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Complex genetic predisposition in adult and juvenile rheumatoid arthritis
BACKGROUND: Rheumatoid arthritis (RA) and juvenile rheumatoid arthritis (JRA) are complex multifactorial diseases caused by environmental influences and an unknown number of predisposing genes. The present study was undertaken in order to investigate association of polymorphisms in candidate genes w...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2004
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC356909/ https://www.ncbi.nlm.nih.gov/pubmed/15018649 http://dx.doi.org/10.1186/1471-2156-5-2 |
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author | Miterski, Bianca Drynda, Susanne Böschow, Gundula Klein, Wolfram Oppermann, Joachim Kekow, Jörn Epplen, Jörg Thomas |
author_facet | Miterski, Bianca Drynda, Susanne Böschow, Gundula Klein, Wolfram Oppermann, Joachim Kekow, Jörn Epplen, Jörg Thomas |
author_sort | Miterski, Bianca |
collection | PubMed |
description | BACKGROUND: Rheumatoid arthritis (RA) and juvenile rheumatoid arthritis (JRA) are complex multifactorial diseases caused by environmental influences and an unknown number of predisposing genes. The present study was undertaken in order to investigate association of polymorphisms in candidate genes with RA and JRA in German subjects. RESULTS: Up to 200 unrelated German RA and JRA patients each and 300–400 healthy controls have been genotyped for HLA-DRB1, TNFa, TNFA -238a/g, TNFA -308a/g, TNFA -857c/t, TNFR1 -609g/t, TNFR1 P12P, TNFR2 del 15bp, IKBL -332a/g, IKBL -132t/a, IKBL C224R, CTLA4 -318c/t, CTLA4 T17A, PTPRC P57P, MIF -173g/c, the MIF and IFNG microsatellites as well as for D17S795, D17S807, D17S1821 by polyacrylamide gel electrophoresis, single-strand conformation polymorphism analysis, restriction fragment length polymorphism analysis or allele specific hybridization. None of the investigated genetic markers is associated with both, RA and JRA, but there are some statistically significant differences between patients and controls that have to be discussed sensibly. CONCLUSIONS: The difficulty in investigating the genetics of complex disorders like RA and JRA may arise from genetic heterogeneity in the clinically defined disease cohorts (and generally limited power of such studies). In addition, several to many genes appear to be involved in the genetic predisposition, each of which exerting only small effects. The number of investigated patients has to be increased to establish the possibility of subdivison of the patients according their clinical symptoms, severity of disease, HLA status and other genetic characteristics. |
format | Text |
id | pubmed-356909 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2004 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-3569092004-03-05 Complex genetic predisposition in adult and juvenile rheumatoid arthritis Miterski, Bianca Drynda, Susanne Böschow, Gundula Klein, Wolfram Oppermann, Joachim Kekow, Jörn Epplen, Jörg Thomas BMC Genet Research Article BACKGROUND: Rheumatoid arthritis (RA) and juvenile rheumatoid arthritis (JRA) are complex multifactorial diseases caused by environmental influences and an unknown number of predisposing genes. The present study was undertaken in order to investigate association of polymorphisms in candidate genes with RA and JRA in German subjects. RESULTS: Up to 200 unrelated German RA and JRA patients each and 300–400 healthy controls have been genotyped for HLA-DRB1, TNFa, TNFA -238a/g, TNFA -308a/g, TNFA -857c/t, TNFR1 -609g/t, TNFR1 P12P, TNFR2 del 15bp, IKBL -332a/g, IKBL -132t/a, IKBL C224R, CTLA4 -318c/t, CTLA4 T17A, PTPRC P57P, MIF -173g/c, the MIF and IFNG microsatellites as well as for D17S795, D17S807, D17S1821 by polyacrylamide gel electrophoresis, single-strand conformation polymorphism analysis, restriction fragment length polymorphism analysis or allele specific hybridization. None of the investigated genetic markers is associated with both, RA and JRA, but there are some statistically significant differences between patients and controls that have to be discussed sensibly. CONCLUSIONS: The difficulty in investigating the genetics of complex disorders like RA and JRA may arise from genetic heterogeneity in the clinically defined disease cohorts (and generally limited power of such studies). In addition, several to many genes appear to be involved in the genetic predisposition, each of which exerting only small effects. The number of investigated patients has to be increased to establish the possibility of subdivison of the patients according their clinical symptoms, severity of disease, HLA status and other genetic characteristics. BioMed Central 2004-02-04 /pmc/articles/PMC356909/ /pubmed/15018649 http://dx.doi.org/10.1186/1471-2156-5-2 Text en Copyright © 2004 Miterski et al; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL. |
spellingShingle | Research Article Miterski, Bianca Drynda, Susanne Böschow, Gundula Klein, Wolfram Oppermann, Joachim Kekow, Jörn Epplen, Jörg Thomas Complex genetic predisposition in adult and juvenile rheumatoid arthritis |
title | Complex genetic predisposition in adult and juvenile rheumatoid arthritis |
title_full | Complex genetic predisposition in adult and juvenile rheumatoid arthritis |
title_fullStr | Complex genetic predisposition in adult and juvenile rheumatoid arthritis |
title_full_unstemmed | Complex genetic predisposition in adult and juvenile rheumatoid arthritis |
title_short | Complex genetic predisposition in adult and juvenile rheumatoid arthritis |
title_sort | complex genetic predisposition in adult and juvenile rheumatoid arthritis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC356909/ https://www.ncbi.nlm.nih.gov/pubmed/15018649 http://dx.doi.org/10.1186/1471-2156-5-2 |
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