Nutrition and Metabolism Branch, International Agency for Research on Cancer, Lyon, France.
Department of Epidemiology and Biostatistics, School of Public Health, Imperial College London, London, United Kingdom.
Br J Cancer. 2024 Nov;131(9):1480-1495. doi: 10.1038/s41416-024-02857-7. Epub 2024 Sep 24.
Adiposity is a known risk factor for certain cancers; however, it is not clear whether the risk of cancer differs between individuals with high adiposity but different metabolic health status. The aim of this systematic literature review and meta-analysis of cohort studies was to evaluate associations between metabolic obesity phenotypes and overall and site-specific cancer risk.
PubMed and Embase databases were used to identify relevant cohort studies up to the 6th of June 2023. Random-effects models were used to estimate summary relative risks (SRRs) and 95% confidence intervals (CIs) for the association between metabolic obesity phenotypes and cancer risk. Certainty of evidence was assessed using the Cochrane methods and the GRADE tool. This study is registered with PROSPERO, number CRD42024549511.
A total of 15,556 records were screened, and 31 publications covering 15 unique cohort studies were included in this analysis. Of these studies, 22 were evaluated as being at low risk of bias and 9 at moderate risk of bias. Compared to metabolically healthy normal-weight individuals (MHNW), metabolically unhealthy overweight/obese (MUOW/OB) individuals had a higher risk of overall (SRR = 1.21, 95% CI = 1.02-1.44, n = 3 studies, high certainty) and obesity-related cancers (SRR = 1.42, 95% CI = 1.15-1.74, n = 3, very low certainty). Specifically, MUOW/OB individuals were at higher risk of cancers of the postmenopausal breast (SRR = 1.32, 95% CI = 1.17-1.48, n = 7, low certainty), colorectum (SRR = 1.24, 95% CI = 1.16-1.31, n = 6, moderate certainty), endometrium (SRR = 2.31, 95% CI = 2.08-2.57, n = 4, high certainty), thyroid (SRR = 1.42, 95% CI = 1.29-1.57, n = 4, moderate certainty), kidney (SRR = 1.71, 95% CI = 1.40-2.10, n = 3, low certainty), pancreas (SRR = 1.35, 95% CI = 1.24-1.47, n = 3, high certainty), liver (SRR = 1.81, 95% CI = 1.36-2.42, n = 2, moderate certainty), gallbladder (SRR = 1.42, 95% CI = 1.17-1.73, n = 2, high certainty), bladder (SRR = 1.36, 95% CI = 1.19-1.56, n = 2, moderate certainty), and stomach (SRR = 1.50, 95% CI = 1.12-2.01, n = 2, high certainty). In addition, we found elevated risks of most of these cancers among individuals classified as MUNW and MHOW/OB phenotypes compared to those with MHNW phenotype. Our stratified analyses according to metabolic obesity phenotypes suggested that the elevated risks of some cancers were stronger in individuals with MUOW/OB versus those with MHOW/OB or MUNW phenotypes.
These findings suggest that both higher adiposity and metabolic dysfunction were independently associated with increased risk of several cancers, with the strongest associations generally observed among those with both metabolic dysfunction and obesity.
肥胖是某些癌症的已知危险因素;然而,高肥胖但代谢健康状况不同的个体的癌症风险是否不同尚不清楚。本系统文献综述和队列研究的目的是评估代谢性肥胖表型与整体和特定部位癌症风险之间的关联。
使用 PubMed 和 Embase 数据库检索截至 2023 年 6 月 6 日的相关队列研究。使用随机效应模型估计代谢性肥胖表型与癌症风险之间的关联的综合相对风险(SRR)和 95%置信区间(CI)。使用 Cochrane 方法和 GRADE 工具评估证据的确定性。本研究在 PROSPERO 注册,编号为 CRD42024549511。
共筛选出 15556 条记录,纳入了 31 篇涵盖 15 项独特队列研究的出版物进行分析。其中 22 项研究被评估为低偏倚风险,9 项研究为中偏倚风险。与代谢健康正常体重的个体(MHNW)相比,代谢不健康超重/肥胖的个体(MUOW/OB)患整体(SRR=1.21,95%CI=1.02-1.44,n=3 项研究,高确定性)和肥胖相关癌症的风险更高(SRR=1.42,95%CI=1.15-1.74,n=3 项研究,极低确定性)。具体而言,MUOW/OB 个体患绝经后乳腺癌(SRR=1.32,95%CI=1.17-1.48,n=7,低确定性)、结直肠癌(SRR=1.24,95%CI=1.16-1.31,n=6,中等确定性)、子宫内膜癌(SRR=2.31,95%CI=2.08-2.57,n=4,高确定性)、甲状腺癌(SRR=1.42,95%CI=1.29-1.57,n=4,中等确定性)、肾癌(SRR=1.71,95%CI=1.40-2.10,n=3,低确定性)、胰腺癌(SRR=1.35,95%CI=1.24-1.47,n=3,高确定性)、肝癌(SRR=1.81,95%CI=1.36-2.42,n=2,中等确定性)、胆囊癌(SRR=1.42,95%CI=1.17-1.73,n=2,高确定性)、膀胱癌(SRR=1.36,95%CI=1.19-1.56,n=2,中等确定性)和胃癌(SRR=1.50,95%CI=1.12-2.01,n=2,高确定性)的风险也更高。此外,我们发现与 MHNW 表型相比,分类为 MUNW 和 MHOW/OB 表型的个体中,这些癌症的风险大多升高。我们根据代谢性肥胖表型进行的分层分析表明,与 MUOW/OB 个体相比,MHOW/OB 或 MUNW 个体的一些癌症风险升高更为明显。
这些发现表明,较高的肥胖和代谢功能障碍都与多种癌症的风险增加独立相关,一般来说,代谢功能障碍和肥胖并存的个体的相关性最强。