2007
DOI: 10.1093/rheumatology/kem041
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Combined tumour necrosis factor-  and tumour necrosis factor receptor genotypes could predict rheumatoid arthritis patients' response to anti-TNF-  therapy and explain controversies of studies based on a single polymorphism

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Cited by 42 publications
(25 citation statements)
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“…After the full-text review, 10 of these 18 articles were excluded because 2 of them were review articles [16,24], 3 articles had no exact statistics about polymorphisms [25][26][27], 1 reported duplicate data [28], 1 was irrelevant to biological agent [29], 3 were not related to TNFRSF polymorphisms [2,30,31]. Finally, in the current study, 8 eligible studies [32][33][34][35][36][37][38][39] that meet the inclusion criteria were included in our biologic-specific meta-analysis.…”
Section: Studies Included In the Meta-analysismentioning
confidence: 99%
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“…After the full-text review, 10 of these 18 articles were excluded because 2 of them were review articles [16,24], 3 articles had no exact statistics about polymorphisms [25][26][27], 1 reported duplicate data [28], 1 was irrelevant to biological agent [29], 3 were not related to TNFRSF polymorphisms [2,30,31]. Finally, in the current study, 8 eligible studies [32][33][34][35][36][37][38][39] that meet the inclusion criteria were included in our biologic-specific meta-analysis.…”
Section: Studies Included In the Meta-analysismentioning
confidence: 99%
“…Therefore, seven of the eight studies containing 929 subjects for TNFRSF1B rs1061622 and five of eight studies involving 564 subjects for TNFRSF1A rs767455 were finally analyzed in our meta-analysis. For TNFRSF1B rs1061622, the subjects in three included studies were of RA [36,38,39], two CD [33,34] and the other two of psoriasis [32,37]. As for TNFRSF1A rs767455, two studies were carried out in RA [35,39], two in CD [33,34] and the other one in psoriasis [35] ( Table 2).…”
Section: Studies Included In the Meta-analysismentioning
confidence: 99%
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“…Two meta-analyses, performed by Lee et al in 20066 and O’Rielly et al in 2009,25 including data of 311 and 692 patients, respectively, suggested that patients with RA carrying the rare A allele had a worse response to anti-TNF therapy than those carrying the common G allele. However, these meta-analyses pooled data with varying response criteria and curiously, did not include studies that did not support a significant effect of this polymorphism on anti-TNF response 16 26. Furthermore, the meta-analysis from O’Rielly did not include three recently published studies accounting for 1551 additional patients with RA treated with anti-TNF agents 2022…”
Section: Introductionmentioning
confidence: 99%
“…No single genetic marker that predicts primary response to TNF-antagonists with replication in all cohorts has so far been identified (Table 1) [45][46][47][48][49][50][51][52][53][54][55][56][57][58][59][60][61][62][63][64]. Pharmacogenetic studies in the field are hampered by clinical heterogeneity of the study populations (e.g.…”
Section: Genetic Biomarkersmentioning
confidence: 99%