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通过双能CT获得的细胞外体积分数描绘了肝纤维化的病因差异。

Extracellular volume fraction obtained by dual-energy CT depicting the etiological differences of liver fibrosis.

作者信息

Ozaki Kumi, Ohtani Takashi, Ishida Shota, Higuchi Shohei, Ishida Tomokazu, Takahashi Kouki, Matta Yuki, KImura Hirohiko, Gabata Toshifumi

机构信息

Department of Radiology, Faculty of Medical Sciences, University of Fukui, 23-3 Matsuoka-Shimoaizuki, Eiheiji, Fukui, 910-1193, Japan.

Department of Radiology, Hamamatsu University School of Medicine, 1-20-1, Handayama, Higashi-Ku, Hamamatsu, 431-3192, Japan.

出版信息

Abdom Radiol (NY). 2023 Jun;48(6):1975-1986. doi: 10.1007/s00261-023-03873-6. Epub 2023 Mar 20.

Abstract

PURPOSE

To assess etiological differences in extracellular volume fraction (ECV) and evaluate its influence on staging performance.

METHODS

A total of 166 patients with normal liver (n = 14) and chronic liver disease related to viral hepatitis (n = 71), alcohol (n = 44), and nonalcoholic steatohepatitis (NASH) (n = 37) underwent dual-energy CT (DECT) of the liver (5-min equilibrium-phase images) between January 2020 and July 2022. The iodine densities of the parenchyma and aorta were measured and ECV was calculated. Comparisons of ECV between each etiology and METAVIR fibrosis stage were statistically analyzed (p < 0.05).

RESULTS

ECV in each etiology and all patients significantly increased with higher fibrosis stage (p < 0.001) and showed a strong or moderate correlation with fibrosis stage (Spearman's ρ; all patients, 0.701; viral hepatitis, 0.638; alcoholic, 0.885; NASH, 0.791). In stages F2-F4, ECV in alcoholic liver disease was significantly larger than those for viral hepatitis and NASH (p < 0.05); however, no significant difference in stage F1 was found among the three etiologies. The cutoff values and areas under the receiver operating characteristic curve (AUC-ROCs) for discriminating fibrosis stage (≥ F1- ≥ F4) were higher for alcohol (cutoff values and AUC-ROC; 20.1% and 0.708 for ≥ F1, 23.8% and 0.990 for ≥ F2, 24.3% and 0.968 for ≥ F3, and 26.6% and 0.961 for ≥ F4, respectively) compared with those for the others.

CONCLUSION

ECV in alcoholic liver disease is higher than that in other etiologies in the advanced stages of fibrosis, and etiological differences in ECV affect the staging performance of fibrosis.

摘要

目的

评估细胞外容积分数(ECV)的病因差异,并评估其对分期性能的影响。

方法

2020年1月至2022年7月期间,共有166例肝脏正常患者(n = 14)以及与病毒性肝炎(n = 71)、酒精(n = 44)和非酒精性脂肪性肝炎(NASH)(n = 37)相关的慢性肝病患者接受了肝脏双能CT(DECT)检查(5分钟平衡期图像)。测量实质和主动脉的碘密度并计算ECV。对各病因与METAVIR纤维化分期之间的ECV进行统计学比较分析(p < 0.05)。

结果

各病因组及所有患者的ECV均随纤维化分期升高而显著增加(p < 0.001),且与纤维化分期呈强或中度相关(Spearman氏ρ;所有患者,0.701;病毒性肝炎,0.638;酒精性,0.885;NASH,0.791)。在F2 - F4期,酒精性肝病的ECV显著大于病毒性肝炎和NASH(p < 0.05);然而,在F1期,三种病因之间未发现显著差异。酒精性肝病在区分纤维化分期(≥F1 - ≥F4)时的临界值和受试者操作特征曲线下面积(AUC - ROC)高于其他病因(≥F1时的临界值和AUC - ROC分别为20.1%和0.708,≥F2时为23.8%和0.990,≥F3时为24.3%和0.968,≥F4时为26.6%和0.961)。

结论

在纤维化晚期,酒精性肝病的ECV高于其他病因,且ECV的病因差异影响纤维化的分期性能。

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