Synopsis
In this lecture,
we provide an overview on the potential of coupling of cutting edge
technologies in quantitative MRI, deep learning and big data analytics fields.
The main goal is to show how those techniques can be applied to discover latent
feature able to accurately characterize disease status and predict progression.
The data-driven extraction of features from relaxation maps and
multidimensional analysis of data from various sources can exploit the real
potential of quantitative MRI technique, to date still hampered by tedious and
time-consuming manual image post-processing pipelines; and deeply underused due
to the handcrafting of too simplistic image representations.
Introduction
Quantitative
compositional MRI plays a central role in Osteoarthritis(OA) research, offering
imaging biomarkers that probe the biochemical composition of the articular
cartilage1.
While
several studies are still limited to analyzing average relaxation time values
of manually defined cartilage compartments2,
there is growing interest in exploring techniques for the automatic analysis of
spatial distribution and extraction of relaxometry patterns able to
characterize subjects and predict disease progression. Extraction of second
order statistical information, or texture analysis3-5, has been widely used to overcome the limitation of
the average ROI-based approaches. However, texture analysis does not address
the problem of studying local differences between two groups, and does not
allow for the extraction of salient patterns that could characterize cartilage
degeneration in a data-driven way. Automation of post-processing pipelines and
more effective feature extraction techniques are needed to exploit the real
potential of compositional MRI techniques which is, to date, still hampered by
tedious and time-consuming manual image post-processing pipelines; and deeply
underused due to the handcrafting of overly-simplistic image representations.
Deep Learning applied to MSK Quantitative MRI: Data-Driven Feature Extraction
In the last few years, Computer Vision has
been drastically accelerated by the usage of machine learning techniques
6-7. With the large
availability of annotated data and processing power, supervised learning can
today accomplish challenges never demonstrated before using the concepts of
transforming data to knowledge by the observation and computational
interpretation of said examples
8-11. Additionally, a completely new concept has changed the
machine-learning field; supervised feature extraction. Conventional machine
learning techniques were limited in their ability to process natural data in
their raw form. For decades, constructing a pattern-recognition or machine
learning system required careful engineering and considerable domain expertise
to design feature extractors able to transform raw data, such as the pixel
values of an image, into a suitable internal representation or feature vector
from which the classifier could detect patterns in the input. In contrast,
representation learning allows a machine to be fed with raw data and to
automatically discover the best representations of the information hidden in
the data needed to accomplish a specified task
12. Deep learning
neural networks are a representation learning method characterized by the usage
of multiple simple, non-linear units to build several interconnected layers.
Each layer aggregates the information at increasing levels of abstraction
starting with simple image elements, such as edges or contrast, to more complex
and semantic aggregations, such as uncovering latent patterns able to
accomplish pattern recognition tasks
13.
The key aspect of deep learning is that these models are not designed to solve
a specific task, but are adaptive to the specific problems, learning directly
from the data and using a general-purpose learning procedure. Deep learning
models were recently applied to solve joint tissues segmentation tasks
14-15 and relaxation time
feature extraction
16-17 showing
promising results in overcoming traditional post processing techniques.
Integration and Analysis of Multidimensional Data: Topological Data Analysis to Study OA
While OA is known as a whole joint
disease, the data analytics more commonly used are often limited to either
univariate analysis or a subset of the variables. However, innovations in the
big data analytics field have brought several multidimensional visualization methods
with which we can compare individual patients as a ‘point-cloud’ in
multidimensional space, overcoming the inherent limitations of single endpoints.
One possible approach considers the usage of data shape or topology
18. Topological data analysis (TDA) explores
relationships between data and data shapes. The fundamental idea of TDA
is that this method acts as a geometric approach to pattern recognition within
data. By extracting fundamental shapes (patterns) in high-dimensional data TDA
provides visualization that can provide novel insights about the data and can
identify meaningful sub-groups. Extracting patterns via shape data analysis is
possible due to three key ideas: 1) coordinate free description, 2) invariance
to small deformations and 3) compactness. The first permits the
generalizability of the insights extracted from
the shape of complex data. The second guarantees robustness to noise while the
last allows complex data to be represented in a simple way. These
characteristics make TDA a valuable tool for a combined analysis of all the OA
features simultaneously, ultimately leading to a more accurate study of risk
factors, pathogenesis and natural history of OA and disease phenotyping
19.
Conclusions
In this lecture, recent innovations in the
fields of image processing, machine learning and multidimensional/multimodal
data analysis to study musculoskeletal disorders will be presented with the aim
of discussing the potentials of coupling cutting edge technologies in
quantitative compositional MRI and machine learning fields to discover new tools
able to automate post-processing, better characterize disease status, and
predict progression.
Acknowledgements
I received funding from NIH-NIAMS K99AR070902 (VP) and GE Healthcare A128218 (SM/VP)References
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