Association of circulating leptin, adiponectin, and resistin concentrations with long-term breast cancer prognosis in a German patient cohort

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作者
Nadia Obi
Audrey Y. Jung
Tabea Maurer
Marianne Huebner
Theron Johnson
Sabine Behrens
Stefanie Jaskulski
Heiko Becher
Jenny Chang-Claude
机构
[1] University Medical Center Hamburg-Eppendorf,Institute for Medical Biometry and Epidemiology
[2] German Cancer Research Center (DKFZ),Division of Cancer Epidemiology/Unit of Genetic Epidemiology
[3] University Cancer Center Hamburg,Cancer Epidemiology
[4] University Medical Center Hamburg-Eppendorf,Department of Statistics and Probability
[5] Michigan State University,Institute for Prevention and Cancer Epidemiology, Faculty of Medicine and Medical Center
[6] University Medical Center,undefined
[7] University of Freiburg,undefined
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Adipokines including leptin, adiponectin and resistin have been linked to risk of obesity-related cancers potentially through low-grade chronic inflammation pathways. We aimed to assess the role of post-diagnosis circulating adipokines on long-term prognosis in a prospective breast cancer cohort. Adipokines were measured in blood collected at baseline shortly after diagnosis (2002–2005) and at follow-up (2009) from 3112 breast cancer patients enrolled in the population-based MARIE study. Half of the patients had measurements at both time-points. All-cause mortality, breast cancer specific mortality and recurrences were ascertained up to June 2015 (11 years median follow-up). Associations with time-varying adipokine concentrations overall and stratified by estrogen and progesterone receptor (ERPR) were evaluated using adjusted proportional hazard regression. At baseline (n = 2700) and follow-up (n = 2027), median concentrations for leptin, adiponectin and resistin were 4.6 and 2.7 ng/ml, 24.4 and 30.0 mg/l, 15.4 and 26.2 ng/ml, respectively. After adjustment, there was no evidence for associations between adipokines and any outcome overall. In ERPR negative tumors, highest vs. lowest quintile of adiponectin was significantly associated with increased breast cancer specific mortality (HR 2.51, 95%CI 1.07–5.92). Overall, post-diagnosis adipokines were not associated with long-term outcomes after breast cancer. In patients with ERPR negative tumors, higher concentrations of adiponectin may be associated with increased breast cancer specific mortality and warrant further investigation.
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