Genome‐wide association study of stage III/IV grade C periodontitis (former aggressive periodontitis) in a Spanish population. (19th April 2021)

• Record Type: Journal Article
• Authors: de Coo, Alicia; Cruz, Raquel; Quintela, Inés; Herrera, David; Sanz, Mariano; Diz, Pedro; Rodríguez Grandío, Segundo; Vallcorba, Nuria; Ramos, Isabel; Oteo, Alfonso; Serrano, Cristina; Esmatges, Alejandro; Enrile, Francisco; Mateos, Leopoldo; García, Roberto; Álvarez‐Novoa, Pablo; Noguerol, Blas; Zabalegui, Ion; Blanco‐Moreno, José; Alonso, Ángel; Lorenzo, Ramón; Carracedo, Angel; Blanco, Juan
• Is Part Of: Journal of clinical periodontology. Volume 48:Number 7(2021)
• Page Start: 896
• Page End: 906
• Publication Date: 2021-04-19
• Subjects: epidemiology -- genome‐wide association study -- periodontitis -- rare variation -- single‐nucleotide polymorphisms; Periodontics -- Periodicals; 617.6
• DOI: 10.1111/jcpe.13460
• Languages: English
• ISSNs: 0303-6979

Abstract

Abstract: Aim: To identify loci associated with stages III/IV, grade C periodontitis (PIII/IV‐C) through a genome‐wide association study (GWAS). Materials and Methods: 441 Caucasian Spanish PIII/IV‐C cases from the SEPA Network of Research Clinics and 1141 controls from the Banco Nacional de ADN were genotyped with "Axiom Spain Biobank Array, " which contains 757836 markers, including rare and low‐frequency Spanish variants. The analysis of the individual association and subsequently the gene‐level analysis with Sequence Kernel Association Test (SKAT) were carried out adjusting for age, sex and PC1 covariates. Pathway Analysis was additionally performed with Ingenuity Pathway Analysis (IPA) software on the top associated genes. Results: In the individual analyses, no genome‐wide significant signals were detected. However, 8 SNPs of 8 loci reached suggestive evidence of association with PIII/IV‐C, including FAT3 rs35709256, CSNK1G2 rs4807188, MYH13 rs2074872, CNTN2 rs116611488, ANTXR1 rs4854545, 8p23.2 rs78672540, ANGPT1 rs13439823 and PLEC rs11993287 ( p < 5 × 10 −6 ). SKAT analysis identified other interesting signals at CNTN2, FBXO44, AP1 M2, RSPO4, KRI1, BPIFB1 and INMT, although their probability does not exceed the multiple‐test correction. IPA indicated significant enrichment of pathways related to cAMP, IL‐2, CD28, VDR/RXR and PI3K/Akt. Conclusions: GWAS found no SNPs significantly associated with PIII/IV‐C.