Salivary Melatonin Levels in Comparison with Disease Features and Antihistamine Use: Prospective Follow-Up of Atopic Dermatitis Patients
5 affiliations
- 1Department of Dermatology and Venereology, Sestre Milosrdnice University Hospital Center, Vinogradska Cesta 29, 10000 Zagreb, Croatia
- 2School of Dental Medicine, University of Zagreb, 10000 Zagreb, Croatia
- 3Department of Clinical Chemistry, Sestre Milosrdnice University Hospital Center, 10000 Zagreb, Croatia
- 4Lipik Special Hospital for Medical Rehabilitation, 34551 Lipik, Croatia
- 5Department of Dental Medicine, Faculty of Dental Medicine and Health Osijek, Josip Juraj Strossmayer University of Osijek, 31000 Osijek, Croatia
Abstract
Background: Atopic dermatitis (AD) is a common inflammatory dermatosis often accompanied by itching and sleep disturbances. Various treatment options exist, including antihistamines (AHs), even though current clinical recommendations do not mention them. Methods: This prospective exploratory study measured and recorded salivary melatonin at two timepoints (T1 and T2) in three groups of participants: those not treated with AHs, those who discontinued H1-AHs, and those for whom H1-AHs were introduced. Also assessed were disease severity (Scoring Atopic Dermatitis/SCORAD and Eczema Area and Severity Index/EASI), pruritus severity (Peak Pruritus Numeric Rating Scale/NRS), and sleep quality (Pittsburgh Sleep Quality Index/PSQI). Results: The EASI scores were significantly inversely correlated with salivary melatonin levels (p = 0.009) at the first timepoint (T1), but not at the second timepoint (T2). At T2, SCORAD correlated with EASI, NRS, and PSQI (ρ = 0.304–0.842; p ≤ 0.022). EASI correlated with NRS and PSQI (ρ = 0.281–0.453; p ≤ 0.035). Those who discontinued AHs showed increased AD severity indicators (SCORAD, EASI, NRS), whereas participants for whom AHs were introduced showed decreases in the same scores. After adjusting for baseline values, a significant main effect was detected for the treatment group for T2 SCORAD scores (p < 0.001, η2 = 0.493). Pairwise comparisons confirmed significant differences among all treatment arms/measures (all p values ≤ 0.023). Changes in melatonin levels between the three groups were not significant when baseline SCORAD values were controlled for. Conclusions: Our exploratory study observed an inverse association between melatonin levels and AD severity at T1, but this was not replicated at T2. This association should be interpreted with caution due to study limitations. Changes in AD severity and pruritus scores following AH initiation or discontinuation were observed, but the study’s non-randomized design and baseline differences between groups preclude a definitive causal inference, and further research on this topic is needed.
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BibTeX
@article{tomasevic2026salivary,
title = {{Salivary Melatonin Levels in Comparison with Disease Features and Antihistamine Use: Prospective Follow-Up of Atopic Dermatitis Patients}},
author = {Renata Tomašević and Milena Hanžek and Tamara Sušić and Mirta Peček and Stjepanka Lešić and Liborija Lugović-Mihić},
journal = {International Journal of Molecular Sciences},
year = {2026},
month = oct,
doi = {10.3390/ijms27209333},
url = {https://www.mdpi.com/1422-0067/27/20/9333},
note = {CC BY 4.0},
}
RIS
TY - JOUR
TI - Salivary Melatonin Levels in Comparison with Disease Features and Antihistamine Use: Prospective Follow-Up of Atopic Dermatitis Patients
AU - Renata Tomašević
AU - Milena Hanžek
AU - Tamara Sušić
AU - Mirta Peček
AU - Stjepanka Lešić
AU - Liborija Lugović-Mihić
PY - 2026
DA - 2026/10/01
JO - International Journal of Molecular Sciences
DO - 10.3390/ijms27209333
UR - https://www.mdpi.com/1422-0067/27/20/9333
AB - Background: Atopic dermatitis (AD) is a common inflammatory dermatosis often accompanied by itching and sleep disturbances. Various treatment options exist, including antihistamines (AHs), even though current clinical recommendations do not mention them. Methods: This prospective exploratory study measured and recorded salivary melatonin at two timepoints (T1 and T2) in three groups of participants: those not treated with AHs, those who discontinued H1-AHs, and those for whom H1-AHs were introduced. Also assessed were disease severity (Scoring Atopic Dermatitis/SCORAD and Eczema Area and Severity Index/EASI), pruritus severity (Peak Pruritus Numeric Rating Scale/NRS), and sleep quality (Pittsburgh Sleep Quality Index/PSQI). Results: The EASI scores were significantly inversely correlated with salivary melatonin levels (p = 0.009) at the first timepoint (T1), but not at the second timepoint (T2). At T2, SCORAD correlated with EASI, NRS, and PSQI (ρ = 0.304–0.842; p ≤ 0.022). EASI correlated with NRS and PSQI (ρ = 0.281–0.453; p ≤ 0.035). Those who discontinued AHs showed increased AD severity indicators (SCORAD, EASI, NRS), whereas participants for whom AHs were introduced showed decreases in the same scores. After adjusting for baseline values, a significant main effect was detected for the treatment group for T2 SCORAD scores (p < 0.001, η2 = 0.493). Pairwise comparisons confirmed significant differences among all treatment arms/measures (all p values ≤ 0.023). Changes in melatonin levels between the three groups were not significant when baseline SCORAD values were controlled for. Conclusions: Our exploratory study observed an inverse association between melatonin levels and AD severity at T1, but this was not replicated at T2. This association should be interpreted with caution due to study limitations. Changes in AD severity and pruritus scores following AH initiation or discontinuation were observed, but the study’s non-randomized design and baseline differences between groups preclude a definitive causal inference, and further research on this topic is needed.
SN - 1422-0067
ER -