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Correlation of hippocampal atrophy with hyperhomocysteinemia in hemodialysis patients: An exploratory pilot study

BACKGROUND: Cognitive impairment is one of the important critical issues in hemodialysis (HD) patients. However, the associating factors of brain atrophy in HD patients have not been fully elucidated. PURPOSE AND METHODS: Brain magnetic resonance imaging (MRI) was performed in 34 of total 72 HD outp...

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Autores principales: Maesato, Kyoko, Ohtake, Takayasu, Mochida, Yasuhiro, Ishioka, Kunihiro, Oka, Machiko, Moriya, Hidekazu, Hidaka, Sumi, Kobayashi, Shuzo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5386238/
https://www.ncbi.nlm.nih.gov/pubmed/28394902
http://dx.doi.org/10.1371/journal.pone.0175102
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author Maesato, Kyoko
Ohtake, Takayasu
Mochida, Yasuhiro
Ishioka, Kunihiro
Oka, Machiko
Moriya, Hidekazu
Hidaka, Sumi
Kobayashi, Shuzo
author_facet Maesato, Kyoko
Ohtake, Takayasu
Mochida, Yasuhiro
Ishioka, Kunihiro
Oka, Machiko
Moriya, Hidekazu
Hidaka, Sumi
Kobayashi, Shuzo
author_sort Maesato, Kyoko
collection PubMed
description BACKGROUND: Cognitive impairment is one of the important critical issues in hemodialysis (HD) patients. However, the associating factors of brain atrophy in HD patients have not been fully elucidated. PURPOSE AND METHODS: Brain magnetic resonance imaging (MRI) was performed in 34 of total 72 HD outpatients in our dialysis center. These MRI images were analyzed by an application software; Voxel-based Specific Regional Analysis System for Alzheimer’s Disease (VSRAD). VSRAD quantitatively calculates the extent of brain atrophy (percent of volume reduction) comparing with a MRI imaging database of 80 age-matched healthy controls. The extent of both hippocampal and whole-brain atrophy was evaluated with possible contributing factors. RESULTS: In all patients, the mean extent of hippocampal atrophy was 27.3%, and the mean extent of whole-brain atrophy was 11.2%. The extent of hippocampal atrophy was significantly correlated with low body mass index (BMI), total serum homocysteine (tHcy) levels, and brachial-ankle pulse wave velocity (baPWV). The extent of whole-brain atrophy showed significant correlations with age, hypoalbuminemia, and baPWV. Based on the multiple regression analysis, tHcy was an independent determinant of hippocampal atrophy (β = 0.460, R(2) = 0.189, P<0.01); while age was an independent determinant of whole-brain atrophy (β = 0.594, R(2) = 0.333, P<0.01). CONCLUSIONS: In this exploratory pilot study, hippocampal atrophy was significantly correlated with hyperhomocysteinemia in HD patients.
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spelling pubmed-53862382017-05-03 Correlation of hippocampal atrophy with hyperhomocysteinemia in hemodialysis patients: An exploratory pilot study Maesato, Kyoko Ohtake, Takayasu Mochida, Yasuhiro Ishioka, Kunihiro Oka, Machiko Moriya, Hidekazu Hidaka, Sumi Kobayashi, Shuzo PLoS One Research Article BACKGROUND: Cognitive impairment is one of the important critical issues in hemodialysis (HD) patients. However, the associating factors of brain atrophy in HD patients have not been fully elucidated. PURPOSE AND METHODS: Brain magnetic resonance imaging (MRI) was performed in 34 of total 72 HD outpatients in our dialysis center. These MRI images were analyzed by an application software; Voxel-based Specific Regional Analysis System for Alzheimer’s Disease (VSRAD). VSRAD quantitatively calculates the extent of brain atrophy (percent of volume reduction) comparing with a MRI imaging database of 80 age-matched healthy controls. The extent of both hippocampal and whole-brain atrophy was evaluated with possible contributing factors. RESULTS: In all patients, the mean extent of hippocampal atrophy was 27.3%, and the mean extent of whole-brain atrophy was 11.2%. The extent of hippocampal atrophy was significantly correlated with low body mass index (BMI), total serum homocysteine (tHcy) levels, and brachial-ankle pulse wave velocity (baPWV). The extent of whole-brain atrophy showed significant correlations with age, hypoalbuminemia, and baPWV. Based on the multiple regression analysis, tHcy was an independent determinant of hippocampal atrophy (β = 0.460, R(2) = 0.189, P<0.01); while age was an independent determinant of whole-brain atrophy (β = 0.594, R(2) = 0.333, P<0.01). CONCLUSIONS: In this exploratory pilot study, hippocampal atrophy was significantly correlated with hyperhomocysteinemia in HD patients. Public Library of Science 2017-04-10 /pmc/articles/PMC5386238/ /pubmed/28394902 http://dx.doi.org/10.1371/journal.pone.0175102 Text en © 2017 Maesato et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Maesato, Kyoko
Ohtake, Takayasu
Mochida, Yasuhiro
Ishioka, Kunihiro
Oka, Machiko
Moriya, Hidekazu
Hidaka, Sumi
Kobayashi, Shuzo
Correlation of hippocampal atrophy with hyperhomocysteinemia in hemodialysis patients: An exploratory pilot study
title Correlation of hippocampal atrophy with hyperhomocysteinemia in hemodialysis patients: An exploratory pilot study
title_full Correlation of hippocampal atrophy with hyperhomocysteinemia in hemodialysis patients: An exploratory pilot study
title_fullStr Correlation of hippocampal atrophy with hyperhomocysteinemia in hemodialysis patients: An exploratory pilot study
title_full_unstemmed Correlation of hippocampal atrophy with hyperhomocysteinemia in hemodialysis patients: An exploratory pilot study
title_short Correlation of hippocampal atrophy with hyperhomocysteinemia in hemodialysis patients: An exploratory pilot study
title_sort correlation of hippocampal atrophy with hyperhomocysteinemia in hemodialysis patients: an exploratory pilot study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5386238/
https://www.ncbi.nlm.nih.gov/pubmed/28394902
http://dx.doi.org/10.1371/journal.pone.0175102
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