ArticleEuropean journal of pediatrics2026
Serum 25-hydroxyvitamin D levels in pediatric atopic dermatitis: seasonal variability and association with disease severity.
Article in European journal of pediatrics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Vitamin D has important immunomodulatory and skin barrier-protective effects that may influence the pathogenesis of atopic dermatitis (AD). However, the relationship between serum 25-hydroxyvitamin D [25(OH)D] levels and AD severity remains controversial. This study aimed to evaluate the association between serum 25(OH)D levels and disease severity assessed by the SCORAD index in pediatric patients with AD and to examine seasonal variability in vitamin D levels. In this retrospective study, pediatric patients diagnosed with AD according to the Hanifin and Rajka criteria were included, and their medical records were reviewed. Serum 25(OH)D levels measured at the time of diagnosis and disease severity assessed using the SCORAD index were recorded. Ordinal logistic regression was performed as the primary analysis to evaluate the association between serum 25(OH)D levels and AD severity across all three severity categories (mild, moderate, severe), adjusting for age, sex, food allergy, and season. As a secondary, clinically oriented analysis, disease severity was dichotomized as mild versus moderate-to-severe, and binary logistic regression together with receiver operating characteristic (ROC) curve analysis was performed to determine an optimal serum 25(OH)D cutoff value for discriminating mild disease. As a sensitivity analysis, a 25(OH)D-by-season interaction was tested within the primary ordinal model. A total of 222 pediatric patients with AD, aged 3 months to 17 years, were included. Based on SCORAD classification, disease severity was mild in 134 patients (60.4%), moderate in 62 (27.9%), and severe in 26 (11.7%). The median serum 25(OH)D level was 19.17 ng/mL (IQR 15.62-27.20). 25(OH)D levels differed significantly across SCORAD severity groups (p < 0.001), with the lowest levels observed in patients with severe disease (median 15.40 ng/mL, IQR 13.42-17.00) and the highest in those with mild disease (median 22.88 ng/mL, IQR 17.60-32.02 ng/mL). Ordinal logistic regression demonstrated that higher serum 25(OH)D levels were independently associated with lower odds of a more severe category (OR = 0.91 per 1 ng/mL increase; 95% CI 0.88-0.94; p < 0.001); food allergy was associated with higher odds of more severe disease (OR = 2.11, 95% CI 1.10-4.05, p = 0.026), and the association between 25(OH)D and severity did not differ significantly across seasons (25(OH)D-by-season interaction, p = 0.74). As a secondary, clinically oriented analysis, binary logistic regression confirmed that higher serum 25(OH)D levels were independently associated with mild AD (OR = 1.095 per 1 ng/mL increase; 95% CI 1.055-1.137; p < 0.001), and ROC analysis identified a cutoff value of 20 ng/mL for discriminating mild disease (AUC = 0.728; sensitivity = 62.7%; specificity = 84.1%). Serum 25(OH)D levels decreased significantly with increasing age (r = - 0.233, p < 0.001), while disease severity was not significantly associated with season.
conclusionLower serum 25(OH)D levels were significantly associated with increased disease severity in pediatric AD. Serum 25(OH)D levels below 20 ng/mL were associated with a higher likelihood of more severe disease. Although serum 25(OH)D levels varied by season, disease severity was not associated with seasonal variation. These findings support an association between vitamin D status and the clinical expression of AD; given the retrospective design, causality cannot be established, and prospective studies are needed to clarify the clinical relevance of monitoring vitamin D status in pediatric AD management. WHAT IS KNOWN: • Vitamin D deficiency is common in children with atopic dermatitis and has been associated with increased disease severity in several studies. • The relationship between serum 25(OH)D levels and AD severity remains inconsistent across geographic regions and patient populations. WHAT IS NEW: • In this Turkish pediatric cohort, serum 25(OH)D levels were independently associated with AD severity after adjustment for age, sex, food allergy, and season. • A serum 25(OH)D cutoff of 20 ng/mL discriminated mild from moderate-to-severe AD, consistent with established clinical thresholds for vitamin D status.
Indexed as
Identifiers
42909638What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.