Suppr超能文献

APC 基因突变与家族性腺瘤性息肉病患者的 pouch 腺瘤的表型相关性。

Genotype-Phenotype Associations of APC Mutations With Pouch Adenoma in Patients With Familial Adenomatous Polyposis.

机构信息

Oncogenetic service at the Department of Gastroenterology, Tel Aviv Sourasky Medical Center.

Faculty of Medicine, Tel Aviv University.

出版信息

J Clin Gastroenterol. 2019 Feb;53(2):e54-e60. doi: 10.1097/MCG.0000000000000950.

Abstract

BACKGROUND

Patients with familial adenomatous polyposis (FAP) may carry various adenomatous polyposis coli (APC) mutations. However, genotype-phenotype correlation for APC mutations is still debated and is yet to be evaluated with regard to pouch polyp formation.

OBJECTIVE

To evaluate the association between APC mutation type and exon location and the outcome of pouch adenoma.

DESIGN SETTING AND PATIENTS

Forty-five FAP patients with defined pathogenic APC mutations, who underwent total proctocolectomy and ileal pouch anal anastomosis were classified by mutation type and location. Analysis was conducted for clinical and endoscopic parameters.

RESULTS

Twenty patients had either indel/deletion mutations and 25 had nonsense/missense mutations. The indel/deletion group was associated with higher prevalence of preoperative hundreds of colonic adenomas (66.7% vs. 30%; P=0.030), lower rates of stapled versus sewn anastomosis (46.7% vs. 76%; P=0.060), of single stage surgery (13.3% vs. 44%; P=0.045) and with higher pouch adenoma formation rate (50% vs. 8%; P=0.002). Twenty-seven were carriers of exons 1 to 14 mutations and 18 were carriers of exon 15 mutations. Carriers of exon 15 mutations had higher prevalence of preoperative hundreds of colonic adenomas (55.6% vs. 22.2%; P=0.003) and a higher tendency for pouch and cuff adenoma formation rate. Adjusted odds ratio for pouch adenoma formation was 8.32 (1.42-48.80; P=0.019) for the indel/deletion group versus nonsense/missense, but no significant independent association was noted with mutation location. The mean number of pouch and cuff adenoma formation (per endoscopy) was higher among carriers of exon 15 mutations, but no significant independent association was noted the with mutation type.

CONCLUSIONS

Type and location of APC mutation are associated with colonic polyp burden, surgical outcome and likelihood of developing pouch adenomas. These findings may contribute to surgical and endoscopic surveillance decisions for FAP patients.

摘要

背景

家族性腺瘤性息肉病(FAP)患者可能携带各种腺瘤性结肠息肉病(APC)突变。然而,APC 突变的基因型-表型相关性仍存在争议,并且尚未针对袋状息肉形成进行评估。

目的

评估 APC 突变类型和外显子位置与袋状腺瘤结局之间的关系。

设计、设置和患者:45 名患有明确致病性 APC 突变的 FAP 患者,他们接受了全直肠结肠切除术和回肠袋肛门吻合术,根据突变类型和位置进行分类。对临床和内镜参数进行了分析。

结果

20 名患者存在插入/缺失突变,25 名患者存在无义/错义突变。缺失/插入组术前存在数百个结肠腺瘤的比例更高(66.7% vs. 30%;P=0.030),吻合方式为吻合钉吻合而非缝合的比例更低(46.7% vs. 76%;P=0.060),一期手术的比例更低(13.3% vs. 44%;P=0.045),袋状腺瘤形成率更高(50% vs. 8%;P=0.002)。27 名患者携带外显子 1 至 14 突变,18 名患者携带外显子 15 突变。携带外显子 15 突变的患者术前存在数百个结肠腺瘤的比例更高(55.6% vs. 22.2%;P=0.003),且更倾向于形成袋状和袖口腺瘤。调整后的比值比(OR)显示,与无义/错义突变相比,缺失/插入组形成袋状腺瘤的风险更高(8.32 [1.42-48.80];P=0.019),但突变位置与腺瘤形成无显著独立关联。携带外显子 15 突变的患者的袋状和袖口腺瘤形成(每次内镜检查)的平均数量更高,但与突变类型无显著独立关联。

结论

APC 突变的类型和位置与结肠息肉负担、手术结果和形成袋状腺瘤的可能性相关。这些发现可能有助于 FAP 患者的手术和内镜监测决策。

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