlabeling delays at the level of the basal ganglia in the same subject as presented in Fig 1. A–C, Rest CBF image, post-acetazolamide CBF image, and CVR image, respectively, with a PLD of 1525 ms. D–F, Rest CBF image, post-ACZ CBF image, and CVR image, respectively, with a PLD of 2525 ms. The upper and lower limits of the color scale are set at 110 and 0 mL/min per 100 g, respectively, for CBF images, and the upper and lower limits for CVR images are set at 70% and 0%, respectively.

View this table:

Table 2:

Regional CBF and regional cerebrovascular reactivity values with acetazolamide injection

Rest rCBF values were significantly lower with a PLD of 2525 ms (44.3–47.8 mL/min per 100 g) than with a PLD of 1525 ms; however, the differences were small. Post-ACZ rCBF values were also significantly lower with a PLD of 2525 ms (58.0–62.4 mL/min per 100 g), and the PLD-dependent difference was more evident. As a result, rCVR was significantly and largely lower with a PLD of 2525 ms (26.9–32.5%).

DISCUSSION

Although SPECT measurements of CBF at rest and after ACZ injection are commonly used for the assessment of CVR,^5,6 they require radiation exposure and long examination times. ASL MR imaging is a safe, rapid method of measuring CBF and is applicable to the assessment of CVR.^{7⇓⇓⇓⇓–12} In the present study, we evaluated cerebrovascular response to ACZ by 3D pseudocontinuous ASL MR imaging. Repeated ASL imaging after ACZ injection demonstrated a CBF increase in the whole brain visually and quantitatively. The number of arms and the NEX determine the acquisition time, and we selected relatively small numbers (4 arms and a NEX of 2) to shorten the acquisition time and attain high temporal resolution. With the use of these imaging parameters, ASL images with acceptable qualities were obtained during an acquisition time of 1 minute, 42 seconds. In ASL assessment of CBF with no vascular suppression, magnetically labeled water in the cerebral vessels may lead to erroneously high CBF values in the superficial areas of the brain.^2,16 The position and size of the ROI may affect calculated rCBF values, depending on the degree of inclusion of superficial high values in the ROI. We used automated software for the ROI setting to avoid operator-dependent variations in rCBF estimates and to improve reproducibility. This software was developed to analyze CBF SPECT¹⁵; however, it was applicable to the analysis of ASL imaging. ROIs determined by use of the reference proton attenuation images for anatomic standardization were visually judged to be appropriate and provided CBF values for each region.

Quantitative analysis of rCBF after ACZ injection showed a rapid increase in CBF, with a peak at approximately 10 minutes and a subsequent slow decrease. Such a detailed assessment of the time course of CBF changes is difficult with the use of methods requiring administration of exogenous contrast agents or radiotracers. Doppler ultrasonography^17,18 and phase-contrast MR imaging¹⁹ have been used to assess the time course of cerebrovascular response to ACZ and have shown temporal changes in blood flow or velocity in the major cerebral arteries that are consistent with temporal changes in rCBF observed in the current study. Planar dynamic imaging after radio-labeled albumin has also revealed similar temporal patterns in alterations of cerebral blood volume representing intravascular volume.²⁰ The present study confirmed the time course of cerebrovascular response to ACZ by assessing brain tissue perfusion instead of an approach from the vessels. CBF SPECT after ACZ injection is commonly performed assuming peak CBF response at 10–15 minutes after injection on the basis of Doppler measurement of the major cerebral arteries; the validity of this timing is supported by the present rCBF measurement.

The PLD is an essential parameter in ASL imaging. The use of a short PLD may diminish labeled water that reaches the brain tissues by the time of data acquisition, whereas the use of a long PLD causes decreased signals caused by relaxation of labeled water. We evaluated the effect of the PLD on the assessment of cerebrovascular response to ACZ by ASL imaging. Although rest rCBF did not differ largely, post-ACZ rCBF and rCVR were definitely lower with a PLD of 2525 ms than with a PLD of 1525 ms. CBF measurement by use of ASL MR imaging is dependent on the arterial arrival time, the time for water labeled in the neck to reach the brain tissues, and this dependence is more pronounced with a short PLD.^2,13 Previous studies with the use of Doppler ultrasonography demonstrated increased blood velocity after ACZ injection in the MCA¹⁷ and internal carotid artery.¹⁸ The administration of ACZ may shorten the arrival time as a result of increased blood velocity and aid early influx of labeled water into the brain tissues, which may enhance ASL signals with a short PLD preferentially and consequently cause overestimation of CVR. The mean CVR values reported in normal subjects range from 25–31% with the use of ¹³³Xe inhalation SPECT,^{18,21⇓–23} from 33.5–35% with the use of ¹⁵O-water positron-emission tomography,^24,25 and from 37.7–54.2% with the use of ASL MR imaging.^9⇓–11 Although the CVR values obtained with the use of a PLD of either 1525 ms (43.8–46.4%, depending on the region) or 2525 ms (26.9–32.5%) in the present study are in the range of the reported values, those obtained with a PLD of 1525 ms as well as those previously reported by use of ASL MR imaging are relatively high; thus, ASL MR imaging probably leads to overestimation of CVR. The method that provides more accurate CVR cannot be concluded because of the lack of a standard reference; however, our results indicate that the influence of the PLD on CVR estimates should be taken into consideration.

Regional differences were not apparent in the temporal patterns of cerebrovascular response to ACZ among cortical regions. Systematic differences among regions were not demonstrated for rest rCBF, post-ACZ rCBF, or rCVR. However, rCVR was more variable among subjects in the posterior cerebral artery region than in the other regions, as indicated by a large SD. A long arrival time has been reported in the posterior cerebral artery region,²⁶ and such difference between carotid and vertebro-basilar circulations may be related to the variability in rCVR in the posterior cerebral artery region. Although the actual cause of the variability in CVR is unclear, our results raise caution in the assessment of CVR in the posterior cerebral artery region by use of ASL imaging.

High repeatability is crucial for evaluation of true changes from 2 measurements. Several reports have focused on the repeatability of CBF measurement by ASL imaging.^{11,14,27⇓⇓–30} Interday repeatability indicates the capability of detecting alterations in CBF in the longitudinal assessment of disease status. CVR can be assessed by ASL imaging before and after ACZ injection in 1 imaging session, and intra-session repeatability is essential for this assessment. Differences in the positioning of the subject, physiologic fluctuations, and instability of the instruments are major factors causing interday variation but not intrasession variation. In the present study, we evaluated intrasession repeatability in addition to interday repeatability. Naturally, intrasession variation was smaller than intersession variation, as shown in a previous study.²⁷ Scanner tuning is commonly performed before each imaging and consists of shimming of the magnetic field, adjustment of the transmit gain, adjustment of the receive gain, and determination of the resonant frequency. It is noteworthy that omission of the tuning between scans reduced the coefficients of variance in rCBF measurement by a factor of 2. Tuning appears to be a major factor in intrasession variation. The peak response to ACZ is attained at approximately 10 minutes after injection. In clinical practice, imaging other than ASL would be performed during the waiting period before the commencement of post-ACZ ASL imaging, resulting in a need for tuning between rest and post-ACZ ASL imaging. Recording the tuning parameters for rest ASL imaging and application of the same parameters to post-ACZ ASL imaging may be helpful to improve the accuracy of assessing CVR to ACZ.

CONCLUSIONS

We performed 3D pseudocontinuous ASL imaging before and after ACZ injection to assess cerebrovascular response to ACZ. The observed time course in rCBF changes supports the previous reports of flow and velocity in the major cerebral arteries and cerebral blood volume. The magnitude of CVR was comparable to that in previous studies. The PLD influenced rest rCBF mildly and post-ACZ rCBF and rCVR severely. It was also suggested that attention should be paid in assessing CVR abnormalities in the posterior cerebral artery region. Intrasession repeatability was favorable, especially when the scanner settings were not changed by tuning between scans. The 3D pseudocontinuous ASL imaging allows evaluation of the distribution, magnitude, and time course of cerebrovascular response without radiation exposure or administration of exogenous contrast agents and is expected to serve as a tool for investigating in vivo physiology and assessing impaired hemodynamics in pathologic conditions.

ACKNOWLEDGMENTS

We thank Tetsuo Hosoda, BS, Fujifilm RI Pharama, for his support in the ROI-based analysis. We also thank Hiroyuki Kabasawa, PhD, Global Applied Science Laboratory, GE Healthcare, for valuable discussion.

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Received September 11, 2013.
Accepted after revision October 14, 2013.

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[1] 1.↵
Hendrikse J,
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American Journal of Neuroradiology

Arterial Spin-Labeling Evaluation of Cerebrovascular Reactivity to Acetazolamide in Healthy Subjects

Abstract

ABBREVIATIONS:

MATERIALS AND METHODS

Subjects

3D ASL Imaging

Calculation of Regional CBF Values

Time Course after ACZ Injection

Repeatability of Rest rCBF Measurement

rCBF and Regional Cerebrovascular Reactivity with Different PLDs

Statistical Analysis

RESULTS

Time Course after ACZ Injection

Repeatability of Rest rCBF Measurement

rCBF and rCVR with Different PLDs

DISCUSSION

CONCLUSIONS

ACKNOWLEDGMENTS

References

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Main menu

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Search

Arterial Spin-Labeling Evaluation of Cerebrovascular Reactivity to Acetazolamide in Healthy Subjects

Abstract

ABBREVIATIONS:

MATERIALS AND METHODS

Subjects

3D ASL Imaging

Calculation of Regional CBF Values

Time Course after ACZ Injection

Repeatability of Rest rCBF Measurement

rCBF and Regional Cerebrovascular Reactivity with Different PLDs

Statistical Analysis

RESULTS

Time Course after ACZ Injection

Repeatability of Rest rCBF Measurement

rCBF and rCVR with Different PLDs

DISCUSSION

CONCLUSIONS

ACKNOWLEDGMENTS

References

In this issue

Citation Manager Formats

Jump to section

Related Articles

Cited By...

More in this TOC Section

Similar Articles

News and Updates

Resources

Opportunities

American Society of Neuroradiology