The effect of 18F-FDG-PET image reconstruction algorithms on the expression of characteristic metabolic brain network in Parkinson’s disease

• Published in: Physica medica Vol. 41; pp. 129 - 135
• Main Authors: Tomše, Petra, Jensterle, Luka, Rep, Sebastijan, Grmek, Marko, Zaletel, Katja, Eidelberg, David, Dhawan, Vijay, Ma, Yilong, Trošt, Maja
• Format: Journal Article
• Language: English
• Published: Italy Elsevier Ltd 01.09.2017
• Subjects: Algorithms; Brain - diagnostic imaging; Brain - metabolism; FDG-PET; Fluorodeoxyglucose F18; Humans; Image Processing, Computer-Assisted; Parkinson Disease - diagnostic imaging; Parkinson Disease - metabolism; Parkinson’s disease; Positron-Emission Tomography; Radiology; Reconstruction algorithms; Reproducibility of Results; Specific metabolic brain networks; FDG-PET; Reconstruction algorithms; Specific metabolic brain networks; Parkinson’s disease
• ISSN: 1120-1797; 1724-191X; 1724-191X
• DOI: 10.1016/j.ejmp.2017.01.018

•Parkinson’s Disease Related Pattern (PDRP) is a robust metabolic biomarker of PD.•PDRP expression is reproducible across FDG-PET reconstruction algorithms (RA).•Different RA may shift PDRP expression but do not affect disease discrimination. To evaluate the reproducibility of the expression of Parkinson’s Disease Related Pattern (PDRP) across multiple sets of 18F-FDG-PET brain images reconstructed with different reconstruction algorithms. 18F-FDG-PET brain imaging was performed in two independent cohorts of Parkinson's disease (PD) patients and normal controls (NC). Slovenian cohort (20 PD patients, 20 NC) was scanned with Siemens Biograph mCT camera and reconstructed using FBP, FBP+TOF, OSEM, OSEM+TOF, OSEM+PSF and OSEM+PSF+TOF. American Cohort (20 PD patients, 7 NC) was scanned with GE Advance camera and reconstructed using 3DRP, FORE-FBP and FORE-Iterative. Expressions of two previously-validated PDRP patterns (PDRP-Slovenia and PDRP-USA) were calculated. We compared the ability of PDRP to discriminate PD patients from NC, differences and correlation between the corresponding subject scores and ROC analysis results across the different reconstruction algorithms. The expression of PDRP-Slovenia and PDRP-USA networks was significantly elevated in PD patients compared to NC (p<0.0001), regardless of reconstruction algorithms. PDRP expression strongly correlated between all studied algorithms and the reference algorithm (r⩾0.993, p<0.0001). Average differences in the PDRP expression among different algorithms varied within 0.73 and 0.08 of the reference value for PDRP-Slovenia and PDRP-USA, respectively. ROC analysis confirmed high similarity in sensitivity, specificity and AUC among all studied reconstruction algorithms. These results show that the expression of PDRP is reproducible across a variety of reconstruction algorithms of 18F-FDG-PET brain images. PDRP is capable of providing a robust metabolic biomarker of PD for multicenter 18F-FDG-PET images acquired in the context of differential diagnosis or clinical trials.