Metabolic syndrome and outcomes following early-stage breast cancer

被引:62
作者
Calip, Gregory S. [1 ,2 ,3 ]
Malone, Kathleen E. [2 ,3 ]
Gralow, Julie R. [4 ]
Stergachis, Andy [2 ,5 ]
Hubbard, Rebecca A. [6 ,7 ]
Boudreau, Denise M. [2 ,7 ,8 ]
机构
[1] Univ Illinois, Ctr Pharmacoepidemiol & Pharmacoecon Res, Chicago, IL 60612 USA
[2] Univ Washington, Dept Epidemiol, Seattle, WA 98195 USA
[3] Fred Hutchinson Canc Res Ctr, Div Publ Hlth Sci, Seattle, WA 98104 USA
[4] Seattle Canc Care Alliance, Seattle, WA USA
[5] Univ Washington, Dept Global Hlth, Seattle, WA 98195 USA
[6] Univ Washington, Dept Biostat, Seattle, WA 98195 USA
[7] Grp Hlth Res Inst, Seattle, WA USA
[8] Univ Washington, Sch Pharm, Seattle, WA 98195 USA
基金
美国国家卫生研究院;
关键词
Breast cancer; Metabolic syndrome; Recurrence; Second primary breast cancer; Mortality; BODY-MASS INDEX; ALL-CAUSE MORTALITY; RISK-FACTORS; DIABETES-MELLITUS; BLOOD-LIPIDS; SERUM-LIPIDS; WOMEN; OBESITY; METAANALYSIS; PROGNOSIS;
D O I
10.1007/s10549-014-3157-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The prevalence of risk factors contributing to metabolic syndrome (MetS) is increasing, and numerous components of MetS are associated with increased primary breast cancer (BC) risk. However, less is known about the relationship of MetS to BC outcomes. The aim of this study was to evaluate whether MetS, characterized by increased weight, hypertension, low HDL-cholesterol, high triglycerides, and diabetes or impaired glucose tolerance, is associated with risk of second breast cancer events (SBCE) and BC-specific mortality. Retrospective cohort study of women diagnosed with incident early-stage (I-II) BC between 1990 and 2008, enrolled in an integrated health plan. Outcomes of interest were SBCE, defined as recurrence or second primary BC, and BC-specific mortality. We used multivariable Cox proportional hazards models to estimate adjusted hazard ratios (HR) and 95 % confidence intervals (CI) for time-varying exposure to MetS components while accounting for potential confounders and competing risks. Among 4,216 women in the cohort, 26 % had a parts per thousand yen3 MetS components and 13 % developed SBCE during median follow-up of 6.3 years. Compared to women with no MetS components, presence of MetS (a parts per thousand yen3 components) was associated with increased risk of SBCE (HR = 1.50, 95 % CI 1.08-2.07) and BC-specific mortality (HR = 1.65, 95 % CI 1.02-2.69). Of the individual components, only increased weight was associated with increased risk of SBCE (HR = 1.26, 95 % CI 1.06-1.49). MetS is associated with modestly increased risk of SBCE and BC-specific mortality. Given the growing population of BC survivors, further research in larger and more diverse populations is warranted.
引用
收藏
页码:363 / 377
页数:15
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