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Polymorphic Variants of V-Maf Musculoaponeurotic Fibrosarcoma Oncogene Homolog B (rs13041247 and rs11696257) and Risk of Non-Syndromic Cleft Lip/Palate: Systematic Review and Meta-Analysis

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dc.contributor.author Imani, Mohammad-Moslem
dc.contributor.author López-Jornet, Pía
dc.contributor.author Pons-Fuster-López, Eduardo
dc.contributor.author Sadeghi, Masoud
dc.date.accessioned 2026-01-19T16:08:22Z
dc.date.available 2026-01-19T16:08:22Z
dc.date.issued 2019-08-01
dc.identifier.citation Imani MM, Lopez-Jornet P, Pons-Fuster López E, Sadeghi M. Polymorphic Variants of V-Maf Musculoaponeurotic Fibrosarcoma Oncogene Homolog B (rs13041247 and rs11696257) and Risk of Non-Syndromic Cleft Lip/Palate: Systematic Review and Meta-Analysis. IJERPH. 5 de agosto de 2019;16(15):2792.
dc.identifier.uri https://sms.carm.es/ricsmur/handle/123456789/23768
dc.description.abstract Background: Non-syndromic cleft lip/palate (NSCL/P) has an etiology, including both genetic and environmental factors. Herein, we evaluated the association of rs13041247 and rs11696257 v-maf musculoaponeurotic fibrosarcoma oncogene homolog B (MAFB) polymorphisms with the risk of NSCL/P in a meta-analysis. Methods: The PubMed/Medline, Scopus, Cochrane Library, Web of Science, and HuGE Navigator databases were systematically searched to retrieve relevant articles published up to January 2019. The Newcastle-Ottawa scale was applied for quality evaluation of retrieved articles. The 95% confidence interval (CI) and crude odds ratio (OR) were calculated for each study using the Review Manager 5.3 software to show the association between MAFB polymorphisms and risk of NSCL/P. The comprehensive meta-analysis 2.0 software was used to calculate the publication bias. In addition, sensitivity analysis was carried out to show the stability of results. Results: Of 102 articles retrieved from the databases, 10 articles were analyzed in this meta-analysis. Ten articles, including eleven studies reporting rs13041247 MAFB polymorphism, included 3082 NSCL/P patients and 4104 controls. Three studies that reported rs11696257 MAFB polymorphism involved 845 NSCL/P patients and 927 controls. The rs11696257 MAFB polymorphism was not associated with the risk of NSCL/P, but the CC and TC genotypes of rs13041247 polymorphism were associated with the risk of NSCL/P. Nevertheless, the C allele and CC and TC genotypes were associated with a significant decline in the risk of NSCL/P in population-based studies. Conclusions: The results of this meta-analysis demonstrated that the risk of NSCL/P was related to rs13041247 polymorphism, not rs11696257 MAFB polymorphism. Well-designed studies are required to assess the interaction of MAFB and other genes with environmental factors in different ethnic groups.
dc.language.iso eng
dc.publisher MDPI
dc.rights Atribución/Reconocimiento 4.0 Internacional
dc.rights.uri https://creativecommons.org/licenses/by/4.0/deed.es *
dc.subject.mesh Cleft Lip/genetics
dc.subject.mesh Cleft Palate/genetics
dc.subject.mesh Genetic Predisposition to Disease
dc.subject.mesh Genetic Variation
dc.subject.mesh Genotype
dc.subject.mesh Humans
dc.subject.mesh MafB Transcription Factor/genetics/metabolism
dc.title Polymorphic Variants of V-Maf Musculoaponeurotic Fibrosarcoma Oncogene Homolog B (rs13041247 and rs11696257) and Risk of Non-Syndromic Cleft Lip/Palate: Systematic Review and Meta-Analysis
dc.type info:eu-repo/semantics/article
dc.identifier.pmid 31387249
dc.relation.publisherversion https://www.mdpi.com/1660-4601/16/15/2792
dc.type.version info:eu-repo/semantics/publishedVersion
dc.identifier.doi 10.3390/ijerph16152792
dc.journal.title International Journal of Environmental Research and Public Health
dc.identifier.essn 1660-4601


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