TY - JOUR
T1 - Electrocardiographic Precordial ST‐Segment Deviations and the Risk of Cardiovascular Death
T2 - Results From the Copenhagen ECG Study
AU - Rasmussen, Peter Vibe
AU - Nielsen, Jonas Bille
AU - Pietersen, Adrian
AU - Graff, Claus
AU - Lind, Bent
AU - Struijk, Johannes Jan
AU - Olesen, Morten Salling
AU - Haunsø, Stig
AU - Køber, Lars
AU - Svendsen, Jesper Hastrup
AU - Holst, Anders Gaarsdal
PY - 2014/6
Y1 - 2014/6
N2 - Background-We sought to perform a study assessing the association between electrocardiographic ST-segment deviations and cardiovascular death (CVD), in relation to sex and age (≥ and < 65 years), in a large primary care population without overt ischemic heart disease. Methods and Results-Using computerized analysis of ECGs from 285 194 persons, we evaluated the association between precordial ST-segment deviations and the risk of CVD. All data on medication, comorbidity, and outcomes were retrieved from Danish registries. After a median follow-up period of 5.8 years, there were 6679 cardiovascular deaths. Increasing ST-depression was associated with an increased risk of CVD in almost all of the precordial leads, with the most robust association seen in lead V5 to V6. ST-elevations in lead V2 to V6 were associated with increased risk of CVD in young women, but not in men. However, STelevations in V1 increased the risk for both genders and age groups, exemplified by a HR of 1.80 (95% CI [1.19 to 2.74], P=0.005) for men < 65 years with ST-elevations ≥150 μV versus a nondeviating ST-segment (-50 μV to +50 μV). In contrast, for men < 65 years, ST-elevations in lead V2 to V3 conferred a decreased risk of CVD with a HR of 0.77 (95% CI [0.62 to 0.96], P < 0.001) for ST-elevations ≥150 μV in V2. Conclusion-We found that ST-depressions were associated with a dose-responsive increased risk of CVD in nearly all the precordial leads. ST-elevations conferred an increased risk of CVD in women and with regard to lead V1 also in men. However, STelevations in V2 to V3 were associated with a decreased risk of CVD in young men.
AB - Background-We sought to perform a study assessing the association between electrocardiographic ST-segment deviations and cardiovascular death (CVD), in relation to sex and age (≥ and < 65 years), in a large primary care population without overt ischemic heart disease. Methods and Results-Using computerized analysis of ECGs from 285 194 persons, we evaluated the association between precordial ST-segment deviations and the risk of CVD. All data on medication, comorbidity, and outcomes were retrieved from Danish registries. After a median follow-up period of 5.8 years, there were 6679 cardiovascular deaths. Increasing ST-depression was associated with an increased risk of CVD in almost all of the precordial leads, with the most robust association seen in lead V5 to V6. ST-elevations in lead V2 to V6 were associated with increased risk of CVD in young women, but not in men. However, STelevations in V1 increased the risk for both genders and age groups, exemplified by a HR of 1.80 (95% CI [1.19 to 2.74], P=0.005) for men < 65 years with ST-elevations ≥150 μV versus a nondeviating ST-segment (-50 μV to +50 μV). In contrast, for men < 65 years, ST-elevations in lead V2 to V3 conferred a decreased risk of CVD with a HR of 0.77 (95% CI [0.62 to 0.96], P < 0.001) for ST-elevations ≥150 μV in V2. Conclusion-We found that ST-depressions were associated with a dose-responsive increased risk of CVD in nearly all the precordial leads. ST-elevations conferred an increased risk of CVD in women and with regard to lead V1 also in men. However, STelevations in V2 to V3 were associated with a decreased risk of CVD in young men.
KW - Adult
KW - Age Factors
KW - Aged
KW - Aged, 80 and over
KW - Cardiovascular Diseases
KW - Denmark
KW - Electrocardiography
KW - Female
KW - Heart
KW - Humans
KW - Male
KW - Middle Aged
KW - Proportional Hazards Models
KW - Risk Factors
KW - Sex Factors
U2 - 10.1161/JAHA.113.000549
DO - 10.1161/JAHA.113.000549
M3 - Journal article
C2 - 24815495
SN - 2047-9980
VL - 3
SP - 1
EP - 16
JO - American Heart Association. Journal. Cardiovascular and Cerebrovascular Disease
JF - American Heart Association. Journal. Cardiovascular and Cerebrovascular Disease
IS - 3
M1 - e000549
ER -