To evaluate the feasibility of using pseudo-continuous arterial spin labeling (pCASL) perfusion in a geriatric population at 1.5-Tesla.
Materials and Methods
In 17 participants (mean age 78.8±1.63 years) we assessed; 1) inter-session repeatability and reliability of resting state perfusion in 27 brain regions; 2) brain activation using finger-tapping as a means to evaluate the ability to detect flow differences; 3) reliability by comparing cerebral blood flow (CBF) with pCASL to CBF with phase contrast (PC-MR).
The CBF (mean±standard deviation (SD)) for the whole brain grey matter (GM) was 40.6±8.4 and 41.4±8.7 ml/100g/min for the first and second scan respectively. The within-subject standard deviation (SDw), the repeatability index (RI) and intra-class correlation coefficient (ICC) across the 27 regions ranged from 1.1 to 7.9, 2.2 to 15.5 and 0.35 to 0.98 respectively. For whole brain GM the SDw, RI and ICC were 1.6, 3.2 and 0.96 respectively. The between-subject standard deviation (SDB) was larger than the SDw for all regions. Comparison of CBF at rest and activation on a voxel level showed significantly higher perfusion during finger tapping in the motor- and somatosensory regions. The mean CBF for whole brain GM was 40.6±8.4 ml/100g/min at rest and 42.6±8.6 ml/100g/min during activation. Finally the reliability of pCASL against the reference standard of PC-MR was high (ICC = 0.80). The mean CBF for whole brain measured with PC-MRI was 54.3±10.1 ml/100g/min and 38.3±7.8 ml/100g/min with pCASL.
The results demonstrate moderate to high levels of repeatability and reliability for most brain regions, comparable to what has been reported for younger populations. The performance of pCASL at 1.5-Tesla shows that region-specific perfusion measurements with this technique are feasible in studies of a geriatric population.
Citation: Sigurdsson S, Forsberg L, Aspelund T, van der Geest RJ, van Buchem MA, Launer LJ, et al. (2015) Feasibility of Using Pseudo-Continuous Arterial Spin Labeling Perfusion in a Geriatric Population at 1.5 Tesla. PLoS ONE 10(12): e0144743. doi:10.1371/journal.pone.0144743
Editor: Jeroen Hendrikse, University Medical Center (UMC) Utrecht, NETHERLANDS
Received: September 1, 2015; Accepted: November 22, 2015; Published: December 14, 2015
This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication
Data Availability: The data cannot be made publicly available since the informed consent signed by the participants, prohibits data sharing on an individual level as the approval for the study by the Icelandic National Bioethics Committee is based on. Requests for the data may be sent to the AGES-Reykjavik Study Executive Committee, contact; MS Gudny Eiriksdottir, email@example.com.
Funding: The authors have no support or funding to report.
Competing interests: The authors have declared that no competing interests exist.
Arterial spin labeling (ASL) can be used to visualize and quantify cerebral blood flow (CBF), an important physiological parameter used in the diagnosis and assessment of neurological disorders as well as for an examination of brain function . Several studies have shown high reliability of ASL techniques [2–5]. Most of these studies have been limited to 3-Tesla field strength and whole brain cortical grey matter (GM). The advantage of increased field strength is higher signal-to-noise ratio (SNR) which results from a combination of higher intrinsic SNR and longer T1-relaxation time of both tissue as well as arterial blood . The ASL signal decays with time constant T1 after labeling . The reported T1-relaxation time of arterial blood at 1.5-Tesla is in the range of 1350 msec to 1530 msec [7, 8], comparable to or even shorter than the arterial transit time for the flow of blood from the labeled region to the imaging region. Arterial transit times in healthy GM can vary between 500 msec and 1500 msec but can be 2000 msec or longer in cerebrovascular disease and in deep white matter (WM). Ideally the post-labeling delay (PLD) should be just longer than the longest arterial transit time. However, due the rapid decay of the ASL signal with time constant T1, it is too costly in terms of SNR to always meet this requirement. This is less of a problem at 3-Tesla field strength where arterial blood T1-relaxation times are longer compared to 1.5-Tesla (approximately 1650 msec) [6, 9].
However, ASL techniques are emerging as a tool for clinical use and the availability of systems at field strength of 1.5-Tesla are more widely available. Further, most extant studies are limited to young subjects. There is a need for reliability studies in older persons where there are specific issues that need to be accounted for when aiming for reliable measures. Older persons are at high risk for neurodegenerative disorders, and more detailed assessment of localized brain regions is needed. Motion artifacts in MR images that degrade their quality and clinical utility may be more likely to occur in older compared to younger adults. Imaging with ASL of older persons is also challenging due to age related morphological alterations of vasculature such as increased vessel tortuosity and damage of arteriole walls  shown to alter transit times and dispersion of blood flow tracers  resulting in inaccuracies in perfusion measurements. Further, age related atherosclerotic vascular disease including steno-occlusive disease can result in longer arterial transit times of blood water .
The objective of this study was to evaluate the feasibility of using pseudo-continuous arterial spin labeling (pCASL) in very old individuals with a commercial 1.5-Tesla MRI system. To our knowledge, there is no other study in the current literature that has assessed pCASL reproducibility in localized brain regions in a geriatric population at 1.5-Tesla.We assessed the following; 1) inter-session repeatability and reliability of resting state perfusion in template driven brain regions including GM and WM with and without white matter hyperintensities (WMH); 2) task-driven brain activation in GM regions as a way to assess the ability of pCASL to detect flow changes; and 3) reliability of pCASL by comparing whole brain CBF values generated with pCASL to whole brain CBF values generated with phase contrast -MRI as a reference standard.
Materials and Methods
The volunteers for this study were recruited from participants in the prospective population based Age Gene/Environment Susceptibility-Reykjavik Study . Repeated pCASL scans were acquired in 17 healthy subjects (7 women and 10 men); age (mean±standard deviation (SD)) 78.8±1.63 years in June 2012. Imaging with pCASL was performed three times; during rest, and then in the same scanning session during activation by bilateral finger tapping. Following this session and a 15 minute pause, each subject was repositioned in the scanner and rescanned during rest. Study subjects were requested to stay awake with eyes closed when the scan was being acquired. The study was approved by the Icelandic National Bioethics Committee, which acts as the Institutional Review Board for the Icelandic Heart Association. Written informed consent was obtained from all participants.
All scans were acquired on a 1.5-Tesla Signa system (General Electrics (GE), Waukesha, WI). In the first session when subjects were at rest, imaging with pCASL was followed with phase contrast (PC)-MRI for quantification of total CBF (tCBF). Anatomical imaging was acquired for brain tissue segmentation. The pCASL imaging was performed with the product sequence from GE , which adheres almost completely to the recently internationally recommended implementation of ASL ; a 3D fast spin echo (FSE) using spiral acquisition and background suppression with a scan time of 5 minutes (TR ⁄TE = 4678 ⁄ 9.8 msec, labeling duration 1500 msec, post labeling delay 1525 msec, 512 sampling points on eight spirals; reconstructed matrix 128x128, three averages, slice thickness 4 mm, FOV 24 cm). A PC-MRI scan (TR ⁄TE = 20⁄6.2 msec; flip-angle, 9°; FOV, 22 cm; matrix, 256x256; slice thickness 5 mm; velocity encoding 100 cm/sec) for measuring mean tCBF was prescribed on a PC-MRI sagittal localizer image perpendicular to the carotid arteries at the level of the mid basilar artery (Fig 1). The anatomical image protocol has been described in detail elsewhere  and included T1-weighted 3D spoiled gradient echo, proton density/T2-weighted FSE and fluid attenuated inversion recovery (FLAIR) sequences.
(a) A PC-MRI scan for measuring mean tCBF was prescribed on a PC-MRI sagittal localizer image perpendicular to the carotid arteries at the level of the mid basilar artery. (b) A representative phase image demonstrating the right and left internal carotid arteries (R.ICA and L.ICA) together with the basilar artery (BA).
Quantification of perfusion.
The quantitative CBF maps were generated using software (v16, M4) on the GE scanner console computer with a method proposed by Wang et al [6, 16]. In brief, the flow was calculated using the following equation: (1) where f is the perfusion, S is the signal on the control- (Sctrl), label- (Slbl) or reference image (Sref), λ is the blood brain partition coefficient (0.9 ml/g), α is the labeling efficiency (assumed to be 0.80), T1b is the T1 of blood (assumed to be 1400 msec). The same T1 of blood was assumed for men and women . The partial saturation of the reference image is corrected by using a T1g of 1200 msec (assumed T1 of GM), tsat is the saturation time (2000 msec), w is the post-labeling delay and τ is the labeling duration.
Brain tissue segmentation.
Whole brain tissue segmentation of GM, WM, WMH and cerebral-spinal-fluid (CSF) was done on intensity normalized and non-uniformity corrected anatomical images in MNI Talairach space, using a trained classifier . Regional segmentation was done by non-linearly warping an atlas of 56 regions to the T1-weighted image (Fig 2). The average CBF values were calculated for 27 regions of interests (ROIs); whole brain, whole brain GM, whole brain WMH, normal appearing WM and total WM in addition to 22 other GM and WM regions excluding WMH. Right and left hemispheric regions were combined into one. Normal appearing WM was defined as white matter without WMH and total WM as white matter including WMH. Whole brain volume was defined as the sum of whole brain GM- and total WM volumes .
For assessing the ability of pCASL to detect flow differences, statistically significant differences in perfusion between brain activation and rest were determined voxel-wise within MNI-space. Testing for significance was performed by permutation testing using the FSL software randomize with 5000 permutations . The permutations were enhanced with Threshold-Free Cluster Enhancement  resulting in a 1-P image, corrected for family-wise error.
Quantification of tCBF.
The PC-MR images were processed using the software package FLOW (Division of Image Processing, Leiden University Medical Center, The Netherlands) . The software quantified the average blood flow volume to the brain (in ml/min) after correcting for background velocity in stationary tissues. The average blood flow volume was subsequently divided by the whole brain volume to generate average whole brain CBF expressed in units of ml/100g/min assuming an average brain density of 1.05 g/ml .
The repeatability and reliability of pCASL was assessed by comparing the CBF measurements from the two scans at rest in the 27 ROIs. Several statistical parameters were included in these assessments that individually or all together have commonly been used in previous studies addressing ASL perfusion repeatability including Bland-Altman plot demonstrating the agreement between the first and second scan at rest for whole brain CBF [2, 4, 21]. The CBF for all ROIs were tested for normal distribution. Subsequently, a paired t-test was used to assess statistically significant difference in mean CBF between the two scans. Secondly, the within-subject SD (SDw), a measure of measurement error was calculated as the square root of the residual mean square within subjects using one-way ANOVA . The between-subject SD (SDB) was calculated in the same way as SDW but from residual between subjects mean square. Third, the repeatability index (RI), defined as the 95% confidence limits for the difference between repeated measurements was calculated using : (2) Fourth, the within-subject coefficient of variation (CoV) which quantifies the measurement error relative to the size of the measurements was calculated by dividing the SDw with the overall mean of CBF for both scans . Lastly, the intraclass correlation coefficient (ICC) was used to estimate the reliability of measurements. The ICC was estimated from a random effects model using PROC MIXED. An ICC close to 1.0 indicates high reliability, ICC values between 0.5 and 0.8 indicate a moderate reliability, whereas a value of 0.5 or lower indicates a randomness of results having limited use in distinguishing subjects .
For assessing the ability of pCASL to detect flow differences, statistically significant differences in perfusion between brain activation and rest were determined voxel-wise after correcting for multiple comparisons.
For the assessment of reliability of pCASL compared to PC-MRI, the ICC was calculated and a paired t-test used to assess difference between whole brain resting mean CBF values generated with the two techniques. Level of significance for all analyses was set to <0.05. All statistical analyses were performed with SAS/STAT®9.2 (SAS Institute Inc).
pCASL—Repeatability and reliability
Study sample characteristics are summarized in Table 1. In addition to volumes for the 27 brain ROIs, Tables 2 and 3 include by region the mean CBF with SDB for the two pCASL scans acquired at rest, and the measures of repeatability and reliability. There was no statistically significant difference between the two resting scans for any of the 27 ROIs except for the occipitotemporal gyrus (p = 0.04). The SDB was larger than SDw in all regions. There was a significant negative correlation between regional volume and SDw (-0.83, <0.0001). Small ROIs had generally greater within-subject variability compared to large ROIs.
The CBF (mean±SD) for the whole brain GM was 40.6±8.4 and 41.4±8.7 ml/100g/min for the first and second scan respectively. The corresponding CBF values for normal WM were 35.2±7.1 and 35.1±6.3 ml/100g/min and for total WM 34.6±7.2 and 34.5±6.5 ml/100g/min (Table 2). The GM/WM CBF ratio based on the first scan in rest was 1.2±0.1. The difference in CBF between normal WM and total WM was statistically significant for both scans (p<0.01).
Women had higher CBF values than men for whole brain (42.3±7.4 vs. 35.8±7.2), whole brain GM (45.2±8.1 vs. 38.0±7.7), whole brain normal WM (37.8±6.5 vs. 33.3±6.4) and whole brain total WM (37.5±6.5 vs. 32.5±6.5). This difference was not statistically significant for any of these regions.
Results of repeatability (SDw, RI, CoV) for whole brain GM were 1.62 ml/100g/min, 4.50 ml/100g/min and 4.10% respectively, for whole brain normal WM 1.34 ml/100g/min, 3.71 ml/100g/min and 3.9% respectively and for whole brain WMH 2.16 ml/100g/min, 5.98 ml/100g/min and 9.11% respectively (representative CBF maps of whole brain CBF for one study participant are shown in Fig 3). Reliability (ICC) for those regions was 0.96, 0.96 and 0.77 respectively (Table 2). A Bland-Altman plot demonstrates the agreement within limits (1.96 standard deviation) between the first and second scan at rest for whole brain CBF in all study subjects (Fig 4).
Representative CBF maps of an 80 year old male participant with whole brain CBF 47.6 and 49.5 ml/100g/min for the first and second scan at rest respectively. (a) First row corresponds to first scan at rest and (b) second row to rescan at rest.
Bland-Altman plot demonstrating the agreement between the first and second scan at rest for whole brain CBF. Solid mid and upper-lower lines are the mean bias and limits of agreement (1.96 standard deviation), respectively. Y-axis displays mean difference between first and second scan and x-axis the average CBF of the first and second scan.
Repeatability in all other regions ranged from 1.72 to 7.91 ml/100g/min, 3.10 to 21.95 ml/100g/min and 4.71 to 14.28% for SDw, RI, CoV respectively. The reliability for these regions varied between 0.35 and 0.97. Variability in CBF was higher in WM regions and subcortical GM compared to cortical GM regions (Tables 2 and 3). Lobar WM reliability was high ranging from 0.91 to 0.96, but lower in the external and internal capsules; 0.65 and 0.49 respectively (Table 3).
Table 4 includes mean pCASL CBF values for scans acquired at rest compared to the activation scans. The mean CBF for whole brain GM was 40.6±8.4 ml/100g/min at rest and 42.6±8.6 ml/100g/min during activation. Of the 17 GM ROIs included in the assessment, six which all were cortical ROIs, showed significantly lower mean CBF at rest compared to activation (p<0.001) (Fig 5A). Comparison of CBF values at rest and activation on a voxel level showed significantly higher perfusion during activation in the motor- and somatosensory regions at threshold p≤0.01 after correcting for multiple comparisons (Fig 5B).
(a) Average CBF maps of the entire study sample (n = 17) of the first scan at rest (Rest 1), rescan at rest (Rest 2) and at activation by bilateral finger-tapping (activation). (b) Comparison of CBF values at rest and activation by finger-tapping on a voxel level showed significantly higher perfusion during activation in the motor and somatosensory regions at threshold p≤0.01.
Reliability of pCASL compared to PC-MRI
The mean CBF for whole brain measured with PC-MRI was 54.3±10.1 ml/100g/min and with pCASL it was 38.3±7.8 ml/100g/min. The difference was statistically significant (p<0.0001). As with pCASL, women showed on average higher mean whole brain CBF with PC-MRI than men (57.3±11.1 vs. 52.3±9.3, ml/100g/min, p = 0.3). Measurements of CBF using pCASL showed high level of reliability when considering CBF using PC-MRI as a reference standard; the ICC between PC-MRI and pCASL was 0.80.
The aim of this study was to evaluate the feasibility of using perfusion imaging with pCASL on a 1.5-Tesla MRI system in an elderly population. The motivation of the study was the increasing clinical use of ASL and great promises of ASL for the assessment of neurodegenerative disorders as evidenced by fast growing literature [6, 25, 26].
The mean CBF estimates at rest for whole brain GM of this study are consistent with values reported in the PET and ASL MRI literature for healthy elderly individuals [5, 25, 27, 28], while estimates for total WM CBF are in the upper range of other ASL studies [21, 28]. Further, the GM/WM CBF ratio (1.2±0.1) was considerably lower in this study compared to results in many other ASL studies, typically reporting ratios between 2 and 4 [28, 29]. However, these studies used 2D readout sequences in contrast to this study, which used a 3D spiral readout sequence. Three previous studies compared 3D- to 2D readout sequences and reported lower ratio in 3D readout; 1.2 vs 2.1 , 1.7 vs 3.9  and 2.2 vs 4.3  due to image blurring  and larger extent of spatial smoothing of a spiral 3D readout compared to 2D readout leading to more contamination of the GM signal to WM and vice versa . Another contributor to inaccuracies in WM CBF values in this study may be related to long blood arrival times in WM and shorter T1 of blood at 1.5-Tesla compared to scanners with higher field strength [9, 33, 34]. Investigators and users of ASL should therefore interpret perfusion in WM with caution. Increasing age additionally contributes to lower GM/WM CBF ratio .
The mean CBF for total WM were significantly lower than mean CBF in normal WM. Hypoperfusion in areas of WMH is consistent with findings in two other studies [35, 36] and show that differences in WMH volume should be accounted for.
Women had on average higher CBF values than men for whole brain regions although this difference was not statistically significant. Higher CBF in women compared to men is in accordance with other ASL perfusion studies [3, 11, 27] and may be explained by lower hematocrit levels in women and therefore longer T1-relaxation time of blood . The quantification of CBF in this study assumed the same T1 of blood in men and women in accordance to the recent paper by Alsop et al on the recommended implementation of ASL perfusion for clinical applications . In the study by Zhang et al , the T1 of blood at 1.5-Tesla was measured as 1430 msec in men and 1530 msec in women. The CBF in whole brain GM in this study was found to be 16% higher in women compared to men on average. After correcting for blood T1 differences in men and women based on these T1 values using the CBF quantification method recommended by Alsop et al  for pCASL, this difference would be reduced to 5%. That together with the fact that the CBF values with PC-MRI were also higher in women compared to men suggests that the longer T1 of blood in women explains most, but not all of the observed sex difference.
Repeatability and reliability
The estimates of inter-session reproducibility and reliability in this study do not suggest increased variability in perfusion of healthy elderly subjects when compared to other ASL studies of younger subjects. In a study by Wang et al , reproducibility of CBF by pulsed ASL at 3 Tesla was assessed in multiple brain regions in 10 healthy young adults and showed inter-session variability ranging from 2.0 to 8.8 (SDw) and ICC ranging from 0.68 to 0.94. The SDw and ICC for whole brain cortical GM was 3.3 and 0.90 respectively. In another study using pCASL at 3-Tesla , the inter-session ICC in 8 young adults ranged from 0.82 to 0.98 for whole brain WM, lobar GM and posterior cingulate gyrus. These results are comparable to the results from this study. Less evidence exists in the current literature on ASL reproducibility in older individuals and results are inconsistent. The ICC in the same study as referenced to above , but in an older group of subjects (n = 14, age range 50–73 years) ranged from 0.80 to 0.96 for the same brain regions. In a recent study addressing inter-session reproducibility at 3-Tesla in older cognitively impaired subjects and normal controls, the ICCs of global brain perfusion were 0.70 and 0.41 for a 3D- and a 2D based pCASL sequences respectively  which is considerably lower compared to this study.
The reproducibility and reliability in the present study was high for most regions. The between-subject SD was up to seven times larger than SDW for all 27 regions, there was no statistically significant difference between the two scans at rest for 26 of the 27 regions and the ICC reflected moderate to high reliability for 24 out of the 27 regions (Tables 2 and 3). Smaller ROI sizes contribute to increased within-subject variability as evidenced by inverse correlation between regional volume and SDW, consistent with the results of Asllani et al .
Smaller SDW compared to SDB is in agreement with previous ASL perfusion regional reproducibility studies [21, 37]. This together with moderate to high ICCs for most regions supports that within-subject effects are a much smaller contributor to variability in perfusion measurements than other sources of variability between subjects, not only in young adults  but also in old individuals. Other sources of variability have been suggested to include variation in neuronal density, individual differences in underlying physiological fluctuations and T1 relaxation time of blood [2, 3, 40].
Another part of this study included brain activation measurements to assess the ability of ASL in detecting flow differences. The results showed clear flow differences between rest and activation in the expected brain regions. The anatomical location of the hand motor area (precentral gyrus) and the sensory receptive area for the sense of touch (postcentral gyrus) have been well established in the literature . The mean CBF difference between the rest and activation scan was statistically significant for 6 out of the 17 GM regions, all but one (occipital lobe) adjacent to or overlapping with the precentral or postcentral gyrus (Table 3). Further, the comparison on a voxel level showed significantly higher perfusion during activation in the motor- and somatosensory regions (Fig 5B).
Reliability of pCASL compared to PC-MRI
The reliability of pCASL was also tested by comparing it to PC-MRI as a reference standard. Flow quantification with PC-MRI is a well-established, robust method  that has been used in at least one previous study  as reference standard in the assessment of ASL perfusion reliability in children and showed a reliability of 0.65 (ICC). In the current study the ICC of pCASL compared to PC-MRI was higher (0.80).
This study has several limitations. Small sample size may explain lack of statistical significance in perfusion sex differences. The non-triggered PC-MRI scan used as a reference standard may contain noise and ghosting due to cardiac pulsation and physiologic fluctuations resulting in inaccuracies in the flow quantification. Further, averaging flow information over the cardiac cycle compared to trigger the scan to the cardiac cycle has been shown to give rise to a loss of information in the periphery of the vessels, resulting in artificially high flow values . The assumed T1-relaxation time of blood in this study (1400 msec) was somewhat low compared to measured T1 of blood in the study by Zhang et al (1430 msec in men and 1530 in women) .
In conclusion, the overall results of this study demonstrate moderate to high level of repeatability and reliability for majority of regions, comparable to what has been reported in younger populations with 3.0 Tesla MRI systems. The performance of pCASL on a 1.5-Tesla system in this study shows that perfusion measurements in brain regions of very old individuals are feasible.
This study is approved by the Icelandic National Bioethics Committee. The researchers are indebted to the participants for their willingness to participate in the study.
Conceived and designed the experiments: SS MJO. Performed the experiments: SS LF. Analyzed the data: SS LF TA. Contributed reagents/materials/analysis tools: MAB MJO RG VG. Wrote the paper: SS MJO. Critical revision of manuscript: SS LF TA RG MAB VG LJL MJO.
- 1. Wintermark M, Sesay M, Barbier E, Borbely K, Dillon WP, Eastwood JD, et al. Comparative Overview of Brain Perfusion Imaging Techniques. Stroke. 2005;36(9):e83–e99. pmid:16100027
- 2. Petersen ET, Mouridsen K, Golay X. The QUASAR reproducibility study, Part II: Results from a multi-center Arterial Spin Labeling test-retest study. NeuroImage. 2009;49(1):104–13. doi: 10.1016/j.neuroimage.2009.07.068. pmid:19660557
- 3. Parkes LM, Rashid W, Chard DT, Tofts PS. Normal cerebral perfusion measurements using arterial spin labeling: Reproducibility, stability, and age and gender effects. Magnetic Resonance in Medicine. 2004;51(4):736–43. pmid:15065246
- 4. Jain V, Duda J, Avants B, Giannetta M, Xie SX, Roberts T, et al. Longitudinal Reproducibility and Accuracy of Pseudo-Continuous Arterial Spin-labeled Perfusion MR Imaging in Typically Developing Children. Radiology. 2012;263(2):527–36. doi: 10.1148/radiol.12111509. pmid:22517961
- 5. Jahng G-H, Song E, Zhu X-P, Matson GB, Weiner MW, Schuff N. Human Brain: Reliability and Reproducibility of Pulsed Arterial Spin-labeling Perfusion MR Imaging1. Radiology. 2005;234(3):909–16. pmid:15734942
- 6. Alsop DC, Detre JA, Golay X, Günther M, Hendrikse J, Hernandez-Garcia L, et al. Recommended implementation of arterial spin-labeled perfusion MRI for clinical applications: A consensus of the ISMRM perfusion study group and the European consortium for ASL in dementia. Magnetic Resonance in Medicine. 2015;73:102–16. doi: 10.1002/mrm.25197. pmid:24715426
- 7. Barth M. ME. Proton NMR relaxation times of human blood samples at 1.5 T and implications for functional MRI. Cell Mol Biol. 1997;43(5):783–91. pmid:9298600
- 8. Zhang X, Petersen ET, Ghariq E, De Vis JB, Webb AG, Teeuwisse WM, et al. In vivo blood T1 measurements at 1.5 T, 3 T, and 7 T. Magnetic Resonance in Medicine. 2013;70(4):1082–6. doi: 10.1002/mrm.24550. pmid:23172845
- 9. Wang J, Alsop DC, Li L, Listerud J, Gonzalez-At JB, Schnall MD, et al. Comparison of quantitative perfusion imaging using arterial spin labeling at 1.5 and 4.0 Tesla. Magnetic Resonance in Medicine. 2002;48(2):242–54. pmid:12210932
- 10. Sonntag WE, Lynch CD, Cooney PT, Hutchins PM. Decreases in Cerebral Microvasculature with Age Are Associated with the Decline in Growth Hormone and Insulin-Like Growth Factor 1*. Endocrinology. 1997;138(8):3515–20. pmid:9231806
- 11. Liu Y, Zhu X, Feinberg D, Guenther M, Gregori J, Weiner MW, et al. Arterial spin labeling MRI study of age and gender effects on brain perfusion hemodynamics. Magnetic Resonance in Medicine. 2012;68(3):912–22. doi: 10.1002/mrm.23286. pmid:22139957
- 12. Mutke MA, Madai VI, von Samson-Himmelstjerna FC, Zaro Weber O, Revankar GS, Martin SZ, et al. Clinical Evaluation of an Arterial-Spin-Labeling Product Sequence in Steno-Occlusive Disease of the Brain. PLoS ONE. 2014;9(2):e87143. doi: 10.1371/journal.pone.0087143. pmid:24516546
- 13. Harris TB, Launer LJ, Eiriksdottir G, Kjartansson O, Jonsson PV, Sigurdsson G, et al. Age, Gene/Environment Susceptibility–Reykjavik Study: Multidisciplinary Applied Phenomics. American Journal of Epidemiology. 2007;165(9):1076–87. pmid:17351290
- 14. Dai W, Garcia D, de Bazelaire C, Alsop DC. Continuous flow-driven inversion for arterial spin labeling using pulsed radio frequency and gradient fields. Magnetic Resonance in Medicine. 2008;60(6):1488–97. doi: 10.1002/mrm.21790. pmid:19025913
- 15. Sigurdsson S, Aspelund T, Forsberg L, Fredriksson J, Kjartansson O, Oskarsdottir B, et al. Brain tissue volumes in the general population of the elderly: The AGES-Reykjavik Study. NeuroImage. 2012;59(4):3862–70. doi: 10.1016/j.neuroimage.2011.11.024. pmid:22119006
- 16. Wang J, Zhang Y, Wolf RL, Roc AC, Alsop DC, Detre JA. Amplitude-modulated Continuous Arterial Spin-labeling 3.0-T Perfusion MR Imaging with a Single Coil: Feasibility Study1. Radiology. 2005;235(1):218–28. pmid:15716390
- 17. Nichols TE, Holmes AP. Nonparametric permutation tests for functional neuroimaging: A primer with examples. Human Brain Mapping. 2002;15(1):1–25. pmid:11747097
- 18. Smith SM, Nichols TE. Threshold-free cluster enhancement: Addressing problems of smoothing, threshold dependence and localisation in cluster inference. NeuroImage. 2009;44(1):83–98. doi: 10.1016/j.neuroimage.2008.03.061. pmid:18501637
- 19. Spilt A, Box FMA, van der Geest RJ, Reiber JHC, Kunz P, Kamper AM, et al. Reproducibility of total cerebral blood flow measurements using phase contrast magnetic resonance imaging. Journal of Magnetic Resonance Imaging. 2002;16(1):1–5. pmid:12112496
- 20. Herscovitch P. What Is the Correct Value for the Brain-Blood Partition Coefficient for Water? J Cereb Blood Flow Metab. 1985;5(1):65–9. pmid:3871783
- 21. Hermes M, Hagemann D, Britz P, Lieser S, Rock Jr, Naumann E, et al. Reproducibility of continuous arterial spin labeling perfusion MRI after 7 weeks. Magnetic Resonance Materials in Physics, Biology and Medicine. 2007;20(2):103–15.
- 22. Bland JM, Altman DG. Statistics Notes: Measurement error proportional to the mean. BMJ. 1996;313(7049):106. pmid:8688716
- 23. Bland JM, Altman DG. Statistics Notes: Measurement error. BMJ. 1996;313(7059):744. pmid:8819450
- 24. Jiang L, Kim M, Chodkowski B, Donahue MJ, Pekar JJ, Van Zijl PCM, et al. Reliability and reproducibility of perfusion MRI in cognitively normal subjects. Magnetic Resonance Imaging. 2010;28(9):1283–9. doi: 10.1016/j.mri.2010.05.002. pmid:20573464
- 25. Zhang Q, Stafford RB, Wang Z, Arnold SE, Wolk DA, Detre JA. Microvascular Perfusion Based on Arterial Spin Labeled Perfusion MRI as a Measure of Vascular Risk in Alzheimer's Disease. Journal of Alzheimer's Disease. 2012;32(3):677–87. doi: 10.3233/JAD-2012-120964. pmid:22886015
- 26. Wolk. Arterial spin labeling MRI: an emerging biomarker for Alzheimer's disease and other neurodegenerative conditions. Curr Opin Neurol. 2012;25(4):421–8. doi: 10.1097/WCO.0b013e328354ff0a. pmid:22610458
- 27. Chen JJ, Rosas HD, Salat DH. Age-associated reductions in cerebral blood flow are independent from regional atrophy. NeuroImage. 2011;55(2):468–78. doi: 10.1016/j.neuroimage.2010.12.032. pmid:21167947
- 28. Xu G, Rowley HA, Wu G, Alsop DC, Shankaranarayanan A, Dowling M, et al. Reliability and precision of pseudo-continuous arterial spin labeling perfusion MRI on 3.0 T and comparison with 15O-water PET in elderly subjects at risk for Alzheimer's disease. NMR in Biomedicine. 2010;23(3):286–93. doi: 10.1002/nbm.1462. pmid:19953503
- 29. Asllani I, Habeck C, Borogovac A, Brown TR, Brickman AM, Stern Y. Separating function from structure in perfusion imaging of the aging brain. Human Brain Mapping. 2009;30(9):2927–35. doi: 10.1002/hbm.20719. pmid:19172645
- 30. Fernández-Seara MA, Wang Z, Wang J, Rao H- Y, Guenther M, Feinberg DA, et al. Continuous arterial spin labeling perfusion measurements using single shot 3D GRASE at 3 T. Magnetic Resonance in Medicine. 2005;54(5):1241–7. pmid:16193469
- 31. Vidorreta M, Wang Z, Rodríguez I, Pastor MA, Detre JA, Fernández-Seara MA. Comparison of 2D and 3D single-shot ASL perfusion fMRI sequences. NeuroImage. 2013;66(0):662–71.
- 32. Mutsaerts HJMM, Steketee RME, Heijtel DFR, Kuijer JPA, van Osch MJP, Majoie CBLM, et al. Inter-Vendor Reproducibility of Pseudo-Continuous Arterial Spin Labeling at 3 Tesla. PLoS ONE. 2014;9(8):e104108. doi: 10.1371/journal.pone.0104108. pmid:25090654
- 33. van Osch MJP, Teeuwisse WM, van Walderveen MAA, Hendrikse J, Kies DA, van Buchem MA. Can arterial spin labeling detect white matter perfusion signal? Magnetic Resonance in Medicine. 2009;62(1):165–73. doi: 10.1002/mrm.22002. pmid:19365865
- 34. van Gelderen P, de Zwart JA, Duyn JH. Pittfalls of MRI measurement of white matter perfusion based on arterial spin labeling. Magnetic Resonance in Medicine. 2008;59(4):788–95. doi: 10.1002/mrm.21515. pmid:18383289
- 35. Brickman AM, Zahra A, Muraskin J, Steffener J, Holland CM, Habeck C, et al. Reduction in cerebral blood flow in areas appearing as white matter hyperintensities on magnetic resonance imaging. Psychiatry Research: Neuroimaging. 2009;172(2):117–20. doi: 10.1016/j.pscychresns.2008.11.006. pmid:19324534
- 36. Bastos-Leite AJ, Kuijer JPA, Rombouts SARB, Sanz-Arigita E, van Straaten EC, Gouw AA, et al. Cerebral Blood Flow by Using Pulsed Arterial Spin-Labeling in Elderly Subjects with White Matter Hyperintensities. American Journal of Neuroradiology. 2008;29(7):1296–301. doi: 10.3174/ajnr.A1091. pmid:18451090
- 37. Wang Y, Saykin AJ, Pfeuffer J, Lin C, Mosier KM, Shen L, et al. Regional reproducibility of pulsed arterial spin labeling perfusion imaging at 3T. NeuroImage. 2011;54(2):1188–95. doi: 10.1016/j.neuroimage.2010.08.043. pmid:20800097
- 38. Kilroy E, Apostolova L, Liu C, Yan L, Ringman J, Wang DJJ. Reliability of two-dimensional and three-dimensional pseudo-continuous arterial spin labeling perfusion MRI in elderly populations: Comparison with 15o-water positron emission tomography. Journal of Magnetic Resonance Imaging. 2014;39(4):931–9. doi: 10.1002/jmri.24246. pmid:24038544
- 39. Asllani I, Borogovac A, Wright C, Sacco R, Brown TR, Zarahn E. An investigation of statistical power for continuous arterial spin labeling imaging at 1.5 T. NeuroImage. 2008;39(3):1246–56. pmid:18036834
- 40. Hodkinson DJ, Krause K, Khawaja N, Renton TF, Huggins JP, Vennart W, et al. Quantifying the test–retest reliability of cerebral blood flow measurements in a clinical model of on-going post-surgical pain: A study using pseudo-continuous arterial spin labelling. NeuroImage: Clinical. 2013;3(0):301–10.
- 41. Yousry TA, Schmid UD, Alkadhi H, Schmidt D, Peraud A, Buettner A, et al. Localization of the motor hand area to a knob on the precentral gyrus. A new landmark. Brain. 1997;120(1):141–57.
- 42. Barkhof F KM, Scheltens P, Sprenger M, Algra P, Valk J. Phase-contrast cine MR imaging of normal aqueductal CSF flow. Effect of aging and relation to CSF void on modulus MR. Acta Radiolo. 1994;35(s):123–30.