儿童癌症幸存者骨密度不足的归因风险及后果
Attributable Risk and Consequences of Bone Mineral Density Deficits in Childhood Cancer Survivors.
作者信息
Goodenough Chelsea G, Baedke Jessica L, Delaney Angela M, Wilson Carmen L, Brinkman Tara M, Im Cindy, Ware Megan E, Inaba Hiroto, Clark Karen L, Armstrong Gregory T, Mulrooney Daniel A, Pui Ching-Hon, Green Daniel M, Merchant Thomas E, Srivastava Deo Kumar, Yasui Yutaka, Hudson Melissa M, Robison Leslie L, Kaste Sue C, Ness Kirsten K, Chemaitilly Wassim
机构信息
Department of Epidemiology and Cancer Control, St Jude Children's Research Hospital, Memphis, Tennessee.
Endocrinology Department, St Jude Children's Research Hospital, Memphis, Tennessee.
出版信息
JAMA Netw Open. 2025 Jan 2;8(1):e2454069. doi: 10.1001/jamanetworkopen.2024.54069.
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.
重要性
缺乏关于儿童癌症幸存者在治疗数十年后骨矿物质密度(BMD)缺陷的严重程度、患病率变化以及相关非骨折后果的数据。
目的
评估幸存者中中度和重度BMD缺陷的风险,并确定BMD缺陷的长期后果。
设计、设置和参与者:这项队列研究使用了来自圣裘德终身(SJLIFE)队列的横断面和纵向数据,这是一个通过回顾性构建并进行前瞻性随访的队列。SJLIFE的参与者是儿童癌症成年幸存者,他们在1962年至2012年期间被诊断出癌症,并且从诊断后存活了5年或更长时间。数据收集于2007年11月至2020年6月,并于2021年1月至2023年11月进行分析。
暴露因素
儿童癌症治疗暴露、临床确定的合并症、物质使用和久坐不动的生活方式。
主要结局和测量指标
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评分进行分类,中度(≤-1 SD)或重度(≤-2 SD)缺陷。多变量逻辑回归估计比值比(OR)、归因分数(AF)以及BMD缺陷与长期后遗症(社会、功能和生活质量[QOL])之间的关联。
结果
在3919名五年幸存者中(中位[范围]年龄,31.7[18.0 - 69.9]岁;2063[52.6%]为男性;105[2.7%]为西班牙裔,607[15.5%]为非西班牙裔黑人,3153[80.4%]为非西班牙裔白人),中度或重度BMD缺陷的患病率分别为21.7%(95%CI,20.4% - 23.0%)和6.9%(�5%CI,6.1% - 7.7%)。治疗暴露(包括诊断时的年龄)、合并症以及吸烟和久坐行为分别解释了中度缺陷的18.5%、10.2%和7.0%以及重度缺陷的55.4%、51.1%和9.9%。重度缺陷与30 Gy或更高剂量的颅脑放疗(CRT)(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(OR,5.28,95%CI,3.68 - 7.56;AF,26.0%)、吸烟(OR,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;AF,6.2%)相关。CRT暴露增加了BMD下降的风险(OR,2.94,95%CI,1.46 - 5.91;AF,8.8%)。有缺陷的幸存者独居和就业的可能性较小,更有可能需要个人护理协助,并报告有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BMD缺陷相关,但包括吸烟、久坐行为、性腺功能减退和生长激素缺乏在内的可改变风险因素提示了可行的干预目标。
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