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rs2476601 in PTPN22 gene in rheumatoid arthritis and periodontitis—a possible interface?

BACKGROUND: Rheumatoid arthritis (RA) and periodontitis (PD) are proven to share common risk markers, including genetic factors. In the present study we focused on genetic variants in PTPN22 (rs2476601), PADI4 (rs2240340), CTLA4 genes (rs3087243) and its impact on RA and PD. MATERIALS AND METHODS: I...

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Autores principales: Schulz, Susanne, Zimmer, Pauline, Pütz, Natalie, Jurianz, Elisa, Schaller, Hans-Günter, Reichert, Stefan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7559817/
https://www.ncbi.nlm.nih.gov/pubmed/33059697
http://dx.doi.org/10.1186/s12967-020-02548-w
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author Schulz, Susanne
Zimmer, Pauline
Pütz, Natalie
Jurianz, Elisa
Schaller, Hans-Günter
Reichert, Stefan
author_facet Schulz, Susanne
Zimmer, Pauline
Pütz, Natalie
Jurianz, Elisa
Schaller, Hans-Günter
Reichert, Stefan
author_sort Schulz, Susanne
collection PubMed
description BACKGROUND: Rheumatoid arthritis (RA) and periodontitis (PD) are proven to share common risk markers, including genetic factors. In the present study we focused on genetic variants in PTPN22 (rs2476601), PADI4 (rs2240340), CTLA4 genes (rs3087243) and its impact on RA and PD. MATERIALS AND METHODS: In the study 111 RA patients and 256 systemically healthy controls were involved. A subdivision of patients and controls was carried out according the severity of periodontitis (no/level 1 PD vs. level 2 PD). RESULTS: I. Evaluating the genetic impact on the occurrence of RA the T allele of rs2476601 (PTPN22) (bivariate: p < 0.001; multivariate: p = 0.018) and T allele of rs2240340 (PADI4) (bivariate: p = 0.006; multivariate: p = 0.070) were associated with an increased vulnerability to RA. II. Investigating the genetic influence on level 2 PD the T allele of rs2476601 (PTPN22) was shown to be associated with a higher susceptibility to PD within the RA group (bivariate: p = 0.043; multivariate: p = 0.024). III. The T allele of rs2476601 (PTPN22) was proven to be a significant marker of RA and level 2 PD comorbidity (bivariate: p < 0.001; multivariate: p = 0.028). CONCLUSIONS: These results support the thesis that genetic variations may represent a possible link between PD and RA. The study increases knowledge about disease-specific and cross-disease genetic pattern.
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spelling pubmed-75598172020-10-16 rs2476601 in PTPN22 gene in rheumatoid arthritis and periodontitis—a possible interface? Schulz, Susanne Zimmer, Pauline Pütz, Natalie Jurianz, Elisa Schaller, Hans-Günter Reichert, Stefan J Transl Med Research BACKGROUND: Rheumatoid arthritis (RA) and periodontitis (PD) are proven to share common risk markers, including genetic factors. In the present study we focused on genetic variants in PTPN22 (rs2476601), PADI4 (rs2240340), CTLA4 genes (rs3087243) and its impact on RA and PD. MATERIALS AND METHODS: In the study 111 RA patients and 256 systemically healthy controls were involved. A subdivision of patients and controls was carried out according the severity of periodontitis (no/level 1 PD vs. level 2 PD). RESULTS: I. Evaluating the genetic impact on the occurrence of RA the T allele of rs2476601 (PTPN22) (bivariate: p < 0.001; multivariate: p = 0.018) and T allele of rs2240340 (PADI4) (bivariate: p = 0.006; multivariate: p = 0.070) were associated with an increased vulnerability to RA. II. Investigating the genetic influence on level 2 PD the T allele of rs2476601 (PTPN22) was shown to be associated with a higher susceptibility to PD within the RA group (bivariate: p = 0.043; multivariate: p = 0.024). III. The T allele of rs2476601 (PTPN22) was proven to be a significant marker of RA and level 2 PD comorbidity (bivariate: p < 0.001; multivariate: p = 0.028). CONCLUSIONS: These results support the thesis that genetic variations may represent a possible link between PD and RA. The study increases knowledge about disease-specific and cross-disease genetic pattern. BioMed Central 2020-10-15 /pmc/articles/PMC7559817/ /pubmed/33059697 http://dx.doi.org/10.1186/s12967-020-02548-w Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Schulz, Susanne
Zimmer, Pauline
Pütz, Natalie
Jurianz, Elisa
Schaller, Hans-Günter
Reichert, Stefan
rs2476601 in PTPN22 gene in rheumatoid arthritis and periodontitis—a possible interface?
title rs2476601 in PTPN22 gene in rheumatoid arthritis and periodontitis—a possible interface?
title_full rs2476601 in PTPN22 gene in rheumatoid arthritis and periodontitis—a possible interface?
title_fullStr rs2476601 in PTPN22 gene in rheumatoid arthritis and periodontitis—a possible interface?
title_full_unstemmed rs2476601 in PTPN22 gene in rheumatoid arthritis and periodontitis—a possible interface?
title_short rs2476601 in PTPN22 gene in rheumatoid arthritis and periodontitis—a possible interface?
title_sort rs2476601 in ptpn22 gene in rheumatoid arthritis and periodontitis—a possible interface?
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7559817/
https://www.ncbi.nlm.nih.gov/pubmed/33059697
http://dx.doi.org/10.1186/s12967-020-02548-w
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