Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/12265
Full metadata record
DC FieldValueLanguage
dc.contributor.authorPriyono, Drajad-
dc.contributor.authorYerizel, Eti-
dc.contributor.authorHarun, Harnavi-
dc.contributor.authorSuharti, Netti-
dc.date.accessioned2025-07-22T01:40:58Z-
dc.date.available2025-07-22T01:40:58Z-
dc.date.issued2025-04-
dc.identifier.citationOriginal Articleen_US
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/12265-
dc.description.abstractBackground: 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.isoen_USen_US
dc.publisherActa Medika Indonesiaen_US
dc.subjectbiomarkersen_US
dc.subjectchronic kidney diseaseen_US
dc.subjectinflammationen_US
dc.subjectRamadan fastingen_US
dc.subjectoxidative stressen_US
dc.titleEffect 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 Studyen_US
dc.typeArticleen_US
Appears in Collections:VOL 57 NO 2 2025

Files in This Item:
File Description SizeFormat 
8.pdf873.08 kBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.