Are encephaloceles neural tube defects?

被引:55
作者
Rowland, Courtney A. [1 ]
Correa, Adolfo [1 ]
Cragan, Janet D. [1 ]
Alverson, Clinton J. [1 ]
机构
[1] Ctr Dis Control & Prevent, Natl Ctr Birth Defects & Dev Disabil, Atlanta, GA 30333 USA
关键词
encephalocele; neural tube defects; spina; bifida; anencephaly; folic acid;
D O I
10.1542/peds.2005-1739
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
OBJECTIVE. Encephalocele is classified as a neural tube defect, but questions have been raised regarding whether its epidemiological characteristics are similar to those of other neural tube defects. DESIGN. We compared characteristics of temporal trends in, and the impact of folic acid grain fortification on, the prevalence of encephalocele, spina bifida, and anencephaly using data from the Metropolitan Atlanta Congenital Defects Program, a population-based birth defects surveillance system. Prevalences of encephalocele, spina bifida, and anencephaly were compared by maternal age, gender, race, birth weight, ascertainment period (1968-1981, 1982-1993, or 1994-2002), and fortification period (1994-1996 [prefortification] and 1998-2002 [postfortification]) using prevalence ratios with 95% confidence intervals. Temporal trends were assessed using Poisson and negative binomial regression models. RESULTS. Prevalence rates of encephalocele (n = 167), spina bifida (n = 650), and anencephaly (n = 431) were 1.4, 5.5, and 3.7 per 10 000 live births, respectively. Encephalocele was similar to anencephaly in showing an increased prevalence among girls and multiple gestation pregnancies and to spina bifida and anencephaly in an annual prevalence decrease between 1968 and 2002 (-1.2% for encephalocele, -4.2% for spina bifida, and -3.6% for anencephaly). With fortification, prevalence decreased for spina bifida but not significantly for encephalocele or anencephaly. CONCLUSIONS. Encephalocele shows more similarities to spina bifida or anencephaly than it shows differences with respect to characteristics, temporal trend, and impact of fortification. Additional studies should be done to explore the etiologic heterogeneity of encephalocele using better markers of folate status and a wider range of risk factors.
引用
收藏
页码:916 / 923
页数:8
相关论文
共 37 条
[21]   East Ireland 1980-1994: epidemiology of neural tube defects [J].
McDonnell, RJ ;
Johnson, Z ;
Delaney, V ;
Dack, P .
JOURNAL OF EPIDEMIOLOGY AND COMMUNITY HEALTH, 1999, 53 (12) :782-788
[22]   Knobloch syndrome:: Novel mutations in COL18A1, evidence for genetic heterogeneity, and a functionally impaired polymorphism in endostatin [J].
Menzel, O ;
Bekkeheien, RCJ ;
Reymond, A ;
Fukai, N ;
Boye, E ;
Kosztolanyi, G ;
Aftimos, S ;
Deutsch, S ;
Scott, HS ;
Olsen, BR ;
Antonarakis, SE ;
Guipponi, M .
HUMAN MUTATION, 2004, 23 (01) :77-84
[23]   CONSTRICTIVE AMNIOTIC BANDS, AMNIOTIC ADHESIONS, AND LIMB-BODY WALL COMPLEX - DISCRETE DISRUPTION SEQUENCES WITH PATHOGENETIC OVERLAP [J].
MOERMAN, P ;
FRYNS, JP ;
VANDENBERGHE, K ;
LAUWERYNS, JM .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1992, 42 (04) :470-479
[24]  
Norman M. G., 1995, CONGENITAL MALFORMAT
[25]  
Ogata A J, 1992, Rev Paul Med, V110, P147
[26]  
Oostra RJ, 1998, AM J MED GENET, V80, P74, DOI 10.1002/(SICI)1096-8628(19981102)80:1<74::AID-AJMG10>3.3.CO
[27]  
2-Q
[28]   Guidelines for case classification for the national birth defects prevention study [J].
Rasmussen, SA ;
Olney, RS ;
Holmes, LB ;
Lin, AE ;
Keppler-Noreuil, KM ;
Moore, CA .
BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY, 2003, 67 (03) :193-201
[29]   FRONTOETHMOIDAL MENINGOENCEPHALOCELE - A COMMON AND SEVERE CONGENITAL ABNORMALITY IN SOUTHEAST-ASIA [J].
RICHARDS, CGM .
ARCHIVES OF DISEASE IN CHILDHOOD, 1992, 67 (06) :717-719
[30]   Survival of infants diagnosed with encephalocele in Atlanta, 1979-98 [J].
Siffel, C ;
Wong, LYC ;
Olney, RS ;
Correa, A .
PAEDIATRIC AND PERINATAL EPIDEMIOLOGY, 2003, 17 (01) :40-48