Increased risk of hip and major osteoporotic fractures in 8463 patients who have undergone stem cell transplantation, a Swedish population-based study.

IF 4.2 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Osteoporosis International Pub Date : 2024-10-01 Epub Date: 2024-07-08 DOI:10.1007/s00198-024-07171-9
Peter Johansson, Hallgerdur Lind Kristjansdottir, Helena Johansson, Dan Mellström, Catharina Lewerin
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引用次数: 0

Abstract

In this retrospective cohort study of adult stem cell transplanted patients (n = 8463), a significant increased risk of both MOF and hip fractures was seen compared with the Swedish population and occurred in mean more than 2 years after stem cell transplantation.

Purpose: To explore the risk for osteoporotic fracture in patients who have undergone hematopoietic stem cell transplantation (HSCT) compared with the Swedish population.

Methods: The risk of osteoporotic fractures was determined in a retrospective population cohort study of adult (≥ 18 years) Swedish patients (n = 8463), who were transplanted with HSCT 1997-2016 and compared with all adults living in Sweden during the same period.

Results: In the total study group (n = 8463), 90 hip fractures (1.1% both in males and females) and 361 major osteoporotic fractures (MOF) (3.2% in men and 6.0% in women) were identified. In the total study population, the ratio of observed and expected number of hip fracture for women was 1.99 (95% CI 1.39-2.75) and for men 2.54 (95% CI 1.91-3.31). The corresponding ratio for MOF in women was 1.36 (CI 1.18-1.56) and for men 1.61 (CI 1.37-1.88). From 2005 onwards, when differentiation in the registry between allo- and auto-HSCT was possible, the observed number of hip fracture and MOF in allo-HSCT (n = 1865) were significantly increased (observed/expected hip fracture 5.24 (95% CI 3.28-7.93) and observed/expected MOF 2.08 (95% CI 1.63-2.62)). Fractures occurred in mean 2.7 (hip) and 2.5 (MOF) years after allo-HSCT. Graft-versus-host disease (GVHD) was not associated with an increased risk of fracture.

Conclusion: Patients who underwent HSCT had an increased risk of both hip and major osteoporotic fracture compared with the Swedish population and occurred in 4.3% of patients. GVHD was not statistically significantly associated with fracture risk.

一项基于瑞典人口的研究发现,8463 名接受干细胞移植的患者发生髋部和主要骨质疏松性骨折的风险增加。
在这项针对成年干细胞移植患者(n = 8463)的回顾性队列研究中,与瑞典人群相比,MOF和髋部骨折的风险显著增加,且平均发生在干细胞移植后2年以上。目的:探讨与瑞典人群相比,接受造血干细胞移植(HSCT)的患者发生骨质疏松性骨折的风险:在一项回顾性人群队列研究中,对1997-2016年接受造血干细胞移植的瑞典成年(≥18岁)患者(n = 8463)进行了骨质疏松性骨折风险测定,并与同期居住在瑞典的所有成年人进行了比较:在所有研究群体(n = 8463)中,发现了90例髋部骨折(男性和女性均为1.1%)和361例重大骨质疏松性骨折(MOF)(男性为3.2%,女性为6.0%)。在所有研究人群中,女性髋部骨折的观察数与预期数的比率为 1.99(95% CI 1.39-2.75),男性为 2.54(95% CI 1.91-3.31)。女性 MOF 的相应比率为 1.36(CI 1.18-1.56),男性为 1.61(CI 1.37-1.88)。从 2005 年起,当登记册可以区分allo-HSCT 和 auto-HSCT 时,allo-HSCT(n = 1865)中观察到的髋部骨折数量和 MOF 显著增加(观察到/预期髋部骨折为 5.24 (95% CI 3.28-7.93) ,观察到/预期 MOF 为 2.08 (95% CI 1.63-2.62))。骨折平均发生在allo-HSCT后2.7年(髋部)和2.5年(MOF)。移植物抗宿主疾病(GVHD)与骨折风险增加无关:结论:与瑞典人口相比,接受造血干细胞移植的患者发生髋部骨折和重大骨质疏松性骨折的风险均有所增加,发生率为4.3%。GVHD与骨折风险在统计学上无明显关联。
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来源期刊
Osteoporosis International
Osteoporosis International 医学-内分泌学与代谢
CiteScore
8.10
自引率
10.00%
发文量
224
审稿时长
3 months
期刊介绍: An international multi-disciplinary journal which is a joint initiative between the International Osteoporosis Foundation and the National Osteoporosis Foundation of the USA, Osteoporosis International provides a forum for the communication and exchange of current ideas concerning the diagnosis, prevention, treatment and management of osteoporosis and other metabolic bone diseases. It publishes: original papers - reporting progress and results in all areas of osteoporosis and its related fields; review articles - reflecting the present state of knowledge in special areas of summarizing limited themes in which discussion has led to clearly defined conclusions; educational articles - giving information on the progress of a topic of particular interest; case reports - of uncommon or interesting presentations of the condition. While focusing on clinical research, the Journal will also accept submissions on more basic aspects of research, where they are considered by the editors to be relevant to the human disease spectrum.
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