AOAzubuike M. Okorie

Azubuike M. Okorie

*This is an algorithmically generated author record based on publicly available information.

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Azubuike M. Okorie has a total of 13 co-authors. Here are the top co-authors by number of shared publications:


Latest Publications

  • Open Access

    PET Imaging of Neurofibromatosis Type 1 with a Fluorine-18 Labeled Tryptophan Radiotracer

    by Xuyi Yue, Erik Stauff, Shriya Boyapati, Sigrid A. Langhans, Wenqi Xu, Sokratis Makrogiannis, Uchenna J. Okorie, Azubuike M. Okorie, Vinay V. R. Kandula, Heidi H. Kecskemethy, et al.

    Neurofibromatosis type 1 (NF1) is a neurocutaneous disorder. Plexiform neurofibromas (PNFs) are benign tumors commonly formed in patients with NF1. PNFs have a high incidence of developing into malignant peripheral nerve sheath tumors (MPNSTs) with a 5-year survival rate of only 30%. Therefore, the accurate diagnosis and differentiation of MPNSTs from benign PNFs are critical to patient management. We studied a fluorine-18 labeled tryptophan positron emission tomography (PET) radiotracer, 1-(2-[18F]fluoroethyl)-L-tryptophan (L-[18F]FETrp), to detect NF1-associated tumors in an animal model. An ex vivo biodistribution study of L-[18F]FETrp showed a similar tracer distribution and kinetics between the wild-type and triple mutant mice with the highest uptake in the pancreas. Bone uptake was stable. Brain uptake was low during the 90-min uptake period. Static PET imaging at 60 min post-injection showed L-[18F]FETrp had a comparable tumor uptake with [1⁸F]fluorodeoxyglucose (FDG). However, L-[18F]FETrp showed a significantly higher tumor-to-brain ratio than FDG (n = 4, p < 0.05). Sixty-minute-long dynamic PET scans using the two radiotracers showed similar kidney, liver, and lung kinetics. A dysregulated tryptophan metabolism in NF1 mice was further confirmed using immunohistostaining. L-[18F]FETrp is warranted to further investigate differentiating malignant NF1 tumors from benign PNFs. The study may reveal the tryptophan–kynurenine pathway as a therapeutic target for treating NF1.


  • Unsupervised learning of probabilistic subspaces for multi-spectral and multi-temporal image-based disaster mapping

    by Azubuike Okorie, Chandra Kambhamettu, Sokratis Makrogiannnis

    Accurate and timely identification of regions damaged by a natural disaster is critical for assessing the damages and reducing the human life cost. The increasing availability of satellite imagery and other remote sensing data has triggered research activities on development of algorithms for detection and monitoring of natural events. Here, we introduce an unsupervised subspace learning-based methodology that uses multi-temporal and multi-spectral satellite images to identify regions damaged by natural disasters. It first performs region delineation, matching, and fusion. Next, it applies subspace learning in the joint regional space to produce a change map. It identifies the damaged regions by estimating probabilistic subspace distances and rejecting the non-disaster changes. We evaluated the performance of our method on seven disaster datasets including four wildfire events, two flooding events, and a earthquake/tsunami event. We validated our results by calculating the dice similarity coefficient (DSC), and accuracy of classification between our disaster maps and ground-truth data. Our method produced average DSC values of 0.833 and 0.736, for wildfires and floods, respectively, and overall DSC of 0.855 for the tsunami event. The evaluation results support the applicability of our method to multiple types of natural disasters.