Optimizing Cholesterol Treatment in Patients With Muscle Complaints.
Identifieur interne : 000519 ( PubMed/Corpus ); précédent : 000518; suivant : 000520Optimizing Cholesterol Treatment in Patients With Muscle Complaints.
Auteurs : Robert S. Rosenson ; Steven Baker ; Maciej Banach ; Kenneth M. Borow ; Lynne T. Braun ; Eric Bruckert ; Liam R. Brunham ; Alberico L. Catapano ; Marshall B. Elam ; G B John Mancini ; Patrick M. Moriarty ; Pamela B. Morris ; Paul Muntner ; Kausik K. Ray ; Erik S. Stroes ; Beth A. Taylor ; Valerie H. Taylor ; Gerald F. Watts ; Paul D. ThompsonSource :
- Journal of the American College of Cardiology [ 1558-3597 ] ; 2017.
English descriptors
- KwdEn :
- Anticholesteremic Agents (adverse effects), Anticholesteremic Agents (therapeutic use), Cardiovascular Diseases (blood), Cardiovascular Diseases (prevention & control), Cholesterol (blood), Humans, Hydroxymethylglutaryl-CoA Reductase Inhibitors (adverse effects), Hydroxymethylglutaryl-CoA Reductase Inhibitors (therapeutic use), Muscle, Skeletal (drug effects), Muscular Diseases (chemically induced), Risk Factors.
- MESH :
- chemical , adverse effects : Anticholesteremic Agents, Hydroxymethylglutaryl-CoA Reductase Inhibitors.
- chemical , blood : Cholesterol.
- chemical , therapeutic use : Anticholesteremic Agents, Hydroxymethylglutaryl-CoA Reductase Inhibitors.
- blood : Cardiovascular Diseases.
- chemically induced : Muscular Diseases.
- drug effects : Muscle, Skeletal.
- prevention & control : Cardiovascular Diseases.
- Humans, Risk Factors.
Abstract
Statins are highly effective for preventing cardiovascular events by reducing low-density lipoprotein cholesterol (LDL-C). However, many patients taking statins report muscle-related symptoms that prevent the use of guideline recommended doses. Patients with reported intolerance to statins have a high risk of cardiovascular events. Clinical strategies that optimize cardiovascular risk reduction through LDL-C lowering need to be applied in patients experiencing intolerable side effects that they attribute to statins. In this paper, the authors review definitions of statin intolerance, propose algorithms to better define statin intolerance, and describe approaches to optimize cardiovascular risk reduction among individuals reporting statin-associated muscle symptoms.
DOI: 10.1016/j.jacc.2017.07.752
PubMed: 28859793
Links to Exploration step
pubmed:28859793Le document en format XML
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<author><name sortKey="Banach, Maciej" sort="Banach, Maciej" uniqKey="Banach M" first="Maciej" last="Banach">Maciej Banach</name>
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</affiliation>
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<author><name sortKey="Baker, Steven" sort="Baker, Steven" uniqKey="Baker S" first="Steven" last="Baker">Steven Baker</name>
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<author><name sortKey="Banach, Maciej" sort="Banach, Maciej" uniqKey="Banach M" first="Maciej" last="Banach">Maciej Banach</name>
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<author><name sortKey="Catapano, Alberico L" sort="Catapano, Alberico L" uniqKey="Catapano A" first="Alberico L" last="Catapano">Alberico L. Catapano</name>
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</affiliation>
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<author><name sortKey="Elam, Marshall B" sort="Elam, Marshall B" uniqKey="Elam M" first="Marshall B" last="Elam">Marshall B. Elam</name>
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</affiliation>
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</affiliation>
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</affiliation>
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</affiliation>
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<author><name sortKey="Taylor, Valerie H" sort="Taylor, Valerie H" uniqKey="Taylor V" first="Valerie H" last="Taylor">Valerie H. Taylor</name>
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</affiliation>
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<author><name sortKey="Watts, Gerald F" sort="Watts, Gerald F" uniqKey="Watts G" first="Gerald F" last="Watts">Gerald F. Watts</name>
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<term>Cardiovascular Diseases (blood)</term>
<term>Cardiovascular Diseases (prevention & control)</term>
<term>Cholesterol (blood)</term>
<term>Humans</term>
<term>Hydroxymethylglutaryl-CoA Reductase Inhibitors (adverse effects)</term>
<term>Hydroxymethylglutaryl-CoA Reductase Inhibitors (therapeutic use)</term>
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<front><div type="abstract" xml:lang="en">Statins are highly effective for preventing cardiovascular events by reducing low-density lipoprotein cholesterol (LDL-C). However, many patients taking statins report muscle-related symptoms that prevent the use of guideline recommended doses. Patients with reported intolerance to statins have a high risk of cardiovascular events. Clinical strategies that optimize cardiovascular risk reduction through LDL-C lowering need to be applied in patients experiencing intolerable side effects that they attribute to statins. In this paper, the authors review definitions of statin intolerance, propose algorithms to better define statin intolerance, and describe approaches to optimize cardiovascular risk reduction among individuals reporting statin-associated muscle symptoms.</div>
</front>
</TEI>
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<Month>Sep</Month>
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<Title>Journal of the American College of Cardiology</Title>
<ISOAbbreviation>J. Am. Coll. Cardiol.</ISOAbbreviation>
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<ArticleTitle>Optimizing Cholesterol Treatment in Patients With Muscle Complaints.</ArticleTitle>
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<Abstract><AbstractText>Statins are highly effective for preventing cardiovascular events by reducing low-density lipoprotein cholesterol (LDL-C). However, many patients taking statins report muscle-related symptoms that prevent the use of guideline recommended doses. Patients with reported intolerance to statins have a high risk of cardiovascular events. Clinical strategies that optimize cardiovascular risk reduction through LDL-C lowering need to be applied in patients experiencing intolerable side effects that they attribute to statins. In this paper, the authors review definitions of statin intolerance, propose algorithms to better define statin intolerance, and describe approaches to optimize cardiovascular risk reduction among individuals reporting statin-associated muscle symptoms.</AbstractText>
<CopyrightInformation>Copyright © 2017 American College of Cardiology Foundation. All rights reserved.</CopyrightInformation>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Rosenson</LastName>
<ForeName>Robert S</ForeName>
<Initials>RS</Initials>
<AffiliationInfo><Affiliation>Department of Medicine, Mount Sinai Heart, Icahn School of Medicine at Mount Sinai, New York, New York. Electronic address: robert.rosenson@mssm.edu.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Baker</LastName>
<ForeName>Steven</ForeName>
<Initials>S</Initials>
<AffiliationInfo><Affiliation>Department of Medicine, Neuromuscular Disease Clinic, McMaster University, Hamilton, Ontario, Canada.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Banach</LastName>
<ForeName>Maciej</ForeName>
<Initials>M</Initials>
<AffiliationInfo><Affiliation>Department of Hypertension, Medical University of Lodz, Lodz, Poland; Cardiovascular Research Centre, University of Zielona Gora, Zielona Gora, Poland.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Borow</LastName>
<ForeName>Kenneth M</ForeName>
<Initials>KM</Initials>
<AffiliationInfo><Affiliation>National Medication Safety, Outcomes and Adherence Program, MediMergent, Rockville, Maryland.</Affiliation>
</AffiliationInfo>
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<Author ValidYN="Y"><LastName>Braun</LastName>
<ForeName>Lynne T</ForeName>
<Initials>LT</Initials>
<AffiliationInfo><Affiliation>Department of Adult Health and Gerentologic Nursing, College of Nursing, Rush University Medical Center, Chicago, Illinois.</Affiliation>
</AffiliationInfo>
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<Author ValidYN="Y"><LastName>Bruckert</LastName>
<ForeName>Eric</ForeName>
<Initials>E</Initials>
<AffiliationInfo><Affiliation>Institute of Cardiometabolism and Nutrition (ICAN), Endocrinology Department, Hopital Pitié Salpetrière, Paris, France.</Affiliation>
</AffiliationInfo>
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<Author ValidYN="Y"><LastName>Brunham</LastName>
<ForeName>Liam R</ForeName>
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<AffiliationInfo><Affiliation>Department of Medicine, University of Vancouver, British Columbia, Canada.</Affiliation>
</AffiliationInfo>
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<Author ValidYN="Y"><LastName>Catapano</LastName>
<ForeName>Alberico L</ForeName>
<Initials>AL</Initials>
<AffiliationInfo><Affiliation>Department of Pharmacological and Biomolecular Sciences, University of Milan, IRCCS Multimedica, Milan, Italy.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Elam</LastName>
<ForeName>Marshall B</ForeName>
<Initials>MB</Initials>
<AffiliationInfo><Affiliation>Departments of Pharmacology and Medicine, University of Tennessee Health Sciences Center, Memphis, Tennessee.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Mancini</LastName>
<ForeName>G B John</ForeName>
<Initials>GBJ</Initials>
<AffiliationInfo><Affiliation>Department of Medicine, Division of Cardiology, University of British Columbia, Vancouver, British Columbia, Canada.</Affiliation>
</AffiliationInfo>
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<Author ValidYN="Y"><LastName>Moriarty</LastName>
<ForeName>Patrick M</ForeName>
<Initials>PM</Initials>
<AffiliationInfo><Affiliation>Division of Clinical Pharmacology, Division of Internal Medicine, University of Kansas Medical Center, Kansas City, Kansas.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Morris</LastName>
<ForeName>Pamela B</ForeName>
<Initials>PB</Initials>
<AffiliationInfo><Affiliation>Department of Medicine, Division of Cardiology, Medical University of South Carolina, Charleston, South Carolina.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Muntner</LastName>
<ForeName>Paul</ForeName>
<Initials>P</Initials>
<AffiliationInfo><Affiliation>Department of Epidemiology, University of Alabama Birmingham, Birmingham, Alabama.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Ray</LastName>
<ForeName>Kausik K</ForeName>
<Initials>KK</Initials>
<AffiliationInfo><Affiliation>Imperial Centre for Cardiovascular Disease Prevention, Department of Primary Care and Public Health, Imperial College London, London, United Kingdom.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Stroes</LastName>
<ForeName>Erik S</ForeName>
<Initials>ES</Initials>
<AffiliationInfo><Affiliation>Department of Vascular Medicine, AMC, Amsterdam, the Netherlands.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Taylor</LastName>
<ForeName>Beth A</ForeName>
<Initials>BA</Initials>
<AffiliationInfo><Affiliation>Department of Kinesiology, University of Connecticut, Storrs, Connecticut; Division of Cardiology, Hartford Hospital, Hartford, Connecticut.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Taylor</LastName>
<ForeName>Valerie H</ForeName>
<Initials>VH</Initials>
<AffiliationInfo><Affiliation>Department of Psychiatry, University of Toronto, Women's College Hospital, Toronto, Ontario, Canada.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Watts</LastName>
<ForeName>Gerald F</ForeName>
<Initials>GF</Initials>
<AffiliationInfo><Affiliation>Cardiometabolic Service, Department of Cardiology, Royal Perth Hospital; School of Medicine, University of Western Australia, Perth, Western Australia.</Affiliation>
</AffiliationInfo>
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<ForeName>Paul D</ForeName>
<Initials>PD</Initials>
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<QualifierName UI="Q000627" MajorTopicYN="N">therapeutic use</QualifierName>
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<QualifierName UI="Q000627" MajorTopicYN="N">therapeutic use</QualifierName>
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<Keyword MajorTopicYN="N">low-density lipoprotein</Keyword>
<Keyword MajorTopicYN="N">myalgia</Keyword>
<Keyword MajorTopicYN="N">myopathy</Keyword>
<Keyword MajorTopicYN="N">statin intolerance</Keyword>
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<PubmedData><History><PubMedPubDate PubStatus="received"><Year>2017</Year>
<Month>05</Month>
<Day>21</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="revised"><Year>2017</Year>
<Month>07</Month>
<Day>20</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="accepted"><Year>2017</Year>
<Month>07</Month>
<Day>21</Day>
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<PubMedPubDate PubStatus="entrez"><Year>2017</Year>
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<Day>2</Day>
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<PubMedPubDate PubStatus="medline"><Year>2017</Year>
<Month>9</Month>
<Day>14</Day>
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<ArticleIdList><ArticleId IdType="pubmed">28859793</ArticleId>
<ArticleId IdType="pii">S0735-1097(17)38966-0</ArticleId>
<ArticleId IdType="doi">10.1016/j.jacc.2017.07.752</ArticleId>
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