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Liver and Kidney Function Biomarkers, Blood Cell Traits and Risk of Severe COVID-19: A Mendelian Randomization Study
Kai Wang1, Minghan Qu1, Lin Ding1
1Department of Epidemiology and Biostatistics, Key Laboratory for Environment and Health, School of Public Health, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Insights
This study used genetic data to find causal links between specific blood and liver markers and severe Coronavirus disease 2019 (COVID-19). Albumin, bilirubin, and several blood cell counts are identified as risk factors for severe COVID-19.
Area of Science:
- Genetics
- Epidemiology
- Internal Medicine
Background:
- The Coronavirus disease 2019 (COVID-19) pandemic presents a significant global health challenge.
- Observational studies suggest associations between abnormal liver function, kidney function, and hematological traits with severe COVID-19 outcomes.
- However, the causal relationships and underlying mechanisms for these associations remain unclear.
Purpose of the Study:
- To investigate the potential causal roles of liver function biomarkers, kidney function biomarkers, and hematological traits in the risk of severe COVID-19.
- To elucidate the genetic basis for the association between these biomarkers and COVID-19 severity.
Main Methods:
- Mendelian randomization analyses were employed to assess causality.
- Genetic association summary statistics from European ancestry populations were utilized.
- Eight liver function biomarkers, one kidney function biomarker, and 14 hematological traits were examined.
Main Results:
- Albumin, direct bilirubin, white blood cell count, neutrophil count, lymphocyte count, and mean corpuscular hemoglobin were found to be causally associated with severe COVID-19 risk.
- Lymphocyte count and mean corpuscular hemoglobin demonstrated independent effects on severe COVID-19 risk.
- These findings provide genetic evidence supporting the link between specific biomarkers and disease severity.
Conclusions:
- Specific liver function and hematological traits are causally linked to the risk of severe COVID-19.
- These causal insights can inform risk stratification strategies for individuals with abnormal biomarker levels.
- Further research is warranted to explore the pathogenic roles of these identified biomarkers in COVID-19.
Abstract:
The pandemic of Coronavirus disease 2019 (COVID-19) has posed an enormous threat to human health. According to observational studies, abnormal liver and kidney functions and blood cell traits were associated with severe COVID-19, yet the causal risk factors for COVID-19 severity and the underlying mechanism remained elusive. We performed Mendelian randomization analyses to assess the potential causal role of eight liver function biomarkers, one kidney function biomarker, and 14 hematological traits on COVID-19 severity using genetic association summary statistics from Europeans. Our findings showed that albumin, direct bilirubin, white blood cell count, neutrophil count, lymphocyte count, and mean corpuscular hemoglobin are casually associated with the risk of severe COVID-19. Notably, lymphocyte count and mean corpuscular hemoglobin had an independent effect on severe COVID-19 risk. These causal evidences provide insights into directions for the risk stratification of individuals with abnormal liver function or blood cell indices and motivate more studies to unveil the roles of these abnormalities in COVID-19 pathogenesis.
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