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Updated: May 3, 2026

Chronic Salmonella Infected Mouse Model
Published on: May 31, 2010
Suboptimal Vitamin D Status Is Associated with Salmonella Infection and Elevated C-Reactive Protein in Hospitalized
Hua-Hsi Hung1, Hung-Chang Lee1,2,3, Chun-Yan Yeung2,3,4
1Department of Pediatric Gastroenterology, Hepatology and Nutrition, MacKay Children's Hospital, Taipei 104217, Taiwan.
Abstract:
Background: Vitamin D contributes to intestinal barrier integrity and innate immune regulation, but its role in susceptibility to Salmonella infection and systemic inflammation in hospitalized pediatric patients with acute gastroenteritis (AGE) remains unclear. Methods: We retrospectively analyzed 70 pediatric patients hospitalized with AGE, examining the associations of admission 25(OH)D levels with culture-confirmed Salmonella infection and C-reactive protein (CRP). Multivariable logistic and linear regression models were adjusted for age and sex. Vitamin D status was classified as sufficient (≥30 ng/mL), suboptimal (<30 ng/mL), or deficient (<20 ng/mL). Results: The median age of the 70 included patients was 3.0 years (IQR: 1.5-6.0, range: 1.0-17 years), and 55.7% were male. Suboptimal vitamin D status was present in 64.3% of patients and was associated with higher median CRP levels (3.84 vs. 1.42 mg/dL, p = 0.025) and a greater prevalence of Salmonella infection (48.9% vs. 24.0%, p = 0.047). In multivariable analysis, suboptimal 25(OH)D levels independently marginally predicted an increased odds of Salmonella infection (adjusted odds ratio 3.11, 95% CI 1.00-9.67; p = 0.051). Serum 25(OH)D levels were inversely associated with natural log-transformed CRP (p = 0.026), with each 1 ng/mL increase corresponding to an estimated 5% reduction in CRP. Furthermore, vitamin D deficiency (<20 ng/mL) was associated with a 3.5-fold increase in CRP compared to levels ≥ 20 ng/mL (p = 0.012). Conclusions: Suboptimal vitamin D status (<30 ng/mL) may be associated with increased susceptibility to Salmonella gastroenteritis, while deficiency (<20 ng/mL) correlates with exacerbated inflammatory burden in hospitalized pediatric patients. These findings suggest a threshold-dependent effect of vitamin D on both mucosal defense and systemic inflammation. Prospective trials are warranted to evaluate the therapeutic potential of vitamin D supplementation in this population.
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