Circulating Adipokine Levels and Endometrial Cancer Risk in the Prostate, Lung, Colorectal, and Ovarian Cancer Screening Trial

被引:54
|
作者
Luhn, Patricia [1 ,2 ]
Dallal, Cher M. [1 ,2 ]
Weiss, Jocelyn M. [3 ]
Black, Amanda [1 ]
Huang, Wen-Yi [1 ]
Lacey, James V., Jr. [5 ]
Hayes, Richard B. [4 ]
Stanczyk, Frank Z. [6 ]
Wentzensen, Nicolas [1 ]
Brinton, Louise A. [1 ]
机构
[1] NCI, Div Canc Epidemiol & Genet, Rockville, MD 20892 USA
[2] NCI, Canc Prevent Fellowship Program, Canc Prevent Div, Rockville, MD 20892 USA
[3] Mt Sinai Adolescent Hlth Ctr, New York, NY USA
[4] NYU, Langone Med Ctr, Dept Populat Hlth, New York, NY USA
[5] Beckman Res Inst City Hope, Duarte, CA USA
[6] Univ So Calif, Dept Obstet & Gynecol, Los Angeles, CA 90089 USA
关键词
BODY-MASS-INDEX; HORMONE-REPLACEMENT THERAPY; LEPTIN LEVELS; INSULIN-RESISTANCE; ADIPONECTIN LEVELS; SERUM ADIPONECTIN; OBESITY; VISFATIN; ASSOCIATION; WOMEN;
D O I
10.1158/1055-9965.EPI-13-0258
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Circulating adipokine levels may be associated with endometrial cancer risk, yet few studies have evaluated these markers prospectively. Methods: We conducted a nested case-control study of postmenopausal women in the Prostate, Lung, Colorectal and Ovarian Cancer Screening Trial (n = 78,216), including 167 incident endometrial cancer cases and 327 controls that were matched on age, study center, race, study year of diagnosis, year of blood draw, time of day of blood draw, and menopausal hormone therapy (MHT) use. Adipokine and estradiol levels were categorized into tertiles (T). ORs and 95% confidence intervals (CIs) for the associations of adiponectin, leptin, and visfatin with endometrial cancer risk were estimated by conditional logistic regression, adjusting for known endometrial cancer risk factors, including body mass index (BMI) and circulating estradiol levels. Results: Adiponectin levels were inversely associated with risk of endometrial cancer [ORT3vsT1 = 0.48; 95% CI, 0.29-0.80); P-trend < 0.01], whereas elevated leptin levels showed a positive association [2.77 (1.60-4.79); P-trend < 0.01]. These results remained significant after adjustment for estradiol, but not after further adjustment for BMI. When analyses were restricted to non-MHT users, associations of adiponectin and leptin were stronger and remained significant after adjustment for estradiol and BMI [0.25 (0.08-0.75); P-trend = 0.01 and 4.72 (1.15-19.38); P-trend = 0.02, respectively]. Nonsignificant positive associations were observed for visfatin. Conclusion: Adipokines may influence endometrial cancer risk through pathways other than estrogen-mediated cell growth in postmenopausal women not currently on MHT. Impact: Understanding how adipokines influence endometrial cancer risk may help to elucidate biological mechanisms important for the observed obesity-endometrial cancer association. (C) 2013 AACR.
引用
收藏
页码:1304 / 1312
页数:9
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