Genetic alteration of SLCO1B3 defines constitutional indocyanine green excretory defect in patients who underwent hepatectomy.

IF 3.9 3区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY
Meguri Tanimoto, Yujiro Nishioka, Yoshinori Inagaki, Takashi Kokudo, Takeaki Ishizawa, Junichi Arita, Nobuhisa Akamatsu, Junichi Kaneko, Kiyoshi Hasegawa
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Abstract

Aim: Constitutional indocyanine green (ICG) excretory defects must be distinguished when assessing liver function. The absence of OATP1B3 expression due to homogenous alterations in the SLCO1B3 gene has been recently reported to induce ICG excretory defects; however, its association with the clinical examinations and the clinical implications of heterogeneous SLCO1B3 gene alteration remain unclear.

Methods: OATP1B3 expression was evaluated in 49 patients who underwent hepatectomy after evaluation of the ICG retention rate at 15 min (ICGR15) and technetium-99 m-galactosyl serum albumin (99mTc-GSA) hepatic scintigraphy. Additionally, alterations in SLCO1B3 were analyzed in patients without OATP1B3 expression. Subsequently, 59 patients who underwent hepatectomy for colorectal liver metastasis (CRLM) were analyzed.

Results: Of 49 patients, 6 (12%) had absent OATP1B3 expression. They had significantly higher ICGR15 value (74.7% vs. 23.5%; p < 0.0001), better modified albumin-bilirubin (ALBI) grade (≤grade 2A, 100% vs. 42%; p = 0.010), more normal 99mTc-GSA hepatic scintigraphy (100% vs. 28%; p = 0.0003), and better pathological liver fibrosis (F0-1, 100% vs. 49%; p = 0.027) compared to those with OATP1B3 expression. Three available frozen blocks of cases without OATP1B3 expression showed homozygous alterations in SLCO1B3. Of 59 patients with CRLM in normal liver background, five (8.5%) had heterozygous insertion in SLCO1B3, however they had no difference in ICGR15 values or other clinical findings compared to the other patients.

Conclusions: Constitutional ICG excretory defects may be defined by the complete absence of OATP1B3 expression. The modified ALBI grade and 99mTc-GSA hepatic scintigraphy were useful for detecting constitutional ICG excretory defects.

SLCO1B3 基因改变决定了接受肝切除术的患者存在吲哚菁绿排泄缺陷。
目的:在评估肝功能时,必须区分吲哚菁绿(ICG)排泄缺陷。最近有报道称,由于 SLCO1B3 基因的同质性改变而导致的 OATP1B3 表达缺失可诱发 ICG 排泄缺陷;然而,其与临床检查的关系以及 SLCO1B3 基因异质性改变的临床意义仍不清楚:方法:在评估了 15 分钟 ICG 保留率(ICGR15)和锝-99 m-半乳糖基血清白蛋白(99mTc-GSA)肝闪烁扫描后,对 49 例接受肝切除术的患者进行了 OATP1B3 表达评估。此外,还分析了无 OATP1B3 表达的患者 SLCO1B3 的变化。随后,对59名因结肠直肠肝转移(CRLM)而接受肝切除术的患者进行了分析:结果:在 49 例患者中,有 6 例(12%)没有 OATP1B3 表达。结果:49 名患者中有 6 人(12%)没有 OATP1B3 表达,他们的 ICGR15 值明显更高(74.7% 对 23.5%;P完全无 OATP1B3 表达可定义为体制性 ICG 排泄缺陷。改良 ALBI 分级和 99mTc-GSA 肝闪烁扫描可用于检测体质性 ICG 排泄缺陷。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Hepatology Research
Hepatology Research 医学-胃肠肝病学
CiteScore
8.30
自引率
14.30%
发文量
124
审稿时长
1 months
期刊介绍: Hepatology Research (formerly International Hepatology Communications) is the official journal of the Japan Society of Hepatology, and publishes original articles, reviews and short comunications dealing with hepatology. Reviews or mini-reviews are especially welcomed from those areas within hepatology undergoing rapid changes. Short communications should contain concise definitive information.
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