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Neurocognitive dysfunction and brain FDG-PET/CT findings in HIV-infected hemophilia patients and HIV-infected non-hemophilia patients
This single-institution cross-sectional study aimed to grasp the prevalence and features of neurocognitive dysfunction in HIV-infected hemophilia patients in Japan. We conducted neuropsychological tests and medical examinations in 56 HIV-infected hemophilia patients who received outpatient treatment...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7082013/ https://www.ncbi.nlm.nih.gov/pubmed/32191714 http://dx.doi.org/10.1371/journal.pone.0230292 |
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author | Imai, Koubun Kimura, Sota Kiryu, Yoko Watanabe, Aki Kinai, Ei Oka, Shinichi Kikuchi, Yoshimi Kimura, Satoshi Ogata, Mikiko Takano, Misao Minamimoto, Ryogo Hotta, Masatoshi Yokoyama, Kota Noguchi, Tomoyuki Komatsu, Kensuke |
author_facet | Imai, Koubun Kimura, Sota Kiryu, Yoko Watanabe, Aki Kinai, Ei Oka, Shinichi Kikuchi, Yoshimi Kimura, Satoshi Ogata, Mikiko Takano, Misao Minamimoto, Ryogo Hotta, Masatoshi Yokoyama, Kota Noguchi, Tomoyuki Komatsu, Kensuke |
author_sort | Imai, Koubun |
collection | PubMed |
description | This single-institution cross-sectional study aimed to grasp the prevalence and features of neurocognitive dysfunction in HIV-infected hemophilia patients in Japan. We conducted neuropsychological tests and medical examinations in 56 HIV-infected hemophilia patients who received outpatient treatment at the AIDS Clinical Center, National Center for Global Health and Medicine. A total of 388 HIV-infected non-hemophilia patients who received outpatient treatment at the same institution were included as a control group. To investigate sites responsible for neurocognitive dysfunction in HIV-infected hemophilia patients using brain FDG-PET/CT scans, the accumulation of FDG in each brain region was compared. Approximately 50% of HIV-infected hemophilia patients had neurocognitive dysfunction. The prevalence of asymptomatic neurocognitive impairment was high (34%). Neurocognitive dysfunction was associated with educational level in HIV-infected hemophilia patients. In the symptomatic group, hemophilic arthropathy and history of cerebrovascular disorders were associated with neurocognitive dysfunction. Left temporal lobe function was reduced in the symptomatic group. |
format | Online Article Text |
id | pubmed-7082013 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-70820132020-03-24 Neurocognitive dysfunction and brain FDG-PET/CT findings in HIV-infected hemophilia patients and HIV-infected non-hemophilia patients Imai, Koubun Kimura, Sota Kiryu, Yoko Watanabe, Aki Kinai, Ei Oka, Shinichi Kikuchi, Yoshimi Kimura, Satoshi Ogata, Mikiko Takano, Misao Minamimoto, Ryogo Hotta, Masatoshi Yokoyama, Kota Noguchi, Tomoyuki Komatsu, Kensuke PLoS One Research Article This single-institution cross-sectional study aimed to grasp the prevalence and features of neurocognitive dysfunction in HIV-infected hemophilia patients in Japan. We conducted neuropsychological tests and medical examinations in 56 HIV-infected hemophilia patients who received outpatient treatment at the AIDS Clinical Center, National Center for Global Health and Medicine. A total of 388 HIV-infected non-hemophilia patients who received outpatient treatment at the same institution were included as a control group. To investigate sites responsible for neurocognitive dysfunction in HIV-infected hemophilia patients using brain FDG-PET/CT scans, the accumulation of FDG in each brain region was compared. Approximately 50% of HIV-infected hemophilia patients had neurocognitive dysfunction. The prevalence of asymptomatic neurocognitive impairment was high (34%). Neurocognitive dysfunction was associated with educational level in HIV-infected hemophilia patients. In the symptomatic group, hemophilic arthropathy and history of cerebrovascular disorders were associated with neurocognitive dysfunction. Left temporal lobe function was reduced in the symptomatic group. Public Library of Science 2020-03-19 /pmc/articles/PMC7082013/ /pubmed/32191714 http://dx.doi.org/10.1371/journal.pone.0230292 Text en © 2020 Imai 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 Imai, Koubun Kimura, Sota Kiryu, Yoko Watanabe, Aki Kinai, Ei Oka, Shinichi Kikuchi, Yoshimi Kimura, Satoshi Ogata, Mikiko Takano, Misao Minamimoto, Ryogo Hotta, Masatoshi Yokoyama, Kota Noguchi, Tomoyuki Komatsu, Kensuke Neurocognitive dysfunction and brain FDG-PET/CT findings in HIV-infected hemophilia patients and HIV-infected non-hemophilia patients |
title | Neurocognitive dysfunction and brain FDG-PET/CT findings in HIV-infected hemophilia patients and HIV-infected non-hemophilia patients |
title_full | Neurocognitive dysfunction and brain FDG-PET/CT findings in HIV-infected hemophilia patients and HIV-infected non-hemophilia patients |
title_fullStr | Neurocognitive dysfunction and brain FDG-PET/CT findings in HIV-infected hemophilia patients and HIV-infected non-hemophilia patients |
title_full_unstemmed | Neurocognitive dysfunction and brain FDG-PET/CT findings in HIV-infected hemophilia patients and HIV-infected non-hemophilia patients |
title_short | Neurocognitive dysfunction and brain FDG-PET/CT findings in HIV-infected hemophilia patients and HIV-infected non-hemophilia patients |
title_sort | neurocognitive dysfunction and brain fdg-pet/ct findings in hiv-infected hemophilia patients and hiv-infected non-hemophilia patients |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7082013/ https://www.ncbi.nlm.nih.gov/pubmed/32191714 http://dx.doi.org/10.1371/journal.pone.0230292 |
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