Key result
Abnormal P-wave terminal force in V1 is linked to ~41% higher odds of cortical infarcts.
Why the study?
Abnormal P-wave parameters are linked to incident dementia independent of AF and ischemic stroke, but the underlying mechanisms remain unclear.
Are abnormal P-wave parameters associated with brain MRI correlates of vascular brain injury in a community-based cohort?
Cross-Sectional (n=1,715)
Yes
Are abnormal P-wave parameters associated with brain MRI correlates of vascular brain injury in a community-based cohort?
Odds Ratio: 1.41 (95% CI 1.14–1.74)
Abnormal P-wave parameters on ECG are associated with subclinical brain infarcts and microhemorrhages on MRI, suggesting a mechanism for the link between atrial myopathy and dementia.
BACKGROUND: Recent evidence indicates that abnormal P-wave parameters (PWPs)-ECG markers of atrial myopathy-are associated with incident dementia, independent of atrial fibrillation (AF) and clinical ischemic stroke. However, the mechanisms remain unclear and may include subclinical vascular brain injury. Hence, we evaluated the association of abnormal PWPs with brain MRI correlates of vascular brain injury in the Atherosclerosis Risk in Communities Neurocognitive Study (ARIC-NCS). METHODS: ARIC-NCS participants who underwent 3T brain MRI scans in 2011-2013 were included. PWPs were measured from standard 12-lead ECGs. Brain MRI outcomes included cortical infarcts, lacunar infarcts, cerebral microhemorrhages, brain volumes, and white matter disease (WMD) volume. We used weighted multivariable logistic and linear regression to evaluate the associations of abnormal PWPs with brain MRI outcomes. RESULTS: Among 1715 participants (mean age, 76.1 years; 61% women; 29% Black), 797 (46%) had ≥1 abnormal PWP. After multivariable adjustment, including adjusting for prevalent AF, abnormal P-wave terminal force in lead V1 (aPTFV1) and prolonged P-wave duration (PPWD) were associated with increased odds of both cortical (OR 1.41; 95% CI, 1.14 to 1.74 and OR 1.30; 95% CI, 1.04 to 1.63, respectively) and lacunar infarcts (OR 1.36; 95% CI, 1.15 to 1.63 and OR 1.37; 95% CI, 1.15 to 1.65, respectively). Advanced interatrial block (aIAB) was associated with higher odds of subcortical microhemorrhage (OR 2.04; 95% CI, 1.36 to 3.06). Other than a significant association between aPTFV1 with lower parietal lobe volume, there were no other significant associations with brain or WMD volume. CONCLUSION: In this exploratory analysis of a US community-based cohort, ECG surrogates of atrial myopathy are associated with a higher prevalence of brain infarcts and microhemorrhage, suggesting subclinical vascular brain injury as a possible mechanism underlying the association of atrial myopathy with dementia.
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Reyes et al. (2023) conducted a cross-sectional in Subclinical vascular brain injury (n=1,715). Abnormal P-wave parameters (aPTFV1, PPWD, aPWA, aIAB) vs. Normal P-wave parameters was evaluated on Cortical infarcts on brain MRI associated with abnormal P-wave terminal force in lead V1 (aPTFV1) (OR 1.41, 95% CI 1.14 to 1.74). Abnormal P-wave terminal force in lead V1 was associated with increased odds of cortical infarcts (OR 1.41) and lacunar infarcts (OR 1.36) on brain MRI.
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