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The association of Metabolic Syndrome and its Components with the Incidence and Survival of Colorectal Cancer: A Systematic Review and Meta-analysis

机译:代谢综合征及其组分与结直肠癌发病率和存活的关联:系统审查和荟萃分析

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Background: This meta-analysis was aimed to quantitatively assess the associations of metabolic syndrome (MetS) and its components with colorectal cancer (CRC). Methods: PubMed, EMBASE and Web of Science databases were systematically searched for eligible studies. A total of 18 studies for CRC incidence and 12 studies for CRC mortality were identified. Results: MetS was associated with an increased risk of CRC incidence and mortality in male (RR: 1.28, 95 % CI 1.16-1.39, and 1.24, 1.18-1.31, respectively) and correlated with an increased risk of CRC incidence in female (RR: 1.21, 1.13-1.30), but not with CRC mortality in female. MetS increased the risk of cancer-specific mortality (RR: 1.72, 1.03-2.42), but not overall mortality. The risk estimates of CRC incidence changed little depending on age, sex, cancer site, the type of studies, ethnicity, publication year, or definition of MetS. As for CRC mortality, further stratified analyses indicated statistical significance in studies with assessing cancer-specific survival outcome, in male, a cohort design, ethnicity of non-Chinese or with definition of MetS as ≥ 3 metabolic abnormalities. Obesity and hyperglycemia are risk factors of CRC incidence in both male and female. Only dysglycemia is the risk factor for CRC mortality. Conclusions: MetS is associated with an increased risk of CRC incidence and cancer-specific mortality, but not overall mortality. In addition, MetS may increase the CRC mortality in male rather than in female. However, since most of the studies on CRC mortality were conducted in Chinese, further studies are needed to clarify this connection.? The author(s).
机译:背景:该元分析旨在定量评估代谢综合征(Mets)及其与结直肠癌(CRC)的组分的关联。方法:系统地搜索有符合条件的研究的软化,Embase和科学数据库网络。鉴定了共有18项CRC发病率的研究和12项CRC死亡的研究。结果:METS与男性(RR:1.28,95%CI 1.16-1.39和1.24,118-1.31和1.24,118-1.31)的CRC发病率和死亡风险增加相关,并与女性CRC发病率的风险增加(RR :1.21,11.13-1.30),但不是女性的CRC死亡率。大都会增加了癌症特异性死亡率的风险(RR:1.72,1.03-2.42),但不是总体死亡率。 CRC发病率的风险估计因年龄,性别,癌症网站,研究类型,种族,出版年份或MET的定义而变化几乎没有变化。对于CRC死亡率,进一步的分层分析表明,在评估癌症特异性生存结果,男性,队列设计,非中文的种族或≥3代谢异常的定义中,评估癌症特异性生存结果的研究表明统计学显着性。肥胖和高血糖是男性和女性CRC发病率的危险因素。只有脱节性血症是CRC死亡率的危险因素。结论:METS与CRC发病率和癌症特异性死亡率的风险增加有关,但不是总体死亡率。此外,METS可能会增加男性而不是女性的CRC死亡率。然而,由于大多数关于CRC死亡率的研究是在中文进行的,因此需要进一步研究来澄清这一联系。?作者。

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