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代谢失调与黑人和白人全国队列的癌症死亡率。

Metabolic dysregulation and cancer mortality in a national cohort of blacks and whites.

机构信息

Departments of Epidemiology, University of Alabama at Birmingham, Birmingham, AL, USA.

Comprehensive Cancer Center, University of Alabama at Birmingham, Birmingham, AL, USA.

出版信息

BMC Cancer. 2017 Dec 15;17(1):856. doi: 10.1186/s12885-017-3807-2.

Abstract

BACKGROUND

We examined the association between metabolic dysregulation and cancer mortality in a prospective cohort of Black and White adults.

METHODS

A total of 25,038 Black and White adults were included in the analysis. Metabolic dysregulation was defined in two ways: 1) using the joint harmonized criteria for metabolic syndrome (MetS) and 2) based on factor analysis of 15 variables characterizing metabolic dysregulation. We estimated hazards ratios (HRs) and 95% confidence intervals (CIs) for the association of MetS and metabolic dysregulation with cancer mortality during follow-up using Cox proportional hazards models.

RESULTS

About 46% of Black and 39% of White participants met the criteria for MetS. Overall, participants with MetS (HR: 1.22, 95% CI: 1.03-1.45) were at increased risk of cancer-related death. In race-stratified analysis, Black participants with MetS had significantly increased risk of cancer mortality compared with those without MetS (HR: 1.32, 95% CI: 1.01-1.72), increasing to more than a 2-fold risk of cancer mortality among those with five metabolic syndrome components (HR: 2.35, 95% CI: 1.01-5.51).

CONCLUSIONS

There are marked racial differences in the prevalence of metabolic dysregulation defined as MetS based on the harmonized criteria. The strong positive associations between MetS and cancer mortality suggests that efforts to improve cancer outcomes in general, and racial disparities in cancer outcomes specifically, may benefit from prevention and management of MetS and its components.

摘要

背景

我们在一项针对黑人和白人成年人的前瞻性队列研究中,研究了代谢失调与癌症死亡率之间的关系。

方法

共有 25038 名黑人和白人成年人纳入分析。代谢失调通过以下两种方式定义:1)使用代谢综合征(MetS)的联合协调标准,2)基于描述代谢失调的 15 个变量的因子分析。我们使用 Cox 比例风险模型估计了 MetS 和代谢失调与随访期间癌症死亡率的关联的风险比(HR)和 95%置信区间(CI)。

结果

大约 46%的黑人参与者和 39%的白人参与者符合 MetS 的标准。总体而言,患有 MetS 的参与者(HR:1.22,95%CI:1.03-1.45)患癌症相关死亡的风险增加。在种族分层分析中,与没有 MetS 的参与者相比,患有 MetS 的黑人参与者的癌症死亡率显著增加(HR:1.32,95%CI:1.01-1.72),而患有五种代谢综合征成分的参与者的癌症死亡率风险增加了两倍以上(HR:2.35,95%CI:1.01-5.51)。

结论

根据协调标准定义的 MetS 代谢失调的流行率存在明显的种族差异。MetS 与癌症死亡率之间的强烈正相关表明,为了改善癌症总体结局,特别是为了改善癌症结局的种族差异,可能需要预防和管理 MetS 及其成分。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5663/5731092/d610c7c7030c/12885_2017_3807_Fig1_HTML.jpg

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