Identification and prediction of association patterns between nutrient intake and anemia using machine learning techniques: results from a cross-sectional study with university female students from Palestine

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dc.identifier.uri http://dx.doi.org/10.15488/17210
dc.identifier.uri https://www.repo.uni-hannover.de/handle/123456789/17338
dc.contributor.author Qasrawi, Radwan
dc.contributor.author Badrasawi, Manal
dc.contributor.author Al-Halawa, Diala Abu
dc.contributor.author Polo, Stephanny Vicuna
dc.contributor.author Khader, Rami Abu
dc.contributor.author Al-Taweel, Haneen
dc.contributor.author Alwafa, Reem Abu
dc.contributor.author Zahdeh, Rana
dc.contributor.author Hahn, Andreas
dc.contributor.author Schuchardt, Jan Philipp
dc.date.accessioned 2024-04-25T07:28:48Z
dc.date.available 2024-04-25T07:28:48Z
dc.date.issued 2024
dc.identifier.citation Qasrawi, R.; Badrasawi, M.; Al-Halawa, D.A.; Polo, S.V.; Khader, R.A. et al.: Identification and prediction of association patterns between nutrient intake and anemia using machine learning techniques: results from a cross-sectional study with university female students from Palestine. In: European Journal of Nutrition (2024), in press. DOI: https://doi.org/10.1007/s00394-024-03360-8
dc.description.abstract Purpose: This study utilized data mining and machine learning (ML) techniques to identify new patterns and classifications of the associations between nutrient intake and anemia among university students. Methods: We employed K-means clustering analysis algorithm and Decision Tree (DT) technique to identify the association between anemia and vitamin and mineral intakes. We normalized and balanced the data based on anemia weighted clusters for improving ML models’ accuracy. In addition, t-tests and Analysis of Variance (ANOVA) were performed to identify significant differences between the clusters. We evaluated the models on a balanced dataset of 755 female participants from the Hebron district in Palestine. Results: Our study found that 34.8% of the participants were anemic. The intake of various micronutrients (i.e., folate, Vit A, B5, B6, B12, C, E, Ca, Fe, and Mg) was below RDA/AI values, which indicated an overall unbalanced malnutrition in the present cohort. Anemia was significantly associated with intakes of energy, protein, fat, Vit B1, B5, B6, C, Mg, Cu and Zn. On the other hand, intakes of protein, Vit B2, B5, B6, C, E, choline, folate, phosphorus, Mn and Zn were significantly lower in anemic than in non-anemic subjects. DT classification models for vitamins and minerals (accuracy rate: 82.1%) identified an inverse association between intakes of Vit B2, B3, B5, B6, B12, E, folate, Zn, Mg, Fe and Mn and prevalence of anemia. Conclusions: Besides the nutrients commonly known to be linked to anemia—like folate, Vit B6, C, B12, or Fe—the cluster analyses in the present cohort of young female university students have also found choline, Vit E, B2, Zn, Mg, Mn, and phosphorus as additional nutrients that might relate to the development of anemia. Further research is needed to elucidate if the intake of these nutrients might influence the risk of anemia. eng
dc.language.iso eng
dc.publisher Berlin ; Heidelberg : Springer
dc.relation.ispartofseries European Journal of Nutrition (2024), in press
dc.rights CC BY 4.0 Unported
dc.rights.uri https://creativecommons.org/licenses/by/4.0
dc.subject Classification and regression tree eng
dc.subject Dietary patterns eng
dc.subject Iron deficiency anemia eng
dc.subject K-means analysis eng
dc.subject Machine learning eng
dc.subject Nutrient intake eng
dc.subject.ddc 630 | Landwirtschaft, Veterinärmedizin
dc.subject.ddc 640 | Hauswirtschaft und Familienleben
dc.subject.ddc 610 | Medizin, Gesundheit
dc.title Identification and prediction of association patterns between nutrient intake and anemia using machine learning techniques: results from a cross-sectional study with university female students from Palestine eng
dc.type Article
dc.type Text
dc.relation.essn 1436-6215
dc.relation.issn 1436-6207
dc.relation.doi https://doi.org/10.1007/s00394-024-03360-8
dc.description.version publishedVersion eng
tib.accessRights frei zug�nglich


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