TNF-α gene polymorphisms in rheumatoid arthritis patients treated with anti-TNF-α agents: preliminary results

Objectives: To study –238 and +489 TNF-α polymorphisms in severe-unresponsive (more than 6 swollen joints and still active disease despite at least 6 months of DMARDs combination therapy) and mild-responsive (less than 3 swollen joints and good response to MTX or other conventional DMARDs) rheumatoi...

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Main Authors: M. Fabris, E. Di Poi, S. Sacco, G. Damante, L. Sinigaglia, G. Ferraccioli
Format: Article
Language:English
Published: PAGEPress Publications 2002-03-01
Series:Reumatismo
Online Access:https://reumatismo.org/index.php/reuma/article/view/53
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spelling doaj-4a99870c170c4fb0b990cd56829ec35c2020-11-24T20:58:39ZengPAGEPress PublicationsReumatismo0048-74492240-26832002-03-0154110.4081/reumatismo.2002.19TNF-α gene polymorphisms in rheumatoid arthritis patients treated with anti-TNF-α agents: preliminary resultsM. FabrisE. Di PoiS. SaccoG. DamanteL. SinigagliaG. FerraccioliObjectives: To study –238 and +489 TNF-α polymorphisms in severe-unresponsive (more than 6 swollen joints and still active disease despite at least 6 months of DMARDs combination therapy) and mild-responsive (less than 3 swollen joints and good response to MTX or other conventional DMARDs) rheumatoid arthritis (RA). Methods: We investigated 100 RA patients (56 with severe and 44 with mild disease activity) and 45 healthy blood donors (HBDs). Genotyping was performed by PCR-restriction fragment lenght polymorphism procedure. Several clinical and serological parameters were also examined. Results: Severe RA patients disclosed the –238 GG genotype in 100% of the cases versus 95.5% in the mild-responsive patients and 91.2% in the HBDs. The +489 GG genotype disclosed only a trend towards a prevalence in severe RA patients. However the +489 A allele seems to associates with early onset, longer disease duration and longer responsiveness to conventional therapy. Conclusion: The -238 AG genotype is absent in severe-unresponsive RA, but present in mild-responsive RA subjects. Thus –238 GG homozygosity associates with severity and unresponsiveness. In contrast the +489 polymorphism does not segregate differently between responsive and unresponsive RA patients.https://reumatismo.org/index.php/reuma/article/view/53
collection DOAJ
language English
format Article
sources DOAJ
author M. Fabris
E. Di Poi
S. Sacco
G. Damante
L. Sinigaglia
G. Ferraccioli
spellingShingle M. Fabris
E. Di Poi
S. Sacco
G. Damante
L. Sinigaglia
G. Ferraccioli
TNF-α gene polymorphisms in rheumatoid arthritis patients treated with anti-TNF-α agents: preliminary results
Reumatismo
author_facet M. Fabris
E. Di Poi
S. Sacco
G. Damante
L. Sinigaglia
G. Ferraccioli
author_sort M. Fabris
title TNF-α gene polymorphisms in rheumatoid arthritis patients treated with anti-TNF-α agents: preliminary results
title_short TNF-α gene polymorphisms in rheumatoid arthritis patients treated with anti-TNF-α agents: preliminary results
title_full TNF-α gene polymorphisms in rheumatoid arthritis patients treated with anti-TNF-α agents: preliminary results
title_fullStr TNF-α gene polymorphisms in rheumatoid arthritis patients treated with anti-TNF-α agents: preliminary results
title_full_unstemmed TNF-α gene polymorphisms in rheumatoid arthritis patients treated with anti-TNF-α agents: preliminary results
title_sort tnf-α gene polymorphisms in rheumatoid arthritis patients treated with anti-tnf-α agents: preliminary results
publisher PAGEPress Publications
series Reumatismo
issn 0048-7449
2240-2683
publishDate 2002-03-01
description Objectives: To study –238 and +489 TNF-α polymorphisms in severe-unresponsive (more than 6 swollen joints and still active disease despite at least 6 months of DMARDs combination therapy) and mild-responsive (less than 3 swollen joints and good response to MTX or other conventional DMARDs) rheumatoid arthritis (RA). Methods: We investigated 100 RA patients (56 with severe and 44 with mild disease activity) and 45 healthy blood donors (HBDs). Genotyping was performed by PCR-restriction fragment lenght polymorphism procedure. Several clinical and serological parameters were also examined. Results: Severe RA patients disclosed the –238 GG genotype in 100% of the cases versus 95.5% in the mild-responsive patients and 91.2% in the HBDs. The +489 GG genotype disclosed only a trend towards a prevalence in severe RA patients. However the +489 A allele seems to associates with early onset, longer disease duration and longer responsiveness to conventional therapy. Conclusion: The -238 AG genotype is absent in severe-unresponsive RA, but present in mild-responsive RA subjects. Thus –238 GG homozygosity associates with severity and unresponsiveness. In contrast the +489 polymorphism does not segregate differently between responsive and unresponsive RA patients.
url https://reumatismo.org/index.php/reuma/article/view/53
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