Associations of Body Fat Distribution and Cardiometabolic Risk of Testicular Cancer Survivors After Cisplatin-Based Chemotherapy

被引:7
作者
Wibmer, Andreas G. [1 ]
Dinh, Paul C., Jr. [2 ]
Travis, Lois B. [2 ,3 ]
Chen, Carol [4 ]
Bromberg, Maria [5 ]
Zheng, Junting [6 ]
Capanu, Marinela [6 ]
Sesso, Howard D. [7 ]
Feldman, Darren R. [5 ]
Vargas, Hebert Alberto [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Radiol, 353 E 68th St, New York, NY 10065 USA
[2] Indiana Univ Sch Med, Dept Med, Indianapolis, IN 46202 USA
[3] Indiana Univ, Fairbanks Sch Publ Hlth, Dept Epidemiol, Indianapolis, IN 46204 USA
[4] Mem Sloan Kettering Canc Ctr, Cardiol Serv, Dept Med, 1275 York Ave, New York, NY 10021 USA
[5] Mem Sloan Kettering Canc Ctr, Genitourinary Serv, Dept Med, 1275 York Ave, New York, NY 10021 USA
[6] Mem Sloan Kettering Canc Ctr, Dept Epidemiol & Biostat, New York, NY 10021 USA
[7] Brigham & Womens Hosp, Dept Med, 75 Francis St, Boston, MA 02115 USA
关键词
LONG-TERM SURVIVORS; SUBCUTANEOUS ADIPOSE-TISSUE; ADVERSE HEALTH OUTCOMES; CARDIOVASCULAR RISK; PRIMARY-CARE; MORBIDITY; DISEASE; OBESITY; MORTALITY; PROFILE;
D O I
10.1093/jncics/pkac030
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background It is unknown how body fat distribution modulates the cardiometabolic risk of testicular cancer survivors after cisplatin-based chemotherapy. Methods For 455 patients enrolled in the Platinum Study at Memorial Sloan Kettering Cancer Center, visceral (VAT) and subcutaneous (SAT) adipose tissue was quantified on prechemotherapy computed tomography. The VAT-to-SAT ratio was calculated as a quantitative measure of central adiposity. Endpoints were incidence of new posthemotherapy cardiometabolic disease (new antihypertensive, lipid-lowering, or diabetes medication), and postchemotherapy Framingham risk scores. Cox models and linear regression with interaction terms were applied. Postchemotherapy body fat distribution was analyzed in 108 patients. All statistical tests were 2-sided. Results The baseline median age was 31 years (interquartile range [IQR] = 26-39 years), body mass index (BMI) was 26 kg/m(2) (IQR = 24-29 kg/m(2)), and the VAT-to-SAT ratio was 0.49 (IQR = 0.31-0.75). The median follow-up was 26 months (IQR = 16-59 months). Higher prechemotherapy VAT-to-SAT ratios inferred a higher likelihood of new cardiometabolic disease among patients with a BMI of 30 kg/m(2) or greater (age-adjusted hazard ratio = 3.14, 95% confidence interval = 1.02 to 9.71, P = .047), but not other BMI groups. The prechemotherapy VAT-to-SAT ratio was associated with postchemotherapy Framingham risk scores in univariate regression analysis (exp(beta)-estimate: 2.10, 95% confidence interval = 1.84 to 2.39, P < .001); in a multivariable model, this association was stronger in younger vs older individuals. BMI increased in most patients after chemotherapy and correlated with increases in the VAT-to-SAT ratio (Spearman r = 0.39, P < .001). Conclusions In testicular cancer survivors, central adiposity is associated with increased cardiometabolic risk after cisplatin-based chemotherapy, particularly in obese or young men. Weight gain after chemotherapy occurs preferentially in the visceral compartment, providing insight into the pathogenesis of cardiovascular disease in this population.
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页数:8
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