Sadim Maureen, Xu Yanfei, Selig Katharina, Paulus Julie, Uthe Regina, Agarwl Surbhi, Dubin Iram, Oikonomopoulou Panagiota, Zaichenko Lesya, McCandlish Silvia Aki, Van Horn Linda, Mantzoros Christos, Ankerst Donna Pauler, Kaklamani Virginia G
Robert H. Lurie Comprehensive Cancer Center, Northwestern University, Chicago, Illinois.
Department of Mathematics, Technical University Munich, Munich, Germany.
Cancer. 2017 Jul 1;123(13):2413-2421. doi: 10.1002/cncr.30628. Epub 2017 Feb 14.
Postdiagnosis weight gain in patients with breast cancer has been associated with increased cancer recurrence and mortality. This study was designed to identify risk factors for weight gain and create a predictive model to identify a high-risk population for targeted interventions.
The weight of 393 patients with breast cancer from the Northwestern Robert H. Lurie Cancer Center was measured over a 2-year period from diagnosis, with body mass index (BMI) change over 18 months as the primary endpoint. Demographics, clinical factors, treatment methods, as well as tumor characteristics were also recorded; and a lifestyle questionnaire was conducted. Blood samples were genotyped for 16 single nucleotide polymorphisms in FTO, adiponectin pathway genes (ADIPOQ, ADIPOR1), and FNDC5. Serum leptin, adiponectin, and irisin levels also were measured.
Mean ± standard deviation 18-month BMI changes were 0.68 ± 1.42, 0.98 ± 1.62, 0.79 ± 1.74, and -0.44 ± 1.58 kg/m for patients ages <40, 40 to 49, 50 to 59, and ≥60 years, respectively. The optimal multivariable model for 18-month BMI change contained the predictors age, height, and endocrine therapy, but only age was statistically significant, with a 0.04 kg/m increase in 18-month BMI change per younger year of age. Single nucleotide polymorphisms in ADIPOR1, FTO, and FNDC5 were associated with 18-month BMI change, and the first 2 remained significant after adjusting for the optimal clinical model (all P < .05).
Women age 60 years and younger at the time of breast cancer diagnosis who have an obesity genetic risk model are at increased risk for weight gain after treatment and should be targeted for weight-maintenance interventions. Cancer 2017;123:2413-21. © 2017 American Cancer Society.
乳腺癌患者诊断后体重增加与癌症复发及死亡率升高相关。本研究旨在确定体重增加的风险因素,并创建一个预测模型以识别需要进行针对性干预的高危人群。
对来自西北大学罗伯特·H·卢里癌症中心的393例乳腺癌患者在确诊后的2年时间里进行体重测量,以18个月内体重指数(BMI)的变化作为主要终点。记录人口统计学信息、临床因素、治疗方法以及肿瘤特征;并进行生活方式问卷调查。对血液样本进行基因分型,检测FTO、脂联素通路基因(ADIPOQ、ADIPOR1)和FNDC5中的16个单核苷酸多态性。同时测量血清瘦素、脂联素和鸢尾素水平。
年龄<40岁、40至49岁、50至59岁和≥60岁患者的18个月平均BMI变化(均值±标准差)分别为0.68±1.42、0.98±1.62、0.79±1.74和 -0.44±1.58 kg/m²。18个月BMI变化的最佳多变量模型包含年龄、身高和内分泌治疗等预测因素,但只有年龄具有统计学意义,年龄每小一岁,18个月BMI变化增加0.04 kg/m²。ADIPOR1、FTO和FNDC5中的单核苷酸多态性与18个月BMI变化相关,在前两个基因中,经最佳临床模型校正后仍具有显著性(所有P<0.05)。
乳腺癌诊断时年龄在60岁及以下且具有肥胖遗传风险模型的女性,治疗后体重增加的风险较高,应针对其进行体重维持干预。《癌症》2017年;123:2413 - 2421。©2017美国癌症协会。