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Association of Serum Phosphate with Efficacy of Statin Therapy in Hemodialysis Patients
Statins are less efficacious in reducing cardiovascular disease risk in patients on dialysis than in the general population. Recent experimental data showed that phosphate excess promotes cellular cholesterol synthesis through 3-hydroxy-3-methylglutaryl CoA (HMG-CoA) reductase activation. Whether th...
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Published in: | Clinical journal of the American Society of Nephrology 2022-04, Vol.17 (4), p.546-554 |
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container_title | Clinical journal of the American Society of Nephrology |
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creator | Massy, Ziad A Merkling, Thomas Wagner, Sandra Girerd, Nicolas Essig, Marie Wanner, Christoph Fellstrom, Bengt C Rossignol, Patrick Zannad, Faiez |
description | Statins are less efficacious in reducing cardiovascular disease risk in patients on dialysis than in the general population. Recent experimental data showed that phosphate excess promotes cellular
cholesterol synthesis through 3-hydroxy-3-methylglutaryl CoA (HMG-CoA) reductase activation. Whether this mechanism might account for the resistance of patients on dialysis to statins has not yet been explored.
In this
analysis, we examined the efficacy of statin treatment according to serum phosphate levels in the patients on dialysis who were participants of the A Study to Evaluate the Use of Rosuvastatin in Subjects on Regular Hemodialysis: An Assessment of Survival and Cardiovascular Events (AURORA) trial using serum phosphate levels at baseline and during the trial course. We first classified the patients by groups of similar phosphate trajectories over time and tested whether phosphate as a longitudinal exposure (summarized by the identified trajectory groups) modulated the occurrence of major adverse cardiovascular events and all-cause death. We replicate the analysis in the Deutsche Diabetes Dialyze Studie (4D) trial.
In the AURORA trial, using multivariable analysis, we found that the treatment effect of statin on major adverse cardiovascular events and all-cause death was significant and protective effects in patients with low values of serum phosphate gradually faded for higher phosphate levels >5 mg/dl. A similar lack of statin treatment efficacy for both outcomes was observed with high baseline phosphate levels (>5 mg/dl). In the 4D trial, we found a comparable but not significant trend toward losing treatment efficacy in the presence of high serum phosphate levels for both outcomes.
Our results demonstrated the limited treatment efficacy of statins in patients on dialysis in the presence of hyperphosphatemia. |
doi_str_mv | 10.2215/CJN.12620921 |
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cholesterol synthesis through 3-hydroxy-3-methylglutaryl CoA (HMG-CoA) reductase activation. Whether this mechanism might account for the resistance of patients on dialysis to statins has not yet been explored.
In this
analysis, we examined the efficacy of statin treatment according to serum phosphate levels in the patients on dialysis who were participants of the A Study to Evaluate the Use of Rosuvastatin in Subjects on Regular Hemodialysis: An Assessment of Survival and Cardiovascular Events (AURORA) trial using serum phosphate levels at baseline and during the trial course. We first classified the patients by groups of similar phosphate trajectories over time and tested whether phosphate as a longitudinal exposure (summarized by the identified trajectory groups) modulated the occurrence of major adverse cardiovascular events and all-cause death. We replicate the analysis in the Deutsche Diabetes Dialyze Studie (4D) trial.
In the AURORA trial, using multivariable analysis, we found that the treatment effect of statin on major adverse cardiovascular events and all-cause death was significant and protective effects in patients with low values of serum phosphate gradually faded for higher phosphate levels >5 mg/dl. A similar lack of statin treatment efficacy for both outcomes was observed with high baseline phosphate levels (>5 mg/dl). In the 4D trial, we found a comparable but not significant trend toward losing treatment efficacy in the presence of high serum phosphate levels for both outcomes.
Our results demonstrated the limited treatment efficacy of statins in patients on dialysis in the presence of hyperphosphatemia.</description><identifier>ISSN: 1555-9041</identifier><identifier>ISSN: 1555-905X</identifier><identifier>EISSN: 1555-905X</identifier><identifier>DOI: 10.2215/CJN.12620921</identifier><identifier>PMID: 35236715</identifier><language>eng</language><publisher>United States: American Society of Nephrology</publisher><subject>Cardiovascular Diseases - etiology ; Cardiovascular Diseases - prevention & control ; Cholesterol ; dialysis ; Humans ; Hydroxymethylglutaryl-CoA Reductase Inhibitors - adverse effects ; hyperphosphatemia ; Life Sciences ; Original ; phosphate ; Phosphates ; Renal Dialysis - adverse effects ; statins</subject><ispartof>Clinical journal of the American Society of Nephrology, 2022-04, Vol.17 (4), p.546-554</ispartof><rights>Copyright © 2022 by the American Society of Nephrology.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><rights>Copyright © 2022 by the American Society of Nephrology 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c455t-428cedcefaf11243ca865f78e17a856e5f6cf6d4d97109af708926e09c875af93</citedby><cites>FETCH-LOGICAL-c455t-428cedcefaf11243ca865f78e17a856e5f6cf6d4d97109af708926e09c875af93</cites><orcidid>0000-0001-5771-5996 ; 0000-0002-5878-0359 ; 0000-0002-3251-3754 ; 0000-0001-9507-5301 ; 0000-0001-8009-3873 ; 0000-0002-3278-2057</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8993469/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8993469/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,4011,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35236715$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-03673637$$DView record in HAL$$Hfree_for_read</backlink><backlink>$$Uhttps://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-475201$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Massy, Ziad A</creatorcontrib><creatorcontrib>Merkling, Thomas</creatorcontrib><creatorcontrib>Wagner, Sandra</creatorcontrib><creatorcontrib>Girerd, Nicolas</creatorcontrib><creatorcontrib>Essig, Marie</creatorcontrib><creatorcontrib>Wanner, Christoph</creatorcontrib><creatorcontrib>Fellstrom, Bengt C</creatorcontrib><creatorcontrib>Rossignol, Patrick</creatorcontrib><creatorcontrib>Zannad, Faiez</creatorcontrib><title>Association of Serum Phosphate with Efficacy of Statin Therapy in Hemodialysis Patients</title><title>Clinical journal of the American Society of Nephrology</title><addtitle>Clin J Am Soc Nephrol</addtitle><description>Statins are less efficacious in reducing cardiovascular disease risk in patients on dialysis than in the general population. Recent experimental data showed that phosphate excess promotes cellular
cholesterol synthesis through 3-hydroxy-3-methylglutaryl CoA (HMG-CoA) reductase activation. Whether this mechanism might account for the resistance of patients on dialysis to statins has not yet been explored.
In this
analysis, we examined the efficacy of statin treatment according to serum phosphate levels in the patients on dialysis who were participants of the A Study to Evaluate the Use of Rosuvastatin in Subjects on Regular Hemodialysis: An Assessment of Survival and Cardiovascular Events (AURORA) trial using serum phosphate levels at baseline and during the trial course. We first classified the patients by groups of similar phosphate trajectories over time and tested whether phosphate as a longitudinal exposure (summarized by the identified trajectory groups) modulated the occurrence of major adverse cardiovascular events and all-cause death. We replicate the analysis in the Deutsche Diabetes Dialyze Studie (4D) trial.
In the AURORA trial, using multivariable analysis, we found that the treatment effect of statin on major adverse cardiovascular events and all-cause death was significant and protective effects in patients with low values of serum phosphate gradually faded for higher phosphate levels >5 mg/dl. A similar lack of statin treatment efficacy for both outcomes was observed with high baseline phosphate levels (>5 mg/dl). In the 4D trial, we found a comparable but not significant trend toward losing treatment efficacy in the presence of high serum phosphate levels for both outcomes.
Our results demonstrated the limited treatment efficacy of statins in patients on dialysis in the presence of hyperphosphatemia.</description><subject>Cardiovascular Diseases - etiology</subject><subject>Cardiovascular Diseases - prevention & control</subject><subject>Cholesterol</subject><subject>dialysis</subject><subject>Humans</subject><subject>Hydroxymethylglutaryl-CoA Reductase Inhibitors - adverse effects</subject><subject>hyperphosphatemia</subject><subject>Life Sciences</subject><subject>Original</subject><subject>phosphate</subject><subject>Phosphates</subject><subject>Renal Dialysis - adverse effects</subject><subject>statins</subject><issn>1555-9041</issn><issn>1555-905X</issn><issn>1555-905X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNpdkU1PAjEQhhujEUVvns1eTQT7vduLCUEUDVES8ePW1NKyNbAl210I_95dERRPM5l53pnJvACcIdjGGLGr7sNjG2GOocBoDxwhxlhLQPa-v80paoDjED4hpJRgdggahGHCY8SOwFsnBK-dKpzPIm-jZ5OXs2iY-jBPVWGipSvSqGet00qvvoGiYrNolJpczVdRlfbNzI-dmq6CC9Gw6pqsCCfgwKppMKc_sQlebnujbr81eLq773YGLU0ZK1oUJ9qMtbHKIoQp0SrhzMaJQbFKGDfMcm35mI5FjKBQNoaJwNxAoZOYKStIE1yu54almZcfcp67mcpX0isnb9xrR_p8IstS0phhiCr8eo1X7KxenBW5mu6odjuZS-XEL2QiBKG83nexHpD-k_U7A1nXYPVYwkm8QL-36dyHkBu7FSAoa-9k5Z3ceFfh539v28Ibs8gXLqyVzQ</recordid><startdate>20220401</startdate><enddate>20220401</enddate><creator>Massy, Ziad A</creator><creator>Merkling, Thomas</creator><creator>Wagner, Sandra</creator><creator>Girerd, Nicolas</creator><creator>Essig, Marie</creator><creator>Wanner, Christoph</creator><creator>Fellstrom, Bengt C</creator><creator>Rossignol, Patrick</creator><creator>Zannad, Faiez</creator><general>American Society of Nephrology</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>1XC</scope><scope>5PM</scope><scope>ADTPV</scope><scope>AOWAS</scope><scope>DF2</scope><orcidid>https://orcid.org/0000-0001-5771-5996</orcidid><orcidid>https://orcid.org/0000-0002-5878-0359</orcidid><orcidid>https://orcid.org/0000-0002-3251-3754</orcidid><orcidid>https://orcid.org/0000-0001-9507-5301</orcidid><orcidid>https://orcid.org/0000-0001-8009-3873</orcidid><orcidid>https://orcid.org/0000-0002-3278-2057</orcidid></search><sort><creationdate>20220401</creationdate><title>Association of Serum Phosphate with Efficacy of Statin Therapy in Hemodialysis Patients</title><author>Massy, Ziad A ; 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Recent experimental data showed that phosphate excess promotes cellular
cholesterol synthesis through 3-hydroxy-3-methylglutaryl CoA (HMG-CoA) reductase activation. Whether this mechanism might account for the resistance of patients on dialysis to statins has not yet been explored.
In this
analysis, we examined the efficacy of statin treatment according to serum phosphate levels in the patients on dialysis who were participants of the A Study to Evaluate the Use of Rosuvastatin in Subjects on Regular Hemodialysis: An Assessment of Survival and Cardiovascular Events (AURORA) trial using serum phosphate levels at baseline and during the trial course. We first classified the patients by groups of similar phosphate trajectories over time and tested whether phosphate as a longitudinal exposure (summarized by the identified trajectory groups) modulated the occurrence of major adverse cardiovascular events and all-cause death. We replicate the analysis in the Deutsche Diabetes Dialyze Studie (4D) trial.
In the AURORA trial, using multivariable analysis, we found that the treatment effect of statin on major adverse cardiovascular events and all-cause death was significant and protective effects in patients with low values of serum phosphate gradually faded for higher phosphate levels >5 mg/dl. A similar lack of statin treatment efficacy for both outcomes was observed with high baseline phosphate levels (>5 mg/dl). In the 4D trial, we found a comparable but not significant trend toward losing treatment efficacy in the presence of high serum phosphate levels for both outcomes.
Our results demonstrated the limited treatment efficacy of statins in patients on dialysis in the presence of hyperphosphatemia.</abstract><cop>United States</cop><pub>American Society of Nephrology</pub><pmid>35236715</pmid><doi>10.2215/CJN.12620921</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0001-5771-5996</orcidid><orcidid>https://orcid.org/0000-0002-5878-0359</orcidid><orcidid>https://orcid.org/0000-0002-3251-3754</orcidid><orcidid>https://orcid.org/0000-0001-9507-5301</orcidid><orcidid>https://orcid.org/0000-0001-8009-3873</orcidid><orcidid>https://orcid.org/0000-0002-3278-2057</orcidid><oa>free_for_read</oa></addata></record> |
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source | American Society of Nephrology; PubMed Central |
subjects | Cardiovascular Diseases - etiology Cardiovascular Diseases - prevention & control Cholesterol dialysis Humans Hydroxymethylglutaryl-CoA Reductase Inhibitors - adverse effects hyperphosphatemia Life Sciences Original phosphate Phosphates Renal Dialysis - adverse effects statins |
title | Association of Serum Phosphate with Efficacy of Statin Therapy in Hemodialysis Patients |
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