Preliminary Study to Identify the Predictive Factors for the Response to Methotrexate Therapy in Patients with Rheumatoid Arthritis

被引:18
作者
Inoue, Sachie [1 ]
Hashiguchi, Masayuki [1 ]
Takagi, Kenji [2 ]
Kawai, Shinichi [2 ]
Mochizuki, Mayumi [1 ]
机构
[1] Keio Univ, Fac Pharm, Div Evaluat & Anal Drug Informat, Minato Ku, Tokyo 1058512, Japan
[2] Toho Univ, Sch Med, Dept Internal Med Omori, Div Rheumatol,Ota Ku, Tokyo 1438541, Japan
来源
YAKUGAKU ZASSHI-JOURNAL OF THE PHARMACEUTICAL SOCIETY OF JAPAN | 2009年 / 129卷 / 07期
关键词
rheumatoid arthritis; methotrexate; methotrexate-polyglutamates; polymorphism; clinical trial; REDUCED FOLATE CARRIER; THYMIDYLATE SYNTHASE; METHYLENETETRAHYDROFOLATE REDUCTASE; COMMON POLYMORPHISMS; POLYGLUTAMATE LEVELS; GENE; PHARMACOKINETICS; SENSITIVITY; EFFICACY; REGION;
D O I
10.1248/yakushi.129.843
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
To identify the major factors predicting the response to Methotrexate (MTX) therapy in rheumatoid arthritis (RA) patients, we evaluated the relationship between the response to MTX and factors such as the concentration of MTX-polyglutamates (MTX-PGs) in erythrocytes (RBCs), genotypes of thymidylate synthase (TYMS) 5'-UTR (2R/3R) and 3'-UTR (-6/+6), 5,10-methylenetetrahydrofolate reductase (MTHFR) C677T and A1298C, and other patient-related factors. Thirty-six Japanese RA patients were enrolled in this cohort study. The concentrations of MTX-PGs in RBCs were measured, and polymorphisms were determined using PCR-RFLP method. As an indicator of the accumulated capacity of MTX-PGs in the RBCs of each patient, the MTX dose/MTX-PGs (AC-MPG, 1/week) was calculated. The response to MTX therapy was assessed using the MTX dose for a >= 50% decrease in CRP level (MTX dose for 50% CRP, mg/week), and the relationships between MTX dose for 50%CRP and various other factors were evaluated using multiple linear regression analysis. The MTX dose was 6.9 +/- 0.3 mg/week and the MTX-PGs concentration in RBCs was 97.3 +/- 8.1 nmol/1 (n=36, blood samples=95, mean +/- S.D.). The range of MTX dose for 50%CRP was 2.0-13.0 mg/week. Most individual AC-MPG levels showed no change during the evaluation period (coefficient of variation=5.9%). Based on the results of multiple linear regression analysis, AC-MPG, TYMS 3'-UTR (-6/+6), and ESR at the start of MTX therapy were associated with the MTX dose for 50%CRP. AC-MPG, TYMS 3'-UTR (-6/+6), and ESR might be the major predictive factors for the response to MTX therapy in Japanese RA patients.
引用
收藏
页码:843 / 849
页数:7
相关论文
共 27 条
[1]
Angelis-Stoforidis P, 1999, CLIN EXP RHEUMATOL, V17, P313
[2]
[Anonymous], 2002, ARTHRITIS RHEUM, V46, P328
[3]
Crom WR, 1992, APPL PHARMACOKINETIC, P1
[4]
Contribution of common polymorphisms in reduced folate carrier and γ-glutamylhydrolase to methotrexate polyglutamate levels in patients with rheumatoid arthritis [J].
Dervieux, T ;
Kremer, J ;
Lein, DO ;
Capps, R ;
Barham, R ;
Meyer, G ;
Smith, K ;
Caldwell, J ;
Furst, DE .
PHARMACOGENETICS, 2004, 14 (11) :733-739
[5]
Polyglutamation of methotrexate with common polymorphisms in reduced folate carrier, aminoimidazole carboxamide ribonucleotide transformylase, and thymidylate synthase are associated with methotrexate effects in rheumatoid arthritis [J].
Dervieux, T ;
Furst, D ;
Lein, DO ;
Capps, R ;
Smith, K ;
Walsh, M ;
Kremer, J .
ARTHRITIS AND RHEUMATISM, 2004, 50 (09) :2766-2774
[6]
HPLC determination of erythrocyte methotrexate polyglutamates after low-dose methotrexate therapy in patients with rheumatoid arthritis [J].
Dervieux, T ;
Lein, DO ;
Marcelletti, J ;
Pischel, K ;
Smith, K ;
Walsh, M ;
Richerson, R .
CLINICAL CHEMISTRY, 2003, 49 (10) :1632-1641
[7]
A CANDIDATE GENETIC RISK FACTOR FOR VASCULAR-DISEASE - A COMMON MUTATION IN METHYLENETETRAHYDROFOLATE REDUCTASE [J].
FROSST, P ;
BLOM, HJ ;
MILOS, R ;
GOYETTE, P ;
SHEPPARD, CA ;
MATTHEWS, RG ;
BOERS, GJH ;
DENHEIJER, M ;
KLUIJTMANS, LAJ ;
VANDENHEUVEL, LP ;
ROZEN, R .
NATURE GENETICS, 1995, 10 (01) :111-113
[8]
Goto Y, 2001, CLIN CANCER RES, V7, P1952
[9]
Pharmacokinetics and pharmacodynamics of methotrexate in non-neoplastic diseases [J].
Grim, J ;
Chládek, J ;
Martínková, J .
CLINICAL PHARMACOKINETICS, 2003, 42 (02) :139-151
[10]
HENDEL J, 1986, J CLIN PHARMACOL, V27, P607