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ISSN 2097-3497 (Online)
CN 22-1108/R
Volume 40 Issue 3
Mar.  2024
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Article Contents

Value of alkaline phosphatase level after ursodeoxycholic acid treatment for one month and baseline red blood cell distribution width in predicting the treatment response of primary biliary cholangitis

DOI: 10.12449/JCH240310
Research funding:

National Natural Science Foundation of China (82000261);

China Public Health Program (GWLM202002);

Key Project of Medical Education Collaborative Innovation Fund of Jiangsu University (JDY2023020)

More Information
  • Corresponding author: ZHANG Pengfei, 316959714@qq.com (ORCID: 0009-0007-4358-886X); TAN Youwen, tyw915@sina.com (ORCID: 0000-0002-5464-1407)
  • Received Date: 2023-10-09
  • Accepted Date: 2023-11-08
  • Published Date: 2024-03-20
  •   Objective  To investigate the value of baseline red cell distribution width (RDW) and alkaline phosphatase (ALP) level after ursodeoxycholic acid (UDCA) treatment for one month in predicting the response to UDCA treatment in patients with primary biliary cholangitis (PBC).  Methods  A retrospective analysis was performed for the data of 127 patients with PBC who were diagnosed in Department of Hepatology, The Third People’s Hospital of Jiangsu University, from January 2015 to July 2022, with data collected at baseline, after one month of treatment, and after one year of follow-up. Based on the Paris-I criteria, the patients were divided into good response group and poor response group, and the two groups were analyzed in terms of clinical and laboratory features and their association with response to UDCA. The Logistic regression method was used to investigate the independent risk factors for response to UDCA treatment. The area under the ROC curve (AUC) was used to determine the optimal cut-off values of related indicators; the patients were divided into two groups based on such values, and the two groups were compared in terms of baseline indicators and response. The independent-samples t test was used for comparison of normally distributed continuous data between two groups, and the Mann-Whitney U test was used for comparison of non-normally distributed continuous data between two groups; the chi-square test was used for comparison of categorical data between two groups.  Results  Compared with the good response group, the poor response group had significantly higher levels of total bilirubin, aspartate aminotransferase/alanine aminotransferase, ALP, RDW, and RDW-CV at baseline and a significantly higher level of ALP after one month of UDCA treatment (Z=-4.792, -3.697, -2.399, -4.102, -3.220, and -4.236, all P<0.05). Compared with the good response group, the poor response group had significantly lower levels of albumin, hemoglobin, lymphocytes, hematocrit, and body mass index at baseline (Z=-3.592, -3.603, -2.602, -3.829, -2.432, all P<0.05), as well as significantly lower levels of prealbumin, albumin/globulin ratio, apolipoprotein A, and free triiodothyronine at baseline (t=4.530, 3.402, 3.485, and 3.639, all P<0.001). Compared with the poor response group, the good response group had a significantly lower proportion of patients with liver cirrhosis, gallstones/cholecystitis, or anemia (χ2=20.815, 3.892, and 12.283, all P<0.05). Baseline RDW (odds ratio [OR]=1.157, 95% confidence interval [CI]: 1.028‍ — ‍1.301, P=0.015) and ALP level after one month of treatment (OR=1.012, 95%CI: 1.005‍ — ‍1.020, P=0.002) were independent risk factors for response to UDCA, with an AUC of 0.713 and 0.720, respectively. The patients with baseline RDW≥upper limit of normal (ULN) and ALP≥2.2×ULN after one month of UDCA treatment had a lower UDCA response rate (42.6% vs 8.2%, χ2=20.813, P<0.001).  Conclusion  Patients with baseline RDW≥ULN and ALP≥2.2×ULN after one month of UDCA treatment tend to have a low biochemical response rate to UDCA.

     

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  • [1]
    GULAMHUSEIN AF, HIRSCHFIELD GM. Primary biliary cholangitis: pathogenesis and therapeutic opportunities[J]. Nat Rev Gastroenterol Hepatol, 2020, 17( 2): 93- 110. DOI: 10.1038/s41575-019-0226-7.
    [2]
    FLOREANI A, GABBIA D, de MARTIN S. Obeticholic acid for primary biliary cholangitis[J]. Biomedicines, 2022, 10( 10). DOI: 10.3390/biomedicines10102464.
    [3]
    YOU H, MA X, EFE C, et al. APASL clinical practice guidance: the diagnosis and management of patients with primary biliary cholangitis[J]. Hepatol Int, 2022, 16( 1): 1- 23. DOI: 10.1007/s12072-021-10276-6.
    [4]
    HARMS MH, LAMMERS WJ, THORBURN D, et al. Major hepatic complications in ursodeoxycholic acid-treated patients with primary biliary cholangitis: Risk factors and time trends in incidence and outcome[J]. Am J Gastroenterol, 2018, 113( 2): 254- 264. DOI: 10.1038/ajg.2017.440.
    [5]
    European Association for the Study of the Liver. EASL Clinical Practice Guidelines: The diagnosis and management of patients with primary biliary cholangitis[J]. J Hepatol, 2017, 67( 1): 145- 172. DOI: 10.1016/j.jhep.2017.03.022.
    [6]
    NEVENS F, ANDREONE P, MAZZELLA G, et al. A placebo-controlled trial of obeticholic acid in primary biliary cholangitis[J]. N Engl J Med, 2016, 375( 7): 631- 643. DOI: 10.1056/NEJMoa1509840.
    [7]
    TANAKA A. Current understanding of primary biliary cholangitis[J]. Clin Mol Hepatol, 2021, 27( 1): 1- 21. DOI: 10.3350/cmh.2020.0028.
    [8]
    BRUNET E, HERNÁNDEZ L, MIQUEL M, et al. Analysis of predictive response scores to treatment with ursodeoxycholic acid in patients with primary biliary cholangitis[J]. Med Clin(Barc), 2019, 152( 10): 377- 383. DOI: 10.1016/j.medcli.2018.08.002.
    [9]
    TERZIROLI BERETTA-PICCOLI B, MIELI-VERGANI G, VERGANI D, et al. The challenges of primary biliary cholangitis: What is new and what needs to be done[J]. J Autoimmun, 2019, 105: 102328. DOI: 10.1016/j.jaut.2019.102328.
    [10]
    ALOMARI M, COVUT F, MOMANI L AL, et al. Evaluation of the United Kingdom-primary biliary cholangitis and global primary biliary cholangitis group prognostic models for primary biliary cholangitis patients treated with ursodeoxycholic acid in the U.S. population[J]. JGH Open, 2020, 4( 2): 132- 139. DOI: 10.1002/jgh3.12223.
    [11]
    SCHATTENBERG JM, PARES A, KOWDLEY KV, et al. A randomized placebo-controlled trial of elafibranor in patients with primary biliary cholangitis and incomplete response to UDCA[J]. J Hepatol, 2021, 74( 6): 1344- 1354. DOI: 10.1016/j.jhep.2021.01.013.
    [12]
    ASLAM H, OZA F, AHMED K, et al. The role of red cell distribution width as a prognostic marker in chronic liver disease: A literature review[J]. Int J Mol Sci, 2023, 24( 4): 3487. DOI: 10.3390/ijms24043487.
    [13]
    LOU Y, WANG M, MAO W. Clinical usefulness of measuring red blood cell distribution width in patients with hepatitis B[J]. PLoS One, 2012, 7( 5): e37644. DOI: 10.1371/journal.pone.0037644.
    [14]
    YANG CY, MA X, TSUNEYAMA K, et al. IL-12/Th1 and IL-23/Th17 biliary microenvironment in primary biliary cirrhosis: implications for therapy[J]. Hepatology, 2014, 59( 5): 1944- 1953. DOI: 10.1002/hep.26979.
    [15]
    WANG H, XU H, WANG X, et al. Red blood cell distribution width to platelet ratio is related to histologic severity of primary biliary cirrhosis[J]. Medicine(Baltimore), 2016, 95( 11): e3114. DOI: 10.1097/MD.0000000000003114.
    [16]
    OWOICHO O, TAPELA K, OLWAL CO, et al. Red blood cell distribution width as a prognostic biomarker for viral infections: prospects and challenges[J]. Biomark Med, 2022, 16( 1): 41- 50. DOI: 10.2217/bmm-2021-0364.
    [17]
    CORTEZ-PINTO H, LIBERAL R, LOPES S, et al. Predictors for incomplete response to ursodeoxycholic acid in primary biliary cholangitis. Data from a national registry of liver disease[J]. United European Gastroenterol J, 2021, 9( 6): 699- 706. DOI: 10.1002/ueg2.12095.
    [18]
    ANGULO P, LINDOR KD, THERNEAU TM, et al. Utilization of the Mayo risk score in patients with primary biliary cirrhosis receiving ursodeoxycholic acid[J]. Liver, 1999, 19( 2): 115- 121. DOI: 10.1111/j.1478-3231.1999.tb00020.x.
    [19]
    PARÉS A, CABALLERÍA L, RODÉS J. Excellent long-term survival in patients with primary biliary cirrhosis and biochemical response to ursodeoxycholic acid[J]. Gastroenterology, 2006, 130( 3): 715- 720. DOI: 10.1053/j.gastro.2005.12.029.
    [20]
    JORGENSEN RA, DICKSON ER, HOFMANN AF, et al. Characterisation of patients with a complete biochemical response to ursodeoxycholic acid[J]. Gut, 1995, 36( 6): 935- 938. DOI: 10.1136/gut.36.6.935.
    [21]
    CARBONE M, NARDI A, FLACK S, et al. Pretreatment prediction of response to ursodeoxycholic acid in primary biliary cholangitis: development and validation of the UDCA Response Score[J]. Lancet Gastroenterol Hepatol, 2018, 3( 9): 626- 634. DOI: 10.1016/S2468-1253(18)30163-8.
    [22]
    ZHANG LN, SHI TY, SHI XH, et al. Early biochemical response to ursodeoxycholic acid and long-term prognosis of primary biliary cirrhosis: results of a 14-year cohort study[J]. Hepatology, 2013, 58( 1): 264- 272. DOI: 10.1002/hep.26322.
    [23]
    MURILLO PEREZ CF, IOANNOU S, HASSANALLY I, et al. Optimizing therapy in primary biliary cholangitis: Alkaline phosphatase at six months identifies one-year non-responders and predicts survival[J]. Liver Int, 2023, 43( 7): 1497- 1506. DOI: 10.1111/liv.15592.
    [24]
    YANG C, GUO G, LI B, et al. Prediction and evaluation of high-risk patients with primary biliary cholangitis receiving ursodeoxycholic acid therapy: an early criterion[J]. Hepatol Int, 2023, 17( 1): 237- 248. DOI: 10.1007/s12072-022-10431-7.
    [25]
    HUANG LX, WANG ZL, JIN R, et al. Incomplete response to ursodeoxycholic acid in primary biliary cholangitis: criteria, epidemiology, and possible mechanisms[J]. Expert Rev Gastroenterol Hepatol, 2022, 16( 11-12): 1065- 1078. DOI: 10.1080/17474124.2022.2153672.
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