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Osteoporosis International

, Volume 28, Issue 4, pp 1413–1422 | Cite as

Long-term effect of aromatase inhibitors on bone microarchitecture and macroarchitecture in non-osteoporotic postmenopausal women with breast cancer

  • A. R. Hong
  • J. H. KimEmail author
  • K. H. Lee
  • T. Y. Kim
  • S. A. Im
  • T. Y. Kim
  • H. G. Moon
  • W. S. Han
  • D. Y. Noh
  • S. W. Kim
  • C. S. Shin
Original Article

Abstract

Summary

In non-osteoporotic postmenopausal women with breast cancer, aromatase inhibitors (AIs) negatively affected bone mineral density (BMD), lumbar spine trabecular bone score (TBS) as a bone microarchitecture index, and hip geometry as a bone macroarchitecture index.

Introduction

AIs increase the risk of fracture in patients with breast cancer. Therefore, we aimed to evaluate the long-term skeletal effects of AIs in postmenopausal women with primary breast cancer.

Methods

We performed a retrospective longitudinal observational study in non-osteoporotic patients with breast cancer who were treated with AIs for ≥3 years (T-score >−2.5). Patients with previous anti-osteoporosis treatment or those who were given bisphosphonate during AI treatment were excluded from the analysis. We serially assessed BMD, lumbar spine TBS, and hip geometry using dual-energy X-ray absorptiometry.

Results

BMD significantly decreased from baseline to 5 years at the lumbar spine (−6.15%), femur neck (−7.12%), and total hip (−6.35%). Lumbar spine TBS also significantly decreased from baseline to 5 years (−2.12%); this change remained significant after adjusting for lumbar spine BMD. The annual loss of lumbar spine BMD and TBS slowed after 3 and 1 year of treatment, respectively, although there was a relatively constant loss of BMD at the femur neck and total hip for up to 4 years. The cross-sectional area, cross-sectional moment of inertia, minimal neck width, femur strength index, and section modulus significantly decreased, although the buckling ratio increased over the treatment period (all P < 0.001); these changes were independent of total hip BMD.

Conclusions

Long-term adjuvant AI treatment negatively influenced bone quality in addition to BMD in patients with breast cancer. This study suggests that early monitoring and management are needed in non-osteoporotic patients with breast cancer who are starting AIs.

Keywords

Aromatase inhibitor Bone mineral density Breast cancer Hip Trabecular bone score 

Notes

Acknowledgments

We appreciate the Medical Research Collaborating Center (MRCC) of Seoul National University Hospital for statistical analysis.

Compliance with ethical standards

The study was conducted in accordance with the Declaration of Helsinki and complies with the current laws of the countries in which it was performed. An independent ethics committee or institutional review board for each study site approved the study protocol. An informed consent was waived due to a retrospective study.

Conflicts of interest

None.

Funding

This study was supported by a grant from Seoul National University Hospital (No. 0420140760 (2014–1293)).

The study was approved by the institutional review board of Seoul National University Hospital (No. H-1601-057-734) and was conducted in accordance with the Declaration of Helsinki. Informed consent from the study participants was waived due to the study’s retrospective nature.

Supplementary material

198_2016_3899_Fig3_ESM.gif (96 kb)
Supplemental Figure 1

Mean percentage changes (± SEM) in bone mineral density (BMD) over time for (A) lumbar spine, (B) femur neck, and (C) total hip and (D) lumbar spine trabecular bone score (TBS) after adjusting for age and body mass index. * P < 0.05, from the baseline; P < 0.05, between time difference after Bonferroni correction. (GIF 95 kb)

198_2016_3899_MOESM1_ESM.tif (2.1 mb)
High Resolution Image (TIFF 2121 kb)
198_2016_3899_MOESM2_ESM.docx (21 kb)
Supplemental Table 1 (DOCX 21 kb)

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Copyright information

© International Osteoporosis Foundation and National Osteoporosis Foundation 2017

Authors and Affiliations

  • A. R. Hong
    • 1
  • J. H. Kim
    • 1
    Email author
  • K. H. Lee
    • 1
  • T. Y. Kim
    • 1
  • S. A. Im
    • 1
  • T. Y. Kim
    • 1
  • H. G. Moon
    • 2
  • W. S. Han
    • 2
  • D. Y. Noh
    • 2
  • S. W. Kim
    • 1
    • 3
  • C. S. Shin
    • 1
  1. 1.Department of Internal MedicineSeoul National University College of MedicineSeoulSouth Korea
  2. 2.Department of SurgerySeoul National University College of MedicineSeoulSouth Korea
  3. 3.Department of Internal MedicineSeoul Metropolitan Government Boramae Medical CenterSeoulSouth Korea

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