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Table of Content

    31 July 2024, Volume 29 Issue 7
    CONTENTS
    2024, 29(7):  0-0. 
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    Liver Cancer
    The time interval between TACE and ablation therapy: A single-center retrospective study on the treatment efficacy for early stage hepatocellular carcinoma
    JING Chang-you, ZHU Tong, ZHANG Yong-hong, LI Jian-jun
    2024, 29(7):  777-801. 
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    Objective To compare the efficacy of combined radiofrequency ablation (RFA) at 0-14 or 15-30 days after transcatheter arterial chemoembolization (TACE) for the treatment of early hepatocellular carcinoma (HCC). Methods A retrospective analysis was conducted on patients with early HCC who underwent combined TACE and RFA treatment at Beijing You'an Hospital, Capital Medical University, between 2011 and 2013. Based on the time interval between TACE and RFA treatment, the study was divided into two groups: Group A (0-14 days) and Group B (15-30 days). The primary endpoints of the study were overall survival (OS) and progression-free survival (PFS), with a multifactorial analysis of factors influencing patient prognosis. Results A total of 56 patients were included in this study. Among them, 22 were classified as BCLC stage 0 and 34 as stage A. By univariate analysis it was indicated that the tumor stage and the degree of liver cirrhosis were correlated with the prognosis of liver cancers (P<0.05). By multifactorial analysis it was identified that the tumor stage (RR=0.045, 95% CI:0.003-0.623, P=0.021) as an independent risk factor affecting the prognosis of HCC treated with combined TACE and RFA therapy. By subgroup analysis it was showed a 5-year survival rate of 78% for Group A and 75% for Group B; the 5-year progression-free survival rates were 14% and 11% for Groups A and B, respectively. The median progression-free survival times were 23 months for Group A and 31 months for Group B, with median overall survival times of 60 months for both groups. There were no statistically significant differences in progression-free1 survival (HR=1.085, P=0.795) and overall survival (HR=0.514, P=0.416) between Groups A and B. Conclusion For HCC patients treated with combined TACE and RFA, better prognosis is associated with earlier tumor staging. The timing interval between TACE and ablation therapy, whether within 14 days or more than 14 days (15-30 days), does not significantly affect the efficacy against hepatocellular carcinoma. RFA within 30 days after TACE is safe and effective.
    An analysis on the short-term and long-term therapeutic effects of tyrosine kinase inhibitors combined with hepatic artery chemoembolization for the treatment of hepatocellular carcinoma
    QIAN Ye-qiang, GAO Lu, YU Chun-lai
    2024, 29(7):  780-783. 
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    Objective To explore the short-term and long-term efficacy of tyrosine kinase inhibitors (TKI) combined with hepatic artery chemoembolization (HAC) for the treatment of hepatocellular carcinoma (HCC). Methods The study focused on 60 HCC patients collected at Zongyang County People's Hospital from June 2019 to June 2021. The patients were divided into a treatment group and a control group with 30 cases in each group using a random number table method. The treatment group received TKIs combined with HAC treatment, while the control group received traditional hepatic artery chemoembolization treatment.The treatment efficacy, liver function, serum AFP levels, survival time, safety, etc, were evaluated. Results Following the treatment, the treatment group exhibited a higher proportion of CR and PR compared to the control group (90.00% vs. 66.67%, P<0.05). After 6 weeks of treatment, the ALT was 40.92 ± 6.09 (U/L), which was lower than the control group's 46.33 ± 8.13 (U/L); After 9 weeks of treatment, the serum AFP level in the control group was 153.25 ± 42.23 μg/L, which was higher than the treatment group's 74.61 ± 18.29 μg/L; The progression free survival of the treatment group was 22.41 ± 2.88 months, with a total survival of 34.18 ± 5.77 months. The progression free survival of the control group was 14.17 ± 3.14 months, the overall survival in the study group was 21.68 ± 5.36 months. There were no statistically significant difference in the incidence of adverse reactions was observed between the two groups (P>0.05). Conclusion The combination of TKIs and HAC treatment for HCC has shown good therapeutic effects in short and long term, which has clinical promotion value.
    The alpha-fetoprotein response and its prognostic evaluation value for patients with advanced hepatocellular carcinoma treated with karelizumab in combination with sorafenib
    ZHANG Yun-jiang, LIANG Liang, ZHANG Dong-cheng
    2024, 29(7):  784-787. 
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    Objective To analysis the alpha-fetoprotein (AFP) response and its prognostic evaluation value of patients with advanced hepatocellular carcinoma (HCC) treated with karelizumab in combination with sorafenib. Methods Sixty patients with intermediate and advanced HCC treated with karelizumab combined with sorafenib who were admitted between April 2019 and April 2021 were categorized into 35 cases in the responding group and 25 cases in the non-responding group according to whether the patients responded to the treatment after 8 months of treatment. The clinicopathologic characteristics and tumor regression of the two groups were compared. Kaplan-Meier survival analysis was used to assess the survival in both groups. To analyze the risk factors affecting the prognosis of patients with middle and advanced HCC using multifactorial Cox regression. Results The hemoglobin level in the responder group was (138.2±23.6) g/L, which was higher than that in the non-responder group [(122.5±21.2) g/L, P<0.05]; the levels of AFP and total bilirubin after treatment in the responder group were (172.3±21.5) ng/mL and (12.3±2.1) μmol/L, respectively, which were lower than that of (468.9± 71.2) ng/mL, (21.2±4.1) μmol/L in the non-responder group [P<0.05]; the rates of early response to AFP, disease remission, and disease control in the responder group were 91.4%, 82.9%, and 37.1%, respectively, which were superior to those of 28.0%, 60.0%, and 12.0% in the mortality group [P<0.05], respectively; As of March 2021, the progression-free survival was 9 months in the responder group and 6 months in the nonresponder group, and overall survival was 13 months in the responder group and 11 months in the nonresponder group, with a total of 20 deaths, 8 in the responder group and 12 in the nonresponder group; The survival rate in the responder group was superior to that in the nonresponder group. The results of multifactorial Cox regression analysis showed that an early response of AFP was an independent risk factor affecting the prognosis of patients with intermediate and advanced HCC (OR=3.511, P<0.05). Conclusion The efficacy of karelizumab combined with sorafenib in the treatment of intermediate and advanced HCC is remarkable, and the early response of AFP has a good application value in evaluating the prognosis of patients.
    An analysis on the efficacy of sequential surgical resection for initial unresectable hepatocellular carcinoma treated with interventional therapy combined with targeted immunotherapy
    DUAN Chang-hu, DUAN Jian-feng, WU Lin, TAI Sheng, LIU Xiao-chen
    2024, 29(7):  788-793. 
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    Objective To evaluate the clinical efficacy and analyze of sequential surgical resection for initial unresectable hepatocellular carcinoma treated with interventional therapy combined with targeted immunotherapy. Methods The clinical data from 10 patients with initial unresectable hepatocellular carcinoma admitted to the 3201 hospital of Xi'an Jiaotong University Health Science Center from June 2021 to May 2023 were retrospectively collected and analysed. Results Of the 10 patients, 8 were male and 2 was female, with a median age of 55 years (33~72 years); there were 6 cases with Child Pugh grade A and 4 cases with grade B; 4 cases with CNLC stage IIb and 6 cases with IIIa; The PS scores of all patients were ≤1; there were 6 cases with cirrhosis and 4 cases without cirrhosis; 6 cases with portal vein cancer thrombus and 4 cases without portal vein cancer thrombus;the maximum tumor diameter before transformation therapy was 13 cm, with 7 cases having AFP>400 ng/mL and 3 cases having AFP<400 ng/mL before treatment; There were 7 cases with hepatitis B, 2 cases with hepatitis C and 1 case without viral hepatitis; The conversion treatment programmes included: 1) TACE combined with anti-angiogenic targeting drugs and immune checkpoint inhibitors in 5 cases, 2) HAIC combined with anti-angiogenic targeting drugs and immune checkpoint inhibitors in 5 cases. During the treatment, there were 4 cases with hypertension, 2 cases with fatigue, and 1 case with diarrhea; the median conversion time were 4 months. The maximum diameter of the tumor after conversion therapy before surgery was 8.8 cm, and the median AFP level after conversion therapy before surgery was 17.2 g/mL, In preoperative imaging assessment (mRECIST), there wereCR in 4 cases, PR in 3 cases, SD in 3 cases; preoperative PS score ≤1 point. After therapy, surgical resection was performed: 3 cases underwent partial hepatectomy, 7 cases underwent semi-hepatic resection; 7 cases underwent laparoscopic surgery, and 3 cases underwent open surgery; The median surgical time was 240 minutes. The median intraoperative blood loss was 400 mL.The median postoperative hospital stay was 8 days, and the median postoperative drainage tube removal time was 7 days. The postoperative pathological results shown that there were 3 cases of pCR, 7 cases of pPR, 8 cases of MVI grade M0, 2 cases of M1 , no case of positive resection margin. Postoperative ascites occurred in 1 case, bile leakage in 1 case, and there were no significant postoperative complications. The median follow-up time after surgery was 8 months, with 1 case experiencing recurrence and no patient died during follow-up. Conclusion Sequential surgical resection for initial unresectable hepatocellular carcinoma treated with interventional therapy combined with targeted immunotherapy is effective and safe.
    The correlation between serum PIVKA-II level and liver function in patients with hepatitis B-associated liver cancer
    KONG Wei-ju, REN Chuan-lu, ZHOU Yu-qi, LI Jing-zheng, HE Qing, YUAN Jun-fei
    2024, 29(7):  794-797. 
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    Objective The abnormal serum PIVKA-II level and liver function in patients with hepatitis B-associated liver cancer were observed and the correlation was analyzed. Methods A total of 137 chronic hepatitis B patients who were enrolled between April 2020 and April 2023 were taken as the chronic hepatitis B group; 35 patients with hepatitis B related cirrhosis admitted during the same period of time were selected as the cirrhosis group; 67 patients with hepatitis B-related liver cancer admitted during the same period of time were selected as the liver cancer group; and 51 healthy subjects who underwent physical examination during the same period of time were selected as the control group. The new industry MAGLUMI X8 chemiluminescence analysis was used to detect the serum PIVKA-Ⅱ level, detect liver function indicators, and ROCHE cobas6000 E602 electrochemiluminescence immunoassay was used to detect alpha fetoprotein (AFP). Graphpad Prism was used to analyze the serum PIVKA-Ⅱ level in the diagnosis of hepatitis B-related liver cancer. Results The levels of serum PIVKA-Ⅱ and AFP were 21.0 (18.0~27.0) and 2.1(1.7~3.3) ng/mL respectively in the control group, 22.0 (12.0~28.0) and 2.3 (1.7~3.4) ng/mL in the chronic hepatitis B group, and 21.0 (15.0~46.0) and 2.5 (1.7~4.0) ng/mL in the cirrhosis group, which were significantly lower than those of 61.1 (22.0~2021.0) and 6.2 (2.5~76.8) ng/mL in the liver cancer group (P<0.05); The serum ALT level in the control group was 16.0 (13.0~26.0)U/L, which was significantly lower than those of 30.0 (18.3~44.0)U/L in the chronic hepatitis B group, 31.5 (20.0~47.3)U/L in cirrhosis group, and 30.5 (20.0~54.0)U/L in liver cancer group [P<0.05]. The serum AST and GGT levels were 19.0 (16.0~22.0) U/L and 24.0 (17.0~35.0) U/L respectively in the control group, 24.0 (20.0~31.0) U/L and 25.5 (17.0~41.7) U/L in the chronic hepatitis B group, which were significantly lower than those of 31.5 (25.0~52.3) U/L, and 53.5 (23.8~99.0) U/L in the cirrhosis group [P<0.05], and 31.5 (21.5~60.0) U/L, and 60.0 (25.8~135.5) U/L in the liver cancer group, [P<0.05]. Spearman correlation analysis showed that serum PIVKA-Ⅱ was positively correlated with AST, GGT and AFP levels (P<0.05) (r=0.173, P=0.004; r=0.323, P<0.001; r=0.286, P<0.001). Using Graphpad prism analysis, compared with the control group, the area under the curve was 0.7523, P<0.05, and the optimal diagnostic cutoff value was 41.00 ng/mL; compared with the chronic hepatitis B group, the area under the curve of PIVKA-Ⅱ was 0.7630, and the optimal diagnostic cutoff value was 43.50 ng/mL. Conclusion The serum PIVKA-Ⅱ level in patients with hepatitis B-related liver cancer is significantly higher than that in patients with hepatitis B and hepatitis B-related cirrhosis, which may have higher diagnostic efficacy for hepatitis B-related liver cancer, and can be used as a reference for clinical diagnosis of hepatitis B-related liver cancer.
    Performance of sound velocity matching technique and shear wave elastography in differentiating atypical hepatic hemangioma from primary hepatocellular carcinoma in 60 patients
    YU Jian, DONG Wen-jian, XIA Jian-xin, PENG Ren-cong
    2024, 29(7):  798-801. 
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    Objective To analyze the sound velocity matching technique and shear wave elastography performance in patients with hepatic hemangioma and their performance in differentiating from primary hepatocellular carcinoma. Methods Sixty patients with hepatic hemangioma confirmed by CT and 40 patients with primary hepatocellular carcinoma confirmed by pathological puncture were selected from July 2019 to July 2020. To compare the performance of sound velocity matching technique and shear wave elastography between the two groups, the value of sound velocity matching technique and shear wave elastography to identify hepatic hemangioma and primary hepatocellular carcinoma were analyzed by the receiver operating characteristic curve (ROC). Results In hepatic hemangioma group, the sound velocity matching value, elastic modulus value, shear wave velocity maximum and mean values were (22.4±3.5) m/s, (16.1±2.5) kPa, (2.7±0.3) m/s, and (2.3±0.2) m/s, respectively, which were significantly lower than those in the hepatocellular carcinoma group [40.6±4.5) m/s, (33.5±2.5) kPa, ( 3.8±0.6) m/s, (3.4±0.4) m/s, P<0.05]. The ROC curve analysis showed that sound velocity matching values, elastic modulus values, shear wave velocity maxima, and mean values were highly valuable in differentiating between hepatic hemangioma and primary hepatocellular carcinoma. Conclusion Sound velocity matching values, elastic modulus values, shear wave velocity maxima, and mean values are of great value in differentiating bewteen hepatic hemangioma and primary hepatocellular carcinoma. The sound velocity matching technique and shear wave elastography can be used to identify hepatic hemangioma from primary hepatocellular carcinoma.
    Liver Fibrosis & Cirrhosis
    Construction and application of a digital management platform for multidisciplinary consultation and management of portal hypertension
    YAN Yu-feng, YUAN Min, HE Yang, TU Chuan-tao, SHI Yu-xin, WANG Lin, WANG Yue, FU Qing-chun
    2024, 29(7):  802-807. 
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    Objective To investigate the development and implementation strategies of a digital management platform for multidisciplinary consultation and management of portal hypertension. Methods The platform integrates digital recognition, data cleansing, structured processing, and artifical intelligentce (AI) algorithms to create a comprehensive disease management system. It details the system's module design, application procedures, and team collaboration mechanisms, demonstrating how multidimensional data analysis and personalized follow-up support meet the diverse and multi-tiered follow-up needs for patients with portal hypertension. Results The platform, utilizing digital technologies, provided personalized treatment plans and long-term dynamic management based on multidisciplinary precise assessments. It included 428 patients, achieving a 94% compliance rate, a 78% revisit rate, and 100% patient satisfaction. It also significantly enhanced the efficiency and motivation of clinical and research teams, leading to multiple projects and municipal awards, fostering medical discipline development and talent cultivation. Conclusion The platform's application effectively strengthens the comprehensive management of portal hypertension patients, enhances patient medical experiences, improves medical quality and safety, advances clinical research, and trains specialized talents, providing empirical and technological support for future medical service model innovation.
    N-Acetylcysteine for liver and kidney function protection during the perioperative period of hepatectomy in the context of liver cirrhosis
    WANG Zhi-gang, YAN Rui-long, YUAN Cui-hua
    2024, 29(7):  808-839. 
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    Objective To investigate the protective effect of N-acetylcysteine (NAC) combined with ulinastatin on liver and kidney function in cirrhosis patients who undergone hepatectomy during perioperative period. Methods A total of 74 patients with cirrhosis who underwent elective partial hepatectomy were selected from January 2021 to March 2023, and were randomly divided into observation group and control group (37 cases each). Control group was treated with ulinastatin injection during perioperative period, and observation group was treated with ulinastatin combined with NAC injection. The changes of inflammatory oxidative stress, liver and kidney function and safety indexes were observed in the two groups. Results The levels of IL-1β at 3 and 7 days after operation in the observation group were 43.59±6.17 μg/L and 35.94±5.10 μg/L, respectively, and TNF-α levles were 26.53±3.91 ng/L and 20.48±3.27 ng/L, respectively. These were significantly lower than the control group's IL-1β levels of 47.92±6.58 μg/L and 39.71±5.76 μg/L, and TNF-α levles of 29.86±4.35 ng/L and 25.61±3.80 ng/L (t=6.524, 6.249, 6.725, 7.314, all P<0.05). At 3 and 7 days post-operation, MDA levels in the observation group were 12.08±2.15 μmol/L and 8.14±1.52 μmol/L, which were lower than the control group's 14.35±2.39 μmol/L and 9.82±1.76 μmol/L. SOD levels in the observation group were 55.04±5.81 U/L and 63.27±6.24 U/L, significantly higher than 52.15±5.46 U/L and 58.79±6.43 U/L in control group (t=6.592, 6.823, 6.739, 6.541, all P<0.05). The levels of ALT, γ-GT, TBil, TBA, SF, RBP and CysC in the observation group were 80.59±6.51 U/L, 59.34±5.62 U/L, 90.15±6.83 U/L, 64.28±5.74 U/L, 21.06±2.37 μmol/L, 15.79±2.08 μmol/L, 11.54±1.90 μmol/L, 9.64±1.57 μmol/L, 385.92±31.70 ng/mL, 351.48±27.09 ng/mL, respectively, all significantly lower than 86.73±7.04 U/L, 67.19±6.47 U/L, 98.74±7.49 U/L, 70.26±6.15 U/L, 22.79±2.51 μmol/L, 17.84±2.35 μmol/L, 12.76±2.02 μmol/L, 10.79±183 μmol/L, 407.59±34.28 ng/mL, 369.85±30.63 ng/mL in the control group. The ALB levels in the observation group were 30.78±2.18 g/L and 32.51±2.46 g/L, which were significantly higher than those in the control group (29.16±2.04 g/L, 30.76±2.17 g/L; t=6.853, 7.128, 6.784, 6.573, 5.487, 6.284, 5.185, 5.384, 6.719, 5.826, 5.438, 5.629, all P<0.05). The levels of RBP and CysC in the observation group were 62.28±5.39 mg/L, 52.06±4.92 mg/L, 2.60±0.52 mg/L, 2.42±0.43 mg/L. It was lower than that of the control group (68.17±5.74 mg/L, 57.48±5.26 mg/L, 2.81±0.59 mg/L, 2.64±0.48 mg/L), with statistically significant difference (t=6.819, 6.793, 6.836, 6.287, all P<0.05). The incidence rates of postoperative infection, HE, PHLF and AKI in the observation group were 2.70%, 2.70%, 0%, and 0%, respectively, significantly lower than those in the control group (8.11%, 10.81%, 2.70%, and 5.41%; χ2=3.284, 3.827, 3.496, 3.608, all P<0.05). Conclusion NAC combined with ulinastatin can inhibit perioperative inflammatory response and oxidative stress in cirrhotic patients who undergone hepatectomy. NAC plays a protective role for liver and kidney function.
    Contrast-enhanced ultrasound perfusion characteristics of different nodules in hepatitis B-related cirrhosis
    FU Peng, TANG Ya-dan, YANG Fang-fang, YANG Li-xin
    2024, 29(7):  813-816. 
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    Objective To analyze the features of different nodules in hepatitis B-related cirrhosis during the contrast-enhanced ultrasound perfusion (CEUS) phase and assess the diagnostic value of CEUS phase analysis technology for these nodules. Methods Pathological examination identified 128 hyperplastic nodules, 16 atypical hyperplastic nodules, and 39 minimal hepatocellular carcinoma (HCC) out of 193 nodules. Ultrasound contrast examination showed 120 hyperplastic nodules, 25 atypical hyperplastic nodules, and 38 minimal HCC out of 183 nodules. Results Three phase enhanced scanning of hyperplastic nodules are mainly manifested as isoechoic-isoechoic-isoechoic enhancement. Atypical hyperplastic nodules mainly exhibited hyperechoic or hypoechoic-isoechoic-isoechoic enhancement. Small HCC is mainly manifested as hyperechoic-isoechoic or hypoechoic enhancement, with these contrast-enhanced ultrasound features being statistically significant (P<0.05). The RBF (regional blood flow) in the three-phase enhanced scanning of hyperplastic nodules were (38.95 ± 13.73) mL/s, (104.82 ± 31.59) mL/s, and (42.93 ± 11.39) mL/s, respectively. The RBV (regional blood flow) were (1281.46 ± 422.08) mL, (1347.25 ± 416.98) mL, and (729.61 ± 218.36) mL, respectively. For atypical hyperplastic nodules, the RBF values were (42.92 ± 12.36) mL/s, (27.26 ± 6.52) mL/s, and (25.17 ± 7.36) mL/s, with RBV values of (1498.63 ± 472.56) mL, (1984.63 ± 315.09) mL, and (603.94 ± 96.83) mL, respectively. For small HCC, the RBF values were (63.19 ± 10.58) mL/s, (28.33 ± 5.96) mL/s, and (18.24 ± 5.13) mL/s, respectively, with RBV values of (3385.26 ± 517.94) mL, (1205.94 ± 256.37) mL, and (372.19 ± 74.35) mL, respectively, showing statistical significance (P<0.05). Pathological examination showed 128 hyperplastic nodules, 16 atypical hyperplastic nodules, and 39 minimal HCC out of 193 nodules. Ultrasound contrast-enhanced examination showed 120 hyperplastic nodules, 25 atypical hyperplastic nodules, and 38 minimal HCC out of 183 nodules. The sensitivity, specificity, accuracy, and Kappa value of contrast-enhanced ultrasound for diagnosing hyperplastic nodules were 0.922, 0.964, 0.934, and 0.850, respectively. For diagnosing atypical hyperplastic nodules, the sensitivity was 0.750, specificity was 0.922, accuracy was 0.907, and the Kappa value was 0.536. For diagnosing small hepatocellular carcinoma, the sensitivity was 0.846, specificity was 0.965, accuracy was 0.940, and the Kappa value was 0.819. Conclusion The analysis of the CEUS shows different enhancement modes for hyperplastic nodules, atypical hyperplastic nodules, and micro HCC in the context of hepatitis B-related cirrhosis. The RBF and RBV values also vary across different perfusion phases. CEUS demonstrates significant value in diagnosing nodules of different natures and and in the early detection of micro HCC.
    Factors and prognostic evaluation of covert hepatic encephalopathy in patients with hepatitis B-related cirrhosis
    WANG Li-hui, LIU Shuang-ping, LU Qiu-yan, SHEN Pei-gen, XU Cheng-run
    2024, 29(7):  817-820. 
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    Objective To explore factors and prognosis of hepatitis B cirrhosis patients complicated with covert hepatic encephalopathy (CHE), and to provide theoretical basis for clinical diagnosis and prognosis improvement of hepatitis B cirrhosis complicated with covert CHE. Methods Between May 2020 and June 2022, 134 patients with hepatitis B cirrhosis were divided into CHE group (n=69) and non-CHE group (n=65). According to the progression of CHE during follow-up, the CHE group was further divided into hepatic encephalopathy (HE) group (n=18) and non-HE group (n=51) . The clinical data and prognosis were compared between CHE and non-CHE groups, and logistic regression analysis was used to analyze the risk factors of CHE patients. Results Comparing the clinical data of CHE group and non-CHE group, age, the proportion of HE, decompensated liver cirrhosis, hepatorenal syndrome, complicated infection, the MELD score and the proportion of liver function class C in CHE group were (58.3±13.1)、37.7%、98.6%、5.8%、50.7%、(10.5±4.6) and 17.4%, respectively, which were significantly higher than those in the non-CHE group [(51.9±12.9)、4.6%、53.8%、1.5%、24.6%、(7.2±2.5) and 1.5% (P<0.05)]. According to logistic regression analysis, age, MELD score, HE history and liver function grade were independent risk factors of CHE. The proportion of grade C of liver function, the proportion of HE history and MELD score in HE patients were 50.0%、61.1% and (14.7±6.3), respectively, which were significantly higher than those in the non-HE group [5.9%、29.4% and (9.5±4.2) (P<0.05)]. Conclusion Patients with hepatitis B cirrhosis complicated with CHE were affected by age, HE history, infection and other factors. Their prognosis were related to liver function grade, HE history and MELD score. Greater clinical attention should be focused on these risk factors to prevent the occurrence of CHE and improve the patients prognosis.
    Efficacy of microecological agents combined with ornithine aspartate in treatment of patients with subclinical hepatic encephalopathy and its influence on liver function and cognitive function
    LI Yan, CHEN Qian, ZHOU Shu-ping, LIU Xin-kuang, XU Bin
    2024, 29(7):  821-824. 
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    Objective To observe the therapeutic effect of microecological agents combined with ornithine aspartate in treatment of patients with subclinical hepatic encephalopathy (SHE) and its influence on liver function and cognitive function. Methods A total of 86 SHE patients were collected from January 2020 to December 2023, and were randomly divided into two groups. The control group (43 cases) received ornithine aspartate treatment, and the observation group (43 cases) received ornithine aspartate combined with microecological agents. Before treatment and 8 weeks after treatment, the blood ammonia, C-reactive protein (CRP), procalcitonin (PCT), and liver function indicators [aspartate aminotransferase (AST), alanine aminotransferase (ALT), γ- Glutamyltransferase (γ- GT) and total bilirubin (TBil)] were measured. The cognitive function was evaluated by the Number Connection Test (NCT-A), NCT-B, and Digital Sign Test (DST). Results Compared to control group after treatment, the blood ammonia (66.69±18.19 μmol/L vs. 87.88±21.35 μmol/L), CRP (6.57±1.43 mg/L vs. 9.56±1.71 mg/L), PCT ( 0.21±0.08 ng/L vs. 0.29±0.09 ng/L), AST(49.14±9.75 U/L vs. 55.21±11.06 U/L), ALT(35.81±5.79 U/L vs. 48.35±7.21 U/L), γ- GT (60.89±9.71 U/L vs. 73.25±11.61 U/L) and TBil (45.61±7.32 U/L vs. 50.37±8.42 U/L) both decreased in the observation group, with statistical significance (all P<0.05). Compared to control group after treatment, the levels of NCT-A (56.68±11.06 vs. 60.01±12.14), NCT-B (67.76±12.83 vs. 71.85±14.69), and DST (105.42±21.68 vs. 126.48±23.41) in the observation group were significantly higher (all P<0.05). There was 4.65% of patients converted to HE in the observation group, significantly lower than the HE conversion rate of 16.28% in control group (P<0.05). Conclusion The combination treatment of microecological agents and ornithine aspartate can reduce blood ammonia and inflammatory factor levels, protect liver and cognitive function in SHE patients, and may reduce the risk of HE conversion.
    The combined value of ultrasounic shear wave elastography and plasma Nrg4 levels in assessing liver fibrosis severity in chronic hepatitis B
    LIU Yan-wu, TIAN Dan, SONG Jing-jing
    2024, 29(7):  825-829. 
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    Objective To explore the value of combining ultrasonic shear wave elastography (SWE) with plasma neuregulin 4 (Nrg4) levels in assessing the degree of liver fibrosis in patients with chronic hepatitis B (CHB). Methods Between June 2020 and June 2022, 116 patients with CHB-related liver fibrosis admitted to our hospital underwent liver biopsy. The liver's Young's modulus value was measured using ultrasound SWE, and the plasma Nrg4 levels were measured using the Elisa method. We analyzes the correlation between liver Young's modulus value and plasma Nrg4 levels with the degree of liver fibrosis. A receiver operating characteristic (ROC) curve was drawn, and the area under the curve (AUC) was used to evaluate the diagnostic efficacy of combining Young's modulus and plasma Nrg4 levels for assessing the degree of liver fibrosis in CHB patients. Results Among the 116 patients with CHB liver fibrosis, there were 33 cases in the F1 phase (28.4%), 38 cases in the F2 phase (32.8%), 26 cases in the F3 phase (22.4%), and 19 cases in the F4 phase (16.4%). The Young's modulus values for patients in the F1, F2, F3, and F4 stages were [(5.2 ± 1.3) kPa, (6.3 ± 1.2) kPa, (8.7 ± 1.4) kPa, and (11.9 ± 1.6) kPa, respectively, P<0.05]. The plasma Nrg4 levels for patients in the F1, F2, F3, and F4 stages were [(6.7 ± 1.2) pg/mL, (4.9 ± 1.0) pg/mL, (3.3 ± 0.9) pg/mL, and (1.9 ± 0.5) pg/mL, respectively(P<0.05)]. Spearman correlation analysis showed that the Young's modulus value was positively correlated with the degree of liver fibrosis (r=0.673, P<0.05), while the plasma Nrg4 level was negatively correlated with the degree of liver fibrosis (r=-0.702, P<0.05). ROC analysis revealed the AUC values of Young's modulus for diagnosing F1, F2, F3, and F4 stages of CHB liver fibrosis were 0.85 (95% CI: 0.75-0.94), 0.83 (95% CI: 0.75-0.92), 0.86 (95% CI: 0.76-0.95), and 0.92 (95% CI: 0.82-1.00), respectively. The AUC values for plasma Nrg4 levels in diagnosing F1, F2, F3, and F4 stages were 0.86 (95% CI: 0.76-0.95), 0.82 (95% CI: 0.74-0.91), 0.88 (95% CI: 0.80-0.97), and 0.92 (95% CI: 0.82-1.00), respectively. The AUC values for diagnosing F1, F2, F3, and F4 stages using the combination of Young's modulus and plasma Nrg4 were 0.92 (95% CI: 0.84-0.99), 0.92 (95% CI: 0.85-0.98), 0.94 (95% CI: 0.88-1.00), and 0.97 (95% CI: 0.91-1.00), respectively. These combined AUC values were significantly higher than those of either Yang's modulus or plasma Nrg4 levels alone (P<0.05). Conclusion The effectiveness of Young's modulus value and plasma Nrg4 levels in diagnosing the degree of liver fibrosis in CHB is significant with the combined diagnostic value being even higher.
    Clinical study of tenofovir alafenamide in the newly treated patients with decompensated hepatitis B cirrhosis
    TANG Hai-tao, WANG Xian, ZHOU Jia-qi, WANG Feng-mei, ZHANG Wen-hua
    2024, 29(7):  830-833. 
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    Objective To investigate the efficacy and safety of Tenofovir alafenamide? (TAF) in the the newly treated patients with decompensated hepatitis B cirrhosis. Methods A total of 72 patients were retrospectively analysed in the study, 34 of whom received TAF treatment and 38 of whom received TDF treatment in Wuwei tumor Hospital of Gansu from October 2021 to October 2023.After 24 weeks and 48 weeks of treatment,we compared the changes in ALT,TBil,Alb, PT, CTP scores, and the proportion of patients with virological response (HBVDNA <20 IU/mL) between the two groups. In terms of safety,we compared changes in Scr and BUN, as well as drug-related adverse events. Results After 48 weeks of treatment, the median ALT was 27.10 U/L in the TAF group, which was significantly lower than the median ALT of 30.90 U/L in the TDF group (P < 0.05). Additionally, the Alb level in the TAF group was 39.73 g/L and 41.69 g/L after 24 and 48 weeks of treatment respectively, and this improvement was superior to the TDF group (P<0.05). The virological response rate of HBV DNA was 97.1% and 81.6% in the TAF and TDF groups after 48 weeks of treatment respectively, indicating a better viral response rate for TAF (P<0.05). The Child-Pugh scores significantly decreased in both groups after 24 and 48 weeks of treatment, but the difference was not statistically significant (P>0.05). Regarding safety, after 48 weeks of TAF treatment. BUN and Scr levels were significantly lower in the TAF group compared to the TDF group (P<0.05). No drug-related adverse events or serious adverse events were reported during the treatment period. Conclusion TAF is effective and safe for patients with decompensated hepatitis B liver cirrhosis.
    Viral Hepatitis
    Research on risk factors for hepatitis B virus (HBV) reactivation in HBeAg-positive pregnant chronic hepatitis B carriers after treatment cessation
    LIU Ming, GUO Yan, CHEN Wen-ting, KUANG Xue-mei, LI Shi-lian, JIE Li, XIA Jie, MAO Qing, ZHU Yan
    2024, 29(7):  834-839. 
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    Objective To observe the dynamic changes of HBV RNA, HBV DNA, qHBsAg, qHBeAg and biochemical parameters from initiated antiviral therapy to 96 weeks postpartum in HBeAg-positive pregnant chronic hepatitis B carriers, and to analyze the risk factors for hepatitis flares within 96 weeks after treatment cessation. Methods Pregnant HBeAg-positive patients receiving antiviral prophylaxis and ceasing treatment postpartum were included. HBV RNA, HBV DNA, qHBsAg, qHBeAg, and biochemical parameters were measured at antiviral therapy baseline, at 36 weeks of gestation, at treatment withdrawal postpartum, and/or at 24 weeks postpartum. Virological and biochemical parameters were regularly examined until 96 weeks postpartum. Results 146 patients with a median treatment duration of 16.4 weeks were enrolled. HBV DNA levels and qHBeAg gradually decreased during antiviral therapy, while HBV RNA gradually increased. qHBsAg levels decreased at 36 weeks of gestation compared to baseline, but increased at treatment withdrawal postpartum. All these indicators rebounded and approached or exceeded baseline levels at 24 weeks postpartum. HBeAg seroconversion at 96 weeks postpartum occurred in 5 patients while none experienced HBsAg clearance. The proportion of hepatitis flares was highest at treatment withdrawal postpartum and 24 weeks postpartum (30.1% vs. 30.8%) but only 14 patients (9.59%) required antiviral intervention due to hepatitis flares. According to whether antiviral treatment was restarted, patients were divided into recurrence group (n=14) and non-recurrence group (n=132). Ten patients in the relapse group experienced hepatitis flares after 6 months of treatment cessation, with a median relapse time of 13.5 months. The difference in the type of antiviral therapy drugs and the magnitude of HBeAg decline from baseline to 36 weeks of gestation between the two groups is statistically significant. Conclusion HBeAg-positive pregnant chronic hepatitis B carriers have a certain proportion of hepatitis flares during receiving antiviral prophylaxis and ceasing treatment. The peak occurs at treatment withdrawal postpartum and at 24 weeks postpartum. However, only a small number of patients require further antiviral intervention. The vast majority (71.4%) of postpartum hepatitis flares occured more than 6 months, so it is recommended to be strengthened long-term regular follow-up after treatment discontinuation. The decline levels of HBeAg from the antiviral baseline to the 36 weeks of gestation are independent risk factors for predicting hepatitis flares after treatment cessation.
    Impact of recombinant human interferon- α2b on serum hepcidin levels in hepatitis C patients: underlying mechanism
    WANG Xue-mei, GONG Fu-qi, ZHENG Jin-na, YU Yan-min, XU Jing, YANG Yong-sheng
    2024, 29(7):  840-843. 
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    Objective To investigate the impact of recombinant human interferon-α2b(rhIFN-α2b) on serum hepcidin levels in hepatitis C patients, and to preliminarily explore its imderlying mechanism. Methods A total of 35 hepatitis C patients from January 2020 to January 2023 were selected and divided into a treatment group (n=20) and an untreated group (n=15) based on whether they received rhIFN-α2b treatment in the last 3 months. Serum hepcidin levels were measured in both groups. Additionally, serum hepcidin, signal transducer and activator of transcription 3 (STAT3), and its phosphorylation(pSTAT3) were measured in hepatogenic HepG2 cells treated with 0, 50,100, 200, and 400ul of rhIFN-α2b for 24 hours. Changes in mRNA expression of STAT3 and correlation analyses were performed. Results Serum hepcidin levels in the treated group was significantly lower (94.91 ± 16.28) ng/mL compared to the untreated group (107.99±17.06) ng/mL, with the difference being statistically significant (t=4.396, P<0.05). HepG2 cells treated with rhIFN-α2b at doses of 0 μL (control group), 50 μL (group 1), 100 μL (group 2), 200 μL (group 3), and 400 μL (group 4) exhibited a dose-dependent decrease in hepcidin. mRNA expression: (1.00±0.23), (0.67±0.12), (0.28±0.04), (0.25±0.03), and (0.17±0.02), respectively. The differences in hepcidin mRNA expression among all groups were statistically significant (P<0.05). Pair comparisons showed that group 4 (400 μL) had significantly lower hepcidin mRNA levels than the control group, group 1, group 2 and group 3. Groups 2 and 3 also had significantly lower levels compared to the control group and group 1. Group 1had significantly lower levels than the control group (P<0.05). STAT3 mRNA expression levels in HepG2 cells for the control group, group 1, group 2, group 3, and group 4 were (0.72±0.11), (0.74±0.12), (0.68±0.09), (0.66±0.06), and (0.66±0.08), respectively, with no statistical differences(P>0.05). The pSTAT3 protein levels for rhIFN-α2b at doses of 50 μL, 100 μL, 200 μL , and 400 μL were (0.76±0.14), (0.65±0.06), (0.57±0.07), and (0.54±0.05), respectively, all lower than the control group. However, there were no significant differences in pSTAT3 protein levels among the treated groups (P>0.05). Conclusion After rhIFN-α2b treatment, the serum hepcidin levels in hepatitis C patients are down-regulated in a dose-dependent manner. This down-regulation may be associated with the inhibition of phosphorylation activation in the STAT3 pathway.
    Other Liver Diseases
    Clinical characteristics of 27 cases of eosinophilic gastroenteritis
    HE Meng, HAN Xiao, JIA Ji-dong, ZHAO Xin-yan, LI Peng
    2024, 29(7):  844-847. 
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    Objective This study aims to summarize the clinical characteristics of eosinophilic gastroenteritis (EGE) to enhance awareness, diagnosis, and management of the disease. Methods We retrospectively collected clinical data from 27 EGE patients diagnosed between January 2016 and March 2023 at Beijing Friendship Hospital, Capital Medical University. Subgroup analyses were performed based on ascites, classification, liver function, spontaneous remission, and prognosis. Results The onset age of the 27 EGE patients was 35.00 years, with a higher prevalence in males (Male: Female ratio, 2.3:1). The stomach and/or duodenum were most commonly affected (70.37%), with the mucosal type being the predominant classification (59.26%). A majority of patients (85.19%) showed elevated peripheral eosinophil (EOS) counts. In subgroup analyses, patients with the serosal type had significantly higher peripheral EOS counts and rates of eosinophilic ascites compared to those with mucosal and muscular types (12.85 vs 8.24 vs 11.11×109/L, P=0.029; 87.50% vs 6.25% vs 0, P<0.001). Patients treated with corticosteroids showed significantly higher peripheral EOS counts, EOS%, and Immunoglobulin E (IgE) levels compared to those with spontaneous remission (2.77 vs 0.56×109/L, P=0.016; 29.30% vs 8.05%, P=0.045; 200.00 vs 20.39 IU/mL, P<0.001). The combination of peripheral EOS count and IgE level demonstrated good predictive power for spontaneous remission (AUC 0.92, 95% CI 0.82-1.00). Conclusion EGE is a rare gastrointestinal inflammatory disease that often involves the stomach and duodenum. Corticosteroid therapy is recommended for patients with elevated peripheral EOS counts and IgE levels.
    Distribution and antibiotic resistance analysis of pathogenic bacteria in bile cultures from 105 patients with common bile duct stones and biliary tract infections
    JIA Li, ZHAO Hua-cai, YANG Xing-ping, LIU Jia
    2024, 29(7):  848-851. 
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    Objective To investigate the distribution and drug resistance of pathogenic bacteria in 105 patients with common bile duct stones complicated by biliary tract infection. Methods A total of 105 patients admitted to our hospital from June 2019 to January 2023 were selected for the study, comprising 58 males and 47 females with an average age of (49.6 ± 10.5) years. Based on the condition of the stones, the patients were divided into two groups: the initial group and the recurrent group. General information about the subjects, including gender, age, clinical presentation, laboratory test results, and imaging examination results, was collected. Endoscopic retrograde cholangiopancreatography (ERCP) was performed by experienced doctors using Olympus electronic duodenoscopy. Following the ERCP procedure, 5-10 mL of bile was collected through the nasobiliary duct. The collected bile samples were transferred into sterile test tubes and sent to our hospital laboratory for bacterial culture and analysis. The bile samples were cultured for 48-72 hours, after which the bacterial strains were isolated and identified using the VITEK 2 Compact fully automatic bacterial analyzer. Drug sensitivity tests on bacterial strains were performed using the paper agar diffusion method. The study observed the subject's history of antibiotic use, the positive rate and distribution of bile strain cultures, and the antibiotic resistance of the bacteria found in the bile. Results Based on the condition of the stones, there were 55 cases in the initial group and 50 cases in the recurrent group. The initial group had a higher rate of antibiotic use, compared to the recurrence group(P<0.05). The positive rates of bile culture in the initial and recurrent groups were 83.6% and 94.0%, respectively, and the disfference was statistically significant (P<0.05). The recurrence group showed a significant increase in Gram-negative bacteria and Escherichia coli, compared to the initial group(P<0.05). There was no significant difference in the distribution of other pathogens between the initial and recurrent groups (P>0.05). Furthermore, the antibiotic resistance rate of pathogens was significantly higher in the recurrent group, with notably enhanced resistance (P<0.05). Conclusion The distribution of pathogens in patients with initial and recurrent common bile duct stones complicated by biliary tract infections is similar. However, pathogen resistance in the recurrent group is higher than in the initial group. Clinical doctors should carefully choose antibiotics based on the patient's stone recurrence and resistance testing results.
    Clinical characteristics and influencing factors of liver function abnormalities in preschool children with infectious mononucleosis
    YUE Yun, MA Li, WANG Wei-guo
    2024, 29(7):  852-856. 
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    Objective To analyze the clinical characteristics and factors influencing liver function abnormalities in preschool children with infectious mononucleosis (IM). Methods A retrospective analysis was conduced on the clinical and laboratory data of 140 preschool children diagnosed with IM and treated at Fuyang People's Hospital from January 2020 to July 2023. Based on alanine aminotransferase (ALT) levels, the children were categorized into a normal liver function group(ALT <50 U/L) and an abnormal liver function group(ALT ≥50 U/L). Basic conditions, clinical symptoms, hospitalization duration, and laboratory indices were compared between the two groups. Statistically significant indices were further analyzed using covariance adjustment and binary regression analysis. Additionally, the clinical value of relevant indices was assessed using receiver operating characteristic (ROC) analysis, with pairwise comparisons of the area under the curve (AUC) to determine statistical significance. Results The incidence of liver function abnormalities in preschool children with IMwas 43.6%. There were no statistically significant differences in age, gender, season of onset, clinical symptoms, and viral load of EBV-positive children between the two groups (P>0.05). Compared to the group with normal liver function, the group with abnormal liver function had significantly higher hospitalization days[7(6,9)d], lymphocyte count[10.10(8.65,14.82)×109/L] and CD8+ T lymphocytes[7690.00(4585.37,11164.50)/uL] (P<0.05), Conversely, the CD4+/CD8+ ratio[0.21(0.17,0.29)], neutrophil count[2.7(2.06,4.12)×109/L], platelet count[199(148,228.5)×109/L], and systemic immune-inflammation index (SII) [46.34(26.63, 93.78)]were significantly lower in the abnormal liver gunction group (P<0.05). Low SII was closely associated with liver function abnormalities in IM preschoolers. The diagnostic efficacy of SII for liver function abnormalities was assessed using ROC curve analysis, with a critical value of 59.13 and an AUC of 0.758, indicating high diagnostic value, superior to CD8+T lymphocytes and CD4+/CD8+ ratio. Conclusion Preschool children with IM and concurrent liver function abnormalities exhibit significant cellular immune dysfunction. Elevated CD8+ T-lymphocytes, low SII and low CD4+/ CD8+ ratio are associated with a high risk of liver abnormalities. These findings suggest that clinical attention should be focused on these immunological markers to better manage and monitor the risk of liver function abnormalitis in IM preschool children.
    Comparison of clinical characteristics and therapeutic effects in autoimmune hepatitis patients presenting with acute and chronic liver injury patterns
    ZHENG Xiang-wei, LI Shi-kun
    2024, 29(7):  857-861. 
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    Objective To compare the clinical features of patients with autoimmune hepatitis (AIH) presenting with acute versus chronic liver injury, and to evaluate the differences in clinical treatment strategies. Methods Ninety-eight patients with AIH admitted to our hospital betwee January 2020 and January 2022 were selected and divided into two groups based on clinical diagnosis: the acute onset group(n=46) and the chronic onset group (n=52). The clinical data of both groups were analyzed, and the efficacy of glucocorticoid treatment was compared between the two groups. Results Upon analysis, jaundice was more commonly observed as an initial symptom in the acute onset group (21.7%) compared to the chronic onset group (7.7%) (P<0.05). Conversely, the percentage of initially asymptomatic patients was higher in the chronic onset group (28.8%) than in the acute onset group(10.9%) (P<0.05). Regarding inflammatory manifestations, hepatic lobular inflammation was more prevalent in the acute onset group (56.5%) than in the chronic onset group (34.6%) (P<0.05), while portal phlebitis was less common in the acute onset group (17.4%)compared to the chronic onset group (55.8%) (P<0.05).The incidence of fibrosis was higher in the chronic onset group (82.7%) than in the acute onset group(65.2%) (P<0.05). Biochemically, the AST level in the chronic onset group was (169.9±10.4) U/L, lower than in the acute onset group [(206.5±13.5) U/L, P<0.05], the ALT level in the chronic onset group was (196.7±11.4) U/L, also lower than in the acute onset group [(279.8±14.7) U/L, P<0.05]. The IgG level in the chronic onset group was (1807.8±122.7)mg/dl, higher than in the acute onset group [(1648.8±110.9) U/L, P<0.05]. After 6 months of treatment, the ALT level in the acute onset group was (20.1±2.0) U/L, lower than in the chronic onset group [(24.7±1.9) U/L, P<0.05], and the IgG level was (941.5±90.1)mg/dl, lower than in the chronic onset group [(1122.7±100.2)mg/dl, P<0.05]. Conclusion Different inflammatory conditions lead to varing degrees of urgency in onset, resulting in differences in initial symptoms and biochemical indicators. Patients with acute onset respond more significantly to standard treatment regimens compared to those with chronic onset. Therefore, timely adjustments to medication are necessary in clinical treatment, taking into account the type of inflammation and the patient's suitability for the treatment regimen.
    Analysis and prediction model of key testing indicators in component transfusion for liver disease
    WU Chun-fang, YANG Sen, XIA Yi-lan, WANG Yue-e, LIN Yong, YAO Yu-rong, CHU Qing
    2024, 29(7):  862-866. 
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    Objective To study the principal component analysis and prediction model of key test indicators in component transfusion for liver disease. Methods A retrospective study was conducted, collecting data from patients with liver disease and those without, who underwent component transfusion from January 2017 to December 2022. Patients were categorized based on the types of transfusion received: suspended red blood cell transfusion, virus-inactivated frozen plasma transfusion, and single-donor platelet transfusion. Genera patient information and pre-transfusion laboratory indicators were gathered, including hemoglobin (Hb), hematocrit (HCT), platelet count , coagulation function indicators, liver function indicators, and transfusion conditions. Differences in these indicators between liver disease and non-liver disease groups were analyzed using T-tests and variance analysis. The suitability of factor analysis was confirmed by the KMO test, Bartlett's sphericity test, and Scree Test. Principal component analysis (PCA) was utilized to observe the variance contribution of each indicator and evaluate their correlations. Receiver operating characteristic (ROC) curve analysis was performed to assess the predictive value of each test indicator for different component transfusions. Results A total of 96 liver disease patients and 216 non-liver disease patients were included in the study. Among the liver disease patients, 57.30% received plasma transfusion (55/96 cases), while 54.20% of the non-liver disease patients received red blood cell transfusion (117/216 cases). The average Hb levels were 70.61 g/L for liver disease patients and 82.82 g/L for non-liver disease patients HCT levels averaged 20.80% and 24.47%, alanine aminotransferase(ALT) were 45.94 U/L and 25.43 U/L, and total bilirubin(TBil) levels were 44.38 μmol/L and 19.31 μmol/L, respectively, for liver disease and non-liver disease groups. These four indicators showed significant differences between the groups (P<0.05). In the plasma transfusion group, the average Hb levels were 73.45 g/L for liver disease patients and 111.43 g/L for non-liver disease patients. HCT levels averaged 21.70% and 31.06%, ALT levels were 59.33 U/L and 28.33 U/L, aspartate aminotransferase(AAT) levels were 44.35 U/L and 22.52 U/L, and INR values were 1.43 and 1.07, respectively, for liver disease and non-liver disease patients. These indicators also showed significant differences (P<0.05). In the platelet transfusion group, the average platelet counts were 36.70×109/L for liver disease patients and 50.76×109/L for non-liver disease patients, ALT levels were 54.20 U/L and 31.19 U/L, PT was 15.95 s and 12.98 s, APTT was 54.42 s and 29.90 s, and INR values were 1.36 and 1.11, respectively, for liver dosease and non-liver disease patients. These five indicators showed significant differences (P<0.05). PCA revealed that the primary and secondary components of pre-transfusion indicators in liver disease patients were blood and liver function indicators, respectively, whereas in non-liver disease patients, the primary components were liver function and coagulation indicators. ROC curve analysis demonstrated that the area under the curve(AUC) for HCT in the red blood cell transfusion group was 0.912; in the plasma transfusion group, the AUCs for INR and PT were 0.964 and 0.953, respectively. In the platelet transfusion group, the AUC for INR was 0.938. Conclusion This study establishes a foundation for correlation analysis and predictive modeling of various pre-transfusion indicators, particularly aiding in the selection of appropriate component transfusions for liver disease patients.