Aberrant lipid profiles and lymphocyte counts in systemic sclerosis population, reassessing predictive value for concurrent cardiovascular diseases.

Front Immunol

Third Hospital of Shanxi Medical University, Shanxi Bethune Hospital, Shanxi Academy of Medical Sciences, Tongji Shanxi Hospital, Taiyuan, China.

Published: March 2025

Objective: To investigate alterations in blood lipid profiles and T cell subsets among systemic sclerosis (SSc) patients, and to assess their potential utility in predicting cardiovascular disease (CVD) risk.

Methods: 105 SSc patients and 80 age- and sex-matched healthy controls (HCs) were enrolled. Flow cytometry was employed to quantify T cell subsets. Multivariate logistic regression analysis investigated the association between blood lipid profile, T cell subsets, SSc occurrence, and CVD risk. Additionally, a prediction model was developed to assess the potential predictive value of CVD risk.

Results: In the SSc patients, low-density lipoprotein cholesterol (LDL-C) (OR = 3.212, 95%CI = 1.132-9.113, = 0.028), ESR (OR = 1.218, 95%CI = 1.086-1.367, = 0.001), CRP (OR = 2.156, 95% CI = 1.393-3.338, = 0.001), T helper (Th)cells (OR = 1.004, 95% CI = 1.001-1.008, = 0.034) were positively correlated with the risk of SSc. Further studies found that absolute increases in Th cells in SSc patients were positively associated with the risk of CVD (OR=1.002, 95%CI=1.001-1.005, =0.011) and were independent predictors of CVD risk in SSc. When Th cells exceeded 866.53 cells/μL, the risk of CVD in SSc patients was greatly increased (<0.001).

Conclusion: Altered lipid profiles and dysregulated Th cell expression in SSc patients, with a significant elevation of Th cells specifically noted in SSc-CVD patients, suggesting that Th cells may serve as a potential predictive biomarker for CVD in SSc patients, thereby aiding in early diagnosis. The underlying mechanism of this association requires further investigation.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11880226PMC
http://dx.doi.org/10.3389/fimmu.2025.1530909DOI Listing

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