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Enhancing thalassemia gene carrier identification in non-anemic populations using artificial intelligence erythrocyte morphology analysis and machine learning.
Zhang, Fan; Zhan, Jieyu; Wang, Yang; Cheng, Jing; Wang, Meinan; Chen, Peisong; Ouyang, Juan; Li, Junxun.
Affiliation
  • Zhang F; Department of Laboratory Science, First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
  • Zhan J; Department of Pediatric, Baiyun District Maternal and Child Healthcare Centre, Guangzhou, China.
  • Wang Y; Department of Laboratory Science, First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
  • Cheng J; Department of Laboratory Science, First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
  • Wang M; IVD Domestic Clinical Application Department, Mindray Biomedical Electronics Co., Ltd, Shenzhen City, China.
  • Chen P; Department of Laboratory Science, First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
  • Ouyang J; Department of Laboratory Science, First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
  • Li J; Department of Laboratory Science, First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Eur J Haematol ; 112(5): 692-700, 2024 May.
Article in En | MEDLINE | ID: mdl-38154920
ABSTRACT

BACKGROUND:

Non-anemic thalassemia trait (TT) accounted for a high proportion of TT cases in South China.

OBJECTIVE:

To use artificial intelligence (AI) analysis of erythrocyte morphology and machine learning (ML) to identify TT gene carriers in a non-anemic population.

METHODS:

Digital morphological data from 76 TT gene carriers and 97 controls were collected. The AI technology-based Mindray MC-100i was used to quantitatively analyze the percentage of abnormal erythrocytes. Further, ML was used to construct a prediction model.

RESULTS:

Non-anemic TT carriers accounted for over 60% of the TT cases. Random Forest was selected as the prediction model and named TT@Normal. The TT@Normal algorithm showed outstanding performance in the training, validation, and external validation sets and could efficiently identify TT carriers in the non-anemic population. The top three weights in the TT@Normal model were the target cells, microcytes, and teardrop cells. Elevated percentages of abnormal erythrocytes should raise a strong suspicion of being a TT gene carrier. TT@Normal could be promoted and used as a visualization and sharing tool. It is accessible through a URL link and can be used by medical staff online to predict the possibility of TT gene carriage in a non-anemic population.

CONCLUSIONS:

The ML-based model TT@Normal could efficiently identify TT carriers in non-anemic people. Elevated percentages of target cells, microcytes, and teardrop cells should raise a strong suspicion of being a TT gene carrier.
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Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Thalassemia / Beta-Thalassemia Limits: Humans Language: En Journal: Eur J Haematol Journal subject: HEMATOLOGIA Year: 2024 Type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Thalassemia / Beta-Thalassemia Limits: Humans Language: En Journal: Eur J Haematol Journal subject: HEMATOLOGIA Year: 2024 Type: Article Affiliation country: China