FRINK Linked Data Fragments server

Matches in SemOpenAlex for { <https://semopenalex.org/work/W2108388631> ?p ?o ?g. }

• W2108388631 endingPage "221" @default.
• W2108388631 startingPage "219" @default.
• W2108388631 abstract "Treatment with angiotensin-converting enzyme inhibitors (ACEIs) or angiotensin receptor blockers (ARBs) slows the progression of proteinuric diabetic kidney disease (1–3). However, the risk of progression remains high despite these medications. In the Reduction of Endpoints in NIDDM with the Angiotensin II Antagonist Losartan trial and the Irbesartan Diabetic Nephropathy Trial, the treatment-induced decrease in albuminuria correlated with overall benefit in terms of risk of CKD progression, and individuals with residual albuminuria despite ARB treatment were at higher risk for progression (1,3). These observations led to the hypothesis that greater reductions in albuminuria with more intensive renin-angiotensin-aldosterone system (RAAS) blockade would further slow progression of diabetic kidney disease (4). There are a number of approaches to intensifying RAAS blockade, including increasing the dose of monotherapy (i.e., supramaximal doses), combining an ACEI with an ARB, adding aliskiren to an ACEI or an ARB, or adding a mineralocorticoid receptor blocker (MRB) to an ACEI or ARB. Each of these treatments reduces albuminuria (5–8), although there are few studies that directly compare the interventions with regard to efficacy or safety. One of the main safety concerns with more intensive RAAS blockade is hyperkalemia. Serum potassium levels are maintained through a combination of internal balance (shifts between extracellular and intracellular spaces) and external balance (intake versus excretion). The major determinants of potassium excretion in the normal kidney are distal delivery of sodium, urinary flow rate, and aldosterone activity (9–11). With loss of functioning nephron mass and declining glomerular filtration, remaining functioning nephrons adapt with an increase in fractional excretion of potassium. This helps maintain normal potassium levels until advanced CKD occurs (10). ACEIs, ARBs, or renin inhibitors increase the risk of hyperkalemia by inhibiting aldosterone as well as by decreasing GFR, which can decrease distal delivery of sodium. Prior studies show that risk factors for hyperkalemia with the use of RAAS blockers are older age, lower eGFR, higher baseline potassium levels, and use of more than one medication that interferes with potassium excretion (12,13). In a recent review of studies of RAAS blockade, Weir and Rolfe found that the incidence of hyperkalemia was <2% in individuals without risk factors for hyperkalemia who received RAAS blockers for hypertension (14). By contrast, the risk of hyperkalemia in patients with CKD or heart failure was 5%–10% in prior studies. Individuals with diabetic nephropathy are more prone to hyperkalemia at higher levels of GFR due to a greater prevalence of hyporeninemic hypoaldosteronism that impairs renal potassium excretion (15). RAAS blockade further exacerbates this risk and the risk is higher with more intensive blockade. In this issue of CJASN, van Buren et al. evaluate whether renal potassium excretion (external balance) explains the higher rate of hyperkalemia with combination RAAS blockade in a secondary analysis of a randomized trial (16). The study, the primary results of which were previously reported (17), was a three-arm, randomized, double-blind study comparing placebo, losartan (100 mg), or spironolactone (25 mg) added to maximal lisinopril (80 mg) in individuals with diabetes and residual overt albuminuria despite maximal-dose lisinopril. Median creatinine clearance on 24-hour urine samples was 64.5 ml/min and median 24-hour urine albumin was approximately 1 g. Compared with placebo, losartan decreased albuminuria by a further 16.8% and spironolactone by 34% at the end of 48 weeks, consistent with prior studies. However, the addition of spironolactone to ACEI therapy also led to significantly greater hyperkalemia. Mean follow-up potassium concentrations were 4.5, 4.7, and 5.0 mEq/L in the placebo, losartan, and spironolactone groups, respectively. In addition to the greater mean potassium with dual-RAAS antagonism, the frequency of clinically significant hyperkalemic events (potassium>6.0 mEq/L) was markedly more common, occurring in 7.4%, 38.5%, and 51.9% in the three groups, respectively. This high rate of hyperkalemia was especially remarkable given the relatively preserved renal filtration function of the participants. Two of the 27 participants in the spironolactone group discontinued the study medication due to recurrent hyperkalemia. Surprisingly, there was no significant difference in the 24-hour urine potassium excretion or fractional excretion of potassium, suggesting that the higher hyperkalemia risk cannot be explained by chronic changes in renal potassium excretion. One potential explanation for the higher risk of clinically significant hyperkalemia is that combination RAAS more severely affects the kidney’s ability to respond to acute increases in potassium intake or to stresses that acutely decrease GFR or distal nephron sodium delivery. This decreased renal “kaliuresis reserve” may not be accurately approximated by 24-hour urine potassium at steady state. Potentially, the effect on this proposed reserve may depend on the degree of RAAS blockade. If the main issue is renal reserve, it may be more difficult to predict which patients with CKD are at higher hyperkalemia risk and would require regular ongoing monitoring of serum potassium levels. More importantly, it implies that we need to develop different approaches to preventing hyperkalemia directed at avoidance of prerenal azotemia and other factors that affect renal perfusion and distal nephron sodium delivery. A larger question is whether determining the precise mechanisms of increased hyperkalemia with combination RAAS blockade is clinically relevant. Results of recently completed large multicenter clinical trials consistently demonstrated an unfavorable risk/benefit profile of this therapeutic approach for preventing progressive renal disease. In the Ongoing Telmisartan Alone and in Combination with Ramipril Global Endpoint Trial, there was no benefit on renal or cardiovascular outcomes with combination therapy, and there was an increased risk of hyperkalemia and AKI (18,19). However, the study included participants at relatively low risk of ESRD, and the absolute rate of hyperkalemia was modest. In the Aliskiren Trial in Type 2 Diabetes Using Cardiorenal Endpoints (8) and the Veterans Affairs Nephropathy in Diabetes study (20), the rate of hyperkalemia (potassium≥6.0 mEq/L) was more than two times higher in the combination RAAS blockade group compared with monotherapy. Importantly, both studies were stopped prematurely for safety concerns. The excess risk of adverse events—and lack of benefit on renal progression—occurred despite decreases in albuminuria. The risk/benefit ratio for preventing progression of proteinuric kidney disease is not clearly answered for MRBs added to maximal ACEI or ARB therapy. Given the different sites of action within the RAAS, one cannot necessarily conclude that such combination therapy would have the same adverse risk/benefit profile as combination ACEI plus ARB therapy. For example, in congestive heart failure, the addition of an MRB to ACEI or ARB treatment reduced all-cause mortality (21), whereas combination ACEI and ARB decreased risk of heart failure admissions without amortality benefit (22). However, caution is needed in the use of such a therapeutic approach in patients with CKD, especially those with impaired GFR, until we have data from long-term randomized trials examining the benefits and risks of MRB added to ACEI or ARB treatment. The risks of widespread MRB therapy were demonstrated after the publication and dissemination of the results of the Randomized Aldactone Evaluation Study (21); compared with the period before release of the study results, the rate of hospital admission for hyperkalemia rose 4-fold, with an associated increase in mortality (23). The results of the analysis by van Buren et al. highlight the importance of careful monitoring of potassium in any CKD patient in whom a mineralocorticoid receptor blocker is to be used in combination with an ACEI or ARB, especially if the patient also has diabetes. van Buren et al. also highlight the importance of careful monitoring and treatment of hyperkalemia in clinical trials of combination MRB plus ACEI/ARB therapy in CKD. Until results of such trials show a favorable effect on CKD progression with an acceptable risk profile, prudence may suggest that this combination be avoided in the absence of documented primary hyperaldosteronism. Disclosures Merck donated the study medication to the US Department of Veterans Affairs for the Veterans Affairs Nephropathy in Diabetes study." @default.
• W2108388631 created "2016-06-24" @default.
• W2108388631 creator A5031256672 @default.
• W2108388631 creator A5089603612 @default.
• W2108388631 date "2014-02-01" @default.
• W2108388631 modified "2023-09-23" @default.
• W2108388631 title "Serum Potassium in Dual Renin-Angiotensin-Aldosterone System Blockade" @default.
• W2108388631 cites W1966840298 @default.
• W2108388631 cites W2029566464 @default.
• W2108388631 cites W2044773944 @default.
• W2108388631 cites W2056893352 @default.
• W2108388631 cites W2056976690 @default.
• W2108388631 cites W2085338982 @default.
• W2108388631 cites W2086158964 @default.
• W2108388631 cites W2093767567 @default.
• W2108388631 cites W2100409734 @default.
• W2108388631 cites W2111945961 @default.
• W2108388631 cites W2126964454 @default.
• W2108388631 cites W2138862624 @default.
• W2108388631 cites W2141386688 @default.
• W2108388631 cites W2145632481 @default.
• W2108388631 cites W2152594920 @default.
• W2108388631 cites W2152798629 @default.
• W2108388631 cites W2155660983 @default.
• W2108388631 cites W2157267479 @default.
• W2108388631 cites W2162368776 @default.
• W2108388631 cites W2323458614 @default.
• W2108388631 cites W2615684303 @default.
• W2108388631 cites W4233762550 @default.
• W2108388631 doi "https://doi.org/10.2215/cjn.12411213" @default.
• W2108388631 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3913249" @default.
• W2108388631 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/24408119" @default.
• W2108388631 hasPublicationYear "2014" @default.
• W2108388631 type Work @default.
• W2108388631 sameAs 2108388631 @default.
• W2108388631 citedByCount "4" @default.
• W2108388631 countsByYear W21083886312016 @default.
• W2108388631 countsByYear W21083886312018 @default.
• W2108388631 countsByYear W21083886312019 @default.
• W2108388631 crossrefType "journal-article" @default.
• W2108388631 hasAuthorship W2108388631A5031256672 @default.
• W2108388631 hasAuthorship W2108388631A5089603612 @default.
• W2108388631 hasBestOaLocation W21083886311 @default.
• W2108388631 hasConcept C126322002 @default.
• W2108388631 hasConcept C134018914 @default.
• W2108388631 hasConcept C170493617 @default.
• W2108388631 hasConcept C178790620 @default.
• W2108388631 hasConcept C185592680 @default.
• W2108388631 hasConcept C198710026 @default.
• W2108388631 hasConcept C2778468042 @default.
• W2108388631 hasConcept C2778525890 @default.
• W2108388631 hasConcept C2908929049 @default.
• W2108388631 hasConcept C517785266 @default.
• W2108388631 hasConcept C71924100 @default.
• W2108388631 hasConcept C84393581 @default.
• W2108388631 hasConceptScore W2108388631C126322002 @default.
• W2108388631 hasConceptScore W2108388631C134018914 @default.
• W2108388631 hasConceptScore W2108388631C170493617 @default.
• W2108388631 hasConceptScore W2108388631C178790620 @default.
• W2108388631 hasConceptScore W2108388631C185592680 @default.
• W2108388631 hasConceptScore W2108388631C198710026 @default.
• W2108388631 hasConceptScore W2108388631C2778468042 @default.
• W2108388631 hasConceptScore W2108388631C2778525890 @default.
• W2108388631 hasConceptScore W2108388631C2908929049 @default.
• W2108388631 hasConceptScore W2108388631C517785266 @default.
• W2108388631 hasConceptScore W2108388631C71924100 @default.
• W2108388631 hasConceptScore W2108388631C84393581 @default.
• W2108388631 hasIssue "2" @default.
• W2108388631 hasLocation W21083886311 @default.
• W2108388631 hasLocation W21083886312 @default.
• W2108388631 hasLocation W21083886313 @default.
• W2108388631 hasLocation W21083886314 @default.
• W2108388631 hasOpenAccess W2108388631 @default.
• W2108388631 hasPrimaryLocation W21083886311 @default.
• W2108388631 hasRelatedWork W1966128948 @default.
• W2108388631 hasRelatedWork W1992220075 @default.
• W2108388631 hasRelatedWork W2006202112 @default.
• W2108388631 hasRelatedWork W2016647631 @default.
• W2108388631 hasRelatedWork W2024736606 @default.
• W2108388631 hasRelatedWork W2033713032 @default.
• W2108388631 hasRelatedWork W2054593959 @default.
• W2108388631 hasRelatedWork W2126797993 @default.
• W2108388631 hasRelatedWork W2132612653 @default.
• W2108388631 hasRelatedWork W2151139437 @default.
• W2108388631 hasVolume "9" @default.
• W2108388631 isParatext "false" @default.
• W2108388631 isRetracted "false" @default.
• W2108388631 magId "2108388631" @default.
• W2108388631 workType "article" @default.