Browsing by Author "Lin, Yuan"
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Item Open Access Quantitative Poly-energetic Reconstruction Schemes for Single Spectrum CT Scanners(2014) Lin, YuanX-ray computed tomography (CT) is a non-destructive medical imaging technique for assessing the cross-sectional images of an object in terms of attenuation. As it is designed based on the physical processes involved in the x-ray and matter interactions, faithfully modeling the physics in the reconstruction procedure can yield accurate attenuation distribution of the scanned object. Otherwise, unrealistic physical assumptions can result in unwanted artifacts in reconstructed images. For example, the current reconstruction algorithms assume the photons emitted by the x-ray source are mono-energetic. This oversimplified physical model neglects the poly-energetic properties of the x-ray source and the nonlinear attenuations of the scanned materials, and results in the well-known beam-hardening artifacts (BHAs). The purpose of this work was to incorporate the poly-energetic nature of the x-ray spectrum and then to eliminate BHAs. By accomplishing this, I can improve the image quality, enable the quantitative reconstruction ability of the single-spectrum CT scanner, and potentially reduce unnecessary radiation dose to patients.
In this thesis, in order to obtain accurate spectrum for poly-energetic reconstruction, I first presented a novel spectral estimation technique, with which spectra across a large range of angular trajectories of the imaging field of view can be estimated with a single phantom and a single axial acquisition. The experimental results with a 16 cm diameter cylindrical phantom (composition: ultra-high-molecular-weight polyethylene [UHMWPE]) on a clinical scanner showed that the averaged absolute mean energy differences and the normalized root mean square differences with respect to the actual spectra across kVp settings (i.e., 80, 100, 120, 140) and angular trajectories were less than 0.61 keV and 3.41%, respectively
With the previous estimation of the x-ray spectra, three poly-energetic reconstruction algorithms are proposed for different clinical applications. The first algorithm (i.e., poly-energetic iterative FBP [piFBP]) can be applied to routine clinical CT exams, as the spectra of the x-ray source and the nonlinear attenuations of diverse body tissues and metal implant materials are incorporated to eliminate BHAs and to reduce metal artifacts. The simulation results showed that the variation range of the relative errors of various tissues across different phantom sizes (i.e., 16, 24, 32, and 40 cm in diameter) and kVp settings (80, 100, 120, 140) were reduced from [-7.5%, 17.5%] for conventional FBP to [-0.1%, 0.1%] for piFBP, while the noise was maintained at the same low level (about [0.3%, 1.7%]).
When iodinated contrast agents are involved and patient motions are not readily correctable (e.g., in myocardial perfusion exam), a second algorithm (i.e., poly-energetic simultaneous algebraic reconstruction technique [pSART]) can be applied to eliminate BHAs and to quantitatively determine the iodine concentrations of blood-iodine mixtures with our new technique. The phantom experiment on a clinical CT scanner indicated that the maximum absolute relative error across material inserts was reduced from 4.1% for conventional simultaneous algebraic reconstruction technique [SART] to 0.4% for pSART.
Extending the work beyond minimizing BHAs, if patient motions are correctable or negligible, a third algorithm (i.e., poly-energetic dynamic perfusion algorithm [pDP]) is developed to retrieve iodine maps of any iodine-tissue mixtures in any perfusion exams, such as breast, lung, or brain perfusion exams. The quantitative results of the simulations with a dynamic anthropomorphic thorax phantom indicated that the maximum error of iodine concentrations can be reduced from 1.1 mg/cc for conventional FBP to less than 0.1 mg/cc for pDP.
Two invention disclosure forms based on the work presented in this thesis have been submitted to Office of Licensing & Ventures of Duke University.
Item Open Access Two-stage genome-wide association study identifies a novel susceptibility locus associated with melanoma.(Oncotarget, 2017-03) Ransohoff, Katherine J; Wu, Wenting; Cho, Hyunje G; Chahal, Harvind C; Lin, Yuan; Dai, Hong-Ji; Amos, Christopher I; Lee, Jeffrey E; Tang, Jean Y; Hinds, David A; Han, Jiali; Wei, Qingyi; Sarin, Kavita YGenome-wide association studies have identified 21 susceptibility loci associated with melanoma. These loci implicate genes affecting pigmentation, nevus count, telomere maintenance, and DNA repair in melanoma risk. Here, we report the results of a two-stage genome-wide association study of melanoma. The stage 1 discovery phase consisted of 4,842 self-reported melanoma cases and 286,565 controls of European ancestry from the 23andMe research cohort and the stage 2 replication phase consisted of 1,804 melanoma cases and 1,026 controls from the University of Texas M.D. Anderson Cancer Center. We performed a combined meta-analysis totaling 6,628 melanoma cases and 287,591 controls. Our study replicates 20 of 21 previously known melanoma-loci and confirms the association of the telomerase reverse transcriptase, TERT, with melanoma susceptibility at genome-wide significance. In addition, we uncover a novel polymorphism, rs187843643 (OR = 1.96; 95% CI = [1.54, 2.48]; P = 3.53 x 10-8), associated with melanoma. The SNP rs187842643 lies within a noncoding RNA 177kb downstream of BASP1 (brain associated protein-1). We find that BASP1 expression is suppressed in melanoma as compared with benign nevi, providing additional evidence for a putative role in melanoma pathogenesis.