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嗅觉缺陷作为非综合征性口面部裂隙表型谱一部分的证据。

Evidence of olfactory deficits as part of the phenotypic spectrum of nonsyndromic orofacial clefting.

作者信息

May Maureen A, Sanchez Carla A, Deleyiannis Frederic W B, Marazita Mary L, Weinberg Seth M

机构信息

From the *Center for Craniofacial and Dental Genetics, Department of Oral Biology, University of Pittsburgh, Pittsburgh, PA; †Cleft Lip and Palate Program, ‡Department of Pediatric Plastic Surgery, and §Department of Otolaryngology, Children's Hospital of Colorado, Aurora, CO; and ∥Department of Human Genetics, ¶Clinical and Translational Science Institute, and #Department of Anthropology, University of Pittsburgh, Pittsburgh, PA.

出版信息

J Craniofac Surg. 2015 Jan;26(1):84-6. doi: 10.1097/SCS.0000000000001242.

Abstract

Improved understanding of the phenotypic spectrum associated with nonsyndromic orofacial clefting (OFC) has the potential to inform efforts to uncover the etiology of this complex trait. Prior studies report that individuals with OFC are characterized by impaired olfactory ability. In this study, we test whether olfactory dysfunction extends to the unaffected parents of children with OFC. The University of Pennsylvania Smell Identification Test was used to measure olfactory ability in a sample of 60 unaffected mothers and fathers with cleft-affected children. The proportion of deficit was compared with reference data obtained from published sex- and age-specific norms on more than 2700 individuals. The proportion of deficit was significantly higher in unaffected parents compared with baseline control subjects (41.7% vs 12.6%; P < 0.001). Of unaffected fathers, 41.7% displayed evidence of deficit compared with 15.1% of male control subjects (P = 0.001), whereas 41.7% of mothers exhibited deficits compared with 10.4% of female control subjects (P < 0.001). Olfactory deficits are present at a high proportion in the unaffected parents of individuals with OFC. This suggests that the deficits observed in affected cases may not simply be a secondary consequence of surgical repair and may instead be an informative phenotype reflecting underlying etiology.

摘要

对非综合征性口面部裂隙(OFC)相关表型谱的深入理解,有可能为揭示这一复杂性状的病因提供信息。先前的研究报告称,患有OFC的个体具有嗅觉能力受损的特征。在本研究中,我们测试嗅觉功能障碍是否也存在于OFC患儿未受影响的父母中。使用宾夕法尼亚大学嗅觉识别测试,对60名有腭裂患儿的未受影响的母亲和父亲进行嗅觉能力测量。将缺陷比例与从超过2700名个体的已发表的性别和年龄特异性标准中获得的参考数据进行比较。与基线对照受试者相比,未受影响的父母中缺陷比例显著更高(41.7%对12.6%;P<0.001)。在未受影响的父亲中,41.7%显示出缺陷证据,而男性对照受试者中这一比例为15.1%(P=0.001),在母亲中,41.7%表现出缺陷,而女性对照受试者中这一比例为10.4%(P<0.001)。在患有OFC个体的未受影响的父母中,嗅觉缺陷比例很高。这表明在受影响病例中观察到的缺陷可能不仅仅是手术修复的次要后果,而可能是反映潜在病因的一个有价值的表型。

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