Key result
Severe orthostatic hypotension and clinically manifest OH were associated with worse cognitive functioning (β: -0.18, 95% CI -0.34 to -0.02, and β: -0.30, 95% CI -0.52 to -0.08, respectively).
Why the study?
Orthostatic hypotension is associated with dementia, but it was unclear which patterns and characteristics of orthostatic hypotension relate to cognition or structural brain injury in hemodynamically impaired patients.
Does orthostatic hypotension associate with worse cognitive functioning and structural brain injury in hemodynamically impaired patients?
Observational (n=337)
Does orthostatic hypotension associate with worse cognitive functioning and structural brain injury in hemodynamically impaired patients?
Mean Difference: -0.12 (95% CI -0.24–0)
Severe and clinically manifest orthostatic hypotension are associated with worse cognitive functioning and lower brain parenchymal fraction in hemodynamically impaired patients.
Association in cross-sectional data should not yet change practice; leaves open causality and need for longitudinal confirmation.
BACKGROUND: Orthostatic hypotension (OH) is associated with an increased risk of dementia, potentially attributable to cerebral hypoperfusion. We investigated which patterns and characteristics of OH are related to cognition or to potentially underlying structural brain injury in hemodynamically impaired patients and healthy reference participants. METHODS: Participants with carotid occlusive disease or heart failure, and reference participants from the Heart-Brain Connection Study underwent OH measurements, neuropsychological assessment and brain MRI. We analyzed the association between OH, global cognitive functioning, white matter hyperintensity (WMH) volume and brain parenchymal fraction with linear regression. We stratified by participant group, severity and duration of OH, chronotropic incompetence and presence of orthostatic symptoms. RESULTS: Of 337 participants (mean age 67.3 ± 8.8 years, 118 (35.0%) women), 113 (33.5%) had OH. Overall, presence of OH was not associated with cognitive functioning (β: -0.12 [-0.24-0.00]), but we did observe worse cognitive functioning in those with severe OH (≥ 30/15 mmHg; β: -0.18 [-0.34 to -0.02]) and clinically manifest OH (β: -0.30 [-0.52 to -0.08]). These associations did not differ significantly by OH duration or chronotropic incompetence, and were similar between patient groups and reference participants. Similarly, both severe OH and clinically manifest OH were associated with a lower brain parenchymal fraction, and severe OH also with a somewhat higher WMH volume. CONCLUSIONS: Severe OH and clinically manifest OH are associated with worse cognitive functioning. This supports the notion that specific patterns and characteristics of OH determine its impact on brain health.
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Starmans et al. (2024) conducted an observational in Hemodynamically impaired patients (carotid occlusive disease or heart failure) (n=337). Orthostatic hypotension vs. No orthostatic hypotension was evaluated on Global cognitive functioning (β -0.12, 95% CI -0.24 to 0.00). Severe orthostatic hypotension and clinically manifest OH were associated with worse cognitive functioning (β: -0.18, 95% CI -0.34 to -0.02, and β: -0.30, 95% CI -0.52 to -0.08, respectively).
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