Laboratory Tests for Suspected Non-Ischemic Cardiomyopathy
For patients with suspected non-ischemic cardiomyopathy, a comprehensive panel of laboratory tests including lipid profile, complete blood count, renal and hepatic function tests, thyroid function, glycemic status, cardiac biomarkers, and specific tests for inflammatory and infiltrative diseases is recommended.
Core Laboratory Tests
The following blood tests are essential in the initial evaluation of suspected non-ischemic cardiomyopathy 1:
Cardiac-specific tests:
- Cardiac troponins (high-sensitivity preferred)
- B-type natriuretic peptide (BNP) or N-terminal pro-BNP (NT-proBNP)
- Creatine kinase-MB (CK-MB)
Basic metabolic and organ function:
- Complete blood count (including hemoglobin)
- Comprehensive metabolic panel
- Renal function (creatinine with estimated GFR)
- Hepatic function tests
- Lipid profile (including LDL-C)
- Glycemic status (HbA1c and/or fasting plasma glucose)
- Thyroid function tests (especially TSH)
Additional Targeted Testing
Based on clinical suspicion and initial findings, the following specialized tests should be considered 1:
Inflammatory markers:
- High-sensitivity C-reactive protein (hs-CRP)
- Erythrocyte sedimentation rate (ESR)
Infectious disease screening:
- HIV testing (in high-risk patients)
- Chagas disease antibodies (in patients from endemic regions) 2
Autoimmune/rheumatologic evaluation:
- Antinuclear antibodies (ANA)
- Rheumatoid factor (RF)
- Anti-cyclic citrullinated peptide (anti-CCP) antibodies
Metabolic and infiltrative disorders:
- Fasting transferrin saturation (to screen for hemochromatosis)
- Serum protein electrophoresis (for amyloidosis)
Biomarker Significance
Cardiac troponins: Elevated levels may indicate ongoing myocardial damage even in non-ischemic settings 3, 4. Troponin I has high specificity for cardiac involvement in inflammatory myopathies.
BNP/NT-proBNP: Elevated levels correlate with ventricular dysfunction severity and predict adverse outcomes in cardiomyopathy 4, 5. These biomarkers are particularly useful for risk stratification.
Matrix metalloproteinases (MMP-2, MMP-9): May help identify early cardiac remodeling in certain cardiomyopathies 2.
Clinical Context and Interpretation
Laboratory findings must be interpreted in conjunction with:
- Clinical presentation (chest pain, dyspnea, fatigue, palpitations)
- ECG findings (conduction abnormalities, ST-T wave changes)
- Imaging results (echocardiography, cardiac MRI)
Important Considerations
Timing of tests: Cardiac biomarkers should be measured immediately upon presentation and results obtained within 60 minutes of blood sampling 1.
Serial measurements: For cardiac troponins, serial measurements (0h/1h or 0h/2h algorithm) are recommended when initial results are inconclusive 1.
Pitfalls to avoid:
Laboratory testing is just one component of the diagnostic approach to non-ischemic cardiomyopathy and should be integrated with appropriate cardiac imaging, particularly echocardiography and cardiac MRI, which are essential for assessing cardiac structure, function, and tissue characterization.