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唇腭裂发病因素的logistic回归分析 被引量:3

A Logistic Regression Analysis on Risk Factors of Cleft Lip and Palate.
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摘要 目的:通过对影响唇腭裂的可疑因素分析,旨在探讨其发病危险因素。方法:对我院2003年CLP及同期省人民医院的非CLP患儿和母亲进行病例对照研究,用非条件logistic回归分析来评价指标。结果:在10项指标中,唇裂伴或不伴腭裂(CL±P)单因素分析中有4项指标具有显著意义(P<0.05),腭裂(CP)发病有5项指标具有显著意义(P<0.05),分别进入Logistic逐步回归方程,结果表明家族史、母亲职业是CL±P发病的危险因素;患儿体重、母亲职业是CP发病的危险因素。结论:遗传因素在CL±P的发病中具有显著意义,怀孕期间患病、用药可导致唇腭裂发病的相对危险度增加。 Objective: The purpose of this study is to evaluate the risk factors of cleft lip and palate (CLP). Methods: 508 CLP mothers and infants accompanied with 134 normal control pairs were studied. A logistic regression model to simple factor and multivariate analysis was used. Results: According to simple factor analysis, 4 factors were significant with cleft lip with or without palate( CL±P) ;5 factors were significant with cleft palate (CP). In the multiple logistic regression model, the family history and mother occupation were involved in CL±P, the infants height and mother occupation were involved in CP. Conclusion: The hereditary factor plays a significant role in CL±P. The relative risk of CLP could increase when mothers suffer from disease and take drugs in the period of pregnancy.
出处 《口腔医学研究》 CAS CSCD 2005年第4期449-451,共3页 Journal of Oral Science Research
关键词 唇裂 腭裂 LOGISTIC回归分析 Cleft lip Cleft palate Logistic regression analysis
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  • 1陈树华,陈江,何力.福建省唇腭裂流行病学研究[J].中华口腔医学杂志,1998,33(1):33-35. 被引量:31
  • 2Laura EM, Terri HB,Andrew CL, et al. Guidelines for the design and analysis of studies on NSCLP in humans [J]. Cleft Palate Craniofac J, 2002, 39(1):93-100
  • 3Hofstee Y,Kors N and Hennekam RCM. Genetic survey of a group of Children with clefting implications for genetic counseling [J]. Cleft Palate- Craniofac J,1993,30(5):447-451
  • 4王安训,黄洪章,潘朝斌,陈伟良,孙良忠.先天性唇腭裂发病危险因素的Logistic回归分析[J].口腔颌面外科杂志,2002,12(2):104-106. 被引量:20
  • 5Chung KC, Kowalaki CP, et al. Maternal cigarette smoking during pregnancy and risk of having a child with cleft lip/palate [J]. Plast Reconstr Surg, 2000, 105(2):485-91
  • 6Spilson SV, Kim HJ, Chung KC. Association between materal diabetes mellitus and newborn oral cleft [J]. Ann Plast Surg, 2001, 47(5):477-481

二级参考文献9

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同被引文献41

  • 1许龙水,唐世杰,孙德麟,谢思田,许道成.粤东地区930例唇腭裂患者临床资料分析[J].中国现代医学杂志,2005,15(3):404-405. 被引量:5
  • 2史晓泓,唐慧,梁怡.新生儿唇腭裂畸形的致病因素研究进展[J].中国妇幼保健,2006,21(7):1006-1007. 被引量:24
  • 3古力巴哈.买买提力,郑雪飞,杨瑞红,刘晓旭.新疆地区先天性唇腭裂发病影响因素的分析[J].口腔颌面外科杂志,2006,16(4):330-332. 被引量:7
  • 4Gritli-Linde A. Molecular control of secondary palate development [ J]. Dev Biol, 2007,301 (2) : 309 -326.
  • 5Ferguson MWJ. Palate development[ J]. Development, 1988,103 (Suppl) : 41 - 60.
  • 6Kaartinen V, Voncken JW, Shuler C, et al. Abnormal lung development and cleft palate in mice lacking TGF-beta 3 indicates defects of epithelialmesenchymal interaction [ J ]. Nat Genet, 1995,11 (4) : 415 - 421.
  • 7Proetzel G, Pawlowski SA, Wiles MV, et al. Transforming growth factor-beta 3 is required for secondary palate fusion [ J ]. Nat Genet, 1995,11 (4) : 409 -414.
  • 8Dudas M, Kim J, Li WY, et al. Epithelial and ectomesenchymal role of the type Ⅰ TGF-beta receptor ALK5 during facial morphogenesis and palatal fusion[J]. Dev Biol, 2006,296(2) : 298 -314.
  • 9Ding Hao, Wu Xiaoli, Bostrom H, et al. A specific requirement for PDGF-C in palate formation and PDGFR-alpha signaling [ J ]. Nat Genet, 2004,36(10) : 1111 -1116.
  • 10Xu Xun, Han Jun, Ito Y, et al. Cell autonomous requirement for Tgfbr2 in the disappearance of medial edge epithelium during palatal fusion [ J ]. Dev Biol, 2006,297( 1 ) : 238 - 248.

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