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http://purl.uniprot.org/citations/37011183http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
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Context

Challenges exist in the management of Glucokinase-maturity-onset diabetes of the young (GCK-MODY), especially during pregnancy.

Objective

This work aimed to evaluate the prevalence of congenital anomaly in newborns from GCK-MODY mothers, and the relationship between fetus genotype and the risk of congenital malformation as well as other adverse pregnancy outcomes.

Methods

Electronic databases including PubMed, EMBASE, and Cochrane database last updated July 16, 2022, were searched. We included observational studies conducted in GCK-MODY complicated by pregnancy, and reporting at least one pregnancy outcome. We extracted data in duplicate, and the risk of bias was evaluated by the Newcastle-Ottawa Quality Assessment Scale (NOS). All statistical analysis was performed by Cochrane Review Manager.

Results

Eight studies were selected in the meta-analysis. Five were of high quality and 3 were of medium quality evaluated by NOS. A total of 257 GCK-MODY mothers and 499 offspring were enrolled. Among them, 370 offspring were divided into 2 groups: GCK-affected offspring (GCK+, n = 238) and GCK-unaffected offspring (GCK-, n = 132). The percentage of congenital malformations in GCK pregnant women's offspring was 2.4%. The risk of congenital malformations was similar between the GCK+ and GCK-group (odds ratio = 0.56; 95% CI, 0.07-4.51; I2 = 0%; P = .59). The risk of macrosomia/large for gestational age, neonatal hypoglycemia, and combined adverse neonatal outcome was significantly lower in offspring with the GCK mutation compared with non-GCK mutation carriers.

Conclusion

The percentage of congenital malformations was 2.4% in GCK-MODY pregnant women's offspring, and newborns with the GCK mutation have lower birth complication than non-GCK mutation carriers."xsd:string
http://purl.uniprot.org/citations/37011183http://purl.org/dc/terms/identifier"doi:10.1210/clinem/dgad188"xsd:string
http://purl.uniprot.org/citations/37011183http://purl.uniprot.org/core/author"Han X."xsd:string
http://purl.uniprot.org/citations/37011183http://purl.uniprot.org/core/author"Ren Q."xsd:string
http://purl.uniprot.org/citations/37011183http://purl.uniprot.org/core/author"Wang Z."xsd:string
http://purl.uniprot.org/citations/37011183http://purl.uniprot.org/core/author"Yang W."xsd:string
http://purl.uniprot.org/citations/37011183http://purl.uniprot.org/core/author"Ji L."xsd:string
http://purl.uniprot.org/citations/37011183http://purl.uniprot.org/core/date"2023"xsd:gYear
http://purl.uniprot.org/citations/37011183http://purl.uniprot.org/core/name"J Clin Endocrinol Metab"xsd:string
http://purl.uniprot.org/citations/37011183http://purl.uniprot.org/core/pages"2739-2746"xsd:string
http://purl.uniprot.org/citations/37011183http://purl.uniprot.org/core/title"Maternal and Infant Outcomes in GCK-MODY Complicated by Pregnancy."xsd:string
http://purl.uniprot.org/citations/37011183http://purl.uniprot.org/core/volume"108"xsd:string
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