Crohn's disease genotypes of patients in remission vs relapses after infliximab discontinuation

被引:0
作者
Cathy Lu [1 ]
Alistair Waugh [1 ]
Robert J Bailey [2 ]
Raeleen Cherry [3 ]
Levinus A Dieleman [1 ]
Leah Gramlich [2 ]
Kata Matic [2 ]
Mario Millan [4 ]
Karen I Kroeker [1 ]
Daniel Sadowski [2 ]
Christopher W Teshima [1 ]
Dennis Todoruk [2 ]
Clarence Wong [2 ]
Karen Wong [1 ]
Richard N Fedorak [1 ]
机构
[1] Division of Gastroenterology,Zeidler Ledcor Center,University of Alberta,Edmonton,AB T6G 2X8,Canada
[2] Division of Gastroenterology,Royal Alexandra Hospital,Edmonton,AB T5H 3V9,Canada  3. Division of Gastroenterology,Grey Nuns Hospital,Edmonton,AB T6L 5X8,Canada 
关键词
Infliximab; Anti-tumor necrosis factor alpha; Crohn’s disease; Inflammatory bowel disease; Genotype;
D O I
暂无
中图分类号
R574.62 [结肠疾病];
学科分类号
1002 ; 100201 ;
摘要
AIM:To investigate genetic differences between Crohn’s disease(CD) patients with a sustained remission vs relapsers after discontinuing infliximab while in corticosteroid-free remission.METHODS:Forty-eight CD patients received infliximab and were in full corticosteroid-free clinical remission but then discontinued infliximab for reasons other than a loss of response,were identified by review of an electronic database and charts.Infliximab-associated remission was defined as corticosteroid-free plus normalization of clinical disease activity [CD activity index(CDAI) < 150] during follow-up visits based on physician global assessments.A CD relapse(loss of infliximab-induced remission) was clinically defined as a physician visit for symptoms of disease activity(CDAI > 220) and a therapeutic intervention with CD medication(s),or a hospitalization with complications related to active CD.Genetic analyses were performed on samples from 14 patients(n = 6 who had a sustained long term remission after stopping infliximab,n = 8 who rapidly relapsed after stopping infliximab).Nucleotide-binding oligomerization domain 2(NOD2)/caspase activation recruitment domain 15(CARD15) polymorphisms(R702W,G908R and L1007fs) and the inflammatory bowel disease 5(IBD5) polymorphisms(IGR2060a1 and IGR3081a1) were analyzed in each group.RESULTS:Five single nucleotide polymorphisms of IBD5 and NOD2/CARD15 genes were successfully analyzed for all 14 subjects.There was no significant increase in frequency of the NOD2/CARD15 polymorphisms(R702W,G908R and L1007fs) and the IBD5 polymorphisms(IGR2060a1 and IGR3081a1) in either group of patients;those whose disease relapsed rapidly or those who remained in sustained long term remission following the discontinuation of infliximab.Nearly a third of patients in full clinical remission who stopped infliximab for reasons other than loss of response remained in sustained clinical remission,while two-thirds relapsed rapidly.There was a marked difference in the duration of clinical remission following discontinuance of infliximab between the two groups.The patients who lost remission did so after 1.0 years ± 0.6 years,while those still in remission were at the time of this study,8.1 years ± 2.6 years post-discontinuation of infliximab,P < 0.001.The 8 patients who had lost remission after discontinuing infliximab had a mean number of 5 infusions(range 3-7),with a mean treatment time of 7.2 mo(range 1.5 mo-15 mo).The mean duration of time from the last infusion of infliximab to the time of loss of remission was 382 d(range 20 d-701 d).The 6 patients who remained in remission after discontinuing infliximab had a mean number of 6 infusions(range 3-12),with a mean treatment duration of 12 mo(range 3.6 mo-32 mo)(P = 0.45 relative to those who lost remission).CONCLUSION:There are no IBD5 or NOD2/CARD15 mutations that predict which patients might have sustained remission and which will relapse rapidly after stopping infliximab.
引用
收藏
页码:5058 / 5064
页数:7
相关论文
共 11 条
[1]  
Role of genetics in prediction of disease course and response to therapy[J]. Severine Vermeire,Gert Van Assche,Paul Rutgeerts. World Journal of Gastroenterology. 2010(21)
[2]  
Safety of infliximab in Crohn's disease: A large single‐center experience[J] . H.Hamzaoglu,J.Cooper,M.Alsahli,K.R.Falchuk,M.A.Peppercorn,R.J.Farrell. Inflamm Bowel Dis . 2010 (12)
[3]  
Maintenance of clinical benefit in Crohn’s disease patients after discontinuation of infliximab: long‐term follow‐up of a single centre cohort[J] . A. W. G.Waugh,S.Garg,K.Matic,L.Gramlich,C.Wong,D. C.Sadowski,M.Millan,R.Bailey,D.Todoruk,R.Cherry,C. W.Teshima,L.Dieleman,R. N.Fedorak. Alimentary Pharmacology & Therapeutics . 2010 (9)
[4]  
Canadian Association of Gastroenterology Clinical Practice Guidelines: The Use of Tumour Necrosis Factor-Alpha Antagonist Therapy in Crohn’s Disease[J] . Daniel C Sadowski,Charles N Bernstein,Alain Bitton,Ken Croitoru,Richard N Fedorak,Anne Griffiths,the CAG Crohn’s Consensus Group. Canadian Journal of Gastroenterology . 2009 (3)
[5]  
IBD: a family affair[J] . R.K Russell,J Satsangi. Best Practice & Research Clinical Gastroenterology . 2004 (3)
[6]  
The safety profile of infliximab in patients with Crohn’s disease: The Mayo Clinic experience in 500 patients[J] . Jean-Frederic Colombel,Edward V. Loftus,William J. Tremaine,Laurence J. Egan,W.Scott Harmsen,Cathy D. Schleck,Alan R. Zinsmeister,William J. Sandborn. Gastroenterology . 2004 (1)
[7]  
Genetics of inflammatory bowel disease: scientific and clinical implications[J] . J Satsangi,J Morecroft,N.B Shah,E Nimmo. Best Practice & Research Clinical Gastroenterology . 2003 (1)
[8]  
Maintenance infliximab for Crohn's disease: the ACCENT I randomised trial[J] . Stephen B Hanauer,Brian G Feagan,Gary R Lichtenstein,Lloyd F Mayer,S Schreiber,Jean Frederic Colombel,Daniel Rachmilewitz,Douglas C Wolf,Allan Olson,Weihang Bao,Paul Rutgeerts. The Lancet . 2002 (9317)
[9]  
Inflammatory Bowel Disease A Positive Response to Infliximab in Crohn Disease: Association with a Higher Systemic Inflammation Before Treatment But Not With -308 TNF Gene Polymorphism[J] . E. Louis,S. Vermeire,P. Rutgeerts,M. De Vos,A. Van Gossum,P. Pescatore,R. Fiasse,P. Pelckmans,H. Reynaert,G. D’Haens,M. Malaise,J. Belaiche. Scandinavian Journal of Gastroenterology . 2002 (7)
[10]   ANCA pattern and LTA haplotype relationship to clinical responses to anti-TNF antibody treatment in Crohn's disease [J].
Taylor, KD ;
Plevy, SE ;
Yang, HY ;
Landers, CJ ;
Barry, MJ ;
Rotter, JI ;
Targan, SR .
GASTROENTEROLOGY, 2001, 120 (06) :1347-1355