No association between polymorphisms in cubilin, a gene of the homocysteine metabolism and the risk of non-syndromic cleft lip with or without cleft palate

• Published in: International journal of immunopathology and pharmacology Vol. 24; no. 2 Suppl; p. 11
• Main Authors: Martinelli, M, Carinci, F, Morselli, P G, Palmieri, A, Girardi, A, Riberti, C, Scapoli, L
• Format: Journal Article
• Language: English
• Published: England 01-04-2011
• Subjects: Cleft Lip - genetics; Cleft Palate - genetics; European Continental Ancestry Group - genetics; Female; Haplotypes; Humans; Italy; Male; Polymorphism, Single Nucleotide; Receptors, Cell Surface - genetics; Italy
• ISSN: 0394-6320
• DOI: 10.1177/03946320110240S203

Epidemiological studies have correlated lower maternal periconceptional levels of plasma folate and cobalamin with increased risk of delivering offspring presenting congenital malformations such as cleft lip with or without cleft palate (CL/P) or neural tube defects. A number of genetic studies aimed at correlating these biochemical levels or the occurrence of malformations with specific genetic defects or polymorphisms have been successfully performed. The cubilin gene (CUBN) codes for a carrier that plays a crucial role in cobalamin cell internalization. CUBN polymorphisms were previously found to be associated with spina bifida occurrence. In this work, a family-based association study was performed to test CUBN involvement in CL/P. A sample of 391 CL/P triads was investigated with three single nucleotide polymorphisms mapping on the cubilin gene. Association tests indicated no significant association between CL/P and marker alleles or marker haplotypes. No evidence of maternal effect and imprinting were obtained. These data suggest that CUBN is not involved in CL/P onset in the investigated Italian population.