Effect of Methotrexate Use and Erythrocyte Methotrexate Polyglutamate on Glycosylated Hemoglobin in Rheumatoid Arthritis

被引:19
作者
de Rotte, Maurits C. F. J. [1 ]
de Jong, Pascal H. P. [1 ]
den Boer, Ethan [1 ]
Pluijm, Saskia M. F. [1 ]
Ozcan, Behiye [1 ]
Weel, Angelique E. A. M. [2 ]
Lindemans, Jan [1 ]
Hazes, Johanna M. W. [1 ]
de Jonge, Robert [1 ]
机构
[1] Erasmus Univ, Med Ctr, NL-3015 CN Rotterdam, Netherlands
[2] Maasstad Hosp, Rotterdam, Netherlands
关键词
IMPROVES INSULIN SENSITIVITY; BETA-CELL FUNCTION; DIABETES-MELLITUS; CARDIOVASCULAR RISK; CONTROLLED-TRIAL; DOUBLE-BLIND; HYDROXYCHLOROQUINE; DISEASE; INFLAMMATION; THERAPY;
D O I
10.1002/art.38652
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. To investigate whether methotrexate (MTX) use, as compared to other therapies, and erythrocyte methotrexate polyglutamate (MTXGlu) concentrations are associated with changes in glycosylated hemoglobin (HbA(1c)) levels in rheumatoid arthritis (RA) patients. Methods. The derivation cohort consisted of patients selected from the Treatment in the Rotterdam Early Arthritis Cohort who fulfilled the 2010 American College of Rheumatology/European League Against Rheumatism classification criteria for RA. Patients were randomized to 6 treatment arms: triple disease-modifying antirheumatic drug (DMARD) therapy (consisting of MTX, sulfasalazine, and hydroxychloroquine [HCQ]) + intramuscular (IM) glucocorticoids, triple DMARD therapy + oral glucocorticoids, MTX + oral glucocorticoid therapy, MTX therapy, oral glucocorticoid therapy, and HCQ therapy. HbA(1c) levels were determined at baseline and at 3 months. Concentrations of erythrocyte MTXGlu(1-5) were measured after 3 months of treatment. Within treatment arms, changes in the level of HbA(1c) were compared by paired t-test. Associations of MTXGlu concentrations with changes in the level of HbA(1c) were tested using multiple linear regression analysis, adjusted for age, sex, body mass index, and comedication. Significant associations were validated using data on RA patients taking MTX who were enrolled in the Methotrexate in Rotterdam cohort. Results. In the derivation cohort, the mean change in HbA(1c) level after 3 months of treatment was -1.9 mmoles/mole (-0.18%) (P = 0.001). Levels of HbA(1c) decreased in 4 of the individual treatment groups, as follows: for the triple DMARD therapy + IM glucocorticoids treatment arm, -5.5 mmoles/mole (-0.50%) (P < 0.001), for the triple DMARD therapy + oral glucocorticoids treatment arm, -3.7 mmoles/mole (-0.34%) (P < 0.001), for the MTX treatment arm, -0.8 mmoles/mole (-0.08%) (P = 0.018), and for the HCQ treatment arm, -2.0 mmoles/mole (-0.19%) (P = 0.175). Increased levels of MTXGlu(2) (beta = -0.20, P = 0.005), MTXGlu(3) (beta = -0.31, P < 0.001), MTXGlu(4) (beta = -0.33, P < 0.001) after treatment, MTXGlu(5) (beta = -0.39, P < 0.001), and total MTXGlu (beta = -0.29, P < 0.001) were associated with decreased levels of HBA(1c). In the validation cohort, levels of HbA(1c) were decreased by 2.6 mmoles/mole (0.23%) (P < 0.001) after treatment, and MTXGlu(3) was associated with decreased levels of HbA(1c) (beta = -0.26, P = 0.018). Conclusion. MTX use and higher concentrations of erythrocyte MTXGlu are associated with decreased levels of HbA(1c) in RA patients. Triple DMARD therapy and HCQ treatment resulted in reduced HbA(1c) levels, and glucocorticoid treatment resulted in increased levels of HbA(1c).
引用
收藏
页码:2026 / 2036
页数:11
相关论文
共 51 条
[1]   2010 Rheumatoid Arthritis Classification Criteria An American College of Rheumatology/European League Against Rheumatism Collaborative Initiative [J].
Aletaha, Daniel ;
Neogi, Tuhina ;
Silman, Alan J. ;
Funovits, Julia ;
Felson, David T. ;
Bingham, Clifton O., III ;
Birnbaum, Neal S. ;
Burmester, Gerd R. ;
Bykerk, Vivian P. ;
Cohen, Marc D. ;
Combe, Bernard ;
Costenbader, Karen H. ;
Dougados, Maxime ;
Emery, Paul ;
Ferraccioli, Gianfranco ;
Hazes, Johanna M. W. ;
Hobbs, Kathryn ;
Huizinga, Tom W. J. ;
Kavanaugh, Arthur ;
Kay, Jonathan ;
Kvien, Tore K. ;
Laing, Timothy ;
Mease, Philip ;
Menard, Henri A. ;
Moreland, Larry W. ;
Naden, Raymond L. ;
Pincus, Theodore ;
Smolen, Josef S. ;
Stanislawska-Biernat, Ewa ;
Symmons, Deborah ;
Tak, Paul P. ;
Upchurch, Katherine S. ;
Vencovsky, Jiri ;
Wolfe, Frederick ;
Hawker, Gillian .
ARTHRITIS AND RHEUMATISM, 2010, 62 (09) :2569-2581
[2]  
Altman DG., 1996, PRACTICAL STAT MED R, V7th
[3]  
Andrews RC, 1999, CLIN SCI, V96, P513, DOI 10.1042/cs0960513
[4]   INHIBITION OF 5-AMINOIMIDAZOLE-4-CARBOXAMIDE RIBOTIDE TRANSFORMYLASE, ADENOSINE-DEAMINASE AND 5'-ADENYLATE DEAMINASE BY POLYGLUTAMATES OF METHOTREXATE AND OXIDIZED FOLATES AND BY 5-AMINOIMIDAZOLE-4-CARBOXAMIDE RIBOSIDE AND RIBOTIDE [J].
BAGGOTT, JE ;
VAUGHN, WH ;
HUDSON, BB .
BIOCHEMICAL JOURNAL, 1986, 236 (01) :193-200
[5]   THE MODERATOR MEDIATOR VARIABLE DISTINCTION IN SOCIAL PSYCHOLOGICAL-RESEARCH - CONCEPTUAL, STRATEGIC, AND STATISTICAL CONSIDERATIONS [J].
BARON, RM ;
KENNY, DA .
JOURNAL OF PERSONALITY AND SOCIAL PSYCHOLOGY, 1986, 51 (06) :1173-1182
[6]   Prednisone plus methotrexate for polymyalgia rheumatica - A randomized, double-blind, placebo-controlled trial [J].
Caporali, R ;
Cimmino, MA ;
Ferraccioli, G ;
Gerli, R ;
Klersy, C ;
Salvarani, C ;
Montecucco, C .
ANNALS OF INTERNAL MEDICINE, 2004, 141 (07) :493-500
[7]   Use of risk stratification to target therapies in patients with recent onset arthritis; design of a prospective randomized multicenter controlled trial [J].
Claessen, Susanne J. J. ;
Hazes, Johanna M. W. ;
Huisman, Margriet A. M. ;
van Zeben, Derkjen ;
Luime, Jolanda J. ;
Weel, Angelique E. A. M. .
BMC MUSCULOSKELETAL DISORDERS, 2009, 10
[8]   THE ANTIINFLAMMATORY MECHANISM OF METHOTREXATE - INCREASED ADENOSINE RELEASE AT INFLAMED SITES DIMINISHES LEUKOCYTE ACCUMULATION IN AN IN-VIVO MODEL OF INFLAMMATION [J].
CRONSTEIN, BN ;
NAIME, D ;
OSTAD, E .
JOURNAL OF CLINICAL INVESTIGATION, 1993, 92 (06) :2675-2682
[9]   Induction therapy with a combination of DMARDs is better than methotrexate monotherapy: first results of the tREACH trial [J].
de Jong, P. H. ;
Hazes, J. M. ;
Barendregt, P. J. ;
Huisman, M. ;
van Zeben, D. ;
van der Lubbe, P. A. ;
Gerards, A. H. ;
de Jager, M. H. ;
de Sonnaville, P. B. ;
Grillet, B. A. ;
Luime, J. J. ;
Weel, A. E. .
ANNALS OF THE RHEUMATIC DISEASES, 2013, 72 (01) :72-78
[10]   Association of Low Baseline Levels of Erythrocyte Folate With Treatment Nonresponse at Three Months in Rheumatoid Arthritis Patients Receiving Methotrexate [J].
de Rotte, M. C. F. J. ;
de Jong, P. H. P. ;
Pluijm, S. M. F. ;
Calasan, M. Bulatovic ;
Barendregt, P. J. ;
van Zeben, D. ;
van der Lubbe, P. A. ;
de Sonnaville, P. B. ;
Lindemans, J. ;
Hazes, J. M. W. ;
de Jonge, R. .
ARTHRITIS AND RHEUMATISM, 2013, 65 (11) :2803-2813