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  1. 原著論文

Principal Component Analysis of Multimodal Neuromelanin MRI and Dopamine Transporter PET Data Provides a Specific Metric for the Nigral Dopaminergic Neuronal Density.

https://repo.qst.go.jp/records/47771
https://repo.qst.go.jp/records/47771
7c9b5354-575b-4b1b-bdec-21aae03bd8e1
Item type 学術雑誌論文 / Journal Article(1)
公開日 2017-04-25
タイトル
タイトル Principal Component Analysis of Multimodal Neuromelanin MRI and Dopamine Transporter PET Data Provides a Specific Metric for the Nigral Dopaminergic Neuronal Density.
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 Kawaguchi, Hiroshi

× Kawaguchi, Hiroshi

WEKO 479377

Kawaguchi, Hiroshi

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Shimada, Hitoshi

× Shimada, Hitoshi

WEKO 479378

Shimada, Hitoshi

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Kodaka, Fumitoshi

× Kodaka, Fumitoshi

WEKO 479379

Kodaka, Fumitoshi

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Suzuki, Masayuki

× Suzuki, Masayuki

WEKO 479380

Suzuki, Masayuki

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Shinotoh, Hitoshi

× Shinotoh, Hitoshi

WEKO 479381

Shinotoh, Hitoshi

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Hirano, Shigeki

× Hirano, Shigeki

WEKO 479382

Hirano, Shigeki

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Kershaw, Jeff

× Kershaw, Jeff

WEKO 479383

Kershaw, Jeff

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Inoue, Yuichi

× Inoue, Yuichi

WEKO 479384

Inoue, Yuichi

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Nakamura, Masaki

× Nakamura, Masaki

WEKO 479385

Nakamura, Masaki

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Sasai, Taeko

× Sasai, Taeko

WEKO 479386

Sasai, Taeko

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Kobayashi, Mina

× Kobayashi, Mina

WEKO 479387

Kobayashi, Mina

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Suhara, Tetsuya

× Suhara, Tetsuya

WEKO 479388

Suhara, Tetsuya

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Ito, Hiroshi

× Ito, Hiroshi

WEKO 479389

Ito, Hiroshi

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川口 拓之

× 川口 拓之

WEKO 479390

en 川口 拓之

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島田 斉

× 島田 斉

WEKO 479391

en 島田 斉

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小高 文聰

× 小高 文聰

WEKO 479392

en 小高 文聰

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鈴木 雅之

× 鈴木 雅之

WEKO 479393

en 鈴木 雅之

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篠遠 仁

× 篠遠 仁

WEKO 479394

en 篠遠 仁

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平野 成樹

× 平野 成樹

WEKO 479395

en 平野 成樹

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Kershaw Jeffrey

× Kershaw Jeffrey

WEKO 479396

en Kershaw Jeffrey

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須原 哲也

× 須原 哲也

WEKO 479397

en 須原 哲也

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伊藤 浩

× 伊藤 浩

WEKO 479398

en 伊藤 浩

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抄録
内容記述タイプ Abstract
内容記述 The loss of dopaminergic (DA) neurons in the substantia nigra (SN) is a major pathophysiological feature of patients with Parkinson's disease (PD). As nigral DA neurons contain both neuromelanin (NM) and dopamine transporter (DAT), decreased intensities in both NM-sensitive MRI and DAT PET reflect decreased DA neuronal density. This study demonstrates that a more specific metric for the nigral DA neuronal density can be derived with multimodal MRI and PET. Participants were 11 clinically diagnosed PD patients and 10 age and gender matched healthy controls (HCs). Two quantities, the NM-related index (RNM) and the binding potential of the radiotracer [18F]FE-PE2I to DAT (BPND) in SN, were measured for each subject using MRI and PET, respectively. Principal component analysis (PCA) was applied to the multimodal data set to estimate principal components. One of the components, PCP, corresponds to a basis vector oriented in a direction where both BPND and RNM increase. The ability of BPND, RNM and PCP to discriminate between HC and PD groups was compared. Correlation analyses between the motor score of the unified Parkinson's disease rating scale and each metric were also performed. PCP, BPND and RNM for PD patients were significantly lower than those for HCs (F = 16.26, P<0.001; F = 6.05, P = 0.008; F = 7.31, P = 0.034, respectively). The differential diagnostic performance between the HC and PD groups as assessed by the area under the receiver-operating characteristic curve was best for PCP (0.94, 95% CI: 0.66-1.00). A significant negative correlation was found between the motor severity score and PCp (R = -0.70, P<0.001) and RNM (R = -0.52, P = 0.015), but not for BPND (R = -0.36, P = 0.110). PCA of multimodal NM-sensitive MRI and DAT PET data provides a metric for nigral DA neuronal density that will help illuminate the pathophysiology of PD in SN. Further studies are required to explore whether PCA is useful for other parkinsonian syndromes.
書誌情報 PloS one

巻 11, 号 3, p. e0151191-1-e0151191-13, 発行日 2016-03
ISSN
収録物識別子タイプ ISSN
収録物識別子 1932-6203
PubMed番号
識別子タイプ PMID
関連識別子 26954690
DOI
識別子タイプ DOI
関連識別子 10.1371/journal.pone.0151191
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