Assessment of anemia recovery using peripheral blood smears by deep semi-supervised learning.

Journal: Annals of hematology
PMID:

Abstract

Monitoring anemia recovery is crucial for clinical intervention. Morphological assessment of red blood cells (RBCs) with peripheral blood smears (PBSs) provides additional information beyond routine blood tests. However, the PBS test is labor-intensive, reliant on manual analysis, and susceptible to variability in expert interpretations. Here we introduce a deep semi-supervised learning method, RBCMatch, to classify RBCs during anemia recovery. Using an acute hemolytic anemic mouse model, PBS images at four different time points during anemia recovery were acquired and segmented into 10,091 single RBC images, with only 5% annotated and used in model training. By employing the semi-supervised strategy Fixmatch, RBCMatch achieved an impressive average classification accuracy of 91.2% on the validation dataset and 87.5% on a held-out dataset, demonstrating its superior accuracy and robustness compared to supervised learning methods, especially when labeled samples are scarce. To characterize the anemia recovery process, principal components (PCs) of RBC embeddings were extracted and visualized. Our results indicated that RBC embeddings quantified the state of anemia recovery, and the second PC had a strong correlation with RBC count and hemoglobin concentration, demonstrating the model's ability to accurately depict RBC morphological changes during anemia recovery. Thus, this study provides a valuable tool for the automatic classification of RBCs and offers novel insights into the assessment of anemia recovery, with the potential to aid in clinical decision-making and prognosis analysis in the future.

Authors

  • Qianming Yan
    Ministry of Education Key Laboratory of Bioinformatics, Center for Synthetic and Systems Biology, Beijing National Research Center for Information Science and Technology, Department of Automation, Tsinghua University, Beijing, China.
  • Yingying Zhang
    Laboratory of Pharmacology, Institute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences, Beijing 100700, P.R. China.
  • Lei Wei
    MOE Key Laboratory of Bioinformatics and Bioinformatics Division of BNRIST, Department of Automation, Tsinghua University, Beijing 100084, China.
  • Xuehui Liu
    State Key Laboratory of Complex, Severe, and Rare Diseases, Haihe Laboratory of Cell Ecosystem, Department of Pathophysiology, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China. liuxuehui@ibms.pumc.edu.cn.
  • Xiaowo Wang
    Ministry of Education Key Laboratory of Bioinformatics; Center for Synthetic and Systems Biology; Bioinformatics Division, Beijing National Research Center for Information Science and Technology; Department of Automation, Tsinghua University, Beijing 100084, China.