Preety Krishnan1, Tejas J Shah2, Akshay Godkhindi2, Rupsa Bhattacharjee3, Stanley Kovil Pichai3, Ajay Krishnan1, Bharat Dave1, and Indrajit Saha3
1Stavya Spine Research Institute, Ahmedabad, India, 2MR, Philips Innovation Campus, Bangalore, India, 3Philips India Limited, Gurgaon, India
Synopsis
Given the prevalence and disease burden of
osteoporosis, it is critical to detect it as early as possible. This is challenging
not only because the disease is typically asymptomatic but also due to known limitations
of the gold standard method of DEXA. The aim of this study was to determine if
alternative approach of 2D texture analysis in L1-L5 lumbar spine on T1W images
can be used to detect osteoporosis. It is demonstrated that such an approach
can indeed be used to clinically detect osteoporosis with an AUC of 0.8.
Background
Osteoporosis is a systemic skeletal disease that causes loss of bone
strength due to low bone mass and deterioration of bone microarchitecture1 leading to increased risk of
bone fractures. Therefore, early detection of osteoporosis is critical for
early intervention to reduce the fracture risk, better disease management and
improved patient quality of life.
Bone mineral density (BMD) measurement is a critical step in diagnosis
of osteoporosis with dual energy x-ray absorptiometry (DEXA) being the gold
standard technique and femoral neck being the gold standard site1. However, there are several
drawbacks with this methodology of BMD measurement including exposure to
ionizing radiation and vulnerability to biased results1.
MRI, on the other hand, is a non-ionizing imaging modality that
provides better soft tissue contrast and can be repeatedly used without any
known side effects to patients. In a clinical scenario, patient typically walks
in with symptoms unrelated to osteoporosis, such as back pain, for which a MRI
exam is often performed2. Also, studies have shown
that bone marrow signal intensity on T1W images is correlated to osteoporosis3.
Texture analysis/Radiomics has been used on MR images for tumor
characterization and grading4. Recent study has shown that
combining MR images of Spine with texture analysis enables detection of
osteoporosis5. In this study, we investigate
the use of a single slice approach on the five lumbar vertebrae, at different
anatomical sites on T1W images for detecting osteoporosis.Methods
In this EC approved study, 91
subjects were evaluated, who underwent routine spine MRI at a 1.5T MRI
scanner (Multiva, Philips Healthcare, Best, The Netherlands) using product whole spine coil and DEXA scans for BMD
measurements. T1W images were acquired using a TSE protocol with the following
parameters ETL: 7, TE/TR 8ms/55.3ms, Voxel size: 0.68 mm/0.93mm/4mm, and a
matrix of 339/247/15 in
frequency/phase/slice direction.
15 patients with considerable
scoliosis and/or spine implants were excluded. Patients were diagnosed with
osteoporosis based on DEXA t-scores and their medical history.
The classification process is
shown in Figure 1.
L1-L5 vertebrae were chosen on Sagittal T1W images as shown in Figure 1.a.
ROIs were drawn manually on L1-L5 vertebrae as shown in Figure 1.
b except in cases where one or multiple lumbar vertebra/e had collapsed.
Texture features were computed using MaZda software (MaZda 4.6, The Technical
University of Lodz, Institute of Electronics)6. The categories of features
that were extracted are shown in Figure 1.c.
The Wavelet features were averaged Eg. WaveEn-S1 = Mean(Wave HH S-1, Wave HL
S-1, Wave LH S-1, Wave LL S-1). Similarly, the GLCM features were averaged eg. AngScMom
= Average of all AngScMoms computed for neighboring pixels. Feature selection
and model generation for classification was done on Python programming
software, version 3.6. The methodology for feature selection and classification
is shown in Figure 1.d
and Figure 1.d
respectively.
For feature selection, a correlation matrix was
generated for all the texture features of which, features with a score of
>0.9 were discarded. Subsequently, Recursive Feature Elimination with Cross
Validation (RFECV) approach was used select features that provided highest
accuracy. For this approach, the entire dataset was used with ten splits using
StratifiedkFold approach and random forest classifier. Feature importance graph
was generated as shown in Figure
3. ROC analysis was then done for four classifier
algorithms Extra Trees, Logistic Regression, MLP and Random Forest. Performance
parameters Area under the curve (AUC), sensitivity, specificity, precision, accuracy
and f1 score were computed using a 10-fold StratifiedKFold cross validation
approach. Model development approach is shown in Figure
2 during which the number of texture features,
used for model generation, are optimized to provide higher precision and
average AUC.Results
76
patients were included for this study; 38 without osteoporosis and 38 with
osteoporosis. A total of 151 texture features were computed using MaZda
software. Haralick and Wavelet features were averaged which reduced the number
of features to 56 are shown in Table
1. 35 features with mutually correlated
information were excluded through correlation matrix. Subsequently, 2 more
features were excluded through RFECV. The final 19 features are listed in Figure
2. The classifier models were then generated for
each of the four classifiers. The model was generated using 9 features shown in
green in Figure
3. The final performance parameters for each of
the classifiers are shown in Table
2.Discussion
Optimal
model performance was achieved using 9 texture features. Results show that Logistic
Regression model has the best performance. The precision of average AUC for the
four models suggests that the 9 texture features, chosen for generation of the
classifier model, are robust and effective irrespective of the classifier
chosen. The performance of the model is improved in comparison to what has been
reported previously. Thus, it is demonstrated that the proposed methodology can
be used in a clinical setting on 1.5T systems on T1-weighted images to detect osteoporosis.Acknowledgements
No acknowledgement found.References
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