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家族性腺瘤性息肉病中基因型预测表型:在手术选择中的实际应用

Genotype predicting phenotype in familial adenomatous polyposis: a practical application to the choice of surgery.

作者信息

Nieuwenhuis Marry H, Bülow Steffen, Björk Jan, Järvinen Heikki J, Bülow Charlotte, Bisgaard Marie Luise, Vasen Hans F A

机构信息

The Netherlands Foundation for the Detection of Hereditary Tumours, Leiden, The Netherlands. m.nieuwenhuis.stoet.nl

出版信息

Dis Colon Rectum. 2009 Jul;52(7):1259-63. doi: 10.1007/DCR.0b013e3181a0d33b.

Abstract

PURPOSE

Genetic information may help preoperatively select patients with familial adenomatous polyposis for either colectomy with ileorectal anastomosis or proctocolectomy with ileal pouch-anal anastomosis. Although complicated, the latter procedure has a low long-term risk of rectal cancer.

METHODS

Data were obtained from four national polyposis registries. On the basis of previously described genotype-phenotype correlations, patients were divided into three genotype groups predicting attenuated, intermediate, and severe polyposis phenotypes. Cumulative risks of secondary proctectomy and rectal cancer after primary colectomy were calculated using the Kaplan-Meier method.

RESULTS

Four hundred and seventy-five polyposis patients with a previous colectomy were included. Cumulative risks of secondary proctectomy 20 years after primary colectomy were 10%, 39%, and 61% in the attenuated, intermediate, and severe genotype groups, respectively (P < 0.05, groups compared separately). Cumulative risks of rectal cancer after primary colectomy were 3.7%, 9.3%, and 8.3%, respectively, in the three groups (P > 0.05, groups compared separately).

CONCLUSION

Mutation analysis may be used to predict the risk of secondary proctectomy after primary colectomy in familial adenomatous polyposis. Patients with severe genotypes have a high risk of reoperation after primary colectomy and will benefit from primary proctocolectomy with ileal pouch-anal anastomosis. The risk of rectal cancer after primary colectomy was not significantly different between the three groups.

摘要

目的

基因信息可能有助于在术前为家族性腺瘤性息肉病患者选择行回肠直肠吻合术的结肠切除术或行回肠袋肛管吻合术的直肠结肠切除术。尽管后一种手术较为复杂,但直肠癌的长期风险较低。

方法

数据来自四个国家息肉病登记处。根据先前描述的基因型-表型相关性,将患者分为预测息肉病表型减弱、中等和严重的三个基因型组。使用Kaplan-Meier方法计算初次结肠切除术后二次直肠切除和直肠癌的累积风险。

结果

纳入了475例曾行结肠切除术的息肉病患者。初次结肠切除术后20年,息肉病表型减弱、中等和严重基因型组二次直肠切除的累积风险分别为10%、39%和61%(P<0.05,各基因型组单独比较)。三组初次结肠切除术后直肠癌的累积风险分别为3.7%、9.3%和8.3%(P>0.05,各基因型组单独比较)。

结论

突变分析可用于预测家族性腺瘤性息肉病患者初次结肠切除术后二次直肠切除的风险。基因型严重的患者初次结肠切除术后再次手术的风险较高,将从初次直肠结肠切除术加回肠袋肛管吻合术中获益。三组初次结肠切除术后直肠癌的风险无显著差异。

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