Frailty and genetic risk predict fracture after lung transplantation

被引:2
|
作者
Macrae, Trisha A. [1 ]
Lazo, Jose [2 ]
Viduya, Judy [2 ]
Florez, Rebecca [2 ]
Dewey, Katherine [2 ]
Gao, Ying [1 ]
Singer, Jonathan P. [1 ]
Hays, Steven R. [1 ]
Golden, Jeffrey A. [1 ]
Kukreja, Jasleen [3 ]
Greenland, John R. [1 ,4 ]
Calabrese, Daniel R. [1 ,4 ,5 ,6 ]
机构
[1] Univ Calif San Francisco, Dept Med, San Francisco, CA USA
[2] Univ Calif San Francisco, Dept Clin Pharm, San Francisco, CA USA
[3] Univ Calif San Francisco, Dept Surg, San Francisco, CA USA
[4] Vet Affairs Hlth Care Syst, Med Serv, San Francisco, CA USA
[5] Univ Calif San Francisco, Dept Med, 4150 Clement St,Box 0111D, San Francisco, CA 94121 USA
[6] Vet Affairs Hlth Care Syst, Med Serv, 4150 Clement St,Box 0111D, San Francisco, CA 94121 USA
基金
美国国家卫生研究院;
关键词
translational research; science; clinical research; practice; lung transplantation; pulmonology; genetics; endocrinology; diabetology; bronchiolitis obliterans (BOS); comorbidities; epidemiology; patient survival; BONE-MINERAL DENSITY; PRIMARY GRAFT DYSFUNCTION; OSTEOPOROSIS; ASSOCIATION; PREVENTION; MORTALITY; DIAGNOSIS; HYPOXIA; IMPACT; HEART;
D O I
10.1016/j.ajt.2022.11.017
中图分类号
R61 [外科手术学];
学科分类号
摘要
Fractures negatively impact quality of life and survival. We hypothesized that recipient frailty score and genetic profile measured before transplant would predict risk of fracture after lung transplant. We conducted a retrospective cohort study of bone mineral density (BMD) and fracture among lung transplant recipients at a single center. The association between predictors and outcomes were assessed by multivariable time-dependent Cox models or regression analysis. Among the 284 participants, osteoporosis and fracture were highly prevalent. Approximately 59% of participants had posttransplant osteopenia, and 35% of participants developed at least 1 fracture. Low BMD was associated with a polygenic osteoporosis risk score, and the interaction between genetic score and BMD predicted fracture. Pretransplant frailty was associated with risk for spine and hip fracture, which were not associated with chronic lung allograft dysfunction or death. Chest fractures were the most frequent type of fracture and conferred a 2.2-fold increased risk of chronic lung allograft dysfunction or death (time-dependent P < .001). Pneumonia, pleural effusions, and acute rejection frequently occurred surrounding chest fracture. Pretransplant frailty and recipient genotype may aid clinical risk stratification for fracture after transplant. Fracture carries significant morbidity, underscoring the importance of surveillance and osteoporosis prevention.
引用
收藏
页码:214 / 222
页数:9
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