Development and validation of machine learning model for predicting treatment responders in patients with primary biliary cholangitis

被引:0
|
作者
Kimura, Naruhiro [1 ]
Takahashi, Kazuya [1 ]
Setsu, Toru [1 ]
Horibata, Yusuke [1 ]
Kaneko, Yusuke [1 ]
Miyazaki, Haruka [1 ]
Ogawa, Kohei [1 ]
Kawata, Yuzo [1 ]
Sakai, Norihiro [1 ]
Watanabe, Yusuke [1 ]
Abe, Hiroyuki [1 ]
Kamimura, Hiroteru [1 ]
Sakamaki, Akira [1 ]
Yokoo, Takeshi [1 ]
Kamimura, Kenya [1 ]
Tsuchiya, Atsunori [1 ]
Terai, Shuji [1 ]
机构
[1] Niigata Univ, Grad Sch Med & Dent Sci, Div Gastroenterol & Hepatol, 1-757 Asahimachi Dori,Chuo Ku, Niigata 9518510, Japan
关键词
biochemical response; machine learning; Paris II criteria; prediction; primary biliary cholangitis; URSODEOXYCHOLIC ACID; BIOCHEMICAL RESPONSE; CIRRHOSIS; PROGNOSIS;
D O I
10.1111/hepr.13966
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
AimsUrsodeoxycholic acid is the first-line treatment for primary biliary cholangitis, and treatment response is one of the factors predicting the outcome. To prescribe alternative therapies, clinicians might need additional information before deciphering the treatment response to ursodeoxycholic acid, contributing to a better patient prognosis. In this study, we developed and validated machine learning (ML) algorithms to predict treatment responses using pretreatment data.MethodsThis multicenter cohort study included collecting datasets from two data samples. Data 1 included 245 patients from 18 hospitals for ML development, and was divided into (i) training and (ii) development sets. Data 2 (iii: test set) included 51 patients from our hospital for validation. An extreme gradient boosted tree predicted the treatment response in the ML model. The area under the curve was used to evaluate the efficacy of the algorithm.ResultsData 1 showed that patients complying with the Paris II treatment response had significantly lower serum alkaline phosphatase and total bilirubin levels than those who did not respond. Three factors, total bilirubin, total protein, and alanine aminotransferase levels were selected as essential variables for prediction. Data 2 showed that patients complying with the Paris II criteria had significantly high prothrombin time and low total bilirubin levels. The area under the curve of extreme gradient boosted tree was good for (ii) (0.811) and (iii) (0.856).ConclusionsWe demonstrated the efficacy of ML in predicting the treatment response for patients with primary biliary cholangitis. Early identification of cases requiring additional treatment with our novel ML model may improve prognosis. image
引用
收藏
页码:67 / 77
页数:11
相关论文
共 50 条
  • [41] Efficacy of Obeticholic Acid Treatment in Patients with Primary Biliary Cholangitis with Cirrhosis
    Vierling, John M.
    Hirschfield, Gideon M.
    Jones, David
    Groszmann, Roberto J.
    Kowdley, Kris V.
    Pencek, Richard
    Marmon, Tonya
    MacConell, Leigh
    [J]. HEPATOLOGY, 2016, 64 : 187A - 187A
  • [42] Mechanism for development of malnutrition in primary biliary cholangitis
    Vasiliy Ivanovich Reshetnyak
    Igor Veniaminovich Maev
    [J]. World Journal of Meta-Analysis, 2022, (03) : 81 - 98
  • [43] SELADELPAR FOR THE TREATMENT OF PRIMARY BILIARY CHOLANGITIS: EXPERIENCE WITH 26 CIRRHOTIC PATIENTS
    Mayo, Marlyn J.
    Bowlus, Christopher L.
    Galambos, Michael
    Neff, Guy
    Trivedi, Palak
    Goel, Aparna
    Odin, Joseph
    Bacon, Bruce R.
    Borg, Brian B.
    Gordon, Stuart C.
    Gulamhusein, Aliya
    Harrison, Stephen
    Levy, Cynthia
    Stanca, Carmen
    Vierling, John M.
    Steinberg, Alexandra
    Varga, Monika
    Nguyen, Jaidyn
    Bergheanu, Sandrin
    Choi, Yun-Jung
    Standen, Mary
    Boudes, Pol
    [J]. GASTROENTEROLOGY, 2019, 156 (06) : S1319 - S1319
  • [44] Development and validation of a machine-learning model for predicting the risk of death in sepsis patients with acute kidney injury
    Dong, Lei
    Liu, Pei
    Qi, Zhili
    Lin, Jin
    Duan, Meili
    [J]. HELIYON, 2024, 10 (09)
  • [45] Ocaliva® is authorized for the Treatment of primary biliary Cholangitis
    Langenbacher, Diane
    [J]. VISCERAL MEDICINE, 2017, 33 (01) : 93 - 93
  • [46] Obeticholic acid for the treatment of primary biliary cholangitis
    Ali, Ahmad H.
    Lindor, Keith D.
    [J]. EXPERT OPINION ON PHARMACOTHERAPY, 2016, 17 (13) : 1809 - 1815
  • [47] New forms of treatment for primary biliary cholangitis
    Hatzis, G.
    Androutsakos, T.
    Vallilas, C.
    Kalisperati, X.
    Chatzis, L.
    [J]. ARCHIVES OF HELLENIC MEDICINE, 2018, 35 (06): : 741 - 756
  • [48] New Treatment Paradigms in Primary Biliary Cholangitis
    Levy, Cynthia
    Manns, Michael
    Hirschfield, Gideon
    [J]. CLINICAL GASTROENTEROLOGY AND HEPATOLOGY, 2023, 21 (08) : 2076 - 2087
  • [49] Primary biliary cholangitis: Epidemiology, prognosis, and treatment
    Trivella, Juan
    John, Binu V.
    Levy, Cynthia
    [J]. HEPATOLOGY COMMUNICATIONS, 2023, 7 (06)
  • [50] Novel Treatment Strategies for Primary Biliary Cholangitis
    Pares, Albert
    [J]. SEMINARS IN LIVER DISEASE, 2017, 37 (01) : 60 - 72