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口腔裂畸形的双胎不一致子女的复发风险:丹麦 1936-2004 年口腔裂畸形双胎队列的基于人群的队列研究。

Recurrence risk for offspring of twins discordant for oral cleft: a population-based cohort study of the Danish 1936-2004 cleft twin cohort.

机构信息

Department of Epidemiology, University of Southern Denmark, Odense, Denmark.

出版信息

Am J Med Genet A. 2010 Oct;152A(10):2468-74. doi: 10.1002/ajmg.a.33608.

DOI:10.1002/ajmg.a.33608
PMID:20799319
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2946514/
Abstract

Our objective in this Danish population-based cohort study was to estimate the recurrence risk of isolated oral cleft (OC) for offspring of the unaffected co-twins of OC discordant twin pairs and to compare this risk to the recurrence risk in the offspring of the affected co-twin as well as to the risk in the background population. During 1936-2004, 207 twin pairs were ascertained, among whom at least one twin had an OC. The index persons were twins discordant for OC who had children (N=117), and their offspring (N=239). The participants were ascertained by linkage between The Danish Facial Cleft Database, The Danish Twin Registry and The Danish Civil Registration System. In the study OC recurrence risk for offspring of the affected and unaffected twin and relative risk were compared to the background prevalence. We found that among 110 children of the 54 OC affected twins, two (1.8%) children had OC corresponding to a significantly increased relative risk (RR=10; 95% CI 1.2-35) when compared to the frequency in the background population. Among the 129 children of the 63 unaffected twins, three (2.3%) children were affected, corresponding to a significantly increased relative risk (RR=13; 95% CI 2.6-36) when compared the background prevalence. We concluded that in OC discordant twin pairs similar increased recurrence risks were found among offspring of both OC affected and OC unaffected twins. This provides further evidence for a genetic component in cleft etiology and is useful information for genetic counseling of twin pairs discordant for clefting.

摘要

在这项丹麦基于人群的队列研究中,我们的目的是估计单侧口腔裂(OC)未受影响的同卵双胞胎的后代发生孤立性 OC 的复发风险,并将这种风险与受影响的同卵双胞胎后代的风险以及背景人群的风险进行比较。在 1936 年至 2004 年间,确定了 207 对双胞胎,其中至少有一个双胞胎患有 OC。索引个体是 OC 不一致的双胞胎,他们有孩子(N=117)及其后代(N=239)。通过丹麦面部裂隙数据库、丹麦双胞胎登记处和丹麦民事登记系统之间的联系确定了参与者。在这项研究中,OC 复发风险的受影响和未受影响的双胞胎及其相对风险与背景患病率进行了比较。我们发现,在 54 名 OC 受影响双胞胎的 110 名儿童中,有 2 名(1.8%)儿童患有 OC,相对风险(RR=10;95%CI 1.2-35)明显高于背景人群的频率。在 63 名未受影响的双胞胎的 129 名儿童中,有 3 名(2.3%)儿童受到影响,相对风险(RR=13;95%CI 2.6-36)明显高于背景患病率。我们得出结论,在 OC 不一致的双胞胎中,OC 受影响和未受影响的双胞胎的后代都发现了类似的复发风险增加。这为裂隙病因学中的遗传因素提供了进一步的证据,并且是对裂隙不一致的双胞胎进行遗传咨询的有用信息。

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Recurrence risk for offspring of twins discordant for oral cleft: a population-based cohort study of the Danish 1936-2004 cleft twin cohort.口腔裂畸形的双胎不一致子女的复发风险:丹麦 1936-2004 年口腔裂畸形双胎队列的基于人群的队列研究。
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本文引用的文献

1
Search for genomic alterations in monozygotic twins discordant for cleft lip and/or palate.在唇腭裂不一致的单卵双胞胎中寻找基因组改变。
Twin Res Hum Genet. 2009 Oct;12(5):462-8. doi: 10.1375/twin.12.5.462.
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A cohort study of recurrence patterns among more than 54,000 relatives of oral cleft cases in Denmark: support for the multifactorial threshold model of inheritance.丹麦一项超过 54000 名唇腭裂病例亲属的复发模式队列研究:对多因素阈值遗传模型的支持。
J Med Genet. 2010 Mar;47(3):162-8. doi: 10.1136/jmg.2009.069385. Epub 2009 Sep 14.
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Rethinking isolated cleft palate: evidence of occult lip defects in a subset of cases.重新审视孤立性腭裂:部分病例中隐匿性唇裂缺陷的证据。
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Unraveling human cleft lip and palate research.解析人类唇腭裂研究。
J Dent Res. 2008 Feb;87(2):119-25. doi: 10.1177/154405910808700202.
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Three-dimensional morphometric analysis of craniofacial shape in the unaffected relatives of individuals with nonsyndromic orofacial clefts: a possible marker for genetic susceptibility.非综合征性口面部裂隙患者未患病亲属的颅面形状三维形态计量学分析:一种可能的遗传易感性标志物。
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6
X-chromosome inactivation patterns in monozygotic twins and sib pairs discordant for nonsyndromic cleft lip and/or palate.单卵双胞胎及非综合征性唇腭裂不一致的同胞对中的X染色体失活模式。
Am J Med Genet A. 2007 Dec 15;143A(24):3267-72. doi: 10.1002/ajmg.a.32098.
7
Subclinical features in non-syndromic cleft lip with or without cleft palate (CL/P): review of the evidence that subepithelial orbicularis oris muscle defects are part of an expanded phenotype for CL/P.非综合征性唇裂伴或不伴腭裂(CL/P)的亚临床特征:关于口轮匝肌上皮下缺陷是CL/P扩展表型一部分的证据综述。
Orthod Craniofac Res. 2007 May;10(2):82-7. doi: 10.1111/j.1601-6343.2007.00386.x.
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Orbicularis oris muscle defects as an expanded phenotypic feature in nonsyndromic cleft lip with or without cleft palate.口轮匝肌缺损作为非综合征性唇裂伴或不伴腭裂的一种扩展表型特征。
Am J Med Genet A. 2007 Jun 1;143A(11):1143-9. doi: 10.1002/ajmg.a.31760.
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Parental craniofacial morphology in cleft lip with or without cleft palate as determined by cephalometry: a meta-analysis.通过头影测量法确定的唇裂伴或不伴腭裂患者父母的颅面形态:一项荟萃分析。
Orthod Craniofac Res. 2006 Feb;9(1):18-30. doi: 10.1111/j.1601-6343.2006.00339.x.
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Cancer risk in persons with oral cleft--a population-based study of 8,093 cases.口腔腭裂患者的癌症风险——一项基于8093例病例的人群研究。
Am J Epidemiol. 2005 Jun 1;161(11):1047-55. doi: 10.1093/aje/kwi132.