Salt Lake City VA Medical Center and University of Utah, Salt Lake City, UT.
Perelman School of Medicine and.
J Clin Rheumatol. 2018 Jun;24(4):203-209. doi: 10.1097/RHU.0000000000000736.
This study reports the effect of disease-modifying therapies for rheumatoid arthritis (RA) on systolic and diastolic blood pressure (SBP, DBP) over 6 months and incident hypertension over 3 years in a large administrative database.
We used administrative Veterans Affairs databases to define unique dispensing episodes of methotrexate, leflunomide, sulfasalazine, hydroxychloroquine, tumor necrosis factor inhibitors, and prednisone among patients with RA. Changes in SBP and DBP in the 6 months before disease-modifying antirheumatic drug initiation were compared with changes observed in the 6 months after initiation. The risk of incident hypertension within 3 years (new diagnosis code for hypertension and prescription for antihypertensive) was also assessed. Multivariable models and propensity analyses assessed the impact of confounding by indication.
A total of 37,900 treatment courses in 21,216 unique patients contributed data. Overall, there were no changes in SBP or DBP in 6 months prior to disease-modifying antirheumatic drug initiation (all P > 0.62). In contrast, there was a decline in SBP (β = -1.08 [-1.32 to -0.85]; P < 0.0001) and DBP (β = -0.48 [-0.62 to -0.33]; P < 0.0001) over the 6 months following initiation. The greatest decline was observed among methotrexate and hydroxychloroquine users. Methotrexate users were 9% more likely to have optimal blood pressure (BP) after 6 months of treatment. Patients treated with leflunomide had increases in BP and a greater risk of incident hypertension compared with patients treated with methotrexate (hazard ratio, 1.53 [1.21-1.91]; P < 0.001).
Blood pressure may improve with treatment of RA, particularly with methotrexate or hydroxychloroquine. Leflunomide use, in contrast, is associated with increases in BP and a greater risk of incident hypertension.
本研究报告了改变类风湿关节炎(RA)疾病的治疗方法对 6 个月内收缩压和舒张压(SBP、DBP)的影响,并在大型行政数据库中报告了 3 年内新发高血压的情况。
我们使用行政退伍军人事务部数据库来定义 RA 患者甲氨蝶呤、来氟米特、柳氮磺胺吡啶、羟氯喹、肿瘤坏死因子抑制剂和泼尼松的独特配药事件。在开始使用疾病修饰抗风湿药物之前的 6 个月内 SBP 和 DBP 的变化与开始后的 6 个月内观察到的变化进行了比较。还评估了 3 年内新发高血压的风险(高血压新诊断代码和抗高血压药物处方)。多变量模型和倾向分析评估了指示性混杂的影响。
共有 37900 个疗程,涉及 21216 个独特患者,提供了数据。总体而言,在开始使用疾病修饰抗风湿药物之前的 6 个月内,SBP 或 DBP 没有变化(均 P > 0.62)。相比之下,在开始后的 6 个月内,SBP 下降(β=-1.08[-1.32 至-0.85];P < 0.0001),DBP 下降(β=-0.48[-0.62 至-0.33];P < 0.0001)。最大的下降发生在甲氨蝶呤和羟氯喹使用者中。使用甲氨蝶呤治疗 6 个月后,有 9%的患者更有可能血压正常。与甲氨蝶呤治疗的患者相比,使用来氟米特治疗的患者血压升高,新发高血压的风险更高(风险比,1.53[1.21-1.91];P < 0.001)。
血压可能会随着 RA 的治疗而改善,特别是使用甲氨蝶呤或羟氯喹。相比之下,来氟米特的使用与血压升高和新发高血压的风险增加有关。