{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,2,27]],"date-time":"2026-02-27T02:52:21Z","timestamp":1772160741236,"version":"3.50.1"},"reference-count":33,"publisher":"Wiley","issue":"1","license":[{"start":{"date-parts":[[2014,9,15]],"date-time":"2014-09-15T00:00:00Z","timestamp":1410739200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Journal of Renal Care"],"published-print":{"date-parts":[[2015,3]]},"abstract":"<jats:title>SUMMARY<\/jats:title>\n                  <jats:sec>\n                    <jats:title>Background<\/jats:title>\n                    <jats:p>Diabetic kidney disease is a common consequence of the development of diabetes. In the United Kingdom 18\u201330% of chronic kidney disease cases and 44% of end\u2010stage renal disease cases in the United States have been attributed to complications of diabetic kidney disease. Angiotensin blockade using angiotensin converting enzyme inhibitors or angiotensin receptor blockers is the standard for slowing the progression of diabetic kidney disease. Evidence suggests that aldosterone antagonism added to standard therapy may be beneficial.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Aim of Review<\/jats:title>\n                    <jats:p>This paper aims to explore the pathophysiological contribution of aldosterone in diabetic kidney disease and review available literature for aldosterone antagonism through mineralocorticoid receptor blockade.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>A comprehensive literature search was conducted. Results were analysed and summarised.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>Nine trials evaluating a total of 535 patients with diabetic kidney disease were identified that evaluated the use of aldosterone antagonists for reducing the signs of diabetic kidney disease. All trials demonstrated a marked decrease in urinary protein excretion when compared to, or added to angiotensin converting enzyme inhibition or angiotensin receptor blockade. The most commonly reported side effect in all of the trials was hyperkalaemia, which occurred in 6.1% of all patients evaluated. Aldosterone antagonists were generally well tolerated in the evaluated patient populations.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusion<\/jats:title>\n                    <jats:p>Aldosterone antagonism may represent a safe and effective complimentary therapy to the use of angiotensin converting enzyme inhibition, or angiotensin receptor blockade, for slowing the progression of diabetic kidney disease.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1111\/jorc.12085","type":"journal-article","created":{"date-parts":[[2014,9,15]],"date-time":"2014-09-15T07:40:03Z","timestamp":1410766803000},"page":"9-18","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":3,"title":["THE ROLE OF ALDOSTERONE ANTAGONISM AGENTS IN DIABETIC KIDNEY DISEASE"],"prefix":"10.1111","volume":"41","author":[{"given":"Eric","family":"Wombwell","sequence":"first","affiliation":[{"name":"University of Missouri\u2010Kansas City School of Pharmacy Kansas City Missouri USA"},{"name":"Centerpoint Medical Center Independence Missouri USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Andrew","family":"Naglich","sequence":"additional","affiliation":[{"name":"University of Missouri\u2010Kansas City School of Pharmacy Kansas City Missouri USA"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2014,9,15]]},"reference":[{"key":"e_1_2_16_2_1","doi-asserted-by":"publisher","DOI":"10.1053\/j.ajkd.2013.01.005"},{"key":"e_1_2_16_3_1","doi-asserted-by":"publisher","DOI":"10.1097\/FJC.0b013e3181ad2190"},{"key":"e_1_2_16_4_1","doi-asserted-by":"publisher","DOI":"10.1038\/ki.2011.48"},{"key":"e_1_2_16_5_1","doi-asserted-by":"publisher","DOI":"10.2215\/CJN.00240106"},{"key":"e_1_2_16_6_1","doi-asserted-by":"publisher","DOI":"10.1016\/S1056-8727(03)00035-7"},{"key":"e_1_2_16_7_1","doi-asserted-by":"publisher","DOI":"10.1172\/JCI118867"},{"key":"e_1_2_16_8_1","doi-asserted-by":"publisher","DOI":"10.3109\/08860220903150312"},{"key":"e_1_2_16_9_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1755-6686.2012.00275.x"},{"key":"e_1_2_16_10_1","volume-title":"Chronic Kidney Disease in England: The Human and Financial Cost","author":"Kerr M.","year":"2012"},{"key":"e_1_2_16_11_1","doi-asserted-by":"publisher","DOI":"10.1097\/HJH.0b013e3283346b62"},{"key":"e_1_2_16_12_1","doi-asserted-by":"publisher","DOI":"10.1681\/ASN.2009070737"},{"key":"e_1_2_16_13_1","doi-asserted-by":"publisher","DOI":"10.2337\/diacare.27.2007.S79"},{"key":"e_1_2_16_14_1","doi-asserted-by":"publisher","DOI":"10.1007\/s10157-010-0298-8"},{"key":"e_1_2_16_15_1","doi-asserted-by":"publisher","DOI":"10.2174\/157339911794273919"},{"key":"e_1_2_16_16_1","unstructured":"NICE. 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