Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/46542
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dc.contributor.authorAkpinar, Kadriye-
dc.contributor.authorAslan, Diler-
dc.contributor.authorFenkci, Semin Melahat-
dc.date.accessioned2023-01-09T21:12:33Z-
dc.date.available2023-01-09T21:12:33Z-
dc.date.issued2021-
dc.identifier.issn0101-2800-
dc.identifier.issn2175-8239-
dc.identifier.urihttps://doi.org/10.1590/2175-8239-JBN-2020-0145-
dc.identifier.urihttps://hdl.handle.net/11499/46542-
dc.description.abstractIntroduction: GFR is estimated by using creatinine and cystatin C to determine renal dysfunction. Our aim was to evaluate estimated GFR (eGFR) based on cystatin C in type 2 diabetic patients with diabetic nephropathy (DN). Methods: Study group included 52 controls (46% male, age: 54.5 +/- 12.4) and 101 diabetic patients (46.5% male, age: 58.2 +/- 11). The diabetics were divided into three subgroups according to 24-hour urine albumin: normal to mildly increased (A1) (n=51), moderately increased (A2) (n=25), severely increased (A3) (n=25) albuminuria. Creatinine clearance (CrCl) was determined. Correlations between CrCl and eGFRs estimated according to the CKD-EPI, MDRD, and Cockcroft- Gault (CG) formulas, and ROC curves were evaluated. Data were analyzed using SPSS 22.0. Results: Only CKD-EPI- cys eGFR was significantly lower in the A1 group than the controls (p=0.021). All GFRs were lower in the A3 group than the control (CKD-EPIcr, MDRD, CKD-EPI- cys, CKD-EPI-crcys: p=0.0001, CG and CrCl: p=0.001) and A1 (for all GFRs p=0.0001) groups. CKD-EPI- cr (p=0.004), MDRD (p=0.01), CG (p=0.037), CKD- EPI-cys (p=0.033), and CKD-EPI-cr-cys (p=0.016) eGFRs in the A2 group were significantly different from the A1 group. All eGFRs showed a moderate correlation with CrCl in the A1group (CKD-EPI-cr and CKD-EPI-crcys: r=0.49, p=0.0001, MDRD: r=0.44, p=0.001, CG r=0.48, p=0.0001: CKDEPI-cys r=0.40, p=0.004). The area under the CKD-EPI-cys ROC curve was the highest and found to be 0.847 (95%CI 0.763-0.931, p=0.0001). Conclusions: Our results showed that the CKD-EPIcys eGFR can be useful in detecting the early stage of DN and more predictive than the others for prediction of DN.en_US
dc.description.sponsorshipPamukkale University Scientific Research Projects Department [2017TIPF018]en_US
dc.description.sponsorshipThis study was supported by the Pamukkale University Scientific Research Projects Department. Grant sponsor: Pamukkale University Scientific Research Projects Department, grant number and date: 2017TIPF018, 26.12.2017.en_US
dc.language.isoenen_US
dc.publisherSoc Brasileira Nefrologiaen_US
dc.relation.ispartofJornal Brasileiro De Nefrologiaen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectDiabetes Mellitusen_US
dc.subjectType 2en_US
dc.subjectDiabetic Nephropathiesen_US
dc.subjectGlomerular Filtration Rateen_US
dc.subjectCystatin Cen_US
dc.subjectSerum Creatinineen_US
dc.subjectKidney-Functionen_US
dc.subjectRenal-Functionen_US
dc.subjectGfren_US
dc.subjectEpidemiologyen_US
dc.subjectPerformanceen_US
dc.subjectClearanceen_US
dc.subjectDiseaseen_US
dc.subjectMarkeren_US
dc.titleAssessment of estimated glomerular filtration rate based on cystatin C in diabetic nephropathyen_US
dc.typeArticleen_US
dc.identifier.volume43en_US
dc.identifier.issue3en_US
dc.identifier.startpage340en_US
dc.identifier.endpage348en_US
dc.authoridAkpinar, Kadriye/0000-0002-6951-8866-
dc.identifier.doi10.1590/2175-8239-JBN-2020-0145-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.authorscopusid57191621440-
dc.authorscopusid7004641773-
dc.authorscopusid6603153570-
dc.identifier.pmid33599678en_US
dc.identifier.scopus2-s2.0-85116173192en_US
dc.identifier.wosWOS:000852619700009en_US
dc.identifier.scopusqualityQ3-
item.languageiso639-1en-
item.cerifentitytypePublications-
item.fulltextWith Fulltext-
item.grantfulltextopen-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeArticle-
crisitem.author.dept14.03. Basic Medical Sciences-
crisitem.author.dept14.03. Basic Medical Sciences-
crisitem.author.dept14.02. Internal Medicine-
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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