Replication analysis of 15 susceptibility loci for nonsyndromic cleft lip with or without cleft palate in an italian population. Issue Volume 106:Issue2(2015) (9th December 2015)

• Record Type: Journal Article
• Authors: Cura, Francesca; Böhmer, Anne C.; Klamt, Johanna; Schünke, Hannah; Scapoli, Luca; Martinelli, Marcella; Carinci, Francesco; Nöthen, Markus M.; Knapp, Michael; Ludwig, Kerstin U.; Mangold, Elisabeth
• Is Part Of: Birth defects research. Volume 106:Issue2(2015)
• Page Start: 81
• Page End: 87
• Publication Date: 2015-12-09
• Subjects: nonsyndromic cleft lip with or without cleft palate -- polymorphism -- genetic loci -- replication study -- association study; Teratology -- Periodicals; Abnormalities, Human -- Research -- Periodicals; Abnormalities, Human -- Periodicals; 616.043
• DOI: 10.1002/bdra.23454
• Languages: English
• ISSNs: 1542-0752

Abstract

Abstract : BACKGROUND: Nonsyndromic cleft lip with or without cleft palate (nsCL/P) is one of the most common congenital malformations in humans. Its average global incidence is 1.7 per 1000 live births, with wide variation according to geographical location and ethnicity. Its etiology involves both genetic and environmental factors. The aim of the present study was to confirm genetic association of a selection of 15 candidate nsCL/P loci using an independent sample of the Italian population. METHODS: At least one single‐nucleotide polymorphism (SNP) for each locus was genotyped in 380 nuclear trios. RESULTS: Transmission disequilibrium analysis revealed significant associations for three variants at two loci (8q24 and 1p22). Two SNPs at 8q24 showed the strongest level of association, the rs987525 ( P TDT = 6.81 × 10 −6 ; homozygous relative risk = 3.60 [95% confidence interval, 2.12–6.13]), and the rs17241253 ( P TDT = 1.03 × 10 −5 ; homozygous relative risk = 3.75 [95% confidence interval, 2.10–6.67]). Four additional loci (at 1q32, 3q12, 8q21, and 10q25) achieved nominally significant p ‐values. Two SNPs at 1p36 achieved p ‐values of < 0.1. The present data suggest that 6 of the 15 analyzed nsCL/P risk loci contribute significantly to nsCL/P risk in the Italian population. These include the 1p22 locus, which previous research has implicated predominantly in Asian populations. CONCLUSION: Different loci, including 8q24 and 1p22 have been found associated with nsCL/P in multiple populations. Further efforts are needed to identify causative variants and transfer knowledge to clinical application, such as personal genetic risk assessment. Birth Defects Research (Part A) 106:81–87, 2016. © 2015 Wiley Periodicals, Inc.