类风湿关节炎患者抗风湿药物治疗期间与左心室质量相关的因素:联合心脏研究

IF 2.1 Q3 PERIPHERAL VASCULAR DISEASE
Anja Linde , Eva Gerdts , Bjørg T. Fevang , Arve Ulvik , Per M. Ueland , Klaus Meyer , Ester Kringeland , Helga Midtbø
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引用次数: 0

摘要

背景:我们探讨了类风湿性关节炎(RA)患者在生物(b)或靶向合成(ts)疾病修饰抗风湿药物(DMARD)治疗期间与左心室(LV)质量指数相关的因素。方法对83例有b/ts DMARD治疗指征的RA门诊患者(55±12岁,71%为女性)在基线和平均随访22个月后进行超声心动图检查。根据指南计算左室质量,并以身高2.7为指标。结果基线时,37%的患者患有高血压,6%的患者患有糖尿病,21%的患者患有肥胖症,100%的患者使用b/ts DMARDs。在随访期间,17%的患者停止了b/tsDMARD治疗。随访期间左室质量指数保持不变(33.1±8.1 g/m2.7 vs. 33.5±7.3 g/m2.7, p = 0.57,平均变化0.3±4.9 g/m2.7)。使用bdmard的患者随访时左室质量指数较低(31.7±6.2 g/m2.7 vs 36.6±8.9 g/m2.7, p = 0.001)。在多变量线性回归分析中,随访时使用bDMARDs (β - 0.22, p = 0.03)与随访时较低的左室质量指数相关,与c反应蛋白(CRP)、年龄、性别和基线时肥胖无关。基线肥胖(β 0.39, p < 0.001)与基线和随访时较高的左室质量指数相关。基线时较高的CRP与基线时较高的左室质量指数相关(β 0.31, p = 0.001),但随访时无相关。结论在接受DMARD治疗的RA患者中,平均左室质量指数在22个月的随访期间保持稳定。肥胖是与较高左室质量指数相关的最强因素,而在整个研究期间使用bDMARD与较低的左室质量指数相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Factors associated with left ventricular mass during disease modifying antirheumatic drug therapy in patients with rheumatoid arthritis: the Joint Heart study

Factors associated with left ventricular mass during disease modifying antirheumatic drug therapy in patients with rheumatoid arthritis: the Joint Heart study

Background

We explored factors associated with left ventricular (LV) mass index during biological (b) or targeted synthetic (ts) disease modifying antirheumatic drug (DMARD) therapy in patients with rheumatoid arthritis (RA).

Methods

Eighty-three outpatients with RA (age 55 ± 12 years, 71% women) with an indication for b/ts DMARD therapy were examined with echocardiography at baseline and after a mean follow-up of 22 months. LV mass was calculated according to guidelines and indexed for height2.7.

Results

At baseline, 37% had hypertension, 6% diabetes, 21% obesity, and 100% were using b/ts DMARDs. During follow-up, 17% discontinued b/tsDMARD treatment. The LV mass index remained unchanged during follow-up (33.1 ± 8.1 g/m2.7 vs. 33.5 ± 7.3 g/m2.7, p = 0.57, mean change 0.3 ± 4.9 g/m2.7). Lower LV mass index at follow-up was observed in patients using bDMARDs at follow-up (31.7 ± 6.2 g/m2.7 vs. 36.6 ± 8.9 g/m2.7, p = 0.001). In multivariable linear regression analyses, use of bDMARDs (β −0.22, p = 0.03) at follow-up were associated with lower LV mass index at follow-up, independent of C-reactive protein (CRP), age, sex, and obesity at baseline. Obesity at baseline (β 0.39, p < 0.001) was associated with a higher LV mass index both at baseline and follow-up. Higher CRP at baseline was associated with higher LV mass index at baseline (β 0.31, p = 0.001), but not at follow-up.

Conclusion

In patients with RA on DMARD treatment, the mean LV mass index remained stable during 22 months of follow-up. Obesity was the strongest factor associated with higher LV mass index, while use of bDMARD throughout the study period was associated with lower LV mass index.
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