Abstract

Objective. To compare the osteoporosis detection rates in postmenopausal women when measuring bone mineral density (BMD) with quantitative computed tomography (QCT) in the spine versus dual X-ray absorptiometry (DXA) in the spine and hip and to investigate the reasons for the discrepancy between the two techniques. Methods. Spinal volumetric BMD was measured with QCT, and areal spinal and hip BMDs were measured with DXA in 140 postmenopausal women. We calculated the osteoporosis detection rate for the two methods. Lumbar CT images of patients who had a discrepancy between QCT and DXA findings were reviewed to evaluate vertebral fractures, spinal degeneration, and abdominal aortic calcification. Results. For the entire 140 patients, the detection rate was 17.1% for DXA and 46.4% for QCT, a significant difference (P < 0.01). Of the 41 patients with conflicting diagnoses, 7 whose diagnosis by QCT was osteoporosis had vertebral fractures even though their DXA findings did not indicate osteoporosis. Varying degrees of spinal degeneration were seen in all of the 41 patients. Conclusion. QCT may avoid the overestimation of BMD by DXA associated with spinal degeneration, abdominal aortic calcification, and other sclerotic lesions. It may be more sensitive than DXA for detecting osteoporosis in postmenopausal women.

Highlights

  • Osteoporosis is characterized by low bone mass and microarchitectural deterioration of bone tissue, leading to increased bone fragility and a consequent increase in fracture risk

  • The trabecular bone mineral density (BMD) of the lumbar spine as measured by quantitative computed tomography (QCT) ranged from −5.0 to 199.4 mg/cm3

  • Our study showed a significant difference in osteoporosis detection rates between Dual X-ray absorptiometry (DXA) and QCT, providing clinical evidence that QCT has a greater diagnostic sensitivity than DXA

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Summary

Introduction

Osteoporosis is characterized by low bone mass and microarchitectural deterioration of bone tissue, leading to increased bone fragility and a consequent increase in fracture risk. Fractures may lead to a decreased quality of life and increased medical costs. Noninvasive techniques for measuring bone mineral density (BMD) play an important role in the clinical diagnosis of osteoporosis and in monitoring its progression. Dual X-ray absorptiometry (DXA) and quantitative computed tomography (QCT) are the most common tools for measuring BMD. DXA determines BMD in two dimensions, including both trabecular and cortical bone, with the results expressed as areal density (grams per square centimeter). QCT allows measurement of volumetric trabecular bone density without superimposition of cortical bone and other tissues, with the results expressed in milligrams per cubic centimeter of calcium hydroxyapatite

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