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Serum calcification propensity is independently associated with disease activity in systemic lupus erythematosus
Suzan Dahdal1, Vasilios Devetzis1, George Chalikias2
1Department of Nephrology and Hypertension lnselspital, Bern University Hospital, University of Bern, Bern, Switzerland.
Insights
The T50 score, a novel blood test for calcification propensity, is closely associated with disease activity in Systemic Lupus Erythematosus (SLE) patients. This finding suggests T50 may serve as an early biomarker for identifying high-risk SLE individuals.
Area of Science:
- Rheumatology
- Cardiovascular Research
- Biomarker Discovery
Background:
- Systemic lupus erythematosus (SLE) is linked to significant cardiovascular issues.
- The T50 score quantifies serum calcification propensity, a predictor of mortality.
- High calcification propensity (low T50) is a key mortality determinant.
Purpose of the Study:
- To investigate the association between T50 score and disease activity in SLE patients.
- To evaluate T50 as a potential biomarker for SLE.
- To identify high-risk SLE patients using T50 levels.
Main Methods:
- Analysis of 168 SLE patients from the Swiss Systemic Lupus Erythematosus Cohort Study (SSCS).
- Assessment of serum calcification propensity using time-resolved nephelometry (T50 score).
- Correlation analysis with disease activity using SELENA-SLEDAI scores.
Main Results:
- The T50 score was influenced by hemoglobin, creatinine, and protein levels.
- Disease activity (SELENA-SLEDAI) was significantly associated with T50 levels.
- A negative association was observed between T50 and SELENA-SLEDAI in patients with active disease (rho = -0.233, P = 0.02).
Conclusions:
- T50 levels are closely associated with SLE disease activity.
- T50 identifies SLE patients with active systemic inflammation.
- T50 shows promise as a biomarker for SLE activity and early risk detection.
Background:
Systemic lupus erythematosus (SLE) is associated with severe cardiovascular complications. The T50 score is a novel functional blood test quantifying calcification propensity in serum. High calcification propensity (or low T50) is a strong and independent determinant of all-cause mortality in various patient populations.
Methods:
A total of 168 patients with ≥ 4 American College of Rheumatology (ACR) diagnostic criteria from the Swiss Systemic lupus erythematosus Cohort Study (SSCS) were included in this analysis. Serum calcification propensity was assessed using time-resolved nephelometry.
Results:
The cohort mainly consisted of female (85%), middle-aged (43±14 years) Caucasians (77%). The major determinants of T50 levels included hemoglobin, serum creatinine and serum protein levels explaining 43% of the variation at baseline. Integrating disease activity (SELENA-SLEDAI) into this multivariate model revealed a significant association between disease activity and T50 levels. In a subgroup analysis considering only patients with active disease (SELENA-SLEDAI score ≥4) we found a negative association between T50 and SELENA-SLEDAI score at baseline (Spearman's rho -0.233, P = 0.02).
Conclusions:
Disease activity and T50 are closely associated. Moreover, T50 levels identify a subgroup of SLE patients with ongoing systemic inflammation as mirrored by increased disease activity. T50 could be a promising biomarker reflecting SLE disease activity and might offer an earlier detection tool for high-risk patients.
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