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Comprehensive elucidation of resting-state functional connectivity in anorexia nervosa by a multicenter cross-sectional study.
Sudo, Yusuke; Ota, Junko; Takamura, Tsunehiko; Kamashita, Rio; Hamatani, Sayo; Numata, Noriko; Chhatkuli, Ritu Bhusal; Yoshida, Tokiko; Takahashi, Jumpei; Kitagawa, Hitomi; Matsumoto, Koji; Masuda, Yoshitada; Nakazato, Michiko; Sato, Yasuhiro; Hamamoto, Yumi; Shoji, Tomotaka; Muratsubaki, Tomohiko; Sugiura, Motoaki; Fukudo, Shin; Kawabata, Michiko; Sunada, Momo; Noda, Tomomi; Tose, Keima; Isobe, Masanori; Kodama, Naoki; Kakeda, Shingo; Takahashi, Masatoshi; Takakura, Shu; Gondo, Motoharu; Yoshihara, Kazufumi; Moriguchi, Yoshiya; Shimizu, Eiji; Sekiguchi, Atsushi; Hirano, Yoshiyuki.
Afiliação
  • Sudo Y; Research Center for Child Mental Development, Chiba University, Chiba, Japan.
  • Ota J; Department of Cognitive Behavioral Physiology, Chiba University, Chiba, Japan.
  • Takamura T; Department of Psychiatry, Chiba University Hospital, Chiba, Japan.
  • Kamashita R; Research Center for Child Mental Development, Chiba University, Chiba, Japan.
  • Hamatani S; Applied MRI Research, Department of Molecular Imaging and Theranostics, Institute for Quantum Medical Science, National Institutes for Quantum Science and Technology, Chiba, Japan.
  • Numata N; United Graduate School of Child Development, Osaka University, Kanazawa University, Hamamatsu University School of Medicine, Chiba University and University of Fukui, Suita, Japan.
  • Chhatkuli RB; Department of Behavioral Medicine, National Institute of Mental Health, National Center of Neurology and Psychiatry, Kodaira, Japan.
  • Yoshida T; Research Center for Child Mental Development, Chiba University, Chiba, Japan.
  • Takahashi J; United Graduate School of Child Development, Osaka University, Kanazawa University, Hamamatsu University School of Medicine, Chiba University and University of Fukui, Suita, Japan.
  • Kitagawa H; Research Center for Child Mental Development, Chiba University, Chiba, Japan.
  • Matsumoto K; United Graduate School of Child Development, Osaka University, Kanazawa University, Hamamatsu University School of Medicine, Chiba University and University of Fukui, Suita, Japan.
  • Masuda Y; Research Center for Child Mental Development, Fukui University, Eiheizi, Japan.
  • Nakazato M; Research Center for Child Mental Development, Chiba University, Chiba, Japan.
  • Sato Y; United Graduate School of Child Development, Osaka University, Kanazawa University, Hamamatsu University School of Medicine, Chiba University and University of Fukui, Suita, Japan.
  • Hamamoto Y; Research Center for Child Mental Development, Chiba University, Chiba, Japan.
  • Shoji T; Applied MRI Research, Department of Molecular Imaging and Theranostics, Institute for Quantum Medical Science, National Institutes for Quantum Science and Technology, Chiba, Japan.
  • Muratsubaki T; United Graduate School of Child Development, Osaka University, Kanazawa University, Hamamatsu University School of Medicine, Chiba University and University of Fukui, Suita, Japan.
  • Sugiura M; Research Center for Child Mental Development, Chiba University, Chiba, Japan.
  • Fukudo S; Department of Psychiatry, Chiba Aoba Municipal Hospital, Chiba, Japan.
  • Kawabata M; Research Center for Child Mental Development, Chiba University, Chiba, Japan.
  • Sunada M; Department of Radiology, Chiba University Hospital, Chiba, Japan.
  • Noda T; Department of Radiology, Chiba University Hospital, Chiba, Japan.
  • Tose K; Department of Psychiatry, School of Medicine, International University of Health and Welfare, Narita, Japan.
  • Isobe M; Department of Psychosomatic Medicine, Tohoku University Hospital, Sendai, Japan.
  • Kodama N; Department of Psychology, Northumbria University, Newcastle-upon-Tyne, UK.
  • Kakeda S; Department of Human Brain Science, Institute of Development, Aging, and Cancer, Tohoku University, Sendai, Japan.
  • Takahashi M; Department of Psychosomatic Medicine, Tohoku University Hospital, Sendai, Japan.
  • Takakura S; Department of Internal Medicine, Nagamachi Hospital, Sendai, Japan.
  • Gondo M; Department of Psychosomatic Medicine, Tohoku University School of Medicine, Sendai, Japan.
  • Yoshihara K; Department of Psychosomatic Medicine, Tohoku University Graduate School of Medicine, Sendai, Japan.
  • Moriguchi Y; Department of Human Brain Science, Institute of Development, Aging, and Cancer, Tohoku University, Sendai, Japan.
  • Shimizu E; Cognitive Sciences Lab, International Research Institute of Disaster Science, Tohoku University, Sendai, Japan.
  • Sekiguchi A; Department of Psychosomatic Medicine, Tohoku University Hospital, Sendai, Japan.
  • Hirano Y; Department of Psychosomatic Medicine, Tohoku University Graduate School of Medicine, Sendai, Japan.
Psychol Med ; : 1-14, 2024 Mar 19.
Article em En | MEDLINE | ID: mdl-38500410
ABSTRACT

BACKGROUND:

Previous research on the changes in resting-state functional connectivity (rsFC) in anorexia nervosa (AN) has been limited by an insufficient sample size, which reduced the reliability of the results and made it difficult to set the whole brain as regions of interest (ROIs).

METHODS:

We analyzed functional magnetic resonance imaging data from 114 female AN patients and 135 healthy controls (HC) and obtained self-reported psychological scales, including eating disorder examination questionnaire 6.0. One hundred sixty-four cortical, subcortical, cerebellar, and network parcellation regions were considered as ROIs. We calculated the ROI-to-ROI rsFCs and performed group comparisons.

RESULTS:

Compared to HC, AN patients showed 12 stronger rsFCs mainly in regions containing dorsolateral prefrontal cortex (DLPFC), and 33 weaker rsFCs primarily in regions containing cerebellum, within temporal lobe, between posterior fusiform cortex and lateral part of visual network, and between anterior cingulate cortex (ACC) and thalamus (p < 0.01, false discovery rate [FDR] correction). Comparisons between AN subtypes showed that there were stronger rsFCs between right lingual gyrus and right supracalcarine cortex and between left temporal occipital fusiform cortex and medial part of visual network in the restricting type compared to the binge/purging type (p < 0.01, FDR correction).

CONCLUSION:

Stronger rsFCs in regions containing mainly DLPFC, and weaker rsFCs in regions containing primarily cerebellum, within temporal lobe, between posterior fusiform cortex and lateral part of visual network, and between ACC and thalamus, may represent categorical diagnostic markers discriminating AN patients from HC.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Psychol Med Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Psychol Med Ano de publicação: 2024 Tipo de documento: Article