論文

査読有り 国際誌
2020年1月

Hepatocyte fraction: correlation with noninvasive liver functional biomarkers.

Abdominal radiology (New York)
  • Yoshifumi Noda
  • ,
  • Satoshi Goshima
  • ,
  • Tomoyuki Okuaki
  • ,
  • Yuta Akamine
  • ,
  • Kimihiro Kajita
  • ,
  • Nobuyuki Kawai
  • ,
  • Hiroshi Kawada
  • ,
  • Yukichi Tanahashi
  • ,
  • Masayuki Matsuo

45
1
開始ページ
83
終了ページ
89
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1007/s00261-019-02238-2

PURPOSE: To evaluate the correlation between HeF obtained from gadoxetic acid-enhanced MR imaging and clinical biomarkers for the assessment of liver function. METHODS: This prospective study was approved by our Institutional Review Board, and written informed consent was obtained from the patients. We recruited 48 patients carrying a known or suspected liver disease to undergo gadoxetic acid-enhanced MR imaging. The new model of the HeF was calculated from ΔR1 values of the liver and spleen. The HeF, quantitative liver-to-spleen contrast ratio (Q-LSC), and ΔT1 value (the reduction rate of the T1 value between the pre- and post-contrast images) were compared with the Child-Pugh and end-stage liver disease (MELD) scores. RESULTS: Among 48 patients, 40 were in Child-Pugh class A and 8 were in class B. The median HeF (P = 0.0001), Q-LSC (P = 0.015), and ΔT1 value (P = 0.0023) in patients in Child-Pugh class A were significantly higher than those in class B. The sensitivities, specificities, and area under the receiver-operating-characteristic curves for differentiating Child-Pugh class A and B were 95.0%, 87.5%, and 0.93 in the HeF; 77.5%, 75.0%, and 0.78 in the Q-LSC; and 57.5%, 100.0%, and 0.84 in the ΔT1 value, respectively. The HeF was significantly correlated with Child-Pugh (r = - 0.58, P < 0.0001) and MELD score (r = - 0.57, P < 0.0001). CONCLUSIONS: The HeF was well correlated with Child-Pugh and MELD score and could be a new biomarker to assess liver function.

リンク情報
DOI
https://doi.org/10.1007/s00261-019-02238-2
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/31552466
ID情報
  • DOI : 10.1007/s00261-019-02238-2
  • ISSN : 2366-004X
  • PubMed ID : 31552466

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