論文

査読有り 国際誌
2020年10月22日

Age-related white matter changes revealed by a whole-brain fiber-tracking method in bipolar disorder compared to major depressive disorder and healthy controls.

Psychiatry and clinical neurosciences
  • Yoshikazu Masuda
  • Go Okada
  • Masahiro Takamura
  • Chiyo Shibasaki
  • Atsuo Yoshino
  • Satoshi Yokoyama
  • Naho Ichikawa
  • Shiho Okuhata
  • Tetsuo Kobayashi
  • Shigeto Yamawaki
  • Yasumasa Okamoto
  • 全て表示

75
2
開始ページ
46
終了ページ
56
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1111/pcn.13166

AIM: Several studies have reported altered age-associated changes in white matter integrity in bipolar disorder (BD). However, little is known as to whether these age-related changes are illness-specific. We assessed disease-specific effects by controlling for age and investigated age-associated changes and Group × Age interactions in white matter integrity among major depressive disorder (MDD) patients, BD patients, and healthy controls. METHODS: Healthy controls (n = 96; age range, 20-77 years), MDD patients (n = 101; age range, 25-78 years), and BD patients (n = 58; age range, 22-76 years) participated in this study. Fractional anisotropy (FA) derived from diffusion tensor imaging in 54 white matter tracts were compared after controlling for the linear and quadratic effect of age using a generalized linear model. Age-related effects and Age × Group interactions were also assessed in the model. RESULTS: The main effect of group was significant in the left column and body of the fornix after controlling for both linear and quadratic effects of age, and in the left body of the corpus callosum after controlling for the quadratic effect of age. BD patients exhibited significantly lower FA relative to other groups. There was no Age × Group interaction in the tracts. CONCLUSION: Significant FA reductions were found in BD patients after controlling for age, indicating that abnormal white matter integrity in BD may occur at a younger age rather than developing progressively with age.

リンク情報
DOI
https://doi.org/10.1111/pcn.13166
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/33090632
PubMed Central
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7894167
ID情報
  • DOI : 10.1111/pcn.13166
  • PubMed ID : 33090632
  • PubMed Central 記事ID : PMC7894167

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