Abstract
Angiogenesis is one of the first stages in fracture healing and bone repair. Therefore, numerous studies evaluating the effect of Mg as a promising degradable, metallic biomaterial on the proliferation and function of endothelial cells have been performed. However, these studies lack methodological homogeneity and therefore differ in fundamental conclusions. Here, Mg-concentration-, donor- and cell age- dependent relations to primary human umbilical cord vein endothelial cells (HUVEC) proliferation and migration were investigated systematically. The generated data were utilized to develop regression models in order to assess and predict the cell response on Mg exposition in a concentration range of 2-20 mM Mg in cell culture medium extract. A concentration of > 2 mM already induced a detrimental effect in the sensitive primary HUVECs. Molecular data quantifying angiogenesis markers supported this finding. An increased migration capacity has been observed at a concentration of 10 mM Mg. We compared linear regression, random forests, support vector machines, neural networks and large language models for the prediction of HUVEC proliferation for a number of scenarios. Using these machine learning methods, we were able to predict the proliferation of HUVECs for missing Mg concentrations and for missing passages with mean absolute errors below 10 % and as low as 8.5 %, respectively. Due to strong differences between the cell behaviour of different donors, information for missing donors can be predicted with mean absolute errors of 15.7 % only. Support vector machines with linear kernel performed best on the tested data, but large language models also showed promising results.