Causes of Global Myocardial Hypokinesis
Global myocardial hypokinesis results from diverse etiologies including dilated cardiomyopathy, stress-induced cardiomyopathy, myocarditis, toxic exposures (especially chemotherapy and alcohol), infiltrative diseases, septic shock, and—less commonly than expected—multivessel coronary artery disease. 1, 2
Primary Cardiac Causes
Cardiomyopathies
- Dilated cardiomyopathy is the most common structural cause, characterized by ventricular dilatation with reduced ejection fraction and both systolic and diastolic dysfunction 1
- Approximately 50% of nonischemic dilated cardiomyopathy cases are idiopathic, typically affecting younger patients 3
- Stress-induced (Takotsubo) cardiomyopathy produces reversible global systolic dysfunction with characteristic apical ballooning, often triggered by acute illness or emotional stress 4, 1
- Hypertrophic cardiomyopathy can present in late stages with dilated, hypokinetic left ventricle and wall thinning 3
Ischemic Heart Disease
- Coronary artery disease remains the leading cause of left ventricular systolic dysfunction in adults, though global hypokinesis shows a possible inverse correlation with triple-vessel disease 1, 2
- Hibernating myocardium (chronically hypoperfused but viable tissue) manifests as hypokinetic segments that can improve after revascularization, even with ejection fractions as low as 15-20% 1, 5
- Myocardial stunning from intermittent ischemia causes reversible ventricular dysfunction 1
- Critical finding: A recent study demonstrated no positive association between global hypokinesis and triple-vessel CAD, suggesting that heart failure and other diagnoses have stronger effects on global hypokinesis than multivessel coronary disease 2
Infectious and Inflammatory Causes
- Myocarditis (viral, bacterial, fungal) can produce both regional and global hypokinesis with myocardial edema mimicking hypertrophic cardiomyopathy 3, 1
- Acute rheumatic fever affects ventricular function 1
- Cardiac sarcoidosis produces segmental hypokinesis with ventricular septal thickening in acute phase, but thinning with global dysfunction in chronic phase 3, 1
- Systemic sclerosis and collagen vascular disorders (lupus, rheumatoid arthritis, polyarteritis nodosa) cause ventricular dysfunction through vasculitis and direct myocardial infiltration 3, 1
Toxic and Metabolic Causes
Cardiotoxic Agents
- Chemotherapeutic agents, particularly anthracyclines (doxorubicin), tyrosine kinase inhibitors, trastuzumab, and interferons induce cardiomyopathy with higher risk at cumulative doses 3, 1
- Alcoholic cardiomyopathy occurs in heavy drinkers with genetic susceptibility, most common in men aged 30-55 years 3, 1
- Cocaine, heroin, and amphetamines cause direct cardiotoxicity 1
- Chronic use of anabolic steroids, tacrolimus, and hydroxychloroquine can cause left ventricular hypertrophy and dysfunction 3, 1
Metabolic Derangements
- Protein, thiamine, and selenium deficiencies 1
- Electrolyte abnormalities: hypocalcemia, hypophosphatemia, hyponatremia, hypokalemia 1
- Endocrine disorders: diabetes mellitus, hypothyroidism, hyperthyroidism 1
Infiltrative Disorders
- Amyloidosis produces characteristic basal-predominant hypokinesis with preserved apical function ("apical sparing" pattern) despite normal ejection fraction 1
- Relative apical sparing of longitudinal strain ≥1.0 has 93% sensitivity and 82% specificity for distinguishing cardiac amyloidosis from controls 3
- Hemochromatosis and storage diseases cause restrictive patterns with associated hypokinesis 1
Acute Hemodynamic and Systemic Causes
Septic Shock
- Global left ventricular hypokinesia occurs in 60% of adult septic shock patients, with 39% presenting at admission (primary) and 21% developing after 24-48 hours of norepinephrine support (secondary) 6
- This reversible dysfunction is usually corrected by adding inotropic agents and is not associated with worse prognosis 6
Pulmonary Embolism
- Acute massive pulmonary embolism causes right ventricular hypokinesis with characteristic apical sparing (McConnell sign) 1
- In severe cases, global dysfunction can occur indicating submassive PE with higher mortality 4
Arrhythmia-Related Causes
- Tachycardia-induced cardiomyopathy from incessant supraventricular tachyarrhythmias or atrial fibrillation with rapid ventricular rates produces reversible global hypokinesis 1
Valvular and Structural Heart Disease
- Chronic aortic stenosis and mitral regurgitation produce progressive ventricular dysfunction through pressure and volume overload 1
- Valvular disease is highly prevalent in heart failure patients: 21% in HFrEF/HFmrEF and 28% in HFpEF 3
Special Populations
- Peripartum cardiomyopathy develops in late pregnancy or first 5 months postpartum, occurring in 1 in 2,500-4,000 births in the United States 3, 1
- Risk factors include age >30 years, nonwhite background, multiparity, hypertension, and preeclampsia 3
- Chagas disease remains the most common cause of nonischemic heart failure in South America 3, 1
Critical Diagnostic Pitfalls
- The designation "idiopathic dilated cardiomyopathy" should only be applied after excluding all specific etiologies through appropriate evaluation 1
- Wall motion abnormalities extending beyond single coronary territories suggest non-ischemic etiologies 3, 1
- Regional wall motion abnormalities can be caused by acute infarction, old infarction, acute ischemia, stunning, hibernation, or non-ischemic conditions like cardiomyopathy and inflammatory diseases 3
- Global hypokinesis shows positive association with heart failure diagnosis but possible inverse correlation with triple-vessel CAD, meaning other causes should be strongly considered 2