• 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

血清瘦素和脂联素水平与 Barrett 食管和胃食管交界处肠化生的风险。

Serum leptin and adiponectin levels and risk of Barrett's esophagus and intestinal metaplasia of the gastroesophageal junction.

机构信息

Nutritional Sciences Program, The University of Washington, Seattle, Washington, USA.

出版信息

Obesity (Silver Spring). 2010 Nov;18(11):2204-11. doi: 10.1038/oby.2009.508. Epub 2010 Jan 28.

DOI:10.1038/oby.2009.508
PMID:20111023
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3125020/
Abstract

Persons diagnosed with Barrett's esophagus (BE) are at increased risk of developing esophageal adenocarcinoma (EA). Obesity is a major risk factor for both BE and EA. The primary purposes of this study were to determine whether circulating levels of leptin and adiponectin, both of which are deregulated in obese states, predict risk of specialized intestinal metaplasia (SIM) occurring in the esophagus (BE) and/or gastroesophageal junction, and evaluate the extent to which they mediate the relationship between obesity and these conditions. In this case-control study, 177 persons newly diagnosed with SIM were compared with 173 general population controls using unconditional logistic regression. Females in the highest tertiles of BMI and waist circumference were at the greatest risk (adjusted odds ratio (OR) = 4.6 (95% confidence interval (CI) = 1.9, 11.6), P(trend) = 0.002; OR = 5.1 (95% CI = 2.0, 13.0), P(trend) = 0.002, respectively) compared to females in the lowest tertiles. Adjustment for leptin and adiponectin attenuated these associations by 52 and 42%, respectively. Males in the highest tertile of waist-to-hip ratio were at the greatest risk (adjusted OR = 2.8 (95% CI = 1.3, 5.9), P(trend) = 0.014) compared to males in the lowest tertile. However, adjustment for leptin and adiponectin did not attenuate these associations. Our study results are consistent with the notion that circulating leptin and adiponectin partially mediate the obesity-BE relationship in women. Leptin and adiponectin's role in the progression from normal epithelium to SIM/BE and on to EA should be further elucidated.

摘要

被诊断患有 Barrett 食管 (BE) 的人患食管腺癌 (EA) 的风险增加。肥胖是 BE 和 EA 的主要危险因素。本研究的主要目的是确定循环中瘦素和脂联素的水平是否可以预测肥胖状态下发生的食管 (BE) 和/或胃食管交界处的特殊肠上皮化生 (SIM) 的风险,以及评估它们在多大程度上调节肥胖与这些疾病之间的关系。在这项病例对照研究中,177 名新诊断为 SIM 的患者与 173 名普通人群对照进行了比较,使用无条件逻辑回归。BMI 和腰围最高三分位的女性风险最大(调整后的优势比 (OR) = 4.6 (95%置信区间 (CI) = 1.9, 11.6),P(trend) = 0.002;OR = 5.1 (95% CI = 2.0, 13.0),P(trend) = 0.002)与 BMI 和腰围最低三分位的女性相比。瘦素和脂联素的调整分别减弱了这些关联的 52%和 42%。腰围与臀围比最高三分位的男性风险最大(调整后的 OR = 2.8 (95% CI = 1.3, 5.9),P(trend) = 0.014)与最低三分位的男性相比。然而,瘦素和脂联素的调整并没有减弱这些关联。我们的研究结果与循环瘦素和脂联素部分调节女性肥胖与 BE 关系的观点一致。瘦素和脂联素在从正常上皮到 SIM/BE 再到 EA 的进展中的作用应进一步阐明。

相似文献

1
Serum leptin and adiponectin levels and risk of Barrett's esophagus and intestinal metaplasia of the gastroesophageal junction.血清瘦素和脂联素水平与 Barrett 食管和胃食管交界处肠化生的风险。
Obesity (Silver Spring). 2010 Nov;18(11):2204-11. doi: 10.1038/oby.2009.508. Epub 2010 Jan 28.
2
Serum adiponectin, resistin, leptin concentration and central adiposity parameters in Barrett's esophagus patients with and without intestinal metaplasia in comparison to healthy controls and patients with GERD.与健康对照者及胃食管反流病(GERD)患者相比,巴雷特食管伴或不伴肠化生患者的血清脂联素、抵抗素、瘦素浓度及中心性肥胖参数。
Hepatogastroenterology. 2012 Nov-Dec;59(120):2395-9. doi: 10.5754/hge12587.
3
Associations of Serum Adiponectin and Leptin With Barrett's Esophagus.血清脂联素和瘦素与巴雷特食管的关联。
Clin Gastroenterol Hepatol. 2015 Dec;13(13):2265-72. doi: 10.1016/j.cgh.2015.02.037. Epub 2015 Feb 28.
4
Association between markers of obesity and progression from Barrett's esophagus to esophageal adenocarcinoma.肥胖标志物与 Barrett 食管向食管腺癌进展的关系。
Clin Gastroenterol Hepatol. 2013 Aug;11(8):934-43. doi: 10.1016/j.cgh.2013.02.017. Epub 2013 Mar 1.
5
Leptin and the risk of Barrett's oesophagus.瘦素与巴雷特食管的风险
Gut. 2008 Apr;57(4):448-54. doi: 10.1136/gut.2007.131243. Epub 2008 Jan 4.
6
Ghrelin and Leptin Have a Complex Relationship with Risk of Barrett's Esophagus.胃饥饿素和瘦素与巴雷特食管风险存在复杂关系。
Dig Dis Sci. 2016 Jan;61(1):70-9. doi: 10.1007/s10620-015-3867-6. Epub 2015 Sep 22.
7
A pilot study of the association of low plasma adiponectin and Barrett's esophagus.血浆脂联素水平降低与巴雷特食管相关性的一项初步研究。
Am J Gastroenterol. 2008 Jun;103(6):1358-64. doi: 10.1111/j.1572-0241.2008.01823.x. Epub 2008 May 28.
8
Associations of diabetes mellitus, insulin, leptin, and ghrelin with gastroesophageal reflux and Barrett's esophagus.糖尿病、胰岛素、瘦素和胃饥饿素与胃食管反流和 Barrett 食管的关系。
Gastroenterology. 2013 Dec;145(6):1237-44.e1-5. doi: 10.1053/j.gastro.2013.08.052. Epub 2013 Aug 30.
9
Abdominal obesity and body mass index as risk factors for Barrett's esophagus.腹型肥胖和体重指数作为巴雷特食管的危险因素。
Gastroenterology. 2007 Jul;133(1):34-41; quiz 311. doi: 10.1053/j.gastro.2007.04.046. Epub 2007 Apr 25.
10
Association of adiponectin multimers with Barrett's oesophagus.脂联素多聚体与巴雷特食管的关联。
Gut. 2009 Dec;58(12):1583-9. doi: 10.1136/gut.2008.171553. Epub 2009 Jun 30.

引用本文的文献

1
Gastro-Oesophageal Reflux Disease Outcomes Following Roux-en-Y Gastric Bypass Surgery in Patients with Obesity: A Systematic Review and Meta-analysis.肥胖患者接受Roux-en-Y胃旁路手术后的胃食管反流病结局:一项系统评价和荟萃分析。
Obes Surg. 2025 Apr 24. doi: 10.1007/s11695-025-07865-x.
2
Gastroesophageal Reflux Disease in Obesity: Bariatric Surgery as Both the Cause and the Cure in the Morbidly Obese Population.肥胖人群中的胃食管反流病:减重手术在病态肥胖人群中既是病因也是治疗方法
J Clin Med. 2023 Aug 25;12(17):5543. doi: 10.3390/jcm12175543.
3
Translating Molecular Biology Discoveries to Develop Targeted Cancer Interception in Barrett's Esophagus.将分子生物学发现转化为巴雷特食管的靶向癌症干预。
Int J Mol Sci. 2023 Jul 11;24(14):11318. doi: 10.3390/ijms241411318.
4
Kyoto international consensus report on anatomy, pathophysiology and clinical significance of the gastro-oesophageal junction.京都胃食管连接部解剖、病理生理学和临床意义国际共识报告
Gut. 2022 Aug;71(8):1488-1514. doi: 10.1136/gutjnl-2022-327281. Epub 2022 Jun 20.
5
Role of Obesity, Physical Exercise, Adipose Tissue-Skeletal Muscle Crosstalk and Molecular Advances in Barrett's Esophagus and Esophageal Adenocarcinoma.肥胖、体育锻炼、脂肪组织-骨骼肌相互作用及分子进展在巴雷特食管和食管腺癌中的作用
Int J Mol Sci. 2022 Apr 1;23(7):3942. doi: 10.3390/ijms23073942.
6
Crossroad between Obesity and Gastrointestinal Cancers: A Review of Molecular Mechanisms and Interventions.肥胖与胃肠道癌症的交叉点:分子机制与干预措施综述
Int J Prev Med. 2021 Feb 24;12:18. doi: 10.4103/ijpvm.IJPVM_266_20. eCollection 2021.
7
Shared genetic architecture and casual relationship between leptin levels and type 2 diabetes: large-scale cross-trait meta-analysis and Mendelian randomization analysis.瘦素水平与2型糖尿病之间的共享遗传结构及因果关系:大规模跨性状荟萃分析和孟德尔随机化分析
BMJ Open Diabetes Res Care. 2020 Apr;8(1). doi: 10.1136/bmjdrc-2019-001140.
8
Adiponectin level changes among Egyptians with gastroesophageal reflux disease.埃及胃食管反流病患者脂联素水平的变化
JGH Open. 2018 Jan 28;2(1):21-27. doi: 10.1002/jgh3.12038. eCollection 2018 Feb.
9
Identification of key pathways and genes in Barrett's esophagus using integrated bioinformatics methods.采用综合生物信息学方法鉴定 Barrett 食管中的关键途径和基因。
Mol Med Rep. 2018 Feb;17(2):3069-3077. doi: 10.3892/mmr.2017.8274. Epub 2017 Dec 12.
10
Globular adiponectin inhibits leptin-stimulated esophageal adenocarcinoma cell proliferation via adiponectin receptor 2-mediated suppression of UHRF1.球形脂联素通过脂联素受体2介导的UHRF1抑制作用来抑制瘦素刺激的食管腺癌细胞增殖。
Mol Cell Biochem. 2017 Jul;431(1-2):103-112. doi: 10.1007/s11010-017-2980-6. Epub 2017 Mar 11.

本文引用的文献

1
Globular adiponectin, acting via adiponectin receptor-1, inhibits leptin-stimulated oesophageal adenocarcinoma cell proliferation.球形脂联素通过脂联素受体-1发挥作用,抑制瘦素刺激的食管腺癌细胞增殖。
Mol Cell Endocrinol. 2008 Mar 26;285(1-2):43-50. doi: 10.1016/j.mce.2008.01.023. Epub 2008 Feb 7.
2
Leptin and the risk of Barrett's oesophagus.瘦素与巴雷特食管的风险
Gut. 2008 Apr;57(4):448-54. doi: 10.1136/gut.2007.131243. Epub 2008 Jan 4.
3
The association of gastric leptin with oesophageal inflammation and metaplasia.胃瘦素与食管炎和化生的关联。
Gut. 2008 Jan;57(1):16-24. doi: 10.1136/gut.2007.131672. Epub 2007 Aug 30.
4
Central adiposity and risk of Barrett's esophagus.中心性肥胖与巴雷特食管的风险
Gastroenterology. 2007 Aug;133(2):403-11. doi: 10.1053/j.gastro.2007.05.026. Epub 2007 May 21.
5
Abdominal obesity and body mass index as risk factors for Barrett's esophagus.腹型肥胖和体重指数作为巴雷特食管的危险因素。
Gastroenterology. 2007 Jul;133(1):34-41; quiz 311. doi: 10.1053/j.gastro.2007.04.046. Epub 2007 Apr 25.
6
Leptin synergistically enhances the anti-apoptotic and growth-promoting effects of acid in OE33 oesophageal adenocarcinoma cells in culture.瘦素协同增强培养的OE33食管腺癌细胞中酸的抗凋亡和促生长作用。
Mol Cell Endocrinol. 2007 Aug 15;274(1-2):60-8. doi: 10.1016/j.mce.2007.05.017. Epub 2007 Jun 2.
7
Activation of Akt is increased in the dysplasia-carcinoma sequence in Barrett's oesophagus and contributes to increased proliferation and inhibition of apoptosis: a histopathological and functional study.在巴雷特食管的发育异常-癌序列中,Akt的激活增加,这有助于增殖增加和细胞凋亡抑制:一项组织病理学和功能研究。
BMC Cancer. 2007 Jun 8;7:97. doi: 10.1186/1471-2407-7-97.
8
Risk factors for Barrett's oesophagus and oesophageal adenocarcinoma: results from the FINBAR study.巴雷特食管和食管腺癌的危险因素:芬兰巴雷特食管研究(FINBAR)结果
World J Gastroenterol. 2007 Mar 14;13(10):1585-94. doi: 10.3748/wjg.v13.i10.1585.
9
Obesity and lifestyle risk factors for gastroesophageal reflux disease, Barrett esophagus and esophageal adenocarcinoma.肥胖与胃食管反流病、巴雷特食管和食管腺癌的生活方式风险因素。
Dis Esophagus. 2006;19(5):321-8. doi: 10.1111/j.1442-2050.2006.00602.x.
10
Leptin stimulates proliferation and inhibits apoptosis in Barrett's esophageal adenocarcinoma cells by cyclooxygenase-2-dependent, prostaglandin-E2-mediated transactivation of the epidermal growth factor receptor and c-Jun NH2-terminal kinase activation.瘦素通过环氧化酶-2依赖性、前列腺素-E2介导的表皮生长因子受体反式激活和c-Jun氨基末端激酶激活,刺激巴雷特食管腺癌细胞增殖并抑制其凋亡。
Endocrinology. 2006 Sep;147(9):4505-16. doi: 10.1210/en.2006-0224. Epub 2006 Jun 1.