• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

成年前饥饿暴露与女性随后结直肠癌风险的关系。

Pre-adult famine exposure and subsequent colorectal cancer risk in women.

机构信息

Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht, The Netherlands and.

School of Public Health, Imperial College London, London, UK.

出版信息

Int J Epidemiol. 2017 Apr 1;46(2):612-621. doi: 10.1093/ije/dyw121.

DOI:10.1093/ije/dyw121
PMID:27585673
Abstract

BACKGROUND

Nutritional deprivation during growth and development may contribute to colorectal cancer (CRC) risk in later life.

METHODS

We studied 7906 women who were aged 0-21 years during the 1944-45 Dutch famine, who enrolled in the Prospect-EPIC study between 1993 and 1997. We used Cox proportional hazard analyses to estimate hazard ratios (HRs) and 95% confidence intervals (CIs) for colorectal (proximal, distal and rectal) cancer risk across self-reported famine exposure and exposure-age categories, while adjusting for potential confounders.

RESULTS

During a median of 17.3 years of follow-up, 245 CRC cases occurred. Moderately and severely famine-exposed women showed a respective 24% and 44% higher CRC risk compared with women who reported no exposure [HR moderate 1.24 (95% CI: 0.93-1.64); HR severe 1.44 (1.03-2.03); P trend 0.027]. This relation attenuated when adjusted for potential confounders [adjusted HR moderate 1.15 (0.87-1.53); HR severe 1.35 (0.96-1.90); P trend 0.091]. Stratified results suggested that severe famine exposure between 10 and 17 years of age was particularly related to CRC risk[adjusted HR moderate 1.39 (0.91-2.11); HR severe 1.76 (1.10-2.83); P trend 0.019; P interaction(famine*10-17yrs) 0.096]. Overall, we found no differences in famine effects across CRC subsites, but age-at-exposure stratified results suggested an increased risk for proximal CRC in those aged 10-17 years during exposure to the famine [adjusted HR moderate 2.14 (1.06-4.32), HR severe 2.96 (1.35-6.46); P trend 0.005]. Overall and within age-at-exposure categories, tests for subsite specific heterogeneity in famine effects were not significant.

CONCLUSIONS

Our findings suggest that severe exposure to a short period of caloric restriction in pre-adult women may relate to CRC risk decades later.

摘要

背景

生长发育过程中的营养剥夺可能导致中老年时期结直肠癌(CRC)的风险增加。

方法

我们研究了 1944-1945 年荷兰饥荒期间年龄在 0-21 岁的 7906 名女性,她们于 1993 年至 1997 年期间参加了前瞻性 EPIC 研究。我们使用 Cox 比例风险分析来估计结直肠(近端、远端和直肠)癌症风险的危险比(HR)和 95%置信区间(CI),跨越自我报告的饥荒暴露和暴露年龄类别,同时调整潜在的混杂因素。

结果

在中位 17.3 年的随访期间,发生了 245 例 CRC 病例。与报告无暴露的女性相比,中度和重度饥荒暴露的女性 CRC 风险分别升高 24%和 44%[中度暴露 HR 1.24(95%CI:0.93-1.64);重度暴露 HR 1.44(1.03-2.03);趋势 P 值 0.027]。当调整潜在混杂因素时,这种关系减弱[调整后的 HR 中度 1.15(0.87-1.53);HR 重度 1.35(0.96-1.90);趋势 P 值 0.091]。分层结果表明,10-17 岁时严重的饥荒暴露与 CRC 风险特别相关[调整后的 HR 中度 1.39(0.91-2.11);HR 重度 1.76(1.10-2.83);趋势 P 值 0.019;P 交互作用(饥荒*10-17 岁)0.096]。总体而言,我们没有发现 CRC 亚部位的饥荒效应存在差异,但根据暴露年龄的分层结果表明,在暴露于饥荒期间年龄为 10-17 岁的人群中,近端 CRC 的风险增加[调整后的 HR 中度 2.14(1.06-4.32),HR 重度 2.96(1.35-6.46);趋势 P 值 0.005]。总体而言和在暴露年龄类别内,对饥荒效应在亚部位特异性方面的差异检验没有显著意义。

结论

我们的研究结果表明,成年前女性严重暴露于短期热量限制可能与几十年后结直肠癌的风险有关。

相似文献

1
Pre-adult famine exposure and subsequent colorectal cancer risk in women.成年前饥饿暴露与女性随后结直肠癌风险的关系。
Int J Epidemiol. 2017 Apr 1;46(2):612-621. doi: 10.1093/ije/dyw121.
2
Breast cancer risk after caloric restriction during the 1944-1945 Dutch famine.1944 - 1945年荷兰饥荒期间热量限制后的乳腺癌风险
J Natl Cancer Inst. 2004 Apr 7;96(7):539-46. doi: 10.1093/jnci/djh087.
3
Famine exposure in the young and the risk of type 2 diabetes in adulthood.幼年饥荒暴露与成年 2 型糖尿病风险。
Diabetes. 2012 Sep;61(9):2255-60. doi: 10.2337/db11-1559. Epub 2012 May 29.
4
Cardiovascular consequences of famine in the young.幼年时期饥荒对心血管的影响。
Eur Heart J. 2012 Feb;33(4):538-45. doi: 10.1093/eurheartj/ehr228. Epub 2011 Aug 25.
5
Diabetes mellitus type 2 and subsite-specific colorectal cancer risk in men and women: results from the Netherlands Cohort Study on diet and cancer.2型糖尿病与男性和女性特定亚部位结直肠癌风险:荷兰饮食与癌症队列研究结果
Eur J Gastroenterol Hepatol. 2016 Aug;28(8):896-903. doi: 10.1097/MEG.0000000000000626.
6
The 1944-1945 Dutch famine and subsequent overall cancer incidence.1944 - 1945年荷兰饥荒与随后的总体癌症发病率。
Cancer Epidemiol Biomarkers Prev. 2005 Aug;14(8):1981-5. doi: 10.1158/1055-9965.EPI-04-0839.
7
Association of famine exposure during early life with the risk of type 2 diabetes in adulthood: a meta-analysis.生命早期饥荒暴露与成年 2 型糖尿病风险的关联:荟萃分析。
Eur J Nutr. 2018 Mar;57(2):741-749. doi: 10.1007/s00394-016-1363-1. Epub 2016 Dec 20.
8
Famine Exposure in Early Life and Risk of Metabolic Syndrome in Adulthood: Comparisons of Different Metabolic Syndrome Definitions.早期生活中的饥荒暴露与成年期代谢综合征风险:不同代谢综合征定义的比较。
J Diabetes Res. 2019 Dec 6;2019:7954856. doi: 10.1155/2019/7954856. eCollection 2019.
9
Early life exposure to famine and colorectal cancer risk: a role for epigenetic mechanisms.早期生活暴露于饥荒与结直肠癌风险:表观遗传机制的作用。
PLoS One. 2009 Nov 23;4(11):e7951. doi: 10.1371/journal.pone.0007951.
10
Famine in the young and risk of later hospitalization for COPD and asthma.年轻时的饥荒与日后患慢性阻塞性肺疾病和哮喘住院的风险
PLoS One. 2013 Dec 23;8(12):e82636. doi: 10.1371/journal.pone.0082636. eCollection 2013.

引用本文的文献

1
Long-term trends in the burden of colorectal cancer in Europe over three decades: a joinpoint regression and age-period-cohort analysis.欧洲三十年来结直肠癌负担的长期趋势:连接点回归和年龄-时期-队列分析
Front Oncol. 2023 Dec 5;13:1287653. doi: 10.3389/fonc.2023.1287653. eCollection 2023.
2
Clinicopathological and Molecular Characteristics of Early-Onset Stage III Colon Adenocarcinoma: An Analysis of the ACCENT Database.早发性 III 期结肠癌的临床病理和分子特征:ACCENT 数据库分析。
J Natl Cancer Inst. 2021 Nov 29;113(12):1693-1704. doi: 10.1093/jnci/djab123.
3
Early-onset colorectal cancer: initial clues and current views.
早发性结直肠癌:初始线索与当前观点。
Nat Rev Gastroenterol Hepatol. 2020 Jun;17(6):352-364. doi: 10.1038/s41575-019-0253-4. Epub 2020 Feb 21.