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乳腺癌女性化疗对骨密度和微结构的影响。

Chemotherapy effects on bone mineral density and microstructure in women with breast cancer.

机构信息

Department of Surgery, Nagasaki University Graduate School of Biomedical Sciences, 1-7-1 Sakamoto-Machi, Nagasaki, 852-8501, Japan.

Department of Orthopedic Surgery, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.

出版信息

J Bone Miner Metab. 2024 Sep;42(5):591-599. doi: 10.1007/s00774-024-01526-2. Epub 2024 Jul 19.

Abstract

INTRODUCTION

Chemotherapy involves the administration of steroids to prevent nausea and vomiting; however, its effect on bone microstructure remains unknown. This study aimed to evaluate the changes in bone mineral density (BMD) and bone microstructure associated with chemotherapy using high-resolution peripheral quantitative computed tomography (HR-pQCT) in women with early breast cancer.

MATERIALS AND METHODS

This prospective single-arm observational study included non-osteoporotic, postmenopausal women with breast cancer. The patients underwent dual-energy X-ray absorptiometry (DXA), HR-pQCT, and tartrate-resistant acid phosphatase-5b (TRACP-5b) or procollagen type-I N-terminal propeptide (P1NP) measurements at baseline, end of chemotherapy, and 6 months after chemotherapy. The primary endpoint was the change in total volumetric BMD at the distal tibia and radius.

RESULTS

Eighteen women were included in the study (median age: 57 years; range: 55-62 years). At 6 months after chemotherapy, HR-pQCT indicated a significant decrease in total volumetric BMD (median: distal tibia -4.5%, p < 0.01; distal radius -2.3%, p < 0.01), cortical volumetric BMD (-1.9%, p < 0.01;  -0.8%, p = 0.07, respectively), and trabecular volumetric BMD (-1.1%, p = 0.09;  -3.0%, p < 0.01, respectively). The DXA BMD also showed a significant decrease in the lumbar spine (median: -4.5%, p < 0.01), total hip (-5.5%, p < 0.01), and femoral neck (-4.2%, p < 0.01). TRACP-5b and P1NP levels were significantly increased at the end of chemotherapy compared to baseline.

CONCLUSION

Postmenopausal women undergoing chemotherapy for early breast cancer experienced significant BMD deterioration in weight-bearing bone, which was further reduced 6 months after chemotherapy.

摘要

简介

化疗涉及使用类固醇来预防恶心和呕吐;然而,其对骨微观结构的影响尚不清楚。本研究旨在使用高分辨率外周定量计算机断层扫描(HR-pQCT)评估早期乳腺癌女性化疗相关的骨矿物质密度(BMD)和骨微观结构变化。

材料和方法

这是一项前瞻性单臂观察性研究,纳入了非骨质疏松、绝经后患有乳腺癌的女性患者。患者在基线、化疗结束时和化疗结束后 6 个月接受双能 X 射线吸收法(DXA)、HR-pQCT 和抗酒石酸酸性磷酸酶-5b(TRACP-5b)或 I 型前胶原氨基端前肽(P1NP)测量。主要终点是远端胫骨和桡骨总容积 BMD 的变化。

结果

该研究纳入了 18 名女性(中位年龄:57 岁;范围:55-62 岁)。化疗结束后 6 个月时,HR-pQCT 显示总容积 BMD 显著下降(远端胫骨:-4.5%,p<0.01;远端桡骨:-2.3%,p<0.01)、皮质容积 BMD(-1.9%,p<0.01;-0.8%,p=0.07)和小梁容积 BMD(-1.1%,p=0.09;-3.0%,p<0.01)。DXA BMD 还显示腰椎(中位数:-4.5%,p<0.01)、全髋(-5.5%,p<0.01)和股骨颈(-4.2%,p<0.01)的 BMD 明显下降。与基线相比,化疗结束时 TRACP-5b 和 P1NP 水平显著升高。

结论

接受早期乳腺癌化疗的绝经后女性承重骨的 BMD 明显恶化,化疗结束后 6 个月时进一步下降。

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