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腹部肥胖的变化会影响息肉切除术后同时性高级结直肠肿瘤发展的风险。

Changes in Abdominal Obesity Affect the Risk of Metachronous Advanced Colorectal Neoplasia Development after Polypectomy.

机构信息

Division of Gastroenterology, Department of Internal Medicine, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul, Korea.

出版信息

Yonsei Med J. 2020 Jul;61(7):579-586. doi: 10.3349/ymj.2020.61.7.579.

DOI:10.3349/ymj.2020.61.7.579
PMID:32608201
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7329737/
Abstract

PURPOSE

The impact of changes in body mass index and waist circumference on the development of metachronous colorectal neoplasia (CRN) after polypectomy has rarely been examined. We evaluated the association between changes in overall/abdominal obesity and metachronous CRN risk.

MATERIALS AND METHODS

We studied patients who underwent ≥1 adenoma removal and surveillance colonoscopy. Patients were classified into the following four groups based on the changes in overall obesity from index to follow-up colonoscopy: non-obesity persisted (group 1), obesity to non-obesity (group 2), non-obesity to obesity (group 3), and obesity persisted (group 4). Patients were also divided into another four groups based on similar changes in abdominal obesity (groups 5-8).

RESULTS

The number of patients in groups 1, 2, 3, and 4 was 5074, 457, 643, and 3538, respectively, and that in groups 5, 6, 7, and 8 was 4229, 538, 656, and 2189, respectively. Group 4 had a significantly higher risk of metachronous CRN compared to groups 1 and 2. However, metachronous advanced CRN (ACRN) risk was not different among groups 1, 2, 3, and 4. Metachronous CRN risk in group 8 (abdominal obesity persisted) was higher than that in groups 5 (non-abdominal obesity persisted) and 7 (non-abdominal obesity to abdominal obesity), and tended to be higher than that in group 6 (abdominal obesity to non-abdominal obesity). Additionally, group 8 had a significantly higher risk of metachronous ACRN compared to groups 5, 6, and 7.

CONCLUSION

Changes in obesity affected the metachronous CRN risk. In particular, changes in abdominal obesity affected the metachronous ACRN risk.

摘要

目的

体重指数和腰围变化对息肉切除后并发结直肠腺瘤(CRN)的影响很少被研究。本研究评估了整体/腹部肥胖变化与结直肠腺瘤复发风险之间的关系。

材料与方法

研究对象为接受了≥1 个腺瘤切除且行随访结肠镜检查的患者。根据从基线到随访结肠镜检查时整体肥胖的变化,患者被分为以下四组:非肥胖持续组(第 1 组)、肥胖至非肥胖组(第 2 组)、非肥胖至肥胖组(第 3 组)和肥胖持续组(第 4 组)。同样,根据腹部肥胖的类似变化,患者被分为另外四组(第 5-8 组)。

结果

第 1、2、3 和 4 组的患者数量分别为 5074、457、643 和 3538 例,第 5、6、7 和 8 组的患者数量分别为 4229、538、656 和 2189 例。与第 1 组和第 2 组相比,第 4 组发生结直肠腺瘤复发的风险显著增加。然而,第 1、2、3 和 4 组之间进展期腺瘤复发(ACRN)的风险无差异。与第 5 组(非腹部肥胖持续)和第 7 组(非腹部肥胖至腹部肥胖)相比,第 8 组(腹部肥胖持续)发生结直肠腺瘤复发的风险更高,且高于第 6 组(腹部肥胖至非腹部肥胖),第 8 组发生 ACRN 的风险也显著高于第 5、6 和 7 组。

结论

肥胖的变化影响了结直肠腺瘤的复发风险。特别是,腹部肥胖的变化影响了结直肠腺瘤进展期腺瘤的复发风险。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a76/7329737/06e820f83737/ymj-61-579-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a76/7329737/0e336e0bf03d/ymj-61-579-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a76/7329737/06e820f83737/ymj-61-579-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a76/7329737/0e336e0bf03d/ymj-61-579-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a76/7329737/06e820f83737/ymj-61-579-g002.jpg

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本文引用的文献

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Clin Gastroenterol Hepatol. 2020 Jan;18(1):163-170. doi: 10.1016/j.cgh.2019.02.018. Epub 2019 Feb 14.
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Association of visceral adiposity and insulin resistance with colorectal adenoma and colorectal cancer.内脏脂肪过多及胰岛素抵抗与结肠直肠腺瘤和结肠直肠癌的关联。
Intest Res. 2019 Jul;17(3):404-412. doi: 10.5217/ir.2018.00072. Epub 2018 Nov 12.
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Abdominal Obesity is More Predictive of Advanced Colorectal Neoplasia Risk Than Overall Obesity in Men: A Cross-sectional Study.
男性中,腹部肥胖比总体肥胖对结直肠高级别肿瘤的发生风险具有更强的预测作用:一项横断面研究。
J Clin Gastroenterol. 2019 Aug;53(7):e284-e290. doi: 10.1097/MCG.0000000000001086.
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Visceral obesity as a risk factor for colorectal adenoma occurrence in surveillance colonoscopy.内脏型肥胖作为结直肠腺瘤发生的危险因素在监测结肠镜检查中的应用。
Gastrointest Endosc. 2018 Jul;88(1):119-127.e4. doi: 10.1016/j.gie.2018.02.040. Epub 2018 Mar 3.
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Abdominal obesity and colorectal cancer risk: systematic review and meta-analysis of prospective studies.腹部肥胖与结直肠癌风险:前瞻性研究的系统评价和荟萃分析。
Biosci Rep. 2017 Dec 12;37(6). doi: 10.1042/BSR20170945. Print 2017 Dec 22.
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