Skip to main content
Top
Published in: Clinical Rheumatology 7/2015

01-07-2015 | Original Article

Predictors of response to TNF-α antagonist therapy in Chinese rheumatoid arthritis

Authors: Rui Ding, Ping Li, Ding Song, Xin Zhang, Liqi Bi

Published in: Clinical Rheumatology | Issue 7/2015

Login to get access

Abstract

This study aimed to investigate the clinical, immunological, and radiologic predictors of response to tumor necrosis factor (TNF)-α antagonist therapy in Chinese rheumatoid arthritis (RA). Ninety RA patients were divided into two groups according to their responsiveness to TNF-α antagonist therapy at 1 month: group A (responders) and group B (non-responders). After 3 months of therapy, all the 90 patients were re-assessed and re-divided into another two groups: group C (responders) and group D (non-responders). Serum samples and clinical characteristics as well as radiographic features were collected at baseline, first month, and third month post-initial administration of TNF-α antagonist. Serum TNF-α, interleukin (IL)-6, IL-8, IL-34, and matrix metalloproteinase (MMP)-3 were measured by enzyme-linked immunosorbent assay (ELISA). Disease activity and Sharp score were evaluated. (1) Comparisons between groups A and B: subjects in group A showed a lower level of erythrocyte sedimentation rate (ESR) and a higher level of albumin (ALB) at baseline than that of group B (p < 0.05). The cutoff value of ALB for prediction was ≥34.9 g/l and that of ESR was ≤55.5 mm/h. (2) Comparisons between groups C and D: group C showed lower levels of ESR, health assessment questionnaire (HAQ), and IL-34 at baseline (p < 0.05). The threshold for prediction were as follows: ESR ≤60 mm/h, HAQ ≤1.3125, and IL-34 ≤194.12 pg/ml. (3) The serum cytokines were positively correlated with C-reactive protein (CRP) and disease activity index, while ALB was negatively correlated with CRP and disease activity. Baseline ALB ≥34.9 g/l or ESR ≤55.5 mm/h might predict a good response at 1-month treatment of TNF-α antagonist, while baseline ESR ≤60 mm/h, HAQ ≤1.3125, and IL-34 ≤194.12 pg/ml might predict a good response at 3-month treatment.
Literature
1.
go back to reference Bathon JM, Martin RW, Fleischmann RM et al (2000) A comparison of etanercept and methotrexate in patients with early rheumatoid arthritis. N Engl J Med 343:1586–1593PubMedCrossRef Bathon JM, Martin RW, Fleischmann RM et al (2000) A comparison of etanercept and methotrexate in patients with early rheumatoid arthritis. N Engl J Med 343:1586–1593PubMedCrossRef
2.
go back to reference Maini RN, Breedveld FC, Kalden JR et al (2004) Sustained improvement over two years in physical function, structural damages, and signs and symptoms among patients with rheumatoid arthritis treated with infliximab and methotrexate. Arthritis Rheum 50:1051–1065PubMedCrossRef Maini RN, Breedveld FC, Kalden JR et al (2004) Sustained improvement over two years in physical function, structural damages, and signs and symptoms among patients with rheumatoid arthritis treated with infliximab and methotrexate. Arthritis Rheum 50:1051–1065PubMedCrossRef
3.
go back to reference Simsek I (2012) Predictors of Response to TNF inhibitors in rheumatoid arthritis—do we have new tools for personalized medicine? Bull NYU Hospital Joint Dis 70:187–190 Simsek I (2012) Predictors of Response to TNF inhibitors in rheumatoid arthritis—do we have new tools for personalized medicine? Bull NYU Hospital Joint Dis 70:187–190
4.
go back to reference Smolen JS, Landewé R, Breedveld FC (2014) EULAR recommendations for the management of rheumatoid arthritis with synthetic and biological disease-modifying antirheumatic drugs: 2013 update. Ann Rheum Dis 73:492–509PubMedCentralPubMedCrossRef Smolen JS, Landewé R, Breedveld FC (2014) EULAR recommendations for the management of rheumatoid arthritis with synthetic and biological disease-modifying antirheumatic drugs: 2013 update. Ann Rheum Dis 73:492–509PubMedCentralPubMedCrossRef
5.
go back to reference der Broeder A, van de Putte L, Rau R et al (2002) A single dose, placebo controlled study of the fully human anti-tumor necrosis factor-alpha antibody adalimumab (D2E7) in patients with rheumatoid arthritis. J Rheumatol 29:2288–2298 der Broeder A, van de Putte L, Rau R et al (2002) A single dose, placebo controlled study of the fully human anti-tumor necrosis factor-alpha antibody adalimumab (D2E7) in patients with rheumatoid arthritis. J Rheumatol 29:2288–2298
6.
go back to reference Salgado E, Maneiro JR, Gomez-Reino JJ (2014) Predictors of response to TNF antagonists. Curr Pharm Des 21:221–232CrossRef Salgado E, Maneiro JR, Gomez-Reino JJ (2014) Predictors of response to TNF antagonists. Curr Pharm Des 21:221–232CrossRef
7.
go back to reference Cuchacovich M, Bueno D, Carvajal R, Bravo N, Aguillón JC, Catalán D, Soto L (2014) Clinical parameters and biomarkers for anti-TNF treatment prognosis in rheumatoid arthritis patients. Clin Rheumatol 33:1707–1714PubMedCrossRef Cuchacovich M, Bueno D, Carvajal R, Bravo N, Aguillón JC, Catalán D, Soto L (2014) Clinical parameters and biomarkers for anti-TNF treatment prognosis in rheumatoid arthritis patients. Clin Rheumatol 33:1707–1714PubMedCrossRef
8.
go back to reference Wright HL, Bucknall RC, Moots RJ et al (2012) Analysis of SF and plasma cytokines provides insights into the mechanisms of inflammatory arthritis and may predict response to therapy. Rheumatology (Oxford) 51:451–459CrossRef Wright HL, Bucknall RC, Moots RJ et al (2012) Analysis of SF and plasma cytokines provides insights into the mechanisms of inflammatory arthritis and may predict response to therapy. Rheumatology (Oxford) 51:451–459CrossRef
9.
go back to reference Fabre S, Dupuy AM, Dossat N et al (2008) Protein biochip array technology for cytokine profiling predicts etanercept responsiveness in rheumatoid arthritis. Clin Exp Immunol 153:188–195PubMedCentralPubMedCrossRef Fabre S, Dupuy AM, Dossat N et al (2008) Protein biochip array technology for cytokine profiling predicts etanercept responsiveness in rheumatoid arthritis. Clin Exp Immunol 153:188–195PubMedCentralPubMedCrossRef
10.
go back to reference Yuasa S, Yamaguchi H, Nakanishi Y et al (2013) Treatment responses and their predictors in patients with rheumatoid arthritis treated with biological agents. J Med Invest 60:77–90PubMedCrossRef Yuasa S, Yamaguchi H, Nakanishi Y et al (2013) Treatment responses and their predictors in patients with rheumatoid arthritis treated with biological agents. J Med Invest 60:77–90PubMedCrossRef
11.
go back to reference Pomirleanu C, Ancuta C, Miu S et al (2013) A predictive model for remission and low disease activity in patients with established rheumatoid arthritis receiving TNF blockers. Clin Rheumatol 32:665–670PubMedCrossRef Pomirleanu C, Ancuta C, Miu S et al (2013) A predictive model for remission and low disease activity in patients with established rheumatoid arthritis receiving TNF blockers. Clin Rheumatol 32:665–670PubMedCrossRef
12.
go back to reference Gonzalez-Alvaro I, Ortiz AM, Tomero EG et al (2007) Baseline serum RANKL levels may serve to predict remission in rheumatoid arthritis patients treated with TNF antagonists. Ann Rheum Dis 66:1675–1678PubMedCentralPubMedCrossRef Gonzalez-Alvaro I, Ortiz AM, Tomero EG et al (2007) Baseline serum RANKL levels may serve to predict remission in rheumatoid arthritis patients treated with TNF antagonists. Ann Rheum Dis 66:1675–1678PubMedCentralPubMedCrossRef
13.
go back to reference Takahashi R, SalkikoIsojima MU et al (2014) Serum anticyclic citrullinated protein antibody titers are correlated with the response to biological agents in patients with rheumatoid arthritis. Open Access Rheumatol: Res Rev 6:57–64 Takahashi R, SalkikoIsojima MU et al (2014) Serum anticyclic citrullinated protein antibody titers are correlated with the response to biological agents in patients with rheumatoid arthritis. Open Access Rheumatol: Res Rev 6:57–64
14.
go back to reference Braun-Moscovici Y, Markovits D, Zinder O et al (2006) Anti-cyclic citrullinated protein antibodies as a predictor of response to anti-tumor necrosis factor-alpha therapy in patients with rheumatoid arthritis. J Rheumatol 33:497–500PubMed Braun-Moscovici Y, Markovits D, Zinder O et al (2006) Anti-cyclic citrullinated protein antibodies as a predictor of response to anti-tumor necrosis factor-alpha therapy in patients with rheumatoid arthritis. J Rheumatol 33:497–500PubMed
15.
go back to reference Nishimoto T, Seta N, Anan R et al (2014) A single nucleotide polymorphism of TRAF1 predicts the clinical response to anti-TNF treatment in Japanese patients with rheumatoid arthritis. Clin Exp Rheumatol 32:211–217PubMed Nishimoto T, Seta N, Anan R et al (2014) A single nucleotide polymorphism of TRAF1 predicts the clinical response to anti-TNF treatment in Japanese patients with rheumatoid arthritis. Clin Exp Rheumatol 32:211–217PubMed
16.
go back to reference Dávila-Fajardo CL, Márquez A, Pascual-Salcedo D et al (2014) Confirmation of -174G/C interleukin-6 gene promoter polymorphism as a genetic marker predicting antitumor necrosis factor treatment outcome. Pharmacogenet Genomics 24:1–5PubMedCrossRef Dávila-Fajardo CL, Márquez A, Pascual-Salcedo D et al (2014) Confirmation of -174G/C interleukin-6 gene promoter polymorphism as a genetic marker predicting antitumor necrosis factor treatment outcome. Pharmacogenet Genomics 24:1–5PubMedCrossRef
17.
go back to reference Kayakabe K, Kuroiwa T, Sakurai N et al (2012) Interleukin-1β measurement in stimulated whole blood cultures is useful to predict response to anti-TNF therapies in rheumatoid arthritis. Rheumatology (Oxford) 51:1639–1643CrossRef Kayakabe K, Kuroiwa T, Sakurai N et al (2012) Interleukin-1β measurement in stimulated whole blood cultures is useful to predict response to anti-TNF therapies in rheumatoid arthritis. Rheumatology (Oxford) 51:1639–1643CrossRef
18.
go back to reference Ribbens C, Andre B, Jaspar JM et al (2000) Matrix metalloproteinase-3 serum levels are correlated with disease activity and predict clinical response in rheumatoid arthritis. J Rheumatol 27:888–893PubMed Ribbens C, Andre B, Jaspar JM et al (2000) Matrix metalloproteinase-3 serum levels are correlated with disease activity and predict clinical response in rheumatoid arthritis. J Rheumatol 27:888–893PubMed
19.
go back to reference Abhishek A, Butt S, Gadsby K et al (2010) Anti-TNF-alpha agents are less effective for the treatment of rheumatoid arthritis in current smokers. J Clin Rheumatol 16:15–18PubMedCrossRef Abhishek A, Butt S, Gadsby K et al (2010) Anti-TNF-alpha agents are less effective for the treatment of rheumatoid arthritis in current smokers. J Clin Rheumatol 16:15–18PubMedCrossRef
20.
go back to reference Coulthard LR, Taylor JC, Eyre S et al (2011) Genetic variants within the MAP kinase signaling network and anti-TNF treatment response in rheumatoid arthritis patients. Ann Rheum Dis 70:98–103PubMedCrossRef Coulthard LR, Taylor JC, Eyre S et al (2011) Genetic variants within the MAP kinase signaling network and anti-TNF treatment response in rheumatoid arthritis patients. Ann Rheum Dis 70:98–103PubMedCrossRef
21.
go back to reference Saevarsdottir S, Wedren S, Seddighzadeh M et al (2011) Patients with early rheumatoid arthritis who smoke are less likely to respond to treatment with methotrexate and tumor necrosis factor inhibitors: observations from the Epidemiological Investigation of Rheumatoid Arthritis and the Swedish Rheumatology Register cohorts. Arthritis Rheum 63:26–36PubMedCrossRef Saevarsdottir S, Wedren S, Seddighzadeh M et al (2011) Patients with early rheumatoid arthritis who smoke are less likely to respond to treatment with methotrexate and tumor necrosis factor inhibitors: observations from the Epidemiological Investigation of Rheumatoid Arthritis and the Swedish Rheumatology Register cohorts. Arthritis Rheum 63:26–36PubMedCrossRef
22.
go back to reference Soderlin MK, Petersson IF, Geborek P (2012) The effect of smoking on response and drug survival in rheumatoid arthritis patients treated with their first anti-TNF drug. Scand J Rheumatol 41:1–9PubMedCrossRef Soderlin MK, Petersson IF, Geborek P (2012) The effect of smoking on response and drug survival in rheumatoid arthritis patients treated with their first anti-TNF drug. Scand J Rheumatol 41:1–9PubMedCrossRef
23.
go back to reference van der Heijde D (2000) How to read radiographs according to the Sharp/van der Heijde method. J Rheumatol 27:261–263PubMed van der Heijde D (2000) How to read radiographs according to the Sharp/van der Heijde method. J Rheumatol 27:261–263PubMed
24.
go back to reference Felson DT, Anderson JJ, Boers M et al (1995) American college of rheumatology. Preliminary definition of improvement in rheumatoid arthritis. Arthritis Rheum 38:727–735PubMedCrossRef Felson DT, Anderson JJ, Boers M et al (1995) American college of rheumatology. Preliminary definition of improvement in rheumatoid arthritis. Arthritis Rheum 38:727–735PubMedCrossRef
25.
go back to reference Ward MM, Guthrie LC, Alba MI (2014) Brief report: rheumatoid arthritis response criteria and patient-reported improvement in arthritis activity: is an American College of Rheumatology twenty percent response meaningful to patients? Arthritis Rheumatol 66:2339–2343PubMedCrossRef Ward MM, Guthrie LC, Alba MI (2014) Brief report: rheumatoid arthritis response criteria and patient-reported improvement in arthritis activity: is an American College of Rheumatology twenty percent response meaningful to patients? Arthritis Rheumatol 66:2339–2343PubMedCrossRef
26.
go back to reference Hyrich KL, Watson KD, Silman AJ et al (2006) Predictors of response to anti-TNF-alpha therapy among patients with rheumatoid arthritis: Results from the British Society for Rheumatology Biologics Register. Rheumatology 45:1558–1565PubMedCrossRef Hyrich KL, Watson KD, Silman AJ et al (2006) Predictors of response to anti-TNF-alpha therapy among patients with rheumatoid arthritis: Results from the British Society for Rheumatology Biologics Register. Rheumatology 45:1558–1565PubMedCrossRef
27.
go back to reference Hwang SJ, Choi B, Kang SS et al (2012) Interleukin-34 produced by human fibroblast-like synovial cells in rheumatoid arthritis supports osteoclastogenesis. Arthritis Res Ther 14:R14PubMedCentralPubMedCrossRef Hwang SJ, Choi B, Kang SS et al (2012) Interleukin-34 produced by human fibroblast-like synovial cells in rheumatoid arthritis supports osteoclastogenesis. Arthritis Res Ther 14:R14PubMedCentralPubMedCrossRef
28.
go back to reference Wijbrandts CA, Dijkgraaf MGW, Kraan MC et al (2008) The clinical response to infliximab in rheumatoid arthritis is in part dependent on pretreatment tumour necrosis factor a expression in the synovium. Ann Rheum Dis 67:1139–1144PubMedCentralPubMedCrossRef Wijbrandts CA, Dijkgraaf MGW, Kraan MC et al (2008) The clinical response to infliximab in rheumatoid arthritis is in part dependent on pretreatment tumour necrosis factor a expression in the synovium. Ann Rheum Dis 67:1139–1144PubMedCentralPubMedCrossRef
Metadata
Title
Predictors of response to TNF-α antagonist therapy in Chinese rheumatoid arthritis
Authors
Rui Ding
Ping Li
Ding Song
Xin Zhang
Liqi Bi
Publication date
01-07-2015
Publisher
Springer London
Published in
Clinical Rheumatology / Issue 7/2015
Print ISSN: 0770-3198
Electronic ISSN: 1434-9949
DOI
https://doi.org/10.1007/s10067-015-2973-3

Other articles of this Issue 7/2015

Clinical Rheumatology 7/2015 Go to the issue
Live Webinar | 27-06-2024 | 18:00 (CEST)

Keynote webinar | Spotlight on medication adherence

Live: Thursday 27th June 2024, 18:00-19:30 (CEST)

WHO estimates that half of all patients worldwide are non-adherent to their prescribed medication. The consequences of poor adherence can be catastrophic, on both the individual and population level.

Join our expert panel to discover why you need to understand the drivers of non-adherence in your patients, and how you can optimize medication adherence in your clinics to drastically improve patient outcomes.

Prof. Kevin Dolgin
Prof. Florian Limbourg
Prof. Anoop Chauhan
Developed by: Springer Medicine
Obesity Clinical Trial Summary

At a glance: The STEP trials

A round-up of the STEP phase 3 clinical trials evaluating semaglutide for weight loss in people with overweight or obesity.

Developed by: Springer Medicine