Guilhem Collier
University of Sheffield
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Publication
Featured researches published by Guilhem Collier.
Magnetic Resonance in Medicine | 2015
Guilhem Collier; Jim M. Wild
Hyperpolarized (HP) 3He and 129Xe are two gases with different fluid dynamic properties, which can be used as tracers for airflow measurement in the lungs with phase contrast velocimetry MRI sequences. In this work, in vivo measurements of velocity maps of airflow in the upper airways and first bronchi of healthy volunteers were obtained with both gases and compared.
NMR in Biomedicine | 2014
Felix Horn; Bilal Tahir; Neil J. Stewart; Guilhem Collier; Graham Norquay; General Leung; Rob H. Ireland; Juan Parra-Robles; Helen Marshall; Jim M. Wild
The purpose of this work was to assess the reproducibility of percentage of ventilated lung volume (PV) measured from hyperpolarized (HP) 3He and 1H anatomical images acquired in the same breath‐hold when compared with PV measured from 3He and 1H images from separate breath‐holds.
Thorax | 2017
Helen Marshall; Alex Horsley; Christopher J. Taylor; Laurie Smith; David Hughes; Felix Horn; Andrew J. Swift; Juan Parra-Robles; Paul Hughes; Graham Norquay; Neil J. Stewart; Guilhem Collier; Dawn Teare; Steve Cunningham; Ina Aldag; Jim M. Wild
Hyperpolarised 3He ventilation-MRI, anatomical lung MRI, lung clearance index (LCI), low-dose CT and spirometry were performed on 19 children (6–16 years) with clinically stable mild cystic fibrosis (CF) (FEV1>−1.96), and 10 controls. All controls had normal spirometry, MRI and LCI. Ventilation-MRI was the most sensitive method of detecting abnormalities, present in 89% of patients with CF, compared with CT abnormalities in 68%, LCI 47% and conventional MRI 22%. Ventilation defects were present in the absence of CT abnormalities and in patients with normal physiology, including LCI. Ventilation-MRI is thus feasible in young children, highly sensitive and provides additional information about lung structure–function relationships.
Magnetic Resonance in Medicine | 2017
Ho-Fung Chan; Neil J. Stewart; Juan Parra-Robles; Guilhem Collier; Jim M. Wild
To demonstrate three‐dimensional (3D) multiple b‐value diffusion‐weighted (DW) MRI of hyperpolarized 3He gas for whole lung morphometry with compressed sensing (CS).
American Journal of Respiratory and Critical Care Medicine | 2017
Laurie Smith; Helen Marshall; Ina Aldag; Felix Horn; Guilhem Collier; David Hughes; Noreen West; Alex Horsley; Christopher J. Taylor; Jim M. Wild
the shortand long-term respiratory outcomes of prematurity and bronchopulmonary dysplasia. Am J Respir Crit Care Med 2015;192: 134–156. 3. Kreiner-Møller E, Chawes BL, Vissing NH, Koppelman GH, Postma DS, Madsen JS, et al. VEGFA variants are associated with pre-school lung function, but not neonatal lung function.Clin Exp Allergy 2013;43:1236–1245. 4. Thébaud B, Ladha F, Michelakis ED, Sawicka M, Thurston G, Eaton F, et al. Vascular endothelial growth factor gene therapy increases survival, promotes lung angiogenesis, and prevents alveolar damage in hyperoxia-induced lung injury: evidence that angiogenesis participates in alveolarization. Circulation 2005;112:2477–2486. 5. Mourani PM, Sontag MK, Younoszai A, Miller JI, Kinsella JP, Baker CD, et al. Early pulmonary vascular disease in preterm infants at risk for bronchopulmonary dysplasia. Am J Respir Crit Care Med 2015;191:87–95. 6. Hathout Y, Brody E, Clemens PR, Cripe L, DeLisle RK, Furlong P, et al. Large-scale serum protein biomarker discovery in Duchenne muscular dystrophy. Proc Natl Acad Sci USA 2015;112:7153–7158. 7. Ganz P, Heidecker B, Hveem K, Jonasson C, Kato S, Segal MR, et al. Development and validation of a protein-based risk score for cardiovascular outcomes among patients with stable coronary heart disease. JAMA 2016;315:2532–2541. 8. Ngo D, Sinha S, Shen D, Kuhn EW, Keyes MJ, Shi X, et al. Aptamer-based proteomic profiling reveals novel candidate biomarkers and pathways in cardiovascular disease. Circulation 2016;134:270–285. 9. SabatineMS. Using aptamer-based technology to probe the plasma proteome for cardiovascular disease prediction. JAMA 2016;315:2525–2526. 10. Rohloff JC, Gelinas AD, Jarvis TC, Ochsner UA, Schneider DJ, Gold L, et al. Nucleic acid ligands with protein-like side chains: modified aptamers and their use as diagnostic and therapeutic agents. Mol Ther Nucleic Acids 2014;3:e201.
Magnetic Resonance in Medicine | 2017
Neil J. Stewart; Felix Horn; Graham Norquay; Guilhem Collier; Denise Yates; Rod Lawson; Helen Marshall; Jim M. Wild
To evaluate the reproducibility of indices of lung microstructure and function derived from 129Xe chemical shift saturation recovery (CSSR) spectroscopy in healthy volunteers and patients with chronic obstructive pulmonary disease (COPD), and to study the sensitivity of CSSR‐derived parameters to pulse sequence design and lung inflation level.
Journal of Magnetic Resonance Imaging | 2018
Neil J. Stewart; Ho-Fung Chan; Paul Hughes; Felix Horn; Graham Norquay; Madhwesha Rao; Denise Yates; Rob H. Ireland; M.Q. Hatton; Bilal Tahir; Paul Ford; Andrew J. Swift; Rod Lawson; Helen Marshall; Guilhem Collier; Jim M. Wild
To support translational lung MRI research with hyperpolarized 129Xe gas, comprehensive evaluation of derived quantitative lung function measures against established measures from 3He MRI is required. Few comparative studies have been performed to date, only at 3T, and multisession repeatability of 129Xe functional metrics have not been reported.
Journal of Magnetic Resonance Imaging | 2018
Paul Hughes; Felix Horn; Guilhem Collier; Alberto Biancardi; Helen Marshall; Jim M. Wild
To develop an image‐processing pipeline for semiautomated (SA) and reproducible analysis of hyperpolarized gas lung ventilation and proton anatomical magnetic resonance imaging (MRI) scan pairs. To compare results from the software for total lung volume (TLV), ventilated volume (VV), and percentage lung ventilated volume (%VV) calculation to the current manual “basic” method and a K‐means segmentation method.
Radiology | 2017
Felix Horn; Helen Marshall; Guilhem Collier; Richard Kay; Salman Siddiqui; Christopher E. Brightling; Juan Parra-Robles; Jim M. Wild
Purpose To assess the magnitude of regional response to respiratory therapeutic agents in the lungs by using treatment response mapping (TRM) with hyperpolarized gas magnetic resonance (MR) imaging. TRM was used to quantify regional physiologic response in adults with asthma who underwent a bronchodilator challenge. Materials and Methods This study was approved by the national research ethics committee and was performed with informed consent. Imaging was performed in 20 adult patients with asthma by using hyperpolarized helium 3 (3He) ventilation MR imaging. Two sets of baseline images were acquired before inhalation of a bronchodilating agent (salbutamol 400 μg), and one set was acquired after. All images were registered for voxelwise comparison. Regional treatment response, ΔR(r), was calculated as the difference in regional gas distribution (R[r] = ratio of inhaled gas to total volume of a voxel when normalized for lung inflation volume) before and after intervention. A voxelwise activation threshold from the variability of the baseline images was applied to ΔR(r) maps. The summed global treatment response map (ΔRnet) was then used as a global lung index for comparison with metrics of bronchodilator response measured by using spirometry and the global imaging metric percentage ventilated volume (%VV). Results ΔRnet showed significant correlation (P < .01) with changes in forced expiratory volume in 1 second (r = 0.70), forced vital capacity (r = 0.84), and %VV (r = 0.56). A significant (P < .01) positive treatment effect was detected with all metrics; however, ΔRnet showed a lower intersubject coefficient of variation (64%) than all of the other tests (coefficient of variation, ≥99%). Conclusion TRM provides regional quantitative information on changes in inhaled gas ventilation in response to therapy. This method could be used as a sensitive regional outcome metric for novel respiratory interventions.
Magnetic Resonance in Medicine | 2018
Ho-Fung Chan; Neil J. Stewart; Graham Norquay; Guilhem Collier; Jim M. Wild
To obtain whole lung morphometry measurements from 129Xe in a single breath‐hold with 3D multiple b‐value 129Xe diffusion‐weighted MRI (DW‐MRI) with an empirically optimized diffusion time and compressed sensing for scan acceleration.