Proteomics landscape and machine learning prediction of long‐term response to splenectomy in primary immune thrombocytopenia

Author:

Sun Ting12,Chen Jia12ORCID,Xu Yuan12ORCID,Li Yang12ORCID,Liu Xiaofan12,Li Huiyuan12,Fu Rongfeng12ORCID,Liu Wei12ORCID,Xue Feng12ORCID,Ju Mankai12,Dong Huan12ORCID,Wang Wentian12ORCID,Chi Ying12,Yang Renchi12,Chen Yunfei12ORCID,Zhang Lei123ORCID

Affiliation:

1. State Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Haihe Laboratory of Cell Ecosystem, CAMS Key Laboratory of Gene Therapy for Blood Diseases, Tianjin Key Laboratory of Gene Therapy for Blood Diseases, Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College Tianjin China

2. Tianjin Institutes of Health Science Tianjin China

3. School of Population Medicine and Public Health, Chinese Academy of Medical Sciences and Peking Union Medical College Beijing China

Abstract

SummaryThis study aimed to identify key proteomic analytes correlated with response to splenectomy in primary immune thrombocytopenia (ITP). Thirty‐four patients were retrospectively collected in the training cohort and 26 were prospectively enrolled as validation cohort. Bone marrow biopsy samples of all participants were collected prior to the splenectomy. A total of 12 modules of proteins were identified by weighted gene co‐expression network analysis (WGCNA) method in the developed cohort. The tan module positively correlated with megakaryocyte counts before splenectomy (r = 0.38, p = 0.027), and time to peak platelet level after splenectomy (r = 0.47, p = 0.005). The blue module significantly correlated with response to splenectomy (r = 0.37, p = 0.0031). KEGG pathways analysis found that the PI3K‐Akt signalling pathway was predominantly enriched in the tan module, while ribosomal and spliceosome pathways were enriched in the blue module. Machine learning algorithm identified the optimal combination of biomarkers from the blue module in the training cohort, and importantly, cofilin‐1 (CFL1) was independently confirmed in the validation cohort. The C‐index of CFL1 was >0.7 in both cohorts. Our results highlight the use of bone marrow proteomics analysis for deriving key analytes that predict the response to splenectomy, warranting further exploration of plasma proteomics in this patient population.

Publisher

Wiley

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