Quantitative Morphologic Findings of the Myocardium in Idiopathic Dilated Cardiomyopathy
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This study assesses the relation between quantitative morphologic findings and left ventricular contractile function in patients with idiopathic dilated cardiomyopathy. Left ventricular endomyocardial catheter biopsy specimens were obtained from 73 patients during diagnostic heart catheterization. All patients had normal coronary arteriograms but abnormal electrocardiograms. Twenty-six patients had normal left ventricular function (ejection fraction greater than or equal to 55%), whereas 47 patients had contractile dysfunction (ejection fraction less than or equal to 54%). Myocardial fiber diameter, volume fraction of interstitial fibrosis, and intracellular volume fraction of myofibrils were determined by light microscopic morphometry. Results of light microscopic morphometry were confirmed by electron microscopic morphometry in 12 patients. The coefficient of variation (analysis of several biopsies from the same patient) was 6% for determination of fiber diameter, 43% for interstitial fibrosis, and 3% for volume fraction of myofibrils. Fiber diameter (r = -0.32, p less than 0.01) and fibrosis (r = -0.47, p less than 0.001) showed a negative correlation, the volume fraction of myofibrils (r = 0.55, p less than 0.001) and calculated myofibrillar mass per 100 g of myocardium (r = 0.64, p less than 0.001) a positive correlation with the ejection fraction. Thus, (1) sampling error is low for determination of fiber diameter and myofibrils but high for evaluation of fibrosis, and (2) a reduction in the volume fraction of myofibrils and an increase in fibrosis are morphologic correlates of left ventricular dysfunction in patients with idiopathic dilated cardiomyopathy.
Saberwal B, Patel K, Klotz E, Herrey A, Seraphim A, Vandermolen S Eur Heart J Imaging Methods Pract. 2025; 3(1):qyaf019.
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Hayashi H, Ko T, Dai Z, Fujita K, Nomura S, Kiyoshima H Bioinformatics. 2024; 40(11).
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Jiao M, Zhang Y, Song X, Xu B Front Immunol. 2024; 15:1354952.
PMID: 38629066 PMC: 11019510. DOI: 10.3389/fimmu.2024.1354952.
Engele L, Van Der Palen R, Egorova A, Bartelings M, Wisse L, Glashan C J Cardiovasc Dev Dis. 2023; 10(4).
PMID: 37103059 PMC: 10143292. DOI: 10.3390/jcdd10040180.
Hung C, Tsai Y, Wu Y, Yeh C, Yang K J Biomed Sci. 2022; 29(1):63.
PMID: 36050716 PMC: 9438287. DOI: 10.1186/s12929-022-00850-x.