Held Julia, Mosheimer-Feistritzer Birgit, Gruber Johann, Mur Erich, Weiss Günter
1Department of Internal Medicine II, Infectious Diseases, Immunology, Rheumatology, Pneumology, Medical University of Innsbruck, Anichstr. 35, A-6020 Innsbruck, Austria.
2Department for Physical Medicine and Rehabilitation, University of Innsbruck, Innsbruck, Austria.
BMC Rheumatol. 2018 Mar 7;2:6. doi: 10.1186/s41927-018-0012-0. eCollection 2018.
Methotrexate (MTX) is well known to affect folic acid metabolism, so MTX treatment can result in alterations of mean corpuscular volume (MCV), which may impact on red cell distribution width (RDW), as MCV levels feed into RDW calculation. We thus questioned whether RDW levels and subsequently its diagnostic utility in RA subjects, as reported before, are influenced by ongoing MTX therapy.We assessed the impact of disease modifying drug (DMARD) treatment, especially MTX, on RDW and evaluated their influence on the predictive value of RDW for cardiovascular (CV) events in patients with rheumatoid arthritis (RA). As far as we know, this is the first study evaluating the influence of MTX on RDW.
Medical treatment, disease activity, laboratory parameters and history of CV events were retrospectively analysed in 385 RA patients at disease onset and at last follow up at our clinic. Additionally, in patients with CV event, data were recorded at last follow up prior the CV event.
Disease parameters and laboratory findings associated with a serious vascular event were older age ( < 0,001), longer disease duration ( = 0,002) and a higher RDW at diagnosis ( = 0,025). No differences in RDW levels became evident with any other treatment regimen beside MTX. MTX treated patients had significantly higher RDW compared to subjects without this drug ( < 0,001). In RA patients without MTX treatment, we found RDW level significantly different between those with versus without a CV event, whereas this difference disappeared in subjects receiving MTX.
MTX impacts on RDW and might therefor reduce its prognostic value for CV events in patients taking MTX, whereas an increased RDW at diagnosis remains an early risk predictor for myocardial infarction and stroke in RA patients.
众所周知,甲氨蝶呤(MTX)会影响叶酸代谢,因此MTX治疗可导致平均红细胞体积(MCV)改变,这可能会影响红细胞分布宽度(RDW),因为MCV水平会纳入RDW计算。因此,我们质疑如之前报道的,RDW水平及其在类风湿关节炎(RA)患者中的诊断效用是否受到正在进行的MTX治疗的影响。我们评估了改善病情抗风湿药(DMARD)治疗,尤其是MTX,对RDW的影响,并评估了它们对类风湿关节炎(RA)患者心血管(CV)事件的RDW预测价值的影响。据我们所知,这是第一项评估MTX对RDW影响的研究。
对在我们诊所发病时和最后一次随访时的385例RA患者的药物治疗、疾病活动度、实验室参数和CV事件病史进行回顾性分析。此外,对于发生CV事件的患者,在CV事件前的最后一次随访时记录数据。
与严重血管事件相关的疾病参数和实验室检查结果包括年龄较大(<0.001)、病程较长(=0.002)以及诊断时RDW较高(=0.025)。除MTX外,其他任何治疗方案的RDW水平均无明显差异。与未使用该药物的受试者相比,接受MTX治疗的患者的RDW显著更高(<0.001)。在未接受MTX治疗的RA患者中,我们发现发生CV事件与未发生CV事件的患者之间RDW水平存在显著差异,而在接受MTX治疗的受试者中这种差异消失。
MTX会影响RDW,因此可能会降低其对接受MTX治疗患者CV事件的预后价值,而诊断时RDW升高仍然是RA患者心肌梗死和中风的早期风险预测指标。