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Temporal changes in total and hippocampal brain volume and cognitive function in patients with chronic heart
Anna Frey1,2, György A Homola1,3, Carsten Henneges1
1Comprehensive Heart Failure Center Würzburg, University and University Hospital Würzburg, Am Schwarzenberg 15, 97078 Würzburg, Germany.
Insights
Heart failure patients with reduced hippocampal volume showed stable cognition over three years, with no accelerated brain atrophy. This suggests mild heart failure does not rapidly worsen brain health.
Area of Science:
- Neurology
- Cardiology
- Gerontology
Background:
- Chronic heart failure (HF) is linked to cognitive decline and brain changes.
- Understanding the mid-term impact of HF on brain structure and function is crucial.
Purpose of the Study:
- To quantify brain volume and cognitive function changes over three years in patients with mild stable heart failure.
- To investigate the association between hippocampal volume and cognitive performance in this cohort.
Main Methods:
- A prospective cohort study of 148 mild HF patients (mean age 64.5 years).
- Assessments included cardiological, neurological, psychological evaluations, and brain MRI over three years.
- Automated quantification of total and hippocampal brain volumes, normalized to intracranial volume.
Main Results:
- Baseline hippocampal volume was ~13% lower than expected.
- Three-year hippocampal volume loss was minimal (-1.8%), comparable to physiological aging.
- Cognitive function remained largely stable, with only 'intensity of attention' showing a decline.
- White matter hyperintensity load increased within normal aging limits.
- Cognitive performance remained associated with hippocampal volume after three years.
Conclusions:
- Mild heart failure patients with reduced baseline hippocampal volume did not exhibit accelerated brain atrophy over three years.
- Cognitive function remained stable, indicating no significant mid-term decline attributable to heart failure progression.
- These findings suggest that mild HF may not lead to rapid mid-term neurocognitive deterioration.
Aims:
We quantified the concurring dynamics affecting total and hippocampal brain volume and cognitive function in patients with chronic heart failure (HF) over a period of three years.
Methods And Results:
A total of 148 patients with mild stable HF entered this monocentric prospective cohort study: mean age 64.5 (10.8) years; 16.2% female; 77% in New York Heart Association functional classes I-II; 128 and 105 patients attended follow-up visits after 1 and 3 years, respectively. The assessment included cardiological, neurological, psychological work-up, and brain magnetic resonance imaging. Total and regional brain volumes were quantified using an operator-independent fully automated approach and reported normalized to the mean estimated intracranial volume. At baseline, the mean hippocampal volume was ∼13% lower than expected. However, the 3-year progressive hippocampal volume loss was small: -62 mm3 [95% confidence interval (CI) -81 to -42, P < 0.0001). This corresponded to a relative change of -1.8% (95% CI -2.3 to -1.2), which was similar in magnitude as observed with physiological aging. Moreover, the load of white matter hypointensities increased within the limits of normal aging. Cognitive function during the 3-year observation period remained stable, with 'intensity of attention' as the only domain declining (LSmean -1.82 points, 95% CI -3.05 to -0.58, P = 0.004). After 3 years, performance in all domains of cognition remained associated with hippocampal volume (r ≥ 0.29).
Conclusion:
In patients with predominantly mild HF, the markedly reduced hippocampal volume observed at baseline was associated with impaired cognitive function, but no accelerated deterioration in cognition and brain atrophy became evident over a mid-term period of three years.
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