# Evaluating the antioxidant and anti-inflammatory effect of melatonin in pediatric hemodialysis patients: a randomized, placebo-controlled trial

**Authors:** Ghadeer Amged Sayed, Radwa Maher El Borolossy, Ragia M. Said, Sara Mahmoud Shaheen

PMC · DOI: 10.1038/s41598-025-34264-0 · Scientific Reports · 2026-01-21

## TL;DR

This study found that melatonin may reduce inflammation and cholesterol in children on hemodialysis, offering potential cardiovascular benefits.

## Contribution

The study provides novel evidence on melatonin's anti-inflammatory and lipid-lowering effects in pediatric hemodialysis patients.

## Key findings

- Melatonin significantly reduced NF-κB levels and improved lipid profiles in pediatric hemodialysis patients.
- Melatonin inhibited the increase in MDA levels, suggesting antioxidant benefits.
- Placebo group showed increased MDA levels, highlighting melatonin's protective role.

## Abstract

Children undergoing chronic hemodialysis are exposed to persistent oxidative stress and systemic inflammation, contributing to long-term cardiovascular complications. Melatonin (MLT) is a pleiotropic hormone with potential antioxidant and anti-inflammatory effects. Due to scarcity of studies on pediatrics this study sought to investigate the effects of MLT on oxidative stress and inflammation in pediatric hemodialysis patients. This prospective, block-randomized, double-blinded, placebo-controlled study aimed at assessing the effect of 5 mg MLT on oxidative stress and inflammation in pediatric hemodialysis patients. Forty eligible patients were randomly allocated into either MLT or placebo group. Serum malondialdehyde (MDA), nuclear factor kappa B (NF-κB) levels and lipid profile were measured at baseline and at the end of the study after 12 weeks. MLT significantly reduced the median percent change of serum NF-κB − 5.404(− 58.25–129.7) with p-value = 0.027 in addition to reduction in median total cholesterol in the MLT group from 163.7(134.5–259.5) at baseline to 144(113–242) at the end of the study with p-value = 0.038 and reduction of low-density lipoprotein levels from 96(78–183) to 78.5(48–171) at the end of the 12 weeks with p-value = 0.002 while there was no significance in the placebo group. Although, there was no statistical significance in serum MDA levels in the MLT group but significant increase in MDA levels in the placebo group was detected. MDA levels increased from 11.79 ± 5.078 to 14.79 ± 4.257 at the end of the study in the placebo group with p-value = 0.048, supplementation appears to have beneficial effects on ameliorating inflammation and reducing serum lipids. Moreover, MLT may have a protective antioxidant effect by reduction and inhibition of elevation of serum MDA levels.

Trial registration: The study was registered on ClinicalTrials.gov (identifier: NCT05570526 https://clinicaltrials.gov/study/NCT05570526), on 6th of October 2022

## Linked entities

- **Proteins:** NFKB1 (nuclear factor kappa B subunit 1)
- **Chemicals:** melatonin (PubChem CID 896), malondialdehyde (PubChem CID 10964)

## Full-text entities

- **Genes:** CAT (catalase) [NCBI Gene 847], SOD1 (superoxide dismutase 1) [NCBI Gene 6647] {aka ALS, ALS1, HEL-S-44, IPOA, SOD, STAHP}, ATHS (atherosclerosis susceptibility (lipoprotein associated)) [NCBI Gene 470] {aka ALP}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, MAP3K20 (mitogen-activated protein kinase kinase kinase 20) [NCBI Gene 51776] {aka AZK, CNM6, MLK7, MLT, MLTK, MLTKalpha}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, PTH (parathyroid hormone) [NCBI Gene 5741] {aka FIH1, PTH1}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}
- **Diseases:** MHD (MESH:D007319), mental retardation (MESH:D008607), kidney dysfunction (MESH:D007674), dyslipidemia (MESH:D050171), autistic (MESH:D001321), inflammation (MESH:D007249), ESRD (MESH:D007676), somnolence (MESH:D006970), ED (MESH:D014652), HD (MESH:D006816), CKD (MESH:D051436), cardiovascular complications (MESH:D002318), death (MESH:D003643), sleep irregularities (MESH:D008599), abdominal pain (MESH:D015746), coronary heart disease (MESH:D003327), Sleep disturbances (MESH:D012893), diabetic (MESH:D003920), nausea (MESH:D009325), MHD.NF-kappaB (OMIM:615561), arteriovenous fistula (MESH:D001164), atherogenic (MESH:D050197), headache (MESH:D006261), malabsorption (MESH:D008286), SLE (MESH:D008180), epileptics (MESH:D004827), RA (MESH:D001172), malignancy (MESH:D009369), gastrointestinal symptoms (MESH:D012817), abdominal discomfort (MESH:D000007), vomiting (MESH:D014839), uremic (MESH:D006463), psychiatric illness (MESH:D001523), hypertension (MESH:D006973), autoimmune conditions (MESH:D001327), skin rash (MESH:D005076)
- **Chemicals:** hydrogen peroxide (MESH:D006861), vitamin D (MESH:D014807), warfarin (MESH:D014859), Tri-glycerides (MESH:D014280), MDA (MESH:D008315), PAP (MESH:D010724), cholesterol (MESH:D002784), TG (MESH:D013866), CHOD (MESH:C064396), ROS (MESH:D017382), starch (MESH:D013213), Amlodipine (MESH:D017311), urea (MESH:D014508), TC (MESH:D013667), potassium (MESH:D011188), Captopril (MESH:D002216), sodium (MESH:D012964), creatinine (MESH:D003404), MLT (MESH:D008550), GPO-PAP (-), NO (MESH:D009569), calcium phosphate (MESH:C020243), calcium (MESH:D002118), superoxide (MESH:D013481), Lipid (MESH:D008055)
- **Species:** Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116]

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## Figures

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## References

2 references — full list in the complete paper: https://tomesphere.com/paper/PMC12877036/full.md

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Source: https://tomesphere.com/paper/PMC12877036