Department of Rheumatology, Karolinska Institutet at Karolinska University Hospital Huddinge, R92, Stockholm 141 86, Sweden.
Arthritis Res Ther. 2010;12(5):R197. doi: 10.1186/ar3169. Epub 2010 Oct 21.
Rheumatoid arthritis (RA) is associated with changes in body composition and bone mineral density (BMD). The purpose of the present study was to evaluate whether anti-TNF treatment in early RA has an impact on body composition and BMD besides that which could be achieved by intensive disease-modifying anti-rheumatic drug (DMARD) combination therapy.
Forty patients with early RA who failed treatment with methotrexate up to 20 mg/week for 3 months were randomised to addition of sulphasalazine and hydroxychloroquine (treatment A) or addition of infliximab (treatment B). At 3, 12 and 24 months, body composition and BMD were assessed by total-body dual-energy X-ray absorptiometry. At the same time points, leptin, adiponectin, apolipoproteins, insulin-like growth factor-1 (IGF-1) and markers of bone remodelling were analysed. Compliance to treatment was considered in the analyses. Data were analysed with a mixed, linear model.
Patients treated with anti-TNF had a significant increase in fat mass at 2 years, 3.8 (1.6 to 5.9) kg, in contrast to patients in treatment A, 0.4 (-1.5 to 2.2) kg (P = 0.040), despite similar reduction in disease activity. Both treatment strategies prevented loss of muscle mass and bone. Leptin concentrations increased significantly in both groups at 2 years and adiponectin increased significantly at 2 years in treatment A and at 1 year in treatment B. There were no significant changes in apolipoproteins or IGF-1. The markers of bone resorption decreased at 12 months in both treatment groups with no significant difference between the treatment groups.
Infliximab therapy increased body fat mass, an effect that was not achieved with the combination of DMARDs, despite a similar reduction in disease activity, and thus seemed to be drug specific. The increase of fat mass was not associated with an exacerbated atherogenic lipid profile. Leptin and adiponectin concentrations increased in both treatment groups. The increase of adiponectin may partially explain the reduced frequency of cardiovascular diseases found when disease activity is reduced in RA.
ISRCTN39045408.
类风湿关节炎(RA)与身体成分和骨密度(BMD)的变化有关。本研究的目的是评估早期 RA 患者接受抗 TNF 治疗是否除了通过强化疾病修饰抗风湿药物(DMARD)联合治疗所能达到的效果外,还会对身体成分和 BMD 产生影响。
40 名接受每周 20mg 甲氨蝶呤治疗 3 个月后治疗失败的早期 RA 患者被随机分为添加柳氮磺胺吡啶和羟氯喹(治疗 A)或添加英夫利昔单抗(治疗 B)。在 3、12 和 24 个月时,通过全身双能 X 射线吸收法评估身体成分和 BMD。同时,分析瘦素、脂联素、载脂蛋白、胰岛素样生长因子-1(IGF-1)和骨重建标志物。分析中考虑了治疗依从性。数据采用混合线性模型进行分析。
接受抗 TNF 治疗的患者在 2 年内脂肪量显著增加,为 3.8(1.6 至 5.9)kg,而治疗 A 的患者仅增加 0.4(-1.5 至 2.2)kg(P=0.040),尽管疾病活动度的降低相似。两种治疗策略均能防止肌肉和骨骼质量的损失。两组患者在 2 年内瘦素浓度显著升高,治疗 A 组在 2 年内和治疗 B 组在 1 年内脂联素浓度显著升高。载脂蛋白或 IGF-1 无明显变化。两组患者在 12 个月时骨吸收标志物均下降,两组间无显著差异。
英夫利昔单抗治疗可增加体脂肪量,而 DMARD 联合治疗则无法达到这一效果,尽管疾病活动度降低相似,但这似乎是药物特异性的。脂肪量的增加与动脉粥样硬化脂质谱恶化无关。两组患者的瘦素和脂联素浓度均升高。脂联素的增加可能部分解释了 RA 患者疾病活动度降低时心血管疾病发病率降低的原因。
ISRCTN39045408。