Effects of Atrial Fibrillation Screening According to N-Terminal Pro-B-Type Natriuretic Peptide: A Secondary Analysis of the Randomized LOOP Study

被引:20
|
作者
Xing, Lucas Yixi [1 ,3 ]
Diederichsen, Soren Zoga [1 ,4 ]
Hojberg, Soren [4 ]
Krieger, Derk W. [5 ,6 ]
Graff, Claus [7 ]
Frikke-Schmidt, Ruth [2 ,8 ]
Olesen, Morten S. [1 ,9 ]
Brandes, Axel [10 ,11 ,12 ]
Kober, Lars [1 ,8 ]
Haugan, Ketil Jorgen [3 ]
Svendsen, Jesper Hastrup [1 ,8 ]
机构
[1] Copenhagen Univ Hosp Rigshosp, Dept Cardiol, Inge Lehmanns Vej 7, DK-2100 Copenhagen, Denmark
[2] Copenhagen Univ Hosp Rigshosp, Dept Clin Biochem, Copenhagen, Denmark
[3] Zealand Univ Hosp Roskilde, Dept Cardiol, Roskilde, Denmark
[4] Copenhagen Univ Hosp Bispebjerg, Dept Cardiol, Copenhagen, Denmark
[5] Mediclin City Hosp, Dept Neurol, Dubai, U Arab Emirates
[6] Mohammed Bin Rashid Univ Med & Hlth Sci, Dept Neurosci, Dubai, U Arab Emirates
[7] Aalborg Univ, Dept Hlth Sci & Technol, Aalborg, Denmark
[8] Univ Copenhagen, Fac Hlth & Med Sci, Dept Clin Med, Copenhagen, Denmark
[9] Univ Copenhagen, Fac Hlth & Med Sci, Biomed Sci, Copenhagen, Denmark
[10] Univ Southern Denmark, Fac Hlth Sci, Dept Clin Res, Odense, Denmark
[11] Univ Hosp Southern Denmark, Esbjerg Hosp, Dept Cardiol, Odense, Denmark
[12] Odense Univ Hosp, Dept Cardiol, Odense, Denmark
关键词
atrial fibrillation; mass screening; natriuretic peptide; ~brain; stroke; BLOOD-PRESSURE; STROKE; RISK; PREVENTION; BIOMARKERS; AGE;
D O I
10.1161/CIRCULATIONAHA.123.064361
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background:Research suggests NT-proBNP (N-terminal pro-B-type natriuretic peptide) to be a strong predictor of incident atrial fibrillation (AF) and stroke. However, its utility in AF screening remains unknown. The aim of this study was to investigate NT-proBNP as a potential marker for screening efficacy with respect to AF yield and stroke prevention. Methods:In the LOOP Study (Atrial Fibrillation Detected by Continuous ECG Monitoring Using Implantable Loop Recorder to Prevent Stroke in High-Risk Individuals), 6004 AF-naive individuals at least 70 years old and with additional stroke risk factors were randomized 1:3 to either screening with an implantable loop recorder (ILR) and initiation of anticoagulation upon detection of AF episodes lasting >= 6 minutes or usual care (control). This post hoc analysis included study participants with available NT-proBNP measurement at baseline. Results:A total of 5819 participants (96.9% of the trial population) were included. The mean age was 74.7 years (SD, 4.1 years) and 47.5% were female. The median NT-proBNP level was 15 pmol/L (interquartile range, 9-28 pmol/L) corresponding to 125 pg/mL (interquartile range, 76-233 pg/mL). NT-proBNP above median was associated with an increased risk of AF diagnosis both in the ILR group (hazard ratio, 1.84 [95% CI, 1.51-2.25]) and the control group (hazard ratio, 2.79 [95% CI, 2.30-3.40]). Participants with NT-proBNP above the median were also at higher risk of clinical events compared with those having lower levels (hazard ratio, 1.21 [95% CI, 0.96-1.54] for stroke or systemic embolism [SE], 1.60 [95% CI, 1.32-1.95] for stroke/SE/cardiovascular death, and 1.91 [95% CI, 1.61-2.26] for all-cause death). Compared with usual care, ILR screening was associated with significant reductions in stroke/SE and stroke/SE/cardiovascular death among participants with NT-proBNP above median (hazard ratio, 0.60 [95% CI, 0.40-0.90] and 0.70 [95% CI, 0.53-0.94], respectively) but not among those with lower levels (P-interaction=0.029 for stroke/SE and 0.045 for stroke/SE/cardiovascular death). No risk reduction in all-cause death was observed in either NT-proBNP subgroup for ILR versus control (P-interaction=0.68). Analyzing NT-proBNP as a continuous variable yielded similar findings. Conclusions:In an older population with additional stroke risk factors, ILR screening for AF was associated with a significant reduction in stroke risk among individuals with higher NT-proBNP levels but not among those with lower levels. These findings should be considered hypothesis generating and warrant further study before clinical implementation.
引用
收藏
页码:1788 / 1797
页数:10
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