Prolonged QTc interval predicts all-cause mortality in patients with rheumatoid arthritis: an association driven by high inflammatory burden

被引:62
作者
Panoulas, Vasileios F. [1 ,2 ]
Toms, Tracey E. [2 ]
Douglas, Karen M. J. [2 ]
Sandoo, Aamer [2 ]
Metsios, George S. [2 ]
Stavropoulos-Kalinoglou, Antonios [2 ]
Kitas, George D. [2 ,3 ]
机构
[1] Imperial Coll Healthcare NHS Trust, Hammersmith Hosp, Dept Cardiol, London W12 0HS, England
[2] Dudley Grp NHS Fdn Trust, Dept Rheumatol, Russells Hall Hosp, Dudley, W Midlands, England
[3] Univ Manchester, Arthrit Res UK Epidemiol Unit, Manchester, Lancs, England
关键词
QTc; prolongation; rheumatoid arthritis; death; sudden cardiac; mortality; C-REACTIVE PROTEIN; SUDDEN CARDIAC DEATH; DIABETES-MELLITUS; POPULATION; DISEASE; COHORT; PREVALENCE; RISK;
D O I
10.1093/rheumatology/ket338
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. RA associates with an increased rate of sudden cardiac death (SCD). A prolonged QTc interval has been associated with arrhythmogenic and SCD in patients with long QT syndrome. Despite the previously reported contemporary association of CRP with SCD, thus far no studies have examined the association of QTc with mortality in RA, a condition characterized by high inflammatory burden. The aim of this study was to examine the role of electrocardiography (QT corrected interval) in predicting all-cause mortality in patients with RA who have an increased rate of SCD and a high inflammatory burden. Methods. Three hundred and fifty-seven RA patients with detailed baseline clinical characterization and 12-lead ECGs were followed up for a mean of 73.0 (s.d. 18.3) months. Linear and Cox regression analyses were used to identify variables that associate with QTc and examine its association with all-cause mortality. Results. The patients' mean age was 60.6 (s.d. 12.0) years, 267 (74.8%) were females and 54 (15.1%) died during the follow-up period. Age (beta = 0.231, P < 0.001), gender (beta = 0.137, P = 0.008) and CRP (beta = 0.144, P = 0.006) associated independently with QTc in RA patients. The crude hazard ratio (HR) for total mortality per 50-ms increase in QTc was 2.17 (95% CI 1.21, 3.90). This association remained significant [HR = 2.18 (95% CI 1.09, 4.35)] after adjustment for identified confounders (cardiovascular and RA specific), but was lost [HR = 1.73 (95% CI 0.83, 3.62)] when CRP was included in the model. Conclusion. A 50-ms increase in QTc interval associates with a doubling of the hazard for all-cause mortality in patients with RA. The observed contemporary association of QTc with CRP levels indicates a potentially hazardous interplay between inflammation and arrhythmogenesis. Future studies are needed to confirm the above findings and explore underlying mechanisms.
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收藏
页码:131 / 137
页数:7
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