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  1. C. 医薬保健学域; 医学類・薬学類・医薬科学類・保健学類
  2. c 10. 学術雑誌掲載論文(医・保健)
  3. 1. 査読済論文(医学・保健)

Idiopathic Normal-Pressure Hydrocephalus: Temporal Changes in ADC during Cardiac Cycle

http://hdl.handle.net/2297/00049383
http://hdl.handle.net/2297/00049383
0a8acfd9-a9d3-4235-b055-c31ddb29a8fd
名前 / ファイル ライセンス アクション
ME-PR-OHNO-N-197.pdf ME-PR-OHNO-N-197 (259.9 kB)
Item type 学術雑誌論文 / Journal Article(1)
公開日 2017-12-12
タイトル
タイトル Idiopathic Normal-Pressure Hydrocephalus: Temporal Changes in ADC during Cardiac Cycle
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
著者 Ohno, Naoki

× Ohno, Naoki

WEKO 13188
e-Rad 30642219
金沢大学研究者情報 30642219
研究者番号 30642219

Ohno, Naoki

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Miyati, Toshiaki

× Miyati, Toshiaki

WEKO 120
e-Rad 80324086
金沢大学研究者情報 80324086
研究者番号 80324086

Miyati, Toshiaki

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Mase, Mitsuhito

× Mase, Mitsuhito

WEKO 69241

Mase, Mitsuhito

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Osawa, Tomoshi

× Osawa, Tomoshi

WEKO 69242

Osawa, Tomoshi

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Kan, Hirohito

× Kan, Hirohito

WEKO 69243

Kan, Hirohito

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Kasai, Harumasa

× Kasai, Harumasa

WEKO 69244

Kasai, Harumasa

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Hara, Masaki

× Hara, Masaki

WEKO 69245

Hara, Masaki

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Shibamoto, Yuta

× Shibamoto, Yuta

WEKO 69246

Shibamoto, Yuta

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Hayashi, Norio

× Hayashi, Norio

WEKO 69247

Hayashi, Norio

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Gabata, Toshifumi

× Gabata, Toshifumi

WEKO 69248

Gabata, Toshifumi

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Matsui, Osamu

× Matsui, Osamu

WEKO 69249

Matsui, Osamu

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著者別表示 大野, 直樹

× 大野, 直樹

大野, 直樹

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宮地, 利明

× 宮地, 利明

宮地, 利明

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書誌情報 Radiology

巻 261, 号 2, 発行日 2011-11
DOI
識別子タイプ DOI
関連識別子 10.1148/radiol.11101860
出版者
出版者 Radiological Society of North America
抄録
内容記述タイプ Abstract
内容記述 Normal-pressure hydrocephalus (NPH) is characterized by a clinical triad of ataxia, incontinence, and dementia, as well as dilated ventricles but normal cerebrospinal fluid (CSF) pressures. In patients with NPH, CSF shunt placement is effective for improving these symptoms (1). NPH has attracted attention as one of the few treatable causes of dementia. Diagnosis of idiopathic NPH (INPH) without a known cause of communicating hydrocephalus, including subarachnoid hemorrhage or meningitis, is particularly difficult (2). Moreover, to clarify the cause of NPH, accurately diagnose NPH, and identify appropriate patients for shunt surgery, several tests have been proposed, including cisternography, the CSF tap test, resistance measures, external lumbar drainage, and intracranial pressure recording, in addition to clinical findings and conventional imaging diagnosis with x-ray computed tomography or magnetic resonance (MR) imaging (3–6). It has also been reported (7) that a single standard for the prognostic evaluation of patients with INPH was lacking and that supplemental tests could increase the predictive accuracy of the prognosis. The CSF tap test is a particularly reliable examination, but it is invasive and has low sensitivity. It has been proposed that MR imaging CSF flow studies can be used to noninvasively obtain information about intracranial mechanical properties in INPH (eg, intracranial compliance) (2,8–12). However, the diagnostic utility of this latter method is still not established.

Arterial inflow into the cranium induces venous and CSF outflow and displacement of the intracranial spinal cord during the cardiac cycle, resulting in pulsatile brain motion (12–14). Brain pulsation (ie, bulk motion) reportedly can give rise to artifactual phase dispersion and may lead to overestimation of the apparent diffusion coefficient (ADC) (15,16). Brockstedt et al (17) reported that ADC was not changed significantly during the cardiac cycle with the single-shot echo-planar imaging (EPI) sequence widely used in diffusion MR imaging. However, they analyzed only two delay times (100 and 400 msec) between the R peaks in the cardiac cycle. To more completely analyze ADC changes during the cardiac cycle, our own group has previously evaluated the temporal change in ADC during the entire cardiac cycle by using an electrocardiographically (ECG)-triggered single-shot diffusion EPI sequence to minimize bulk motion effect. As a result, we revealed in a previous study that white matter ADC changed significantly over the cardiac cycle and that such changes were synchronized with the arterial inflow (volume loading) at systole (18). We further hypothesize that changes in ADC during the cardiac cycle are related to the biomechanical properties of intracranial tissues; hence, observed temporal changes in ADC in diseases such as INPH that are characterized by low intracranial compliance (12) may well be different than those in other diseases. Therefore, the purpose of our study was to determine whether temporal changes in ADC over the cardiac cycle were different in patients with INPH as compared with patients with ex vacuo ventricular dilatation and healthy control subjects.
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