AI Article Synopsis

  • Statistical shape modeling (SSM) is a key technique in biology and medicine for analyzing anatomical shapes, supported by advancements in imaging and open-source tools.
  • Limited evaluation of these tools in clinical settings highlights the need for systematic assessments of their performance, particularly in areas like implant design and lesion screening.
  • The study compares popular SSM tools (ShapeWorks, Deformetrica, SPHARM-PDM) using various metrics, revealing that ShapeWorks and Deformetrica are more consistent and effective in capturing clinically relevant shape variability compared to SPHARM-PDM.

Article Abstract

Statistical shape modeling (SSM) is widely used in biology and medicine as a new generation of morphometric approaches for the quantitative analysis of anatomical shapes. Technological advancements of in vivo imaging have led to the development of open-source computational tools that automate the modeling of anatomical shapes and their population-level variability. However, little work has been done on the evaluation and validation of such tools in clinical applications that rely on morphometric quantifications(e.g., implant design and lesion screening). Here, we systematically assess the outcome of widely used, state-of-the-art SSM tools, namely ShapeWorks, Deformetrica, and SPHARM-PDM. We use both quantitative and qualitative metrics to evaluate shape models from different tools. We propose validation frameworks for anatomical landmark/measurement inference and lesion screening. We also present a lesion screening method to objectively characterize subtle abnormal shape changes with respect to learned population-level statistics of controls. Results demonstrate that SSM tools display different levels of consistencies, where ShapeWorks and Deformetrica models are more consistent compared to models from SPHARM-PDM due to the groupwise approach of estimating surface correspondences. Furthermore, ShapeWorks and Deformetrica shape models are found to capture clinically relevant population-level variability compared to SPHARM-PDM models.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8792348PMC
http://dx.doi.org/10.1016/j.media.2021.102271DOI Listing

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