Accelerated atherosclerosis in systemic lupus erythematosus: Role of fibroblast growth factor 23- phosphate axis
International Journal of Nephrology and Renovascular Disease Aug 31, 2021
Ammar Y, Mohamed A, Khalil G, et al. - Among systemic lupus erythematosus (SLE) patients, there exists a key role of FGF23 (fibroblast growth factor-23)-phosphate axis in accelerated atherosclerotic cardiovascular disease (ACVD), and including serum phosphorus and intact FGF23 (iFGF23) in ACVD risk profile evaluation of these patients is recommended.
This study involved three study groups of predominantly middle-aged females: SLE [without lupus nephritis (LN)], LN, or controls.
Carotid ultrasonography was conducted.
Among study groups, differences in common carotid artery intima-media thickness (CC-IMT), internal carotid resistive index and serum iFGF23 (LN>SLE>controls) were evident.
A significant positive correlation of serum iFGF23 with serum phosphorus, CC-IMT and plaque score was found in both SLE and LN cases.
Cumulative steroid dose in SLE and serum iFGF23 in LN patients was revealed as the strongest predictor of increased CC-IMT, in the multivariate analysis.
Hyperphosphatemia in SLE and proteinuria in LN patients were found as the most significant independent predictors of elevated serum iFGF23.
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