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Atrophy of the parahippocampal gyrus is prominent in heart failure patients without dementia

AIMS: The exacerbation of heart failure (HF) induces brain damage and cognitive impairment (CI), which frequently attenuates the effects of treatment. However, it is not clear whether HF patients without clinical dementia demonstrate increased risk of CI. We examined whether local atrophy in the par...

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Autores principales: Meguro, Tomomi, Meguro, Yuko, Kunieda, Takeyoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5695180/
https://www.ncbi.nlm.nih.gov/pubmed/28925598
http://dx.doi.org/10.1002/ehf2.12192
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author Meguro, Tomomi
Meguro, Yuko
Kunieda, Takeyoshi
author_facet Meguro, Tomomi
Meguro, Yuko
Kunieda, Takeyoshi
author_sort Meguro, Tomomi
collection PubMed
description AIMS: The exacerbation of heart failure (HF) induces brain damage and cognitive impairment (CI), which frequently attenuates the effects of treatment. However, it is not clear whether HF patients without clinical dementia demonstrate increased risk of CI. We examined whether local atrophy in the parahippocampal gyrus, a potential predictor of CI, is prominent in HF patients without clinical dementia. METHODS AND RESULTS: Twenty stable HF patients with a history of admission due to decompensated HF or presentation of apparent pulmonary congestion following chest X‐ray and 17 controls were enrolled in this observational, analytical, cross‐sectional, case‐control study. Patients with dementia were excluded from this study based on the results of cognitive assessment. Three‐dimensional T1 weighted magnetic resonance image analysis was performed to evaluate the severity of local brain atrophy using software based on statistical parametric mapping. Z‐score values were calculated to evaluate the severity of atrophy in the total brain and parahippocampal gyrus. The severity of total brain atrophy was similar between HF patients (8.0 ± 2.9%) and controls (6.5 ± 3.1%). However, the Z‐score was significantly higher in the HF group (1.12 ± 0.49) in comparison with the control group (0.63 ± 0.36, P = 0.002). The Z‐score value did not correlate with age, ejection fraction, left atrial dimension, left ventricular dimensions, or brain natriuretic peptides in the HF group but did correlate with the Clinical Frailty Scale. CONCLUSIONS: Local atrophy in the parahippocampal gyrus was prominent in HF patients without clinical dementia. This finding showed that HF patients without dementia feature a potential risk for developing CI.
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spelling pubmed-56951802018-02-14 Atrophy of the parahippocampal gyrus is prominent in heart failure patients without dementia Meguro, Tomomi Meguro, Yuko Kunieda, Takeyoshi ESC Heart Fail Original Research Articles AIMS: The exacerbation of heart failure (HF) induces brain damage and cognitive impairment (CI), which frequently attenuates the effects of treatment. However, it is not clear whether HF patients without clinical dementia demonstrate increased risk of CI. We examined whether local atrophy in the parahippocampal gyrus, a potential predictor of CI, is prominent in HF patients without clinical dementia. METHODS AND RESULTS: Twenty stable HF patients with a history of admission due to decompensated HF or presentation of apparent pulmonary congestion following chest X‐ray and 17 controls were enrolled in this observational, analytical, cross‐sectional, case‐control study. Patients with dementia were excluded from this study based on the results of cognitive assessment. Three‐dimensional T1 weighted magnetic resonance image analysis was performed to evaluate the severity of local brain atrophy using software based on statistical parametric mapping. Z‐score values were calculated to evaluate the severity of atrophy in the total brain and parahippocampal gyrus. The severity of total brain atrophy was similar between HF patients (8.0 ± 2.9%) and controls (6.5 ± 3.1%). However, the Z‐score was significantly higher in the HF group (1.12 ± 0.49) in comparison with the control group (0.63 ± 0.36, P = 0.002). The Z‐score value did not correlate with age, ejection fraction, left atrial dimension, left ventricular dimensions, or brain natriuretic peptides in the HF group but did correlate with the Clinical Frailty Scale. CONCLUSIONS: Local atrophy in the parahippocampal gyrus was prominent in HF patients without clinical dementia. This finding showed that HF patients without dementia feature a potential risk for developing CI. John Wiley and Sons Inc. 2017-07-17 /pmc/articles/PMC5695180/ /pubmed/28925598 http://dx.doi.org/10.1002/ehf2.12192 Text en © 2017 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of the European Society of Cardiology. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Research Articles
Meguro, Tomomi
Meguro, Yuko
Kunieda, Takeyoshi
Atrophy of the parahippocampal gyrus is prominent in heart failure patients without dementia
title Atrophy of the parahippocampal gyrus is prominent in heart failure patients without dementia
title_full Atrophy of the parahippocampal gyrus is prominent in heart failure patients without dementia
title_fullStr Atrophy of the parahippocampal gyrus is prominent in heart failure patients without dementia
title_full_unstemmed Atrophy of the parahippocampal gyrus is prominent in heart failure patients without dementia
title_short Atrophy of the parahippocampal gyrus is prominent in heart failure patients without dementia
title_sort atrophy of the parahippocampal gyrus is prominent in heart failure patients without dementia
topic Original Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5695180/
https://www.ncbi.nlm.nih.gov/pubmed/28925598
http://dx.doi.org/10.1002/ehf2.12192
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