News Release

New discoveries in lupus research

University of Houston expert identifies biomarkers for heart disease and for children with lupus nephritis

Peer-Reviewed Publication

University of Houston

Chandra Mohan, M.D., Ph.D., Hugh Roy and Lillie Cranz Cullen Endowed Professor of biomedical engineering at the University of Houston Cullen College of Engineering

image: Chandra Mohan, M.D., Ph.D., Hugh Roy and Lillie Cranz Cullen Endowed Professor of biomedical engineering at the University of Houston, has identified two sets of biomarkers in lupus patients - one for those who will get heart disease and one for children who will get lupus nephritis. view more 

Credit: University of Houston

Two separate findings by a University of Houston nationally recognized expert in systemic lupus erythematosus (SLE or lupus), a chronic autoimmune disease that affects multiple organs including the kidneys, skin, joints and heart, are being reported in scientific and medical journals.  

Chandra Mohan, M.D., Ph.D., Hugh Roy and Lillie Cranz Cullen Endowed Professor of biomedical engineering in the UH Cullen College of Engineering, has identified blood biomarkers that predict which lupus patients will develop heart disease in the future and found new urine biomarkers for diagnosing lupus nephritis (LN) in children with lupus. 

Lupus and Cardiovascular Disease 

Lupus is associated with an increased incidence of acute and chronic cardiovascular disease as compared to the general population.  

Mohan’s team, in collaboration with Dr. Maureen McMahon at UCLA, used a comprehensive metabolomic screen of baseline sera from lupus patients to identify metabolites that predict future carotid plaque progression, following eight to nine years of follow-up. Nine patients had SLE without plaque progression, eight had SLE and went on to develop atherosclerotic plaques, and eight patients were controls who did not have SLE.  

“The arachidonic acid pathway metabolites, leukotriene B4 (LTB4) and 5-hydroxyeicosatetraenoic acid (5-HETE), and the oxidized lipids 9/13-hydroxyoctodecadienoic acid (HODE) were found to be significantly altered (p < 0.05 and fold-change >2) in SLE patients compared to SLE patients without plaque progression,” reports Mohan in Frontiers in Cardiovascular Medicine. “SLE patients also exhibited significantly altered levels of branched chain amino acid (BCAA) metabolites and plasmalogens compared to the non-SLE controls.” 

Taken together with the rich literature on these metabolites, the findings suggest that the identified metabolites may not only be prognostic of cardiovascular disease development in SLE patients, but they may also be active drivers of atheroma formation. Early identification of these high risk SLE patients may help institute preventive measures early in the disease course. 

The first author, Sahar Baig, is an undergraduate student at UH. 

Children and lupus nephritis 

Lupus nephritis, or inflammation of the kidneys, is one of the most severe complications for SLE patients. Kidney disease is a leading cause of death among SLE patients – roughly a quarter of all lupus patients succumb to end-stage renal disease. 

Mohan’s team, on a mission to discover non-invasive biomarkers of LN to replace painful serial kidney biopsies in children, is reporting his recent findings in Frontiers in Immunology

Together with collaborator, Dr. Scott E. Wenderfer at Texas Children’s Hospital, Mohan’s team evaluated the performance of ten urine protein markers of diverse nature including cytokines, chemokines and adhesion molecules in distinguishing disease activity in childhood SLE among 84 pediatric patients. 

“Urine concentrations of ALCAM, KIM-1, PF4 and VCAM-1 were significantly higher in active LN patients compared to active non-renal SLE, inactive SLE and healthy controls, with strong diagnostic potential” Mohan reports.  

“Urinary ALCAM, PF4, and VCAM-1 are potential biomarkers for predicting kidney disease activity in cSLE and hold potential as surrogate markers of nephritis flares and prognosis in these patients,” he said. 

The lead author on this paper was Dr. Samar Soliman at Minia University in Egypt. Other clinical contributors were Dr. Larry A. Greenbaum, Emory University and Dr. Sherene Mason, University of Connecticut School of Medicine. 

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