Intermediate monocytes in blood correlate with subclinical vascular changes in lupus nephritis.
Abstract
Atherosclerosis cardiovascular disease (ASCVD)- related mortality is higher in patients with lupus nephritis (LN) compared with those without nephritis (11.7 vs 3.6 per 100 patient- years).1 Accelerated atheroscle- rosis risk in LN cannot be fully explained by traditional risk factors. Many hypothe- sise that dysregulated cytokine profiles and altered cellular subsets may trigger endothe- lial dysfunction and plaque destabilisation, accelerating atherosclerosis risk in LN.2 We recently established that moderate- severe renal arteriosclerosis (ASCL) in kidney biop- sies is a marker of premature endothelial dysfunction in LN and is associated with three times higher 10- year clinical ASCVD occur- rence, underscoring its role as potential proxy for clinical ASCVD.3 Yet, long- term moni- toring of renal ASCL is difficult, as it requires baseline and repeat invasive kidney biopsies. Therefore, a cellular surrogate biomarker of renal vascular changes that may predict clin- ical ASCVD risk is needed in LN.
Authors: | Garg S, McCoy SS, Hartel I, Muhlstock A, Raval AN, Bartels C, |
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Journal: | Lupus Sci Med; 2025 Feb 6;12(1):e001432 doi:10.1136/lupus-2024-001432 |
Year: | 2025 |
PubMed: | PMID: 39914992 (Go to PubMed) |