儿童癌症幸存者骨矿物质密度缺陷的归因风险和后果。

IF 10.5 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL
Chelsea G Goodenough, Jessica L Baedke, Angela M Delaney, Carmen L Wilson, Tara M Brinkman, Cindy Im, Megan E Ware, Hiroto Inaba, Karen L Clark, Gregory T Armstrong, Daniel A Mulrooney, Ching-Hon Pui, Daniel M Green, Thomas E Merchant, Deo Kumar Srivastava, Yutaka Yasui, Melissa M Hudson, Leslie L Robison, Sue C Kaste, Kirsten K Ness, Wassim Chemaitilly
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引用次数: 0

摘要

重要性:在儿童癌症幸存者中,骨密度(BMD)缺陷的严重程度和变化的患病率以及治疗后数十年相关的非骨折后果的数据缺乏。目的:评估幸存者中度和重度骨密度缺陷的风险,并确定骨密度缺陷的长期后果。设计、环境和参与者:该队列研究使用St Jude Lifetime (SJLIFE)队列的横断面和纵向数据,这是一个回顾性构建的前瞻性随访队列。SJLIFE的参与者是1962年至2012年间诊断出的儿童癌症的成年幸存者,并在诊断后存活5年或更长时间。数据收集时间为2007年11月至2020年6月,分析时间为2021年1月至2023年11月。暴露:儿童癌症治疗暴露,临床确定的合并症,物质使用和久坐的生活方式。主要结果和测量方法:使用腰椎定量计算机断层扫描评估BMD,并根据年龄和性别特异性z评分分为中度(≤-1 SD)或重度(≤-2 SD)缺陷。多变量logistic回归估计了优势比(ORs)、归因分数(AFs)和BMD缺陷与长期后遗症(社会、功能和生活质量[QOL])之间的关系。结果:在3919名5年幸存者中(年龄中位数为31.7[18.0-69.9]岁;男性2063人[52.6%];105名[2.7%]西班牙裔,607名[15.5%]非西班牙裔黑人,3153名[80.4%]非西班牙裔白人),中度或重度骨密度缺陷的患病率分别为21.7% (95% CI, 20.4%-23.0%)和6.9% (95% CI, 6.1%-7.7%)。治疗暴露(包括诊断时的年龄)、合并症、吸烟和久坐行为解释了中度缺陷的18.5%、10.2%和7.0%,严重缺陷的55.4%、51.1%和9.9%。严重的缺陷与30 Gy或更高的颅脑放疗(CRT)相关(or, 5.22;95% ci, 3.74-7.30;AF, 33.0%),睾丸或盆腔放疗(or, 1.70, 95% CI, 1.19-2.44;AF, 11.5%),性腺功能减退(OR, 3.27, 95% CI, 2.35-4.55;AF, 25.1%),生长激素缺乏症(OR, 5.28, 95% CI, 3.68-7.56;房颤,26.0%),吸烟(或者1.71,95% CI, 1.21 - -2.43;AF, 6.7%)和久坐行为(OR, 2.06, 95% CI, 1.15-3.69;房颤,6.2%)。CRT暴露增加骨密度下降的风险(OR, 2.94, 95% CI, 1.46-5.91;房颤,8.8%)。有缺陷的幸存者不太可能独自生活和就业,更有可能需要个人护理援助,并报告抑郁症状和生活质量差。结论和相关性:虽然治疗暴露与长期骨密度缺陷有关,但可改变的危险因素,包括吸烟、久坐行为、性腺功能减退和生长激素缺乏,是可行的干预目标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Attributable Risk and Consequences of Bone Mineral Density Deficits in Childhood Cancer Survivors.

Importance: Data characterizing the severity and changing prevalence of bone mineral density (BMD) deficits and associated nonfracture consequences among childhood cancer survivors decades after treatment are lacking.

Objective: To evaluate risk for moderate and severe BMD deficits in survivors and to identify long-term consequences of BMD deficits.

Design, setting, and participants: This cohort study used cross-sectional and longitudinal data from the St Jude Lifetime (SJLIFE) cohort, a retrospectively constructed cohort with prospective follow-up. Participants in SJLIFE are adult survivors of childhood cancer who were diagnosed between 1962 and 2012 and survived 5 years or more from diagnosis. Data were collected from November 2007 to June 2020 and analyzed from January 2021 to November 2023.

Exposures: Childhood cancer therapy exposures, clinically ascertained comorbid conditions, substance use, and sedentary lifestyle.

Main outcomes and measures: BMD was evaluated using lumbar quantitative computed tomography and classified by age- and sex-specific z scores with moderate (≤-1 SD) or severe (≤-2 SD) deficits. Multivariable logistic regression estimated odds ratios (ORs), attributable fractions (AFs), and associations between BMD deficits and long-term sequelae (social, functional, and quality of life [QOL]).

Results: Among 3919 five-year survivors (median [range] age, 31.7 [18.0-69.9] years; 2063 [52.6%] male; 105 [2.7%] Hispanic, 607 [15.5%] non-Hispanic Black, and 3153 [80.4%] non-Hispanic White), prevalence of moderate or severe BMD deficits were 21.7% (95% CI, 20.4%-23.0%) and 6.9% (95% CI, 6.1%-7.7%), respectively. Treatment exposures (including age at diagnosis), comorbid conditions, and smoking and sedentary behavior explained 18.5%, 10.2%, and 7.0% of moderate and 55.4%, 51.1%, and 9.9% of severe deficits. Severe deficits were associated with 30 Gy or greater cranial radiotherapy (CRT) (OR, 5.22; 95% CI, 3.74-7.30; AF, 33.0%), testicular or pelvic radiation (OR, 1.70, 95% CI, 1.19-2.44; AF, 11.5%), hypogonadism (OR, 3.27, 95% CI, 2.35-4.55; AF, 25.1%), growth hormone deficiency (OR, 5.28, 95% CI, 3.68-7.56; AF, 26.0%), smoking (OR, 1.71, 95% CI, 1.21-2.43; AF, 6.7%), and sedentary behavior (OR, 2.06, 95% CI, 1.15-3.69; AF, 6.2%). CRT exposure increased risk for declining BMD (OR, 2.94, 95% CI, 1.46-5.91; AF, 8.8%). Survivors with deficits were less likely to live alone and to be employed and more likely to require personal care assistance and to report depressive symptoms and poor QOL.

Conclusions and relevance: While treatment exposures were associated with long-term BMD deficits, modifiable risk factors, including smoking, sedentary behavior, hypogonadism, and growth hormone deficiency, suggest feasible targets for intervention.

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来源期刊
JAMA Network Open
JAMA Network Open Medicine-General Medicine
CiteScore
16.00
自引率
2.90%
发文量
2126
审稿时长
16 weeks
期刊介绍: JAMA Network Open, a member of the esteemed JAMA Network, stands as an international, peer-reviewed, open-access general medical journal.The publication is dedicated to disseminating research across various health disciplines and countries, encompassing clinical care, innovation in health care, health policy, and global health. JAMA Network Open caters to clinicians, investigators, and policymakers, providing a platform for valuable insights and advancements in the medical field. As part of the JAMA Network, a consortium of peer-reviewed general medical and specialty publications, JAMA Network Open contributes to the collective knowledge and understanding within the medical community.
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