Clinical question: When do you get statin induced myopathy?

Slides:



Advertisements
Similar presentations
Statins in Renal Failure Andrea Fox Sunnybrook Health Science Center May 2010.
Advertisements

© 2006 National Lipid Association Statin Safety: Key Conclusions and Recommendations of the NLA.
Drugs in dyslipidaemias
Statin Drugs Cholesterol lowering drugs. Individual level risk factors for cardiovascular disease High Blood Pressure High Blood Cholesterol Tobacco Use.
1. 2 The primary Objective of IDEAL LDL-C Simvastatin mg/d Atorvastatin 80 mg/d risk CHD In stable CHD patients IDEAL: The Incremental Decrease.
LDL Cholesterol Goals and Cutpoints for Therapeutic Lifestyle Changes (TLC) and Drug Therapy in Different Risk Categories Risk Category LDL Goal (mg/dL)
Anti-Hypercholesterolemic Agents  Biosynthesis and Metabolism of Cholesterol  What is arteriosclerosis? - Link between arteriosclerosis and cholesterol.
DYSLIPIDEMIA IN ADULTS WITH DIABETES* 2003 Clinical Practice Guidelines for the Prevention and Management of Diabetes in Canada *Updated in Leiter.
Livalo (Pitavastatin)
Background: Focus on P-gp Questions:
Kirk Mykytyn, Ph.D. Department of Pharmacology
Agents Used to Treat Hyperlipidemia. Hyperlipidemia 2 Atherosclerosis – accumulation of fatty substances on the inner wall of large and medium sized arteries.
New Agents Heather Kertland, PharmD.
Drug - Food Interactions
Hperlipidemia:- Treatment and Management Presented by:- Dr. Tewari.
Antihyperlipidemia.
2013 ACC/AHA Guideline on the Treatment of Blood Cholesterol to Reduce Atherosclerotic Cardiovascular Risk in Adults: A Report of the American College.
Slide 1 EZT 2002-W-6022-SS Ezetimibe Co-administered with Statins: Efficacy and Tolerability Copyright © 2003 MSP Singapore Company, LLC. All rights reserved.
Praluent® - alirocumab
Inhibition of Cholesterol Biosynthesis By Peter Riedell Medicinal Chemistry Dr. Buynak April 6, 2006.
Pharmacoeconomics and Outcomes Research Dean G. Smith, Ph.D. October 10, 2005 UM Student Chapter.
Incremental Decrease in Clinical Endpoints Through Aggressive Lipid Lowering (IDEAL) Trial IDEAL Trial Presented at The American Heart Association Scientific.
Case 15 Andrea De Mesa. Patient history A 44 y/o male, single, undergoes cardiovascular screening on advice of his attending physician. He is a smoker.
Step 3 P-treatment: Drug Class Selection. Pharmacological and Non- Pharmacological Management Dyslipidemia drug therapyLifestyle modification Smoking.
Chapter 19 Agents Used to Treat Hyperlipidemia. Hyperlipidemia 2 Atherosclerosis – accumulation of fatty substances on the inner wall of large and medium.
Statin Induce Myotoxicity
HYPERLIPIDEMIA Dan O’Connell, MD Montefiore Family Medicine August 2004.
Endocrinologic & Metabolic Drugs Advisory Committee Meeting
B-1 Pravastatin-Aspirin Combination René Belder, M.D. Executive Director Clinical Design and Evaluation, Metabolics Pharmaceutical Research Institute Bristol-Myers.
Sprout Pharmaceuticals Inc. FDA Approval Date: August 18, 2015
HYPERLIPIDEMIA Applied Therapeutics Dr. Riyadh Mustafa Al-Salih.
Mosby items and derived items © 2007, 2005, 2002 by Mosby, Inc., an affiliate of Elsevier Inc. CHAPTER 28 Antilipemic Drugs.
Hyperlipidemia Hyperlipidemia and hyperlipoproteinemia are general terms for elevated concentrations of lipids and lipoproteins in the blood. hypercholesterolemia.
TM © 1999 Professional Postgraduate Services ® Perspectives on Lipid-Lowering Therapy With HMG-CoA Reductase Inhibitors.
IMPACT OF INTRODUCTION OF STATINS TO THE PRIVATE AND STATE SECTORS IN SRI LANKA ON UTILISATION, COST AND PRESCRIPTION PATTERN Galappatthy P Cooray BPR.
Manufacturer: Amgen Inc FDA Approval Date: August 27, 2015
1 The Role of Exposure-Response Evaluation in Drug Development and Regulatory Decisions Case Study: Rosuvastatin Hae-Young Ahn, Ph.D. Office of Clinical.
Chapter 21 Agents Used in the Treatment of Hyperlipidemia.
1 Update to Post Exclusivity Pediatric Adverse Event Review: Atorvastatin Pediatric Advisory Committee Meeting November 16, 2006 Jean Temeck, MD, Acting.
2013 ACC/AHA Guideline on the Treatment of Blood Cholesterol to Reduce Atherosclerotic Cardiovascular Risk in Adults Scott W. Rypkema, M.D.
Anti hyperlipidemic drugs (lipid lowering drugs) Department of Pharmacology Faculty of Medicine AIMST UNIVERSITY 5 September 2012.
HYPERLIPIDEMIA  Coronary heart disease (CHD) is the cause of about half of all deaths. The incidence of CHD is correlated with elevated levels of low-density.
Drugs Used in Hyperlipidemia
Hyperlipidemias.
PGx Logical Overview.
Statins induced myopathy
Factors Affecting Drug Activity
Adverse events for rosuvastatin
Muscle pain with taking statin
Anti-Hypercholesterolemic Agents
Statin Myopathy (AHA/ACC/NHLBI)
2013 ACC/AHA Guideline on Treatment of Blood Cholesterol to Reduce Atherosclerotic Cardiovascular Risk in Adults.
Formative Test.
Intensive Statin Recommendations
Senior Medical Director, Cardiovascular
Anti-Hypercholesterolemic Agents
Drugs for Hyperlipidemias
Biosynthesis and Metabolism of Cholesterol
Antilipidaemic agents
Drug induced myopathy Edition
Patients aged 85yrs and over
Cardiovascular System
PCP View: ACC/AHA Guidelines: Role of Moderate Intensity Statins
Section 7: Aggressive vs moderate approach to lipid lowering
Drug - Food Interactions
Rational Order of Laboratory Tests in Cardiovascular Diseases
Major classes of drugs to reduce lipids
Pandemic Lipid Edition
ATP III Guidelines Drug Therapy FUTURE RESEARCH.
Section 6: Update on lipid treatment guidelines
Presentation transcript:

Clinical question: When do you get statin induced myopathy?

HMG-CoA Reductase Inhibitors 1987: first approved for the treatment of hypercholesterolemia Prevention of primary and secondary CHD First generation: -simvastatin (Zocor), lovastatin (Mevacor), pravastatin (Pravachol) Second generation: -fluvastatin (Lescol) Third generation: -atorvastatin (Lipitor), rosuvastatin (Crestor), cerivastatin (Baycol)

Number of adverse reactions associated with HMG CoA reductase inhibitors reported to the WHO International Information System Database AgentTNRArthralgia (%) Myalgia (%) PN (%) Neuropathy (%) Rhabdo (%) Myopathy (%) Atorvastatin Cerivastatin Fluvastatin Lovastatin Pravastatin Simvastatin NA 0.6 NA NA Drug Safety. June 2000; 22

Symptoms/Duration of Onset of Myopathy diffuse muscle weakness, weakness of the limbs, weakness after exertion Onset is usually within weeks to months but may occur at any time during therapy Review: mean duration before symptom onset=6.3 months (range months), 2/3 had onset within six months mean time to resolution of symptoms after statin discontinuation=2.3 months ( months) Archives of Internal Medicine. December 2005; Vol. 165(22):

Mechanism of Statin Induced Myotoxicity Depletion of secondary metabolites of Mevalonate pathway (Ubiquinone or coenzyme 10)-Ubiquinone is involved in mitochondrial electron transfer and serves as an important intermediary in the oxidative phosphorylation pathway: less CoQ10=less recovery=more weakness Inconclusive: decrease in serum ubiquinone does not necessarily =decrease in intracellular ubiquinone More research is needed Other theories: Induction of apoptotic cell death or Changes in the Cl- channel conductance within the myocyte, which leads to alteration in muscle cell membrane properties American Journal Of Health System Pharmacy. March Vol 61(5):

Complicating Risk Factors for Statin Induced Myopathy Patient Characteristics Sex: F>M Age Patient size Hepatic dysfunction Renal insufficiency Hypothyroidism Diet (grapefruit juice) Statin Properties High systemic exposure High bioavailability Low protein binding Potential for drug- drug interactions, particularly those with CYP450 interactions American Journal of Medicine. 2004; Vol. 116:

Drug Interactions Fold increase of statin AUC Simvastatin LovastatinAtorvastatinFluvastatinCerivastatinPravastatin Rosuvastatin Itraconazole <1.5-- Erythromyin, clarithro <1.5<2- Verapamil, diltiazem 3-8 ?-?-- Cylcosporine Gemfibrozil2-3 < Grapefruit juice <1.5-- Clinical Pharmacology & Therapeutics. December (6): ,

Clinical evaluation Evaluate extent of muscle soreness/weakness-compared to baseline or prior to initiation of therapy Obtain serum CK level and compare to baseline –If normal or moderately elev. CK levels (3-10 times the ULN), symptoms and CK values may be monitored without discontinuation of drug –If serum CK levels continue to increase, a reduction in dose or temporary discontinuation of the drug is necessary –If serum CK levels exceed 10x the ULN, both the statin and any other precipitating agent should be discontinued regardless of the patient’s symptoms American Journal Of Health System Pharmacy. March Vol 61(5):

CK analysis Other cause of muscle soreness/pain: –Exercise or strenuous work –Muscle damage resulting from trauma, sepsis, inflammatory diseases –Hypothyroidism-obtain a TSH level Recent literature suggests that CK elevations do not always correlate with muscle damage If all other etiologies are excluded, the possiblility of statin induced myopathy in the presence of normal CK values should be considered. American Journal Of Health System Pharmacy. March Vol 61(5):

Final Analysis Since the mechanism of statin induced myopathy is not well defined, no preventative measure is available Important to recognize factors that place patients at increased risk, for example, the risk is substantially increased for most statins when used concurrently with drugs that interfere with CYP450 hepatic metabolism Initiate therapy at lowest therapeutic dose Patient education-awareness of potential myotoxic effects and the signs of myopathy Routine monitoring of CK levels has not been shown to be necessary, but a baseline CK level prior to initiating therapy can be useful for reference purposes. Until further evidence is available, widespread use of ubiquinone is not warranted