Nozaki Yuji, Nagare Yasuaki, Hino Shoichi, Yano Tomohiro, Kishimoto Kazuya, Shimazu Hideki, Ikoma Shinya, Kinoshita Koji, Funauchi Masanori
Department of Nephrology and Rheumatology, Kinki University Faculty of Medicine, Osaka-Sayama, Osaka, Japan.
Nihon Rinsho Meneki Gakkai Kaishi. 2010;33(3):135-41. doi: 10.2177/jsci.33.135.
To predict the response of patients with rheumatoid arthritis (RA) to infliximab, patient profile and laboratory findings were compared to determine whether there was any association with the clinical course of the disease, and the clinical significance of serum rheumatoid factor (RF) in the response to this treatment was considered. Sixty-two RA patients were treated with infliximab, 87.9% of whom were positive for RF. At baseline and 12 months after the start of treatment, RF titers were significantly lower in the low-CRP group (CRP at 12 months<0.3 mg/dl) compared with that in the high-CRP group (CRP at 12 months >1.5 mg/dl). Furthermore, at baseline and 12 months, RF titers were significantly lower in the good-CRP-response group (DeltaCRP>or=1.5 mg/d) compared with the poor-CRP-response group (DeltaCRP<or=0.3 mg/d). The percent changes in RF and CRP from baseline were correlated throughout the clinical course. The duration of disease in good-CRP-response group was shorter than that in poor-CRP-response group significantly. The rate of positivity for HLA-DR4 in good response group tends to be higher than that in poor-CRP-response group. We concluded that several factors, including disease duration, positivity for HLA-DR4, and the serum RF titer at baseline, might predict the patient response to infliximab.
为预测类风湿关节炎(RA)患者对英夫利昔单抗的反应,对患者资料和实验室检查结果进行比较,以确定其与疾病临床进程是否存在关联,并探讨血清类风湿因子(RF)在该治疗反应中的临床意义。62例RA患者接受了英夫利昔单抗治疗,其中87.9%的患者RF呈阳性。在基线及治疗开始后12个月时,低CRP组(12个月时CRP<0.3mg/dl)的RF滴度显著低于高CRP组(12个月时CRP>1.5mg/dl)。此外,在基线及12个月时,良好CRP反应组(ΔCRP≥1.5mg/d)的RF滴度显著低于不良CRP反应组(ΔCRP≤0.3mg/d)。在整个临床过程中,RF和CRP相对于基线的变化百分比呈相关性。良好CRP反应组的病程显著短于不良CRP反应组。良好反应组中HLA-DR4的阳性率倾向于高于不良CRP反应组。我们得出结论,包括病程、HLA-DR4阳性以及基线时血清RF滴度等多个因素可能预测患者对英夫利昔单抗的反应。