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结直肠癌与自我报告的牙齿发育不全

Colorectal cancer and self-reported tooth agenesis.

作者信息

Lindor Noralane M, Win Aung Ko, Gallinger Steven, Daftary Darshana, Thibodeau Stephen N, Silva Renato, Letra Ariadne

机构信息

Department of Health Sciences Research, Mayo Clinic, 13400 East Shea Blvd,, Scottsdale, AZ 85259, USA.

出版信息

Hered Cancer Clin Pract. 2014 Mar 10;12(1):7. doi: 10.1186/1897-4287-12-7.

DOI:10.1186/1897-4287-12-7
PMID:24607150
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3975307/
Abstract

BACKGROUND

Germline mutations in APC and AXIN2 are both associated with colon neoplasia as well as anomalous dental development. We tested the hypothesis that congenitally missing teeth may occur more commonly in individuals diagnosed with colorectal cancer than in individuals without this diagnosis.

METHODS

Via a survey conducted on 1636 individuals with colorectal cancer (CRC) and 2788 individuals with no colorectal cancer from the Colon Cancer Family Registry, self-reported information on congenitally missing teeth was collected. The frequency of missing teeth between cases and controls was compared using Pearson's chi-squared test or Fisher's exact test.

RESULTS

4.8% of cases and 5.7% of controls reported having at least one missing tooth (p = 0.20). When we stratified by recruitment site, gender, and mutation status where available, frequency of missing teeth was not statistically significantly different between cases and controls.

CONCLUSIONS

This study did not provide support for there being a general predisposition to missing teeth among a large cohort of CRC patients. The study neither addresses nor excludes the possibility, however, that individuals presenting with notable hypodontia/oligodontia might still have an increased risk for colorectal neoplasia.

摘要

背景

APC和AXIN2的胚系突变均与结肠肿瘤形成以及牙齿发育异常有关。我们检验了这样一个假设,即与未被诊断为结直肠癌的个体相比,被诊断为结直肠癌的个体先天性缺牙可能更常见。

方法

通过对来自结肠癌家族登记处的1636例结直肠癌患者和2788例非结直肠癌患者进行调查,收集了关于先天性缺牙的自我报告信息。使用Pearson卡方检验或Fisher精确检验比较病例组和对照组之间缺牙的频率。

结果

4.8%的病例和5.7%的对照报告至少有一颗牙齿缺失(p = 0.20)。当我们按招募地点、性别和可用的突变状态进行分层时,病例组和对照组之间的缺牙频率没有统计学显著差异。

结论

本研究没有为一大群结直肠癌患者普遍存在缺牙倾向提供支持。然而,该研究既未涉及也未排除这样一种可能性,即表现出明显少牙症/无牙症的个体结直肠肿瘤形成的风险可能仍然增加。

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本文引用的文献

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Association of AXIN2 with non-syndromic oral clefts in multiple populations.AXIN2 与多种人群中非综合征性口腔裂的关联性。
J Dent Res. 2012 May;91(5):473-8. doi: 10.1177/0022034512440578. Epub 2012 Feb 27.
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Colorectal and other cancer risks for carriers and noncarriers from families with a DNA mismatch repair gene mutation: a prospective cohort study.携带 DNA 错配修复基因突变的家族中携带者和非携带者的结直肠癌和其他癌症风险:一项前瞻性队列研究。
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Genetic basis for tooth malformations: from mice to men and back again.牙齿畸形的遗传学基础:从老鼠到人,再回到老鼠。
Clin Genet. 2011 Oct;80(4):319-29. doi: 10.1111/j.1399-0004.2011.01762.x. Epub 2011 Aug 23.
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AXIN2-associated autosomal dominant ectodermal dysplasia and neoplastic syndrome.AXIN2 相关的常染色体显性遗传性外胚层发育不良及肿瘤综合征。
Am J Med Genet A. 2011 Apr;155A(4):898-902. doi: 10.1002/ajmg.a.33927. Epub 2011 Mar 17.
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Germline MutY human homologue mutations and colorectal cancer: a multisite case-control study.种系MutY人类同源物突变与结直肠癌:一项多中心病例对照研究。
Gastroenterology. 2009 Apr;136(4):1251-60. doi: 10.1053/j.gastro.2008.12.050. Epub 2008 Dec 27.
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Genetic basis of tooth agenesis.牙齿发育不全的遗传基础。
J Exp Zool B Mol Dev Evol. 2009 Jun 15;312B(4):320-42. doi: 10.1002/jez.b.21277.
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AXIS inhibition protein 2, orofacial clefts and a family history of cancer.轴抑制蛋白2、口面部裂隙与癌症家族史。
J Am Dent Assoc. 2009 Jan;140(1):80-4. doi: 10.14219/jada.archive.2009.0022.
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Axis inhibition protein 2 (AXIN2) polymorphisms and tooth agenesis.轴抑制蛋白2(AXIN2)多态性与牙齿发育不全
Arch Oral Biol. 2009 Jan;54(1):45-9. doi: 10.1016/j.archoralbio.2008.08.002. Epub 2008 Sep 14.
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