Association between baseline serum glucose, triglycerides and total cholesterol, and prostate cancer risk categories

被引:53
作者
Arthur, Rhonda [1 ]
Moller, Henrik [1 ]
Garmo, Hans [1 ,2 ]
Holmberg, Lars [1 ,2 ,3 ]
Stattin, Par [4 ,5 ,6 ]
Malmstrom, Hakan [7 ]
Lambe, Mats [3 ,8 ,9 ]
Hammar, Niklas [7 ,10 ]
Walldius, Goran [11 ]
Robinson, David [4 ,5 ,6 ]
Jungner, Ingmar [12 ,13 ]
Van Hemelrijck, Mieke [1 ,7 ]
机构
[1] Kings Coll London, Canc Epidemiol Grp, Div Canc Studies, London, England
[2] Reg Canc Ctr, Uppsala, Sweden
[3] Univ Uppsala Hosp, Dept Surg Sci, Uppsala, Sweden
[4] Umea Univ, Fac Med, Dept Surg & Perioperat Sci, Uppsala, Sweden
[5] Umea Univ, Fac Med, Dept Urol, Uppsala, Sweden
[6] Umea Univ, Fac Med, Dept Androl, Uppsala, Sweden
[7] Karolinska Inst, Inst Environm Med, Unit Epidemiol, Stockholm, Sweden
[8] Karolinska Inst, Dept Med Epidemiol, Stockholm, Sweden
[9] Karolinska Inst, Dept Biostat, Stockholm, Sweden
[10] AstraZeneca Sverige, Sodertalje, Sweden
[11] Karolinska Inst, Inst Environm Med, Dept Cardiovasc Epidemiol, Stockholm, Sweden
[12] Karolinska Inst, Dept Clin Epidemiol Unit, Stockholm, Sweden
[13] CALAB Res, Stockholm, Sweden
基金
瑞典研究理事会;
关键词
Glucose; prostate cancer; total cholesterol; triglycerides; APOLIPOPROTEIN-A-I; BODY-MASS INDEX; METABOLIC SYNDROME; DIABETES-MELLITUS; ANTIGEN LEVELS; TOTAL TESTOSTERONE; LIPID PROFILE; SWEDISH MALES; MEN; PREVENTION;
D O I
10.1002/cam4.665
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Lifestyle-related risk factors such as hyperglycemia and dyslipidemia have been associated with several cancers. However, studies exploring their link with prostate cancer (PCa) clinicopathological characteristics are sparse and inconclusive. Here, we investigated the associations between serum metabolic markers and PCa clinicopathological characteristics. The study comprised 14,294 men from the Swedish Apolipoprotein MOrtality RISk (AMORIS) cohort who were diagnosed with PCa between 1996 and 2011. Univariate and multivariable logistic regression were used to investigate the relation between glucose, triglycerides and total cholesterol and PCa risk categories, PSA, Gleason score, and T-stage. Mean age at time of PCa diagnosis was 69 years. Men with glucose levels >6.9 mmol/L tend to have PSA<4 mu g/L, while those with glucose levels of 5.6-6.9 mmol/L had a greater odds of PSA>20 mu g/L compared to PSA 4.0-9.9 mu g/L. Hypertriglyceridemia was also positively associated with PSA>20 mu g/L. Hyperglycemic men had a greater odds of intermediate-and high-grade PCa and advanced stage or metastatic PCa. Similarly, hypertriglyceridemia was positively associated with high-grade PCa. There was also a trend toward an increased odds of intermediate risk localized PCa and advanced stage PCa among men with hypertriglyceridemia. Total cholesterol did not have any statistically significant association with any of the outcomes studied. Our findings suggest that high serum levels of glucose and triglycerides may influence PCa aggressiveness and severity. Further investigation on the role of markers of glucose and lipid metabolism in influencing PCa aggressiveness and severity is needed as this may help define important targets for intervention.
引用
收藏
页码:1307 / 1318
页数:12
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