Key result
Deep terminal P-wave negativity in V1 is linked to ~63% greater stroke risk.
Why the study?
The study aimed to determine the association between deep terminal negativity of the P-wave in V1 (DTNPV1), a simpler P-wave index, and the risk of stroke.
Does deep terminal negativity of the P-wave in V1 (DTNPV1) associate with an increased risk of stroke in the general population?
Cross-Sectional (n=7,732)
Yes
Does deep terminal negativity of the P-wave in V1 (DTNPV1) associate with an increased risk of stroke in the general population?
Deep terminal negativity of the P-wave in V1 is an easily measurable ECG marker associated with an increased prevalence of stroke, independent of traditional cardiovascular risk factors.
Answers are grounded in this paper and cite their sources.
DTNPV1 on routine ECG may flag higher stroke risk; hypothesis-generating and should not yet change practice.
BACKGROUND: Deep terminal negativity of the P-wave in V1 (DTNPV1) was considered if the absolute value of the depth of the negative phase was >100 μV in the presence of a biphasic P-wave in V1. In this study, we aimed to determine the association between DTNPV1, a simpler P-wave index, and the risk of stroke. METHODS: We compared P-wave indices between participants with and without a self-reported history of stroke in the United States Third National Health and Nutrition Examination Survey (NHANES III). The association between DTNPV1 and stroke was quantified with logistic regression models. RESULTS: In total, 7732 participants were included (307 with a history of stroke). Patients with stroke had deeper terminal negativity of the P-wave in V1 (52.3 ± 33.9 μV vs. 41.4 ± 27.0 μV, p < .001). After adjustment, DTNPV1 was associated with an increased risk of stroke (OR: 1.63, 95% CI: 1.03-2.60, p = .038). This association appeared to be stronger in people aged <75 years (interaction p = .023), and in those without heart failure (interaction p = .018) or ischemic heart disease (interaction p = .014). In contrast to the participants with 0 or ≥2 risk factors, in those with 1 risk factor, stroke prevalence was significantly different among the three categories of terminal negativity of the P-wave (0 μV, >0 μV but ≤100 μV and > 100 μV) in V1 (2.8%, 3.3%, and 10.3%, respectively, p = .005). CONCLUSION: In NHANES III, DTNPV1 was associated with a higher prevalence of stroke, suggesting that DTNPV1 might be a convenient marker to distinguish the risk of stroke.
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Shen et al. (2022) conducted a cross-sectional in Stroke (n=7,732). Deep terminal negativity of the P-wave in V1 (DTNPV1) vs. No DTNPV1 was evaluated on Prevalence of stroke (OR 1.63, 95% CI 1.03-2.60, p=0.038). Deep terminal negativity of the P-wave in V1 (DTNPV1) was associated with a significantly increased risk of stroke (OR 1.63) compared to individuals without DTNPV1.
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