PLoS ONE (Jan 2020)

Neurocognitive dysfunction and brain FDG-PET/CT findings in HIV-infected hemophilia patients and HIV-infected non-hemophilia patients.

  • Koubun Imai,
  • Sota Kimura,
  • Yoko Kiryu,
  • Aki Watanabe,
  • Ei Kinai,
  • Shinichi Oka,
  • Yoshimi Kikuchi,
  • Satoshi Kimura,
  • Mikiko Ogata,
  • Misao Takano,
  • Ryogo Minamimoto,
  • Masatoshi Hotta,
  • Kota Yokoyama,
  • Tomoyuki Noguchi,
  • Kensuke Komatsu

DOI
https://doi.org/10.1371/journal.pone.0230292
Journal volume & issue
Vol. 15, no. 3
p. e0230292

Abstract

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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.