Myocardium diseases Flashcards
(50 cards)
LVEF in dilated cardiomyopathy
<40%
LVEF in hypertrophic cardiomyopathy
50-80%
LVEF in restrictive cardiomyopathy
45-90%
Mechanism of HF in dilated cardiomyopathy
Impairment of contractility –> systolic dysfunction
Mechanism of HF in hypertrophic cardiomyopathy
Impairment of compliance –> diastolic dysfunction
Mechanism of HF in restrictive cardiomyopathy
Impairment of compliance –> diastolic dysfunction
Causes of dilated cardiomyopathy
Genetic
Alcohol
Peripartum
Myocarditis
Hemochromatosis
Chronic anemia
Doxorubicin (Adriamycin) toxicity
Sarcoidosis
Idiopathic
Causes of hypertrophic cardiomyopathy
Genetic
Friedreich ataxia
Storage disease
Infants of diabetic mother
Causes of restrictive cardiomyopathy
Amyloidosis
Radiation-induced fibrosis
Idiopathic
Indirect myocardial dysfunctions in dilated cardiomyopathy
IHD
Valvular heart disease
HTN heart disease
Congenital heart disease
Indirect myocardial dysfunctions in hypertrophic cardiomyopathy
HTN heart disease
Aortic stenosis
Indirect myocardial dysfunction in restrictive cardiomyopathy
Pericardial constriction
Characterized by ventricular chamber enlargement with impaired systolic contractile function.
Dilated cardiomyopathy
Genetic mutations that cause dilated cardiomyopathy
Mutations in proteins for sarcolemma, cytoskeleton, and nuclear envelope (laminin)
Mutation in TTN –> encodes titin
Inheritance of genetic dilated cardiomyopathy
Autosomal dominant
Takotsubo cardiomyopathy falls under what cardiomyopathy type?
Dilated
Causes of excess catecholamine production that can result in dilated cardiomyopathy
Pheochromocytoma
Cocaine or dopamine use
Intense autonomic stimulation
Emotional duress –> Takotsubo
Complications of dilated cardiomyopathy
Secondary mitral regurgitation
Abnormal cardiac rhythms
Embolism from intracardiac thrombi
Microscopy of heart in dilated cardiomyopathy
Hypertrophied with enlarged nuclei
Interstitial and endocardial fibrosis of a variable degree
Abnormally thickened ventricular wall with abnormal diastolic relaxation. Due to sarcomeric alterations, defective energy transfer, and/or exaggerated response of myocardial fibroblasts.
Hypertrophic cardiomyopathy
Inheritance of genetic causes of hypertrophic cardiomyopathy
Autosomal dominant with variable penetrance
Genetic mutations associated with hypertrophic cardiomyopathy
Sarcomeric proteins –> missense
Beta-myosin heavy chain
Cardiac TnT
Alpha-tropomyosin
Myosin binding protein C (MYBP-C)
Affect of sarcomeric alterations in hypertrophic cardiomyopathy
Abnormal cardiac contraction causing a secondary compensatory hypertrophy
Affect of myofiber disarray in HOCM without outflow obstruction
Ventricular arrhythmias
Myocyte hypertrophy