Literature DB >> 20104597

Risk factors for non-syndromic holoprosencephaly in the National Birth Defects Prevention Study.

Eric A Miller1, Sonja A Rasmussen, Anna Maria Siega-Riz, Jaime L Frías, Margaret A Honein.   

Abstract

Holoprosencephaly (HPE) is a complex structural brain anomaly that results from incomplete cleavage of the forebrain. The prevalence of HPE at birth is low, and risk factors have been difficult to identify. Using data from a large multi-state population-based case-control study, we examined risk factors for non-syndromic HPE. Data from maternal telephone interviews were available for 74 infants with HPE and 5871 controls born between 1997 and 2004. Several characteristics and exposures were examined, including pregnancy history, medical history, maternal diet and use of nutritional supplements, medications, tobacco, alcohol, and illegal substances. We used chi(2)-tests and logistic regression (excluding women with pre-existing diabetes) to examine associations with HPE. Except for diet (year before pregnancy) and sexually transmitted infections (STIs) (throughout pregnancy), most exposures were examined for the time period from the month before to the third month of pregnancy. HPE was found to be associated with pre-existing diabetes (chi(2) = 6.0; P = 0.01), aspirin use [adjusted odds ratio (aOR) = 3.4; 95% confidence interval (CI) 1.6-6.9], lower education level (aOR = 2.5; 95%CI 1.1-5.6), and use of assisted reproductive technologies (ART) (crude OR = 4.2; 95%CI 1.3-13.7). Consistent maternal folic acid use appeared to be protective (aOR = 0.4; 95%CI 0.2-1.0), but the association was of borderline statistical significance. While some of these findings support previous observations, other potential risk factors identified warrant further study. 2010 Wiley-Liss, Inc.

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Year:  2010        PMID: 20104597     DOI: 10.1002/ajmg.c.30244

Source DB:  PubMed          Journal:  Am J Med Genet C Semin Med Genet        ISSN: 1552-4868            Impact factor:   3.908


  25 in total

Review 1.  Cyclopia: an epidemiologic study in a large dataset from the International Clearinghouse of Birth Defects Surveillance and Research.

Authors:  Iêda M Orioli; Emmanuelle Amar; Marian K Bakker; Eva Bermejo-Sánchez; Fabrizio Bianchi; Mark A Canfield; Maurizio Clementi; Adolfo Correa; Melinda Csáky-Szunyogh; Marcia L Feldkamp; Danielle Landau; Emanuele Leoncini; Zhu Li; R Brian Lowry; Pierpaolo Mastroiacovo; Margery Morgan; Osvaldo M Mutchinick; Anke Rissmann; Annukka Ritvanen; Gioacchino Scarano; Elena Szabova; Eduardo E Castilla
Journal:  Am J Med Genet C Semin Med Genet       Date:  2011-10-17       Impact factor: 3.908

2.  Diabetic embryopathy: a developmental perspective from fertilization to adulthood.

Authors:  M Castori
Journal:  Mol Syndromol       Date:  2013-02

Review 3.  Modeling anterior development in mice: diet as modulator of risk for neural tube defects.

Authors:  Claudia Kappen
Journal:  Am J Med Genet C Semin Med Genet       Date:  2013-10-04       Impact factor: 3.908

4.  Minimal evidence for a direct involvement of twisted gastrulation homolog 1 (TWSG1) gene in human holoprosencephaly.

Authors:  Emily F Kauvar; Ping Hu; Daniel E Pineda-Alvarez; Benjamin D Solomon; Amalia Dutra; Evgenia Pak; Brooke Blessing; Virginia Proud; Alan L Shanske; Cathy A Stevens; Jill A Rosenfeld; Lisa G Shaffer; Erich Roessler; Maximilian Muenke
Journal:  Mol Genet Metab       Date:  2010-12-21       Impact factor: 4.797

5.  New findings for phenotype-genotype correlations in a large European series of holoprosencephaly cases.

Authors:  Sandra Mercier; Christèle Dubourg; Nicolas Garcelon; Boris Campillo-Gimenez; Isabelle Gicquel; Marion Belleguic; Leslie Ratié; Laurent Pasquier; Philippe Loget; Claude Bendavid; Sylvie Jaillard; Lucie Rochard; Chloé Quélin; Valérie Dupé; Véronique David; Sylvie Odent
Journal:  J Med Genet       Date:  2011-09-22       Impact factor: 6.318

Review 6.  Holoprosencephaly: signaling interactions between the brain and the face, the environment and the genes, and the phenotypic variability in animal models and humans.

Authors:  Anna Petryk; Daniel Graf; Ralph Marcucio
Journal:  Wiley Interdiscip Rev Dev Biol       Date:  2014-10-22       Impact factor: 5.814

Review 7.  Holoprosencephaly: recommendations for diagnosis and management.

Authors:  Emily F Kauvar; Maximilian Muenke
Journal:  Curr Opin Pediatr       Date:  2010-12       Impact factor: 2.856

8.  Maternal exposures in the National Birth Defects Prevention Study: Time trends of selected exposures.

Authors:  April L Dawson; Hilda Razzaghi; Annelise Arth; Mark A Canfield; Samantha E Parker; Jennita Reefhuis
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2015-04-17

9.  Cyclopia: isolated and with agnathia-otocephaly complex.

Authors:  Lin Tun Wai; Suresh Chandran
Journal:  BMJ Case Rep       Date:  2017-08-30

10.  Holoprosencephaly: antenatal and postnatal diagnosis and outcome.

Authors:  Chandrasekaran Kaliaperumal; Sam Ndoro; Tafadzwa Mandiwanza; F Reidy; F McAuliffe; John Caird; Darach Crimmins
Journal:  Childs Nerv Syst       Date:  2016-01-15       Impact factor: 1.475

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