Publication:
The liver-kidney axis: Is serum leptin a potential link in non-alcoholic fatty liver disease-associated chronic kidney disease?

dc.contributor.authorCanbakan M.
dc.contributor.authorBakkaloglu O. K.
dc.contributor.authorAtay K.
dc.contributor.authorKoroglu E.
dc.contributor.authorTuncer M. M.
dc.contributor.authorCANBAKAN İ. B.
dc.contributor.authorŞENTÜRK H.
dc.contributor.institutionauthorŞENTÜRK, HAKAN
dc.date.accessioned2023-02-22T21:31:13Z
dc.date.available2023-02-22T21:31:13Z
dc.date.issued2023-01-01
dc.description.abstract© 2023 Pan-Arab Association of GastroenterologyBackground and study aims: Non-alcoholic fatty liver disease (NAFLD) is an independent risk factor for chronic kidney disease (CKD). Previous studies argued that leptin levels increase significantly with the progression of CKD. But the association between leptin and CKD has not been investigated in patients with NAFLD. Therefore, we conducted this study to establish whether increased leptin level is associated with CKD in NAFLD patients. Patients and methods: In our prospective study with a follow up period of six months thirty-five teetotaller biopsy-proven NAFLD patients were divided as groups with mild, versus advanced, fibrosis. Liver fibrosis was also assessed with Fibroscan. Serum leptin levels were measured by radioimmunoassay. For insulin resistance we used the homeostasis model assessment method (HOMA-IR). For the kidney function, we used the abbreviated formula Modification of Diet in Renal Disease (MDRD) formula, which estimates GFR. For statistical analysis, Student\"s-t test, Mann-Whitney test, linear regression-binary logistic regression analyses and the ROC curve analysis were used. Results: Advanced fibrosis and increased HOMA-IR were risk factors for decreased eGFR. Leptin correlated inversely with advanced fibrosis (p: 0.03) and low leptin was a risk factor for CKD (p: 0.02). In ROC curve analysis, advanced fibrosis and low leptin were risk factors for decreased eGFR (p: 0.007 and 0.004, respectively). Low leptin level was dependently associated with decreased eGFR. Conclusion: Advanced fibrosis in NAFLD patients is a risk factor for CKD. Leptin correlated inversely with advanced fibrosis. Unlike the previous studies, which were not performed in NAFLD patients, we found decreased leptin in NAFLD patients with decreased eGFR. Low leptin level was found to be a dependent predictor for differentiating NAFLD patients with high risk for CKD.
dc.identifier.citationCanbakan M., Bakkaloglu O. K., Atay K., Koroglu E., Tuncer M. M., CANBAKAN İ. B., ŞENTÜRK H., "The liver-kidney axis: Is serum leptin a potential link in non-alcoholic fatty liver disease-associated chronic kidney disease?", Arab Journal of Gastroenterology, 2023
dc.identifier.doi10.1016/j.ajg.2023.01.001
dc.identifier.issn1687-1979
dc.identifier.pubmed36764893
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85147888218&origin=inward
dc.identifier.urihttps://hdl.handle.net/20.500.12645/37102
dc.relation.ispartofArab Journal of Gastroenterology
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectTıp
dc.subjectDahili Tıp Bilimleri
dc.subjectİç Hastalıkları
dc.subjectGastroenteroloji-(Hepatoloji)
dc.subjectSağlık Bilimleri
dc.subjectMedicine
dc.subjectInternal Medicine Sciences
dc.subjectInternal Diseases
dc.subjectGastroenterology and Hepatology
dc.subjectHealth Sciences
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectGASTROENTEROLOJİ VE HEPATOLOJİ
dc.subjectClinical Medicine (MED)
dc.subjectCLINICAL MEDICINE
dc.subjectGASTROENTEROLOGY & HEPATOLOGY
dc.subjectGastroenteroloji
dc.subjectGastroenterology
dc.subjectChronic kidney disease
dc.subjecteGFR
dc.subjectLeptin
dc.subjectMDRD
dc.subjectNon-alcoholic fatty liver disease
dc.titleThe liver-kidney axis: Is serum leptin a potential link in non-alcoholic fatty liver disease-associated chronic kidney disease?
dc.typeArticle
dspace.entity.typePublication
local.avesis.ida095efc8-29e9-4aa0-8da3-c09d4b949100
local.indexed.atPubMed
relation.isAuthorOfPublication278fcf63-3b92-4368-bff6-f140ebd9aeb3
relation.isAuthorOfPublication.latestForDiscovery278fcf63-3b92-4368-bff6-f140ebd9aeb3

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