Andy Aitken
King's College London
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Featured researches published by Andy Aitken.
Neuroradiology | 2012
Yawu Liu; Valtteri Julkunen; Teemu Paajanen; Eric Westman; Lars-Olof Wahlund; Andy Aitken; Tomasz Sobow; Patrizia Mecocci; Magda Tsolaki; Bruno Vellas; Sebastian Muehlboeck; Christian Spenger; Simon Lovestone; Andrew Simmons; Hilkka Soininen
IntroductionThe aim of this study was to determine whether years of schooling influences regional cortical thicknesses and volumes in Alzheimer’s disease (AD), mild cognitive impairment (MCI), and healthy age-matched controls.MethodsUsing an automated image analysis pipeline, 33 regional cortical thickness and 15 regional volumes measures from MRI images were determined in 121 subjects with MCI, 121 patients with AD, and 113 controls from AddNeuroMed study. Correlations with years of schooling were determined and more highly and less highly educated subjects compared, controlling for intracranial volume, age, gender, country of origin, cognitive status, and multiple testing.ResultsAfter controlling for confounding factors and multiple testing, in the control group, subjects with more education had larger regional cortical thickness in transverse temporal cortex, insula, and isthmus of cingulate cortex than subjects with less education. However, in the AD group, the subjects with more education had smaller regional cortical thickness in temporal gyrus, inferior and superior parietal gyri, and lateral occipital cortex than the subjects with less education. No significant difference was found in the MCI group.ConclusionEducation may increase regional cortical thickness in healthy controls, leading to increased brain reserve, as well as helping AD patients to cope better with the effects of brain atrophy by increasing cognitive reserve.
Medical Physics | 2013
Andy Aitken; Daniel Giese; Charalampos Tsoumpas; Paul Schleyer; Sebastian Kozerke; Claudia Prieto; Tobias Schaeffter
PURPOSE Ultrashort echo time (UTE) MRI has been proposed as a way to produce segmented attenuation maps for PET, as it provides contrast between bone, air, and soft tissue. However, UTE sequences require samples to be acquired during rapidly changing gradient fields, which makes the resulting images prone to eddy current artifacts. In this work it is demonstrated that this can lead to misclassification of tissues in segmented attenuation maps (AC maps) and that these effects can be corrected for by measuring the true k-space trajectories using a magnetic field camera. METHODS The k-space trajectories during a dual echo UTE sequence were measured using a dynamic magnetic field camera. UTE images were reconstructed using nominal trajectories and again using the measured trajectories. A numerical phantom was used to demonstrate the effect of reconstructing with incorrect trajectories. Images of an ovine leg phantom were reconstructed and segmented and the resulting attenuation maps were compared to a segmented map derived from a CT scan of the same phantom, using the Dice similarity measure. The feasibility of the proposed method was demonstrated in in vivo cranial imaging in five healthy volunteers. Simulated PET data were generated for one volunteer to show the impact of misclassifications on the PET reconstruction. RESULTS Images of the numerical phantom exhibited blurring and edge artifacts on the bone-tissue and air-tissue interfaces when nominal k-space trajectories were used, leading to misclassification of soft tissue as bone and misclassification of bone as air. Images of the tissue phantom and the in vivo cranial images exhibited the same artifacts. The artifacts were greatly reduced when the measured trajectories were used. For the tissue phantom, the Dice coefficient for bone in MR relative to CT was 0.616 using the nominal trajectories and 0.814 using the measured trajectories. The Dice coefficients for soft tissue were 0.933 and 0.934 for the nominal and measured cases, respectively. For air the corresponding figures were 0.991 and 0.993. Compared to an unattenuated reference image, the mean error in simulated PET uptake in the brain was 9.16% when AC maps derived from nominal trajectories was used, with errors in the SUV max for simulated lesions in the range of 7.17%-12.19%. Corresponding figures when AC maps derived from measured trajectories were used were 0.34% (mean error) and -0.21% to +1.81% (lesions). CONCLUSIONS Eddy current artifacts in UTE imaging can be corrected for by measuring the true k-space trajectories during a calibration scan and using them in subsequent image reconstructions. This improves the accuracy of segmented PET attenuation maps derived from UTE sequences and subsequent PET reconstruction.
IEEE Transactions on Nuclear Science | 2012
Christian Buerger; Charalampos Tsoumpas; Andy Aitken; Andrew P. King; Paul Schleyer; Volkmar Schulz; Paul Marsden; Tobias Schaeffter
In hybrid PET/MR systems, attenuation maps can be derived from MR to correct for attenuation in PET. However, MR-based attenuation correction (AC) in abdominal applications remains challenging (i) because of poor signal from important tissue types in common MR sequences (e.g., cortical bone) and (ii) because of respiratory motion which results in misalignments between the derived attenuation maps and the PET emissions. Furthermore, respiratory motion also leads to motion-blurring artefacts in the final PET reconstructions. In this paper, we compute an MR-based 4D attenuation map including cortical bone by combining an Ultrashort Echo Time (UTE) acquisition with a subject-specific motion model derived from a second near real-time 3D MR image acquisition. This model allows us to create attenuation maps at any respiratory position which are used for AC in the reconstruction of different respiratory resolved PET images. The inverse of the model is used for motion compensation (MC) of these images. We demonstrate our approach on MR data from 5 healthy volunteers including 3 manually inserted artificial lesions. The impact of bone tissue and respiratory motion on AC is investigated in PET simulations (i) by misclassifying bone to soft tissue in the attenuation maps leading to errors of up to 26.0% in mean uptake for lesions close to bone, and (ii) by using a non-moving attenuation map leading to errors of up to 24.2%. The impact of respiratory motion on MC showed errors of up to 50.7% in areas of strong motion if MC was not performed. The results show that the effect of motion has to be considered both for attenuation correction and for motion-compensating PET emissions. This additive effect of motion is larger than the effect of a wrong AC.
Magnetic Resonance in Medicine | 2015
Andy Aitken; Markus Henningsson; René M. Botnar; Tobias Schaeffter; Claudia Prieto
To develop a flexible image navigator for 3D coronary MR angiography that allows respiratory motion of variable complexity to be compensated for on different temporal scales.
ieee nuclear science symposium | 2011
Christian Buerger; Andy Aitken; Charalampos Tsoumpas; Andrew P. King; Volkmar Schulz; Paul Marsden; Tobias Schaeffter
In hybrid imaging systems where positron emission tomography (PET) is combined with magnetic resonance (MR) imaging, attenuation maps can be derived from MR to correct for attenuation in PET. However, MR-based attenuation correction (AC) remains challenging especially for tissue types showing poor signal in common MR sequences, such as bone. To overcome this problem, Ultra-short Echo Time (UTE) sequences have been proposed. Another challenge is given by respiratory motion which results in misalignments between the derived attenuation maps and the PET emissions. In this paper we address both issues. We compute a 4D attenuation map including bone from MR by combining a respiratory gated UTE acquisition with a subject-specific motion model derived from a second short dynamic acquisition. We demonstrate our approach on an MR-derived time-averaged PET simulation from three healthy volunteers, including three artificial lesions. The impact of bone on AC is simulated by excluding bone from the derived 4D map leading to errors of up to 26.0%. The impact of respiratory motion is simulated by using a non-moving 3D map, showing an error of up to 24.2%. These results indicate that a consideration of both bone tissue and respiratory motion is crucial to ensure accurate MR-based PET AC.
Dementia and geriatric cognitive disorders extra | 2013
Teemu Paajanen; Tuomo Hänninen; Andy Aitken; Merja Hallikainen; Eric Westman; L.-O. Wahlund; Tomasz Sobow; P. Mecocci; Magda Tsolaki; Bruno Vellas; Sebastian Muehlboeck; Christian Spenger; Simon Lovestone; Andrew Simmons; H. Soininen
Background: Sensitive cognitive global scores are beneficial in screening and monitoring for prodromal Alzheimers disease (AD). Early cortical changes provide a novel opportunity for validating established cognitive total scores against the biological disease markers. Methods: We examined how two different total scores of the Consortium to Establish a Registry for Alzheimers Disease (CERAD) battery and the Mini-Mental State Examination (MMSE) are associated with cortical thickness (CTH) in mild cognitive impairment (MCI) and prodromal AD. Cognitive and magnetic resonance imaging (MRI) data of 22 progressive MCI, 78 stable MCI, and 98 control subjects, and MRI data of 103 AD patients of the prospective multicenter study were analyzed. Results: CERAD total scores correlated with mean CTH more strongly (r = 0.34-0.38, p < 0.001) than did MMSE (r = 0.19, p = 0.01). Of those vertex clusters that showed thinning in progressive MCI, 60-75% related to the CERAD total scores and 3% to the MMSE. Conclusion: CERAD total scores are sensitive to the CTH signature of prodromal AD, which supports their biological validity in detecting early disease-related cognitive changes.
Journal of Magnetic Resonance | 2014
Rw Chan; Constantin von Deuster; Daniel Giese; Christian T. Stoeck; Jack Harmer; Andy Aitken; David Atkinson; Sebastian Kozerke
Archive | 2013
Andy Aitken; Christoph Kolbitsch; Tobias Schaeffter; Claudia Prieto Vasquez
Archive | 2014
Andy Aitken; Markus Henningsson; Tobias Schaeffter; Claudia Prieto Vasquez
Archive | 2014
Andy Aitken; Markus Henningsson; Tobias Schaeffter; Claudia Prieto Vasquez