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Risk Factors for Hematopoietic Stem Cell Transplantation-Associated Bone Loss

Journal

TRANSPLANTATION AND CELLULAR THERAPY
Volume 27, Issue 3, Pages 212-221

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.bbmt.2020.10.002

Keywords

Bone; Bone marrow transplantation; Graft-versus-host disease; Hematopoietic stem cell transplantation; Bone loss; Risk factor

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Hematopoietic stem cell transplantation is a preferred treatment for many hematologic diseases, but can lead to complications such as bone loss post-transplant. The exact mechanism of post-HSCT bone loss is not yet known, but factors such as treatment-related complications, endocrine abnormalities, and lifestyle issues have been identified. However, guidelines have been formulated to prevent and treat post-HSCT bone loss effectively.
Hematopoietic stem cell transplantation (HSCT), including bone marrow transplantation, is the treatment of choice for many hematologic diseases, including hematologic malignancies and different types of anemia. The use of HSCT is increasing annually, mainly because advanced research that has been conducted in this area has exponentially expanded the indications for HSCT and significantly improved transplantation techniques and supportive care practices. Collectively, these improvements have led to an increase in the overall survival of HSCT patients. However, as post-HSCT survival is increasing, awareness of the potential late complications of HSCT is also growing. Unpredictable bone loss is one of the major post-HSCT complications that can cause significant morbidity and impair the quality of life of survivors. Although the exact mechanism of post-HSCT bone loss is not yet known, previous studies have suggested that numerous factors, including destructive preparative regimens (eg, high-dose chemotherapy, total body irradiation), treatment-related complications (eg, graft-versus-host disease), endocrine abnormalities (eg, diabetes mellitus, thyroid dysfunction, adrenal insufficiency), lack of physical activity, and the underlying disease itself are responsible for HSCT-associated bone loss. Sufficient data have been collected to suggest that post-HSCT bone loss can be prevented and treated using the same preventive and treatment modalities as used for the general population. Various guidelines have been formulated to help keep a check on HSCT recipients' deteriorating bone health. (C) 2020 The American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc. All rights reserved.

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