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To continue or Not to Continue statin therapy in patients with diagnosed CHF?. Erin Woodard Mercer University October 2011. Chronic Heart Failure (CHF).
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To continue or Not to Continue statin therapy in patients with diagnosed CHF? Erin Woodard Mercer University October 2011
Chronic Heart Failure (CHF) • Complex clinical syndrome resulting from any structural or functional cardiac disorder that impairs ability of ventricle to fill with or eject blood • Pericardium, myocardium, endocardium • Systolic dysfunction • EF < 40% • Impaired LV contractility • Dilated LV • Diastolic dysfunction • Normal EF • Impaired LV filling • Contractility preserved • In most patients, abnormalities of systolic and diastolic dysfunction coexist, regardless of EF.
CHF Overview • Clinical Presentation • Dyspnea • Fatigue • Lead to limiting exercise tolerance & excess fluid retention pulmonary congestion and peripheral edema • Epidemiology • CAD • HTN • Dilated cardiomyopathy • There is no single diagnostic test for HF because it is largely a clinical diagnosis that is based on a careful history and physical examination.
CHF Overview Cont. • Symptomatic disorder • NYHA Functional assessment • Progressive disorder
NYHA Classification • Class I (asymptomatic): Patients with no limitation of activities due to their HF; they suffer no symptoms from ordinary activities. • Class II (mild): Slight limitation of physical activity. Comfortable at rest, but ordinary physical activity results in fatigue, palpitation, or dyspnea. • Class III (moderate): Patients with marked limitation of activity due to their HF; they are comfortable only at rest. • Class IV (severe): Patients who have to be at complete rest, confined to bed or chair due to their HF; any physical activity brings on discomfort and symptoms occur at rest.
CHF Treatment Jessup M et al. N Engl J Med 2003;348:2007-18.
Known benefit and part of first-line treatment for patients with CAD HMG-coA reductase inhibitors Increase presentation of LDL receptors Total Cholesterol Desirable <200 mg/dL Borderline high 200 – 239 mg/dL High >240 mg/dL Treat CAD and prevent events decrease new onset HF Statins – Friend vs Foe
Lipoprotein – Endotoxin Hypothesis • Hypothesize optimum lipoprotein concentration • Serum lipoproteins to modulate the inflammatory immune function • CHF patients have increased serum cytokine increased endotoxins • Circulating cholesterol – and triglyceride rick lipoproteins are natural nonspecific buffers of endotoxins • Bind and detox bacterial LPS • Patients with CHF, a non-lipid-lowering statin (with immunomodulatory and anti-inflammatory actions) could be as effective or even more beneficial than a lipid-lowering statin • Patients with CAD should be treated differently from patients with ischemic CHF
Ubiquinone hypothesis • Inhibition of mevalonate synthesis decreases ubiquinone • Ubiquinone most abundant in heart • Essential component of mitochondrial respiratory chain ATP • Deleterious effects on cardiac muscles • CHF patients found to have depleted ubiquinone levels • Addition of CoQ helpful?
Selenoprotein hypothesis • Reduction of mevalonate reduction of isopentenyl-pyrophosphate • Interfere with enzyme isopentenylation of Sec-tRNA preventing maturation
Vredevoe DL et al. Skin test anergy in advanced heart failure secondary to either ischemic or idiopathic dilated cardiomyopathy. Am J Cardiol 1998:82:323-8.
Vrederoe - 1998 • Skin test anergy in advanced HF secondary to either ischemic or idopathic dilated cardiomyopathy • 222 patients enrolled followed for 1 year • Skin testing in NYHA functional class III,IV and assess mortality • Primary endpoints • Skin test anergy • Mortality
Vrederoe - 1998 • Results • Skin test anergy occurred in 45% of HF patients • More with NYHA class IV • HF patients significantly less reactive for 3 antigens • Mortality • Increased with lack of ACEi, dec CO, dec lipids • Significant differences in lipid values for TC, LDL, and TG (all lower in anergy) • Lower levels of lipids were predictors of higher mortality • Idiopathic: no significance • Ischemic: decreased lipids and increased mortality • Only 1 year follow – up
Rauchhaus M, Koloczek V et al. Inflammatory cytokines and the possible immunological role for lipoproteins in chronic heart failure. Int J Cardiology 2000; 76:125-33
Rauchhaus - 2000 • Goal: Observe fasting cholesterol, LDL, HDL, & TG in patient with CHF in relation to concentrations of tumor necrosis factor-alpha (TNFa), soluble TNF receptor-1 and -2 and a ratio potentially indicating recent endotoxin bioactivity (sCD14/TC) • 58 CHF patients and 19 controls • Hypothesis – lipoprotein bind endotoxin as natural buffer
Rauchhaus - 2000 • Results • sTNF-R1 and sCD14 were higher in CHF patients than controls where as TNFalpha and sTNF-R2 were not. • Increase cholesterol decreased TNFalpha • TC <200 poor outcome • Limited small sample size, short term F/U
Horwich TB et al. Low serum total cholesterol is associated with marked increase in mortality in advanced heart failure. J Card Failure 2002; 8:216-24
Horwich - 2002 • 1134 patients with advanced HF regardless of etiology (NYHA class III, IV) • Purpose • Describe correlation between cholesterol and baseline patient characteristics important in prognosis • Investigate relationship between lipids, lipoproteins, and HF mortality • Excluded patients LVEF <40% • Primary endpoint • Death or urgent heart transplant
Horwich - 2002 • Results • Patients divided into quintiles based on baseline lipids • 1 and 5 year survival rates (death or urgent heart transplant) • Lowest death/urgent heart transplant at TC 190-205 • Decreased TC worse outcomes HF • More severe symptoms CHF • Increased LDL, HDL, TG longer survival • < 25% with TC <129 survived >5yr • > 50% with TC>190 survived >5yr • Confirmed findings of small sample trial
Mortality based on Quintile of total cholesterol • Similar lipidlowering therapy • 14% in each group • Drug unspecified Horwich TB et al. Low serum total cholesterol is associated with marked increase in mortality in advanced heart failure. J Card Failure 2002; 8:216-24
Rauchhaus et al. Relationship between cholesterol and survival in patients with chronic heart failure. JACC 2003; 42: 11
Rauchhaus - 2003 • Report on 2 cohort studies • 114 patients with CHF recruited to metabolic study and followed for minimum 12 months (derivation study) • 303 unselected patients with CHF (validation study) • Purpose • Relationship between endogenous lipoproteins and survival was explored
Rauchhaus - 2003 • Results • “reciever operator curve analysis” showed 201mg/dL • Decreased serum cholesterol = increased sTNF receptor-1 levels
Theoretical Harm • Lower total cholesterol (<190mg/dl) indicative of poor prognosis for CHF patients in NYHA class III and IV • CAD lead to CHF • Statin is proven outcomes to treat CAD and prevent coronary event • Statin has been shown to prevent new onset CHF • Statin decreasing levels of TC lead to poor prognosis? • Statin used after diagnosis NYHA class III, IV? • Studies and evaluation needed to describe risk/benefit in pharmacologically induced low TC (statin) vs naturally low TC
Kjeckshus, J. et al. Rosuvastatin in Older Patients with Systolic Heart Failure. New Engl J Med 2007; 357:2248-61. “CORONA” Controlled Rosuvastatin Multinational Trial in Heart Failure *supported by AstraZeneca*
CORONA - 2007 • Large randomized placebo controlled study • Total of 5011 patients, >60yo • NYHA class II,III, or IV ischemic, systolic heart failure • EF of no more than 40% • Investigator thought no need for cholesterol-lowering drug • Hypothesized beneficial effects of rosuvastatin would outweigh any theoretical hazards • improve survival, reduce morbidity, increase well-being • Study drug: • 10mg of rosuvastatin vs placebo, 35 month follow up • Primary Outcome • Death from composite of cardiovascular causes, nonfatal MI, nonfatal stroke
CORONA - 2007 • Results: • Baseline TC 5.35mmol/L • Baseline LDL 3.54mmol/L (137) 1.96mmol/L (76) at 3 months • Baseline HDL 1.24mmol/L (48) 1.29mmol/L (50) at 3 months • Baseline TG 2.01mmol/L (178) 1.56mmol/L (138) at 3 months • Baseline hsCRP 3.1mg/L 2.1mg/L • Conclusion • No significant reduction in primary outcome of deaths from any cause • Significantly fewer hospitalizations of any type in rosuvastatin group than placebo group (for cardiovascular causes and heart failure) NNT = 55
GISSI-HF Investigators. Effect of rosuvastatin in patietns with chronic heart failure: a randomised, double-blind, placebo-controlled trial. The Lancet; 372: 1231- 1239. “GISSI/HF” Gruppo Italiano per lo Studio della Sopravvivenza nell’Infarto miocardico trial *Funded by Societa Prodotti Antibiotici (SPA;Italy), Pfizer, Sigma Tau, and AstraZeneca
GISSI/HF – 2008 • Randomized, double-blind placebo controlled trial Italy. • CHF class II-IV irrespective of LVEF • Intervention: rosuvastatin 10mg vs placebo • Followed for 3 – 9 year • Primary endpoint • Time to death • Time to death + time to admission to hospital for cardiovascular reasons • Intent- to-treat
GISSI/HF – 2008 • Results • Conclusion • Rosuvastatin 10mg daily did not affect clinical outcoems in patients with chronic heart failure of any cause, in whom drug was safe
Low TC a Cause or Consequence? • Association between Total Cholesterol (TC) and all-cause mortality • Positive at 40 yo • Negligible at 50 – 70 yo • Negative at age 80 + • Incidence/prevalence of CHF increasing steeply with age • CHF patient untreated with statin naturally have cholesterol levels decrease?
Discussion Points • Most individuals on statin d/t CAD treatment • Take them off? • Titrate down? Decrease aggressive tx? • Those individuals not already on a statin with prior need • Start statin? • Goal of increasing TC? • Leave it alone? Benefit vs. risk?
Other References Hunt SA, Abraham WT, Chin MH, et al. 2009 focused update incorporated into the ACC/AHA 2005 guidelines for the diagnosis and management of chronic heart failure in the adult. JACC 2009;53(15):e1-90.