首页 | 官方网站   微博 | 高级检索  
     


Prospective associations between serum biomarkers of lipid metabolism and overall,breast and prostate cancer risk
Authors:Mathilde His  Laurent Zelek  Mélanie Deschasaux  Camille Pouchieu  Emmanuelle Kesse-Guyot  Serge Hercberg  Pilar Galan  Paule Latino-Martel  Jacques Blacher  Mathilde Touvier
Affiliation:1. EREN, SMBH Paris 13, Sorbonne Paris Cité Research Center, Nutritional Epidemiology Research Team, Inserm (U1153), Inra, Cnam, Paris 13 University, 74 rue Marcel Cachin, 93017, Bobigny Cedex, France
2. Oncology Department, Avicenne Hospital, 93017, Bobigny Cedex, France
3. Public Health Department, Avicenne Hospital, 93017, Bobigny Cedex, France
4. Diagnosis and Therapeutic Center, H?tel-Dieu Hospital, 75004, Paris, France
Abstract:Experimental studies provided evidence about mechanisms by which cholesterol, especially high density lipoprotein cholesterol (HDL-C), could influence carcinogenesis, notably through antioxidant and anti-inflammatory properties. However, prospective studies that investigated the associations between specific lipid metabolism biomarkers and cancer risk provided inconsistent results. The objective was to investigate the prospective associations between total cholesterol (T-C), HDL-C, low density lipoprotein cholesterol, apolipoproteins A1 (apoA1) and B, and triglycerides and overall, breast and prostate cancer risk. Analyses were performed on 7,557 subjects of the Supplémentation en Vitamines et Minéraux Antioxydants Study, a nationwide French cohort study. Biomarkers of lipid metabolism were measured at baseline and analyzed regarding the risk of first primary incident cancer (N = 514 cases diagnosed during follow-up, 1994–2007), using Cox proportional hazards models. T-C was inversely associated with overall (HR1mmol/L increment = 0.91, 95 % CI 0.82–1.00; P = 0.04) and breast (HR1mmol/L increment = 0.83, 95 % CI 0.69–0.99; P = 0.04) cancer risk. HDL-C was also inversely associated with overall (HR1mmol/L increment = 0.61, 95 % CI 0.46–0.82; P = 0.0008) and breast (HR1mmol/L increment = 0.48, 95 % CI 0.28–0.83; P = 0.009) cancer risk. Consistently, apoA1 was inversely associated with overall (HR1g/L increment = 0.56, 95 % CI 0.39–0.82; P = 0.003) and breast (HR1g/L increment = 0.36, 95 % CI 0.18–0.73; P = 0.004) cancer risk. This prospective study suggests that pre-diagnostic serum levels of T-C, HDL-C and ApoA1 are associated with decreased overall and breast cancer risk. The confirmation of a role of cholesterol components in cancer development, by further large prospective and experimental studies, may have important implications in terms of public health, since cholesterol is already crucial in cardiovascular prevention.
Keywords:
本文献已被 SpringerLink 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司    京ICP备09084417号-23

京公网安备 11010802026262号