ArticleMolecular and cellular biochemistry2026
Association between vitamin D status, lymphocyte subsets, and triglycerides in men: an observational study.
Article in Molecular and cellular biochemistry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
Vitamin D plays an important role in immune regulation, yet the relationships among vitamin D status, lymphocyte subsets, and triglycerides (TG) remain incompletely understood. This study aimed to evaluate the associations between serum 25-hydroxyvitamin D [25(OH)D] concentrations, lymphocyte count and subsets, and to examine whether TG statistically contributes to these associations through an indirect pathway. A retrospective cross-sectional analysis was performed in 351 male individuals (mean age 50.22 ± 9.36 years) who underwent routine health screenings. Serum 25(OH)D, TG, lymphocyte count, and lymphocyte subsets (CD3+, CD4+, CD8+, B cells, NK cells) were measured. Pearson correlation, restricted cubic spline, and indirect-effect (mediation) analyses were conducted with adjustment for age, season, physical activity, eGFR, and total bilirubin. 25(OH)D was analyzed as a continuous variable. Serum 25(OH)D was negatively correlated with lymphocyte count (r = - 0.188), CD3 + T cells (r = - 0.209), and CD4 + T cells (r = - 0.218) (all p < 0.01). TG levels were positively correlated with these parameters (r = 0.219, 0.234, and 0.237, respectively; all p < 0.01) and negatively correlated with 25(OH)D (r = - 0.298, p < 0.01). Mediation analysis showed statistically significant indirect effects of TG on the associations between 25(OH)D and lymphocyte count (indirect effect - 3.6, 95% CI -6.7 to - 0.9; 25.4% of the total effect) and between 25(OH)D and CD4 + T-cell count (- 2.0, 95% CI -3.7 to - 0.6; 21.9%), alongside smaller but statistically significant direct effects; these cross-sectional estimates are compatible with, but do not establish, a mediating role of TG. In extended models additionally adjusted for body mass index, fasting plasma glucose, HDL-C and LDL-C, these indirect effects were attenuated (lymphocyte count: -2.4, 95% CI -4.9 to - 0.2; CD3 + T-cell count: -1.7, 95% CI -3.8 to - 0.02), and after further adjustment for smoking and alcohol consumption the bootstrap confidence intervals included zero. Triglycerides may statistically contribute to the association between vitamin D status and selected lymphocyte populations, particularly CD4 + T cells; however, these indirect effects were attenuated after adjustment for metabolic covariates and were no longer statistically significant in the most comprehensively adjusted model. Because of the cross-sectional design, these findings are hypothesis-generating and require confirmation in longitudinal and interventional studies before any clinical relevance can be inferred.
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