ACE and SGLT2 inhibitors: the future for non-diabetic and diabetic proteinuric renal disease. (April 2017)
- Record Type:
- Journal Article
- Title:
- ACE and SGLT2 inhibitors: the future for non-diabetic and diabetic proteinuric renal disease. (April 2017)
- Main Title:
- ACE and SGLT2 inhibitors: the future for non-diabetic and diabetic proteinuric renal disease
- Authors:
- Perico, Norberto
Ruggenenti, Piero
Remuzzi, Giuseppe - Abstract:
- Highlights: Current strategies to prevent or revert renal disease progression in proteinuric nephropathies focus on reduction of abnormal protein trafficking through the glomerular capillary wall. Blockade of the renin-angiotensin system (RAS) by means of ACE inhibitors and/or ARBs is the most effective treatment to slow renal disease progression. Combination therapy with ACEi and ARBs inhibits the RAS more efficiently than does each agent alone through an addictive effect, but requires close monitoring of patients. Novel treatment strategies, especially for diabetic kidney disease are on the horizon, including sodium–glucose linked cotransporter-2 (SGLT2) inhibitors, but investigating their renoprotective efficacy is still in infancy. Abstract : Most chronic nephropathies progress relentlessly to end-stage kidney disease. Research in animals and humans has helped our understanding of the mechanisms of chronic kidney disease progression. Current therapeutic strategies to prevent or revert renal disease progression focus on reduction of urinary protein excretion and blood pressure control. Blockade of the renin-angiotensin system (RAS) with angiotensin-converting enzyme inhibitors and/or angiotensin II type 1 receptor blockers is the most effective treatment to achieve these purposes in non-diabetic and diabetic proteinuric renal diseases. For those individuals in which nephroprotection by RAS blockade is only partial, sodium–glucose linked cotransporter-2 (SGLT2) inhibitorsHighlights: Current strategies to prevent or revert renal disease progression in proteinuric nephropathies focus on reduction of abnormal protein trafficking through the glomerular capillary wall. Blockade of the renin-angiotensin system (RAS) by means of ACE inhibitors and/or ARBs is the most effective treatment to slow renal disease progression. Combination therapy with ACEi and ARBs inhibits the RAS more efficiently than does each agent alone through an addictive effect, but requires close monitoring of patients. Novel treatment strategies, especially for diabetic kidney disease are on the horizon, including sodium–glucose linked cotransporter-2 (SGLT2) inhibitors, but investigating their renoprotective efficacy is still in infancy. Abstract : Most chronic nephropathies progress relentlessly to end-stage kidney disease. Research in animals and humans has helped our understanding of the mechanisms of chronic kidney disease progression. Current therapeutic strategies to prevent or revert renal disease progression focus on reduction of urinary protein excretion and blood pressure control. Blockade of the renin-angiotensin system (RAS) with angiotensin-converting enzyme inhibitors and/or angiotensin II type 1 receptor blockers is the most effective treatment to achieve these purposes in non-diabetic and diabetic proteinuric renal diseases. For those individuals in which nephroprotection by RAS blockade is only partial, sodium–glucose linked cotransporter-2 (SGLT2) inhibitors could be a promising new class of drugs to provide further renoprotective benefit when added on to RAS blockers. … (more)
- Is Part Of:
- Current opinion in pharmacology. Volume 33(2017)
- Journal:
- Current opinion in pharmacology
- Issue:
- Volume 33(2017)
- Issue Display:
- Volume 33, Issue 2017 (2017)
- Year:
- 2017
- Volume:
- 33
- Issue:
- 2017
- Issue Sort Value:
- 2017-0033-2017-0000
- Page Start:
- 34
- Page End:
- 40
- Publication Date:
- 2017-04
- Subjects:
- Pharmacology -- Periodicals
Pharmaceutical Preparations -- Periodicals
Drug Therapy -- Periodicals
Biopharmaceutics -- Periodicals
Pharmacologie -- Périodiques
Pharmacology
Periodicals
615.105 - Journal URLs:
- http://www.sciencedirect.com/science/journal/14714892 ↗
http://www.clinicalkey.com/dura/browse/journalIssue/14714892 ↗
http://www.clinicalkey.com.au/dura/browse/journalIssue/14714892 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.coph.2017.03.006 ↗
- Languages:
- English
- ISSNs:
- 1471-4892
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3500.776920
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 2696.xml