Department of Rheumatology, Clinical Research Unit, Russell's Hall Hospital, Dudley Group of Hospitals NHS Foundation Trust, Dudley, West Midlands, DY1 2HQ, UK.
Rheumatol Int. 2010 Jun;30(8):1125-9. doi: 10.1007/s00296-009-1345-1. Epub 2010 Jan 12.
A number of mediators are involved in the inflammatory processes that affect joints and vascular wall of patients with rheumatoid arthritis (RA). Tumour necrosis factor alpha (TNFa) is one such mediator, and it is widely regarded as an important target for anti-rheumatic treatment. Most recent studies show that anti-TNFa medication suppresses inflammation and reduces overall activity of RA. The aim of the current study was to investigate changes of mean platelet volume (MPV) in response to the 3-month anti-TNFa therapy in RA. Twenty-one RA patients without established cardiovascular disease were recruited for anti-TNFa therapy and underwent thorough clinical and laboratory evaluation at baseline, 2 weeks, and 12 weeks. Anti-TNFa therapy resulted in a significant (p = 0.01) increase in MPV over the duration of the study (7.7 +/- 0.9, 7.8 +/- 1.1, and 8.4 +/- 1.1 fL at baseline, 2 weeks, and 12 weeks, respectively). The results of the study expand perspectives of the use of MPV in conditions associated with high-grade inflammation, particularly RA, for monitoring anti-inflammatory treatment. More prospective studies with large numbers of patients are warranted to ascertain associations of high and low values of MPV with diverse markers of inflammation and vascular pathology.
许多介质参与影响类风湿关节炎(RA)患者关节和血管壁的炎症过程。肿瘤坏死因子-α(TNFa)就是这样一种介质,它被广泛认为是抗风湿治疗的重要靶点。最近的大多数研究表明,抗 TNFa 药物可抑制炎症并降低 RA 的整体活动度。本研究旨在探讨 RA 患者接受 3 个月抗 TNFa 治疗后平均血小板体积(MPV)的变化。招募了 21 名无明确心血管疾病的 RA 患者进行抗 TNFa 治疗,并在基线、2 周和 12 周时进行了全面的临床和实验室评估。抗 TNFa 治疗在研究期间导致 MPV 显著增加(p=0.01)(分别为 7.7+/-0.9、7.8+/-1.1 和 8.4+/-1.1 fL)。该研究结果扩展了 MPV 在与高度炎症相关的情况下(特别是 RA)的应用前景,用于监测抗炎治疗。需要更多的前瞻性研究,以确定 MPV 的高低值与炎症和血管病理的各种标志物之间的关联。