A Three-Gene Peripheral Blood Potential Diagnosis Signature for Acute Rejection in Renal Transplantation

被引:4
作者
Wang, Yicun [1 ,2 ]
Zhang, Di [1 ,2 ]
Hu, Xiaopeng [1 ,2 ]
机构
[1] Capital Med Univ, Beijing Chao Yang Hosp, Dept Urol, Beijing, Peoples R China
[2] Capital Med Univ, Inst Urol, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
renal transplantation; acute rejection; diagnostic signature; peripheral blood; gene expression; T-cell mediated rejection; immune cell analysis; ALLOGRAFT SURVIVAL; KIDNEY; RISK;
D O I
10.3389/fmolb.2021.661661
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: Acute rejection (AR) remains a major issue that negatively impacts long-term allograft survival in renal transplantation. The current study aims to apply machine learning methods to develop a non-invasive diagnostic test for AR based on gene signature in peripheral blood. Methods: We collected blood gene expression profiles of 251 renal transplant patients with biopsy-proven renal status from three independent cohorts in the Gene Expression Omnibus database. After differential expression analysis and machine learning algorithms, selected biomarkers were applied to the least absolute shrinkage and selection operator (LASSO) logistic regression to construct a diagnostic model in the training cohort. The diagnostic ability of the model was further tested in validation cohorts. Gene set enrichment analysis and immune cell assessment were also conducted for further investigation. Results: A novel diagnostic model based on three genes (TSEN15, CAPRIN1 and PRR34-AS1) was constructed in the training cohort (AUC = 0.968) and successfully verified in the validation cohort (AUC = 0.925) with high accuracy. Moreover, the diagnostic model also showed a promising value in discriminating T cell-mediated rejection (TCMR) (AUC = 0.786). Functional enrichment analysis and immune cell evaluation demonstrated that the AR model was significantly correlated with adaptive immunity, especially T cell subsets and dendritic cells. Conclusion: We identified and validated a novel three-gene diagnostic model with high accuracy for AR in renal transplant patients, and the model also performed well in distinguishing TCMR. The current study provided a promising tool to be used as a precise and cost-effective non-invasive test in clinical practice.
引用
收藏
页数:12
相关论文
共 43 条
  • [1] Accelerating Novel Candidate Gene Discovery in Neurogenetic Disorders via Whole-Exome Sequencing of Prescreened Multiplex Consanguineous Families
    Alazami, Anas M.
    Patel, Nisha
    Shamseldin, Hanan E.
    Anazi, Shamsa
    Al-Dosari, Mohammed S.
    Alzahrani, Fatema
    Hijazi, Hadia
    Alshammari, Muneera
    Aldahmesh, Mohammed A.
    Salih, Mustafa A.
    Faqeih, Eissa
    Alhashem, Amal
    Bashiri, Fahad A.
    Al-Owain, Mohammed
    Kentab, Amal Y.
    Sogaty, Sameera
    Al Tala, Saeed
    Temsah, Mohamad-Hani
    Tulbah, Maha
    Aljelaify, Rasha F.
    Alshahwan, Saad A.
    Seidahmed, Mohammed Zain
    Alhadid, Adnan A.
    Aldhalaan, Hesham
    AlQallaf, Fatema
    Kurdi, Wesam
    Alfadhel, Majid
    Babay, Zainab
    Alsogheer, Mohammad
    Kaya, Namik
    Al-Hassnan, Zuhair N.
    Abdel-Salam, Ghada M. H.
    Al-Sannaa, Nouriya
    Al Mutairi, Fuad
    El Khashab, Heba Y.
    Bohlega, Saeed
    Jia, Xiaofei
    Nguyen, Henry C.
    Hammami, Rakad
    Adly, Nouran
    Mohamed, Jawahir Y.
    Abdulwahab, Firdous
    Ibrahim, Niema
    Naim, Ewa A.
    Al-Younes, Banan
    Meyer, Brian F.
    Hashem, Mais
    Shaheen, Ranad
    Xiong, Yong
    Abouelhoda, Mohamed
    [J]. CELL REPORTS, 2015, 10 (02): : 148 - 161
  • [2] Random forests
    Breiman, L
    [J]. MACHINE LEARNING, 2001, 45 (01) : 5 - 32
  • [3] Autosomal-Recessive Mutations in the tRNA Splicing Endonuclease Subunit TSEN15 Cause Pontocerebellar Hypoplasia and Progressive Microcephaly (vol 99, pg 228, 2016)
    Breuss, Martin W.
    Sultan, Tipu
    James, Kiely N.
    Rosti, Rasim O.
    Scott, Eric
    Musaev, Damir
    Furia, Bansri
    Reis, Andre
    Sticht, Heinrich
    Al-Owain, Mohammed
    Alkuraya, Fowzan S.
    Reuter, Miriam S.
    Abou Jamra, Rami
    Trotta, Christopher R.
    Gleeson, Joseph G.
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2016, 99 (03) : 785 - 785
  • [4] Integrative Analysis of Prognostic Biomarkers for Acute Rejection in Kidney Transplant Recipients
    Cao, Yue
    Alexander, Stephen, I
    Chapman, Jeremy R.
    Craig, Jonathan C.
    Wong, Germaine
    Yang, Jean Y. H.
    [J]. TRANSPLANTATION, 2021, 105 (06) : 1225 - 1237
  • [5] Long-Term Outcomes after Acute Rejection in Kidney Transplant Recipients: An ANZDATA Analysis
    Clayton, Philip A.
    McDonald, Stephen P.
    Russ, Graeme R.
    Chadban, Steven J.
    [J]. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2019, 30 (09): : 1697 - 1707
  • [6] Noninvasive methods to assess the risk of kidney transplant rejection
    Cravedi, Paolo
    Mannon, Roslyn B.
    [J]. EXPERT REVIEW OF CLINICAL IMMUNOLOGY, 2009, 5 (05) : 535 - 546
  • [7] Machine Learning in Medicine
    Deo, Rahul C.
    [J]. CIRCULATION, 2015, 132 (20) : 1920 - 1930
  • [8] A molecular classifier for predicting future graft loss in late kidney transplant biopsies
    Einecke, Gunilla
    Reeve, Jeff
    Sis, Banu
    Mengel, Michael
    Hidalgo, Luis
    Famulski, Konrad S.
    Matas, Arthur
    Kasiske, Bert
    Kaplan, Bruce
    Halloran, Philip F.
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 2010, 120 (06) : 1862 - 1872
  • [9] Non-invasive approaches in the diagnosis of acute rejection in kidney transplant recipients, part II: omics analyses of urine and blood samples
    Erpicum, Pauline
    Hanssen, Oriane
    Weekers, Laurent
    Lovinfosse, Pierre
    Meunier, Paul
    Tshibanda, Luaba
    Krzesinski, Jean-Marie
    Hustinx, Roland
    Jouret, Francois
    [J]. CLINICAL KIDNEY JOURNAL, 2017, 10 (01) : 106 - 115
  • [10] PRR34-AS1 overexpression promotes protection of propofol pretreatment against ischemia/reperfusion injury in a mouse model after total knee arthroplasty via blockade of the JAK1-dependent JAK-STAT signaling pathway
    Fang, Hua
    Zhang, Fang-Xiang
    Li, Hua-Feng
    Yang, Miao
    Liao, Ren
    Wang, Ru-Rong
    Wang, Quan-Yun
    Zheng, Peng-Cheng
    Zhang, Jian-Ping
    [J]. JOURNAL OF CELLULAR PHYSIOLOGY, 2020, 235 (03) : 2545 - 2556