Departments of Pharmacy Practice (Mses Varghese and Meka and Dr Adela) and Pharmaceutical Analysis (Ms Jala and Dr Borkar).
National Institute of Pharmaceutical Education and Research, Guwahati, India.
Am J Obstet Gynecol MFM. 2023 Feb;5(2):100829. doi: 10.1016/j.ajogmf.2022.100829. Epub 2022 Dec 1.
Hypertensive disorders of pregnancy account for 3% to 10% of maternal-fetal morbidity and mortality worldwide. This condition has been considered one of the leading causes of maternal deaths in developing countries, such as India.
This study aimed to discover hypertensive disorders of pregnancy-specific candidate urine metabolites as markers for hypertensive disorders of pregnancy by applying integrated metabolomics and machine learning approaches.
The targeted urinary metabolomics study was conducted in 70 healthy pregnant controls and 133 pregnant patients having hypertension as cases. Hypertensive disorders of pregnancy-specific metabolites for disease prediction were further extracted using univariate and multivariate statistical analyses. For machine learning analysis, 80% of the data were used for training (79 for hypertensive disorders of pregnancy and 42 for healthy pregnancy) and validation (27 for hypertensive disorders of pregnancy and 14 for healthy pregnancy), and 20% of the data were used for test sets (27 for hypertensive disorders of pregnancy and 14 for healthy pregnancy).
The statistical analysis using an unpaired t test revealed 44 differential metabolites. Pathway analysis showed mainly that purine and thiamine metabolism were altered in the group with hypertensive disorders of pregnancy compared with the healthy pregnancy group. The area under the receiver operating characteristic curves of the 5 most predominant metabolites were 0.98 (adenosine), 0.92 (adenosine monophosphate), 0.89 (deoxyadenosine), 0.81 (thiamine), and 0.81 (thiamine monophosphate). The best prediction accuracies were obtained using 2 machine learning models (95% for the gradient boost model and 98% for the decision tree) among the 5 used models. The machine learning models showed higher predictive performance for 3 metabolites (ie, thiamine monophosphate, adenosine monophosphate, and thiamine) among 5 metabolites. The combined accuracies of adenosine from all models were 98.6 in the training set and 95.6 in the test set. Moreover, the predictive performance of adenosine was higher than other metabolites. The relative feature importance of adenosine was also observed in the decision tree and the gradient boost model.
Among other metabolites, adenosine and thiamine metabolites were found to differentiate participants with hypertensive disorders of pregnancy from participants with healthy pregnancies; hence, these metabolites can serve as a promising noninvasive marker for the detection of hypertensive disorders of pregnancy.
妊娠高血压疾病占全球孕产妇发病率和死亡率的 3%至 10%。这种情况被认为是发展中国家(如印度)产妇死亡的主要原因之一。
本研究旨在通过整合代谢组学和机器学习方法,发现妊娠高血压疾病特异性候选尿液代谢物作为妊娠高血压疾病的标志物。
对 70 名健康孕妇对照和 133 名患有高血压的孕妇病例进行靶向尿液代谢组学研究。使用单变量和多变量统计分析进一步提取用于疾病预测的妊娠高血压疾病特异性代谢物。对于机器学习分析,80%的数据用于训练(79 例妊娠高血压疾病和 42 例健康妊娠)和验证(27 例妊娠高血压疾病和 14 例健康妊娠),20%的数据用于测试集(27 例妊娠高血压疾病和 14 例健康妊娠)。
使用非配对 t 检验的统计分析显示 44 种差异代谢物。途径分析显示,与健康妊娠组相比,妊娠高血压疾病组嘌呤和硫胺素代谢主要发生改变。5 种主要代谢物的受试者工作特征曲线下面积分别为 0.98(腺苷)、0.92(单磷酸腺苷)、0.89(脱氧腺苷)、0.81(硫胺素)和 0.81(单磷酸硫胺素)。在 5 种使用的模型中,2 种机器学习模型(梯度提升模型为 95%,决策树为 98%)获得了最佳预测准确性。机器学习模型在 5 种代谢物中对 3 种代谢物(即硫胺素单磷酸、单磷酸腺苷和硫胺素)的预测性能更高。在训练集中,所有模型中腺苷的综合准确率为 98.6%,在测试集中为 95.6%。此外,腺苷的预测性能高于其他代谢物。在决策树和梯度提升模型中也观察到了腺苷的相对特征重要性。
与其他代谢物相比,发现腺苷和硫胺素代谢物可区分妊娠高血压疾病患者和健康妊娠患者;因此,这些代谢物可作为妊娠高血压疾病检测的有前途的非侵入性标志物。