TY - JOUR
T1 - Use of MR-based trabecular bone microstructure analysis at the distal radius for osteoporosis diagnostics
T2 - A study in post-menopausal women with breast cancer and treated with aromatase inhibitor
AU - Baum, Thomas
AU - Karampinos, Dimitrios C.
AU - Seifert-Klauss, Vanadin
AU - Pencheva, Tsvetelina D.
AU - Jungmann, Pia M.
AU - Rummeny, Ernst J.
AU - Müller, Dirk
AU - Bauer, Jan S.
PY - 2016/1/1
Y1 - 2016/1/1
N2 - Purpose. Treatment with aromatase inhibitor (AI) is recommended for post-menopausal women with hormone-receptor positive breast cancer. However, AI therapy is known to induce bone loss leading to osteoporosis with an increased risk for fragility fractures. The purpose of this study was to investigate whether changes of magnetic resonance (MR)-based trabecular bone microstructure parameters as advanced imaging biomarker can already be detected in subjects with AI intake but still without evidence for osteoporosis according to dual energy X-ray absorptiometry (DXA)-based bone mineral density (BMD) measurements as current clinical gold standard. Methods. Twenty-one postmenopausal women (62±6 years of age) with hormone-receptor positive breast cancer, ongoing treatment with aromatase inhibitor for 23±15 months, and no evidence for osteoporosis (current DXA T-score greater than -2.5) were recruited for this study. Eight young, healthy women (24±2 years of age) were included as controls. All subjects underwent 3 Tesla magnetic resonance imaging (MRI) of the distal radius to assess the trabecular bone microstructure. Results. Trabecular bone microstructure parameters were not significantly (p>0.05) different between subjects with AI intake and controls, including apparent bone fraction (0.42±0.03 vs. 0.42±0.05), trabecular number (1.95±0.10 mm-1 vs 1.89±0.15 mm-1), trabecular separation (0.30±0.03 mm vs0.31±0.06 mm), trabecular thickness (0.21±0.01 mm vs 0.22±0.02 mm), and fractal dimension (1.70±0.02 vs. 1.70±0.03). Conclusion. These findings suggest that the initial deterioration of trabecular bone microstructure as measured by MRI and BMD loss as measured by DXA occur not sequentially but rather simultaneously. Thus, the use of MR-based trabecular bone microstructure assessment is limited as early diagnostic biomarker in this clinical setting.
AB - Purpose. Treatment with aromatase inhibitor (AI) is recommended for post-menopausal women with hormone-receptor positive breast cancer. However, AI therapy is known to induce bone loss leading to osteoporosis with an increased risk for fragility fractures. The purpose of this study was to investigate whether changes of magnetic resonance (MR)-based trabecular bone microstructure parameters as advanced imaging biomarker can already be detected in subjects with AI intake but still without evidence for osteoporosis according to dual energy X-ray absorptiometry (DXA)-based bone mineral density (BMD) measurements as current clinical gold standard. Methods. Twenty-one postmenopausal women (62±6 years of age) with hormone-receptor positive breast cancer, ongoing treatment with aromatase inhibitor for 23±15 months, and no evidence for osteoporosis (current DXA T-score greater than -2.5) were recruited for this study. Eight young, healthy women (24±2 years of age) were included as controls. All subjects underwent 3 Tesla magnetic resonance imaging (MRI) of the distal radius to assess the trabecular bone microstructure. Results. Trabecular bone microstructure parameters were not significantly (p>0.05) different between subjects with AI intake and controls, including apparent bone fraction (0.42±0.03 vs. 0.42±0.05), trabecular number (1.95±0.10 mm-1 vs 1.89±0.15 mm-1), trabecular separation (0.30±0.03 mm vs0.31±0.06 mm), trabecular thickness (0.21±0.01 mm vs 0.22±0.02 mm), and fractal dimension (1.70±0.02 vs. 1.70±0.03). Conclusion. These findings suggest that the initial deterioration of trabecular bone microstructure as measured by MRI and BMD loss as measured by DXA occur not sequentially but rather simultaneously. Thus, the use of MR-based trabecular bone microstructure assessment is limited as early diagnostic biomarker in this clinical setting.
KW - Aromatase inhibitor
KW - Magnetic resonance imaging
KW - Osteoporosis
KW - Trabecular bone microstructure
UR - http://www.scopus.com/inward/record.url?scp=84970002248&partnerID=8YFLogxK
U2 - 10.11138/ccmbm/2016.13.1.029
DO - 10.11138/ccmbm/2016.13.1.029
M3 - Article
AN - SCOPUS:84970002248
SN - 1724-8914
VL - 13
SP - 29
EP - 32
JO - Clinical Cases in Mineral and Bone Metabolism
JF - Clinical Cases in Mineral and Bone Metabolism
IS - 1
ER -