Literature DB >> 12728131

Fertility treatments and craniosynostosis: California, Georgia, and Iowa, 1993-1997.

Jennita Reefhuis1, Margaret A Honein, Gary M Shaw, Paul A Romitti.   

Abstract

OBJECTIVE: Craniosynostosis, a malformation caused by premature closure of 1 or more cranial sutures, is a rare birth defect usually of unknown cause; however, it is often associated with advanced maternal age. Because fertility treatments are also associated with increased maternal age, this study investigated the possible association between fertility treatments and craniosynostosis.
METHODS: Data from the Birth Defect Risk Factor Surveillance study were used, which included infants who were delivered from 1993 through 1997 in California, Georgia, and Iowa. Cases were defined as infants who had nonfamilial, nonsyndromic craniosynostosis and were ascertained through existing birth defect surveillance systems. Controls, infants without birth defects, were selected from the same regions and time period.
RESULTS: Mothers of 99 case infants and 777 control infants from the 3 study locations participated in this study by completing a telephone interview. Unadjusted analyses showed associations with craniosynostosis for mothers who had used clomiphene citrate (odds ratio[OR]: 3.8; 95% confidence interval [CI]: 1.1-12.3), artificial insemination (OR: 4.2; 95% CI: 0.8-9.4), or assisted reproductive techniques (OR: 4.2; 95% CI: 0.5-27.3).
CONCLUSIONS: This is the first study that has found associations between fertility treatments and craniosynostosis. However, the numbers are small; therefore, the results should be viewed with caution.

Entities:  

Mesh:

Year:  2003        PMID: 12728131

Source DB:  PubMed          Journal:  Pediatrics        ISSN: 0031-4005            Impact factor:   7.124


  10 in total

Review 1.  Isolated sagittal craniosynostosis: definition, classification, and surgical indications.

Authors:  Luca Massimi; Massimo Caldarelli; Gianpiero Tamburrini; Giovanna Paternoster; Concezio Di Rocco
Journal:  Childs Nerv Syst       Date:  2012-08-08       Impact factor: 1.475

Review 2.  Genetic advances in craniosynostosis.

Authors:  Wanda Lattanzi; Marta Barba; Lorena Di Pietro; Simeon A Boyadjiev
Journal:  Am J Med Genet A       Date:  2017-02-04       Impact factor: 2.802

3.  Craniosynostosis and risk factors related to thyroid dysfunction.

Authors:  S L Carmichael; C Ma; S A Rasmussen; M L Cunningham; M L Browne; C Dosiou; E J Lammer; G M Shaw
Journal:  Am J Med Genet A       Date:  2015-02-05       Impact factor: 2.802

4.  Activation of the IGF1 pathway mediates changes in cellular contractility and motility in single-suture craniosynostosis.

Authors:  Zeinab Al-Rekabi; Marsha M Wheeler; Andrea Leonard; Adriane M Fura; Ilsa Juhlin; Christopher Frazar; Joshua D Smith; Sarah S Park; Jennifer A Gustafson; Christine M Clarke; Michael L Cunningham; Nathan J Sniadecki
Journal:  J Cell Sci       Date:  2015-12-11       Impact factor: 5.285

5.  Fetal constraint as a potential risk factor for craniosynostosis.

Authors:  Pedro A Sanchez-Lara; Suzan L Carmichael; John M Graham; Edward J Lammer; Gary M Shaw; Chen Ma; Sonja A Rasmussen
Journal:  Am J Med Genet A       Date:  2010-02       Impact factor: 2.802

6.  Differential expression of extracellular matrix-mediated pathways in single-suture craniosynostosis.

Authors:  Brendan D Stamper; Sarah S Park; Richard P Beyer; Theo K Bammler; Frederico M Farin; Brig Mecham; Michael L Cunningham
Journal:  PLoS One       Date:  2011-10-19       Impact factor: 3.240

7.  Secondary bicoronal synostosis after metopic craniosynostosis surgical reconstruction.

Authors:  Arash Esmaeli; Farideh Nejat; Zohreh Habibi; Mostafa El Khashab
Journal:  J Pediatr Neurosci       Date:  2014 Sep-Dec

Review 8.  The clinical manifestations, molecular mechanisms and treatment of craniosynostosis.

Authors:  Eloise Stanton; Mark Urata; Jian-Fu Chen; Yang Chai
Journal:  Dis Model Mech       Date:  2022-04-22       Impact factor: 5.732

9.  Study of environmental and genetic factors in children with craniosynostosis: A case-control study.

Authors:  Mayadhar Barik; Minu Bajpai; Rashmi Ranjan Das; Shasanka Shekhar Panda
Journal:  J Pediatr Neurosci       Date:  2013-05

10.  Mutational identification of fibroblast growth factor receptor 1 and fibroblast growth factor receptor 2 genes in craniosynostosis in Indian population.

Authors:  Rajeev Kumar Pandey; Minu Bajpai; Abid Ali; Sukanya Gayan; Amit Singh
Journal:  Indian J Hum Genet       Date:  2013-10
  10 in total

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