Letter to the editor regarding: ‘Construction of a predictive model for relapse of primary autoimmune hemolytic anemia: a retrospective cohort study’
Rong Zhou, Mengyuan Shen, Jiannong Wu

Abstract
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TopicsBlood groups and transfusion · Erythrocyte Function and Pathophysiology · Hepatitis B Virus Studies
To the editor
We read with great interest the article by Pan Li et al. titled ‘Construction of a predictive model for relapse of primary autoimmune hemolytic anemia: a retrospective cohort study’ [1]. The nomogram model constructed in this study can effectively predict the risk of relapse within one year for patients with primary AIHA, which helps in the early identification of high-risk patients and optimization of treatment strategies. However, we have some clinical considerations about this article.
Firstly, the necessity of subgroup analysis. There are three subtypes of primary AIHA, and the pathological mechanisms and treatment plans of different subtypes vary significantly [2], Additionally, the treatment plan usually needs to be adjusted accordingly based on individual factors. This study only focus on overall analysis of all patients with AIHA, which may not be sufficient to comprehensively assess the risk of relapse within one year after remission of primary AIHA. Future research could conduct subgroup analyses based on classification, whether first-line hormone treatment was used, and characteristics of drug resistance, to enhance the applicability and comprehensiveness of the study.
Secondly, there are still shortcomings in the selection of variables included in this study. This study analyzed 22 risk factors for relapse, and the variables included largely relied on single test results and qualitative results of events (such as hemoglobin at admission, whether glucocorticoids were used, and DAT positive results), making it difficult to fully present their dynamic characteristics and impact on the predictive model results. It is also important to consider including more dynamic indicators, such as the duration of first-line glucocorticoid treatment and the rate of change of Hb after therapy [3]. Additionally, monitoring the frequency of follow-up visits could provide a preliminary assessment of patient compliance. Furthermore, as the authors mentioned, DAT results (C3 and IgG) may change over time, and the frequency of C3 and IgG and their trends may more accurately reflect the risk of relapse for patients.
Furthermore, sample issue is a significant limitation of this study. The data came from only two hospitals located in the same city, with a lack of severe or fatal cases. The differences in region-related medical resources may affect the outcome and Severe AIHA patients more emphasis on personalized treatment strategies [4], Moreover, this study lacks the support of an external independent database. It is suggested to combine multi - center online data from different geographical locations to break geographical restrictions and expand sample data.
Finally, this study is based on retrospective data over a one-year period. Considering the close relationship between disease relapse and time factors, future research designs should adopt prospective research methods and extend the follow-up period to obtain more comprehensive data. This will help improve the accuracy of the relapse model assessment and broaden clinical applicability.
In summary, the author team has provided a machine learning-driven quantitative assessment model for predicting the relapse risk of primary autoimmune hemolytic anemia. We hope that the above points will be recognized and adopted to further enhance the clinical applicability of the research results.
The reference list from the paper itself. Each links out to its DOI / PubMed record.
- 1Li P, Zhong C, Huang X, et al. Construction of a predictive model for relapse of primary autoimmune hemolytic anemia: a retrospective cohort study. Ann Med. 2025;57(1):2506482. doi: 10.1080/07853890.2025.2506482.40401462 PMC 12100961 · doi ↗ · pubmed ↗
- 2Loriamini M, Cserti-Gazdewich C, Branch DR. Autoimmune hemolytic anemias: classifications, pathophysiology, diagnoses and management. Int J Mol Sci. 2024;25(8):4296. doi: 10.3390/ijms 25084296.38673882 PMC 11049952 · doi ↗ · pubmed ↗
- 3Li TX, Sun FT, Ji BJ. Correlation of Ig G subclass with blood cell parameters in patients with autoimmune hemolytic anemia. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2019;27(1):197–201. doi: 10.7534/j.issn.1009-2137.2019.01.032.30738470 · doi ↗ · pubmed ↗
- 4Mulder FVM, Evers D, de Haas M, et al. Severe autoimmune hemolytic anemia; epidemiology, clinical management, outcomes and knowledge gaps. Front Immunol. 2023;14:1228142. doi: 10.3389/fimmu.2023.1228142.37795092 PMC 10545865 · doi ↗ · pubmed ↗
