1.Assessment of myocardial metaiodobenzylguanidine uptake and its relation to left ventricular systolic and diastolic functional parameters in dilated cardiomyopathy.
Jong Won HA ; Jong Doo LEE ; Namsik CHUNG ; Yangsoo JANG ; Sang Ho CHO ; Byung Soo KIM ; Se Joong RIM ; Won Heum SHIM ; Seung Yun CHO ; Sung Soon KIM
Yonsei Medical Journal 1999;40(3):199-206
The purpose of this study was to assess the relation between myocardial metaiodobenzylguanidine (MIBG) uptake and left ventricular systolic and diastolic functional parameters, both of which are known as predictors of prognosis in patients with dilated cardiomyopathy. Echocardiography and iodine-123-MIBG myocardial scintigraphy were performed in 35 patients of dilated cardiomyopathy with normal sinus rhythm. Mean myocardial MIBG uptake in the patient group at early and delayed images were significantly lower than those in normal control subjects (10.6 +/- 1.1, 9.8 +/- 1.2 vs 12.4 +/- 1.0, 12.1 +/- 1.0, p < 0.01). There were, however, no significant differences of mean MIBG uptake in the lung and mediastinum between the two groups (p > 0.05). There were no significant correlations between myocardial MIBG uptake, expressed as the ratio of heart/mediastinum MIBG activity at delayed image, and left ventricular systolic and diastolic functional parameters ?left ventricular ejection fraction, left ventricular end-diastolic dimension, peak velocity of early diastolic filling (E velocity), deceleration time of E wave, cardiac output, left ventricular end-diastolic pressure?. In conclusion, the myocardial uptake of MIBG is decreased in patients with dilated cardiomyopathy assessed by iodine-123-MIBG myocardial scintigraphy. There were, however, no significant correlations between myocardial MIBG uptake and left ventricular systolic and diastolic functional parameters derived from echocardiography.
3-Iodobenzylguanidine/pharmacokinetics*
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Adult
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Aged
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Cardiomyopathy, Congestive/physiopathology*
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Cardiomyopathy, Congestive/metabolism
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Diastole
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Female
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Human
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Male
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Middle Age
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Myocardium/metabolism*
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Systole
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Ventricular Function, Left/physiology*
2.The Origin of Proinflammatory Cytokines in Patients with Idiopathic Dilated Cardiomyopathy.
Hyuk Jae CHANG ; Jaehoon CHUNG ; Byoung Joo CHOI ; Tae Young CHOI ; So Yeon CHOI ; Myeong Ho YOON ; Gyo Seung HWANG ; Joon Han SHIN ; Seung Jea TAHK ; Byung Il William CHOI
Journal of Korean Medical Science 2003;18(6):791-796
Proinflammatory cytokines and their receptors are increased in the peripheral blood of patients with heart failure. We measured cytokines and their receptors in systemic artery (SA), coronary sinus (CS) and infra-renal inferior vena cava (IVC), in order to investigate their origin and influential factors. Thirty patients with idiopathic dilated cardiomyopathy were performed echocardiography at admission, and right heart catheterization after stabilization. Blood was drawn from 3 sites for measurement of tumor necrosis factor-alpha (TNF-alpha), interleukin-6 (IL-6) and soluble tumor necrosis factor- receptor (sTNFR) I, II. TNF-alpha at CS (3.25+/-0.34 pg/mL) was higher than those of SA (1.81+/-0.39 pg/mL) and IVC (1.88+/-0.38 pg/mL, p<0.05). IL-6 at CS (18.3+/-3.8 pg/mL) was higher than that of SA (5.8+/-1.2 pg/mL, p<0.01). The levels of sTNFR I, II showed increasing tendency in sequence of SA, IVC and CS. TNF-alpha and sTNFR I, II from all sites were proportional to worsening of functional classes at admission (p<0.05). E/Ea by Doppler study at admission, which reflects left ventricular end-diastolic pressure (LVEDP) was positively correlated with TNF-alpha from SA (R=0.71, p<0.01), CS (R=0.52, p<0.05) and IVC (R=0.46, p<0.05). Thus, elevated LVEDP during decompensation might cause cytokine release from myocardium in patients with idiopathic dilated cardiomyopathy.
Adult
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Aged
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Cardiomyopathy, Congestive/*blood/*immunology
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Female
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Heart/anatomy & histology
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Hemodynamic Processes
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Human
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Interleukin-6/*blood
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Male
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Middle Aged
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Receptors, Tumor Necrosis Factor/*blood
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Statistics
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Tumor Necrosis Factor/*metabolism
3.Expression of a recombinant branched chain alpha-oxo acid dehydrogenase complex E2 (BCOADC-E2) in insect cells and its immunoreactivity to autoimmune sera.
Sang Mi LEE ; Soon Hee KO ; Jeong Eu PARK ; Sang Hoon CHA
Experimental & Molecular Medicine 1998;30(2):65-71
Preparation of a pure autoantigen by way of recombinant DNA technology has an important value in an accurate diagnosis or prognosis of an autoimmune disease. BCOADC-E2 subunit, a mitochondrial protein, has been known to be the autoantigen of primary biliary cirrhosis (PBC), a chronic autoimmune liver disease, as well as idiopathic dilated cardiomypathy (IDCM), a chronic autoimmune heart disease. Recombinant form of this molecule had been expressed in E. coli but with low yield and severe degradation. Furthermore, sera from IDCM patients failed to recognized BCOADC-E2 molecule produced in prokaryotic expression system. In this study, a recombinant bovine BCOADC-E2 fusion protein has been expressed in insect cells using baculovirus expression system and analyzed anti-BCOADC-E2 reactivity in sera from patients with PBC or with IDCM. Optimal production of the recombinant fusion protein has been achieved at 20 multiplicity of infection (MOI), and the protein was affinity-purified using metal-binding resins. The affinity-purified BCOADC-E2 protein was successfully recognized by sera from PBC patients, but not by sera from IDCM patients suggesting that the different auto-immune response against BCOADC-E2 is needed to be elucidated in terms of epitope recognition.
Acetyltransferases/metabolism
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Acetyltransferases/immunology
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Acetyltransferases/genetics*
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Animal
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Baculoviridae/genetics
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Cardiomyopathy, Congestive/immunology
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Cattle
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Human
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Immune Sera
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Insects/cytology*
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Ketone Oxidoreductases/metabolism
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Ketone Oxidoreductases/immunology*
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Ketone Oxidoreductases/genetics*
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Liver Cirrhosis, Biliary/immunology
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Multienzyme Complexes/metabolism
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Multienzyme Complexes/immunology*
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Multienzyme Complexes/genetics*
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Protein Engineering/methods
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Recombinant Proteins/isolation & purification
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Recombinant Proteins/immunology
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Recombinant Proteins/genetics*