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肥胖与组织学亚型相关的肾细胞癌风险:一项巢式病例对照研究及荟萃分析。

Obesity and renal cell carcinoma risk by histologic subtype: A nested case-control study and meta-analysis.

作者信息

Callahan Catherine L, Hofmann Jonathan N, Corley Douglas A, Zhao Wei K, Shuch Brian, Chow Wong-Ho, Purdue Mark P

机构信息

Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, Maryland, United States.

Division of Research, Kaiser Permanente Northern California, Oakland, California, United States.

出版信息

Cancer Epidemiol. 2018 Oct;56:31-37. doi: 10.1016/j.canep.2018.07.002. Epub 2018 Jul 18.

Abstract

BACKGROUND

Although obesity is an established risk factor for renal cell carcinoma (RCC), it is unclear whether this relationship varies across histologic subtypes.

METHODS

We conducted a nested case-control study within the Kaiser Permanente Northern California (KPNC) health care network, and meta-analysis combining our results with those of previously published studies. Our KPNC study included 685 RCC cases [421 clear cell; 65 papillary; 24 chromophobe; 35 other; 141 not otherwise specified (NOS)] and 4266 controls. Subtype-specific odds ratios (ORs) and 95% confidence intervals (CIs) for categories of body mass index (BMI) and were computed from the case-control data using polytomous logistic regression. Findings from this and other relevant studies were combined by meta-analysis using a random effects model.

RESULTS

In the KPNC study, obesity (BMI ≥ 30 kg/m) was associated with clear cell RCC (OR 1.5, 95% CI 1.1-2.1) and chromophobe RCC (OR 2.5, 95%CI 0.8-8.1), but not with papillary RCC (OR 1.0, 95% CI 0.5-1.9). In meta-analysis including three additional studies, a similar pattern of summary relative risks (SRR) for obesity was observed across subtypes (clear cell: SRR 1.8, 95% CI 1.5-2.2; chromophobe: SRR 2.2, 95% CI 1.3-3.7; papillary, SRR 1.2, 95% CI 0.8-1.6).

CONCLUSIONS

These findings support the hypothesis that histologic subtypes of RCC possess distinct etiologic pathways, with obesity important for the development of clear cell and, possibly, chromophobe RCC, but not papillary RCC.

摘要

背景

虽然肥胖是肾细胞癌(RCC)已确定的危险因素,但这种关系是否因组织学亚型而异尚不清楚。

方法

我们在北加利福尼亚州凯撒医疗集团(KPNC)医疗网络内进行了一项巢式病例对照研究,并将我们的结果与先前发表的研究结果进行荟萃分析。我们的KPNC研究包括685例RCC病例[421例透明细胞型;65例乳头状型;24例嫌色细胞型;35例其他类型;141例未另行指定(NOS)]和4266例对照。使用多分类逻辑回归从病例对照数据中计算体重指数(BMI)类别对应的亚型特异性比值比(OR)和95%置信区间(CI)。使用随机效应模型通过荟萃分析将本研究及其他相关研究的结果合并。

结果

在KPNC研究中,肥胖(BMI≥30kg/m²)与透明细胞RCC(OR 1.5,95%CI 1.1 - 2.1)和嫌色细胞RCC(OR 2.5,95%CI 0.8 - 8.1)相关,但与乳头状RCC无关(OR 1.0,95%CI 0.5 - 1.9)。在纳入另外三项研究的荟萃分析中,各亚型肥胖的汇总相对风险(SRR)呈现相似模式(透明细胞型:SRR 1.8,95%CI 1.5 - 2.2;嫌色细胞型:SRR 2.2,95%CI 1.3 - 3.7;乳头状型,SRR 1.2,95%CI 0.8 - 1.6)。

结论

这些发现支持以下假设,即RCC的组织学亚型具有不同的病因途径,肥胖对透明细胞型以及可能的嫌色细胞型RCC的发生发展很重要,但对乳头状RCC不重要。

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Obesity, Inflammation, and Cancer.肥胖、炎症与癌症。
Annu Rev Pathol. 2016 May 23;11:421-49. doi: 10.1146/annurev-pathol-012615-044359.
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Multilevel Genomics-Based Taxonomy of Renal Cell Carcinoma.基于多组学的肾细胞癌分类法
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