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DC Field | Value | Language |
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dc.contributor.author | Priyono, Drajad | - |
dc.contributor.author | Yerizel, Eti | - |
dc.contributor.author | Harun, Harnavi | - |
dc.contributor.author | Suharti, Netti | - |
dc.date.accessioned | 2025-07-22T01:40:58Z | - |
dc.date.available | 2025-07-22T01:40:58Z | - |
dc.date.issued | 2025-04 | - |
dc.identifier.citation | Original Article | en_US |
dc.identifier.uri | http://localhost:8080/xmlui/handle/123456789/12265 | - |
dc.description.abstract | Background: Chronic kidney disease (CKD) is a global health problem with increasing prevalence. This study aims to analyze the effect of Ramadan fasting on important biomarkers in CKD patients. Methods: A prospective cohort study was conducted on 30 CKD patients with stages 1, 2, and 3A who underwent Ramadan fasting. Measurements of MDA, PARP, SIRT1, NR1D1, and TGF-β levels were carried out before fasting, 2 weeks during fasting, and after fasting using the Enzyme-linked immunosorbent assay (ELISA) method. Results: There were significant decreases in urea, fasting blood glucose, HbA1C, and uric acid levels (p<0.05). MDA and SIRT1 decreased significantly (p<0.001), while PARP and NR1D1 increased significantly (p<0.001). TGF-β also showed a decrease. There were no significant changes in lipid profiles, creatinine, and albumin. Conclusion: Ramadan fasting has significant effects on several biochemical parameters and biological markers in early-stage CKD patients. These changes indicate potential improvements in oxidative stress, cell autophagy, inflammation regulation, and circadian rhythm. Further studies are needed to evaluate the long-term effects and clinical implications of these findings in CKD management. | en_US |
dc.language.iso | en_US | en_US |
dc.publisher | Acta Medika Indonesia | en_US |
dc.subject | biomarkers | en_US |
dc.subject | chronic kidney disease | en_US |
dc.subject | inflammation | en_US |
dc.subject | Ramadan fasting | en_US |
dc.subject | oxidative stress | en_US |
dc.title | Effect of Ramadan Fasting on Malondialdehyde, Poly (ADPRibose) Polymerase, Sirtuin 1, Nuclear Receptor Subfamily 1 Group D Member 1, and Transforming Growth Factor Beta in Chronic Kidney Disease: A Prospective Cohort Study | en_US |
dc.type | Article | en_US |
Appears in Collections: | VOL 57 NO 2 2025 |
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