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Outer-Boundary Assisted Segmentation and Quantification of Trabecular Bones by an Imagej Plugin
Published on: March 14, 2018
Trabecular bone mineral density measurement using thoracic and lumbar quantitative computed tomography.
Matthew J Budoff1, Walid Khairallah, Dong Li
1Los Angeles Biomedical Research Institute at Harbor UCLA, Torrance, CA 90502, USA. mbudoff@labiomed.org
Academic Radiology
|November 25, 2011
Summary
Thoracic spine bone mineral density (BMD) measured during cardiac CT scans strongly correlates with lumbar spine BMD. This method allows for osteoporosis assessment without extra radiation exposure.
Area of Science:
- Radiology
- Osteoporosis Research
- Quantitative CT
Background:
- Assessing bone mineral density (BMD) is crucial for osteoporosis diagnosis.
- Current methods often require separate scans, increasing patient burden and radiation dose.
- Cardiac CT imaging presents an opportunity to assess thoracic spine BMD non-invasively.
Purpose of the Study:
- To evaluate the agreement between bone mineral density (BMD) in lumbar (L) and individual thoracic (T) vertebrae.
- To identify a standard thoracic spine level for BMD assessment using cardiac computed tomography (CT) images.
Main Methods:
- Simultaneous chest and abdomen CT scans were performed on 300 subjects.
- Vertebral BMD was measured using QCT 5000 and NVivo systems with a calibration phantom (T1-L5).
- Associations between lumbar (L1-L3) and thoracic BMD (3T) were evaluated.
Main Results:
- BMD values decreased from T1 to L3, then increased in L4 and L5.
- 3T BMD was significantly higher than L1-L3 BMD in both genders (P < .001).
- High correlations were found between 3T and L1-L3 BMD (r=0.91-0.93), and between L1-L3 and individual thoracic vertebrae (r=0.62-0.98).
Conclusions:
- Thoracic spine BMD (3T) is highly correlated with lumbar spine BMD (L1-L3).
- Thoracic BMD can be measured during cardiac and lung CT scans without additional patient burden or radiation.
- This reproducible method is valuable for large cohort studies on osteoporosis prevalence and progression.
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