Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/17990
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dc.contributor.authorMacIsaac, Richard J-
dc.contributor.authorJerums, George-
dc.contributor.authorEkinci, Elif I-
dc.date.accessioned2018-07-02T03:59:01Z-
dc.date.available2018-07-02T03:59:01Z-
dc.date.issued2018-03-
dc.identifier.citationAdvances in Chronic Kidney Disease 2018; 25(2): 141-148en_US
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/17990-
dc.description.abstractImproving strategies to prevent the development and progression of CKD is a highly desirable outcome for all involved in the care of patients with diabetes. This is because CKD is a major factor contributing to morbidly and mortality in patients with diabetes. Furthermore, diabetes is the leading cause of ESRD in most developed countries. Although tight glucose control is now an established modality for preventing the development and progression of albuminuria, evidence is now accumulating to suggest that it can also ameliorate glomerular filtration rate loss and possibly progression to ESRD. These benefits of intensive glucose control appear to be most pronounced when applied to patients with the early stages of CKD. Recently, medications that belong to the sodium glucose cotransporter-type 2 inhibitor and the glucagon-like peptide-1 receptor analogue classes have been shown to reduce progression of CKD in patients with type 2 diabetes and relatively well-preserved kidney function. Here, we review the evidence from observational and interventional clinical studies that link good glucose control with the primary prevention of diabetic kidney disease with a focus on preventing early glomerular filtration rate loss.en_US
dc.language.isoeng-
dc.subjectChronicen_US
dc.subjectDiabetesen_US
dc.subjectDiseaseen_US
dc.subjectGlucoseen_US
dc.subjectKidneyen_US
dc.titleGlycemic Control as Primary Prevention for Diabetic Kidney Disease.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleAdvances in Chronic Kidney Diseaseen_US
dc.identifier.affiliationDepartment of Endocrinology & Diabetes, St Vincent's Hospital Melbourne, Australiaen_US
dc.identifier.affiliationDepartment of Medicine, University of Melbourne, Victoria, Australiaen_US
dc.identifier.affiliationEndocrinologyen_US
dc.identifier.doi10.1053/j.ackd.2017.11.003en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0003-2372-395Xen_US
dc.identifier.pubmedid29580578-
dc.type.austinJournal Article-
dc.type.austinReview-
local.name.researcherEkinci, Elif I
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.languageiso639-1en-
crisitem.author.deptEndocrinology-
crisitem.author.deptEndocrinology-
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