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  1. 原著論文

Possibility of Enlargement in Left Medial Temporal Areas Against Cerebral Amyloid Deposition Observed During Preclinical Stage.

https://repo.qst.go.jp/records/86137
https://repo.qst.go.jp/records/86137
a1169d8c-b5b8-4744-b572-a0c72800af2b
Item type 学術雑誌論文 / Journal Article(1)
公開日 2022-05-16
タイトル
タイトル Possibility of Enlargement in Left Medial Temporal Areas Against Cerebral Amyloid Deposition Observed During Preclinical Stage.
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
アクセス権
アクセス権 metadata only access
アクセス権URI http://purl.org/coar/access_right/c_14cb
著者 Imabayashi, Etsuko

× Imabayashi, Etsuko

WEKO 1071237

Imabayashi, Etsuko

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Ishii, Kenji

× Ishii, Kenji

WEKO 1071238

Ishii, Kenji

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Toyohara, Jun

× Toyohara, Jun

WEKO 1071239

Toyohara, Jun

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Wagatsuma, Kei

× Wagatsuma, Kei

WEKO 1071240

Wagatsuma, Kei

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Sakata, Muneyuki

× Sakata, Muneyuki

WEKO 1071241

Sakata, Muneyuki

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Tago, Tetsuro

× Tago, Tetsuro

WEKO 1071242

Tago, Tetsuro

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Ishibashi, Kenji

× Ishibashi, Kenji

WEKO 1071243

Ishibashi, Kenji

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Kojima, Narumi

× Kojima, Narumi

WEKO 1071244

Kojima, Narumi

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Kohda, Noriyuki

× Kohda, Noriyuki

WEKO 1071245

Kohda, Noriyuki

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M Tokumaru, Aya

× M Tokumaru, Aya

WEKO 1071246

M Tokumaru, Aya

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Kim, Hunkyung

× Kim, Hunkyung

WEKO 1071247

Kim, Hunkyung

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Etsuko, Imabayashi

× Etsuko, Imabayashi

WEKO 1071248

en Etsuko, Imabayashi

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Jun, Toyohara

× Jun, Toyohara

WEKO 1071249

en Jun, Toyohara

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Tetsuro, Tago

× Tetsuro, Tago

WEKO 1071250

en Tetsuro, Tago

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抄録
内容記述タイプ Abstract
内容記述 Neurodegenerative changes in the preclinical stage of Alzheimer's disease (AD) have recently been the focus of attention because they may present a range of treatment opportunities. A total of 134 elderly volunteers who lived in a local community were investigated and grouped into preclinical and mild cognitive impairment stages according to the Clinical Dementia Rating test; we also estimated amyloid deposition in the brain using positron emission tomography (PET). A significant interaction between clinical stage and amyloid PET positivity on cerebral atrophy was observed in the bilateral parietal lobe, parahippocampal gyri, hippocampus, fusiform gyrus, and right superior and middle temporal gyri, as previously reported. Early AD-specific voxel of interest (VOI) analysis was also applied and averaged Z-scores in the right, left, bilateral, and right minus left medial temporal early AD specific area were computed. We defined these averaged Z-scores in the right, left, bilateral, and right minus left early AD specific VOI in medial temporal area as R-MedT-Atrophy-score, L-MedT-Atrophy-score, Bil-MedT-Atrophy-score, and R_L-MedT-Atrophy-score, respectively. It revealed that the R_L-MedT-Atrophy-scores were significantly larger in the amyloid-positive than in the amyloid-negative cognitively normal (CN) elderly group, that is, the right medial temporal areas were smaller than left in amyloid positive CN group and these left-right differences were significantly larger in amyloid positive than amyloid negative CN elderly group. The L-MedT-Atrophy-score was slightly larger ( = 0.073), that is, the left medial temporal area was smaller in the amyloid-negative CN group than in the amyloid-positive CN group. Conclusively, the left medial temporal area could be larger in CN participants with amyloid deposition than in those without amyloid deposition. The area under the receiver operating characteristic curve for differentiating amyloid positivity among CN participants using the R_L-MedT-Atrophy-scores was 0.73; the sensitivity and specificity were 0.828 and 0.606, respectively. Although not significant, a negative correlation was observed between the composite cerebral standardized uptake value ratio in amyloid PET images and L-MedT-Atrophy-score in CN group. The left medial temporal volume might become enlarged because of compensatory effects against AD pathology occurring at the beginning of the amyloid deposition.
書誌情報 Frontiers in aging neuroscience

巻 14, p. 847094, 発行日 2022-04
ISSN
収録物識別子タイプ ISSN
収録物識別子 1663-4365
PubMed番号
識別子タイプ PMID
関連識別子 35517046
DOI
識別子タイプ DOI
関連識別子 10.3389/fnagi.2022.847094
関連サイト
識別子タイプ DOI
関連識別子 https://doi.org/10.3389/fnagi.2022.847094
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