Wednesday, August 27, 2008
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Antiretrovirals: congestive cardiomyopathy in paediatric patients: 3 case reports.
Page: 9 (Source: Reactions Weekly)... MORE...
POSTED 08/23/2008 at 05:12 AM --


The study of cu and zn serum levels in idiopathic dilated cardiomyopathy (idcmp) patients and its comparison with healthy volunteers.

The Study of Cu and Zn Serum Levels in Idiopathic Dilated Cardiomyopathy (IDCMP) Patients and its Comparison with Healthy Volunteers.

Biol Trace Elem Res. 2008 Aug 22;

Authors: Salehifar E, Shokrzadeh M, Ghaemian A, Aliakbari S, Saeedi Saravi SS

Changes in the cupper (Cu) and zinc (Zn) concentrations have been reported previously in idiopathic dilated cardiomyopathy (IDCMP). As a result of controversial results, the aim of this study was to compare the Zn and Cu concentrations and Zn/Cu ratio of IDCMP patients to healthy volunteers. In addition, the correlation of Cu and Zn levels with age has been evaluated. The study population consisted of 18 IDCMP patients and 27 healthy volunteers. IDCMP patients had normal angiography with echocardiography supporting cardiomyopathy without pericardial and valvular diseases. Exclusion criteria were renal or hepatic insufficiency, alcohol usage, and intake of supplements containing Cu or Zn within 1 week ago. Cu and Zn levels have been assayed with atomic absorption spectrophotometry. Statistical analysis was performed with SPSS 10 software with independent sample t test for comparing the level of Cu and Zn of IDCMP patients with normal subjects and Pearson correlation to determine the correlation between numeric data. P < 0.05 was considered as significant differences. There was a trend for a lower Zn level in IDCMP patients compared to healthy volunteers. (0.97 +/- 0.25 mg/l vs. 1.12 +/- 0.42 mg/l, respectively). The mean Cu levels of IDCMP and normal subjects were 1.33 +/- 0.20 mg/l and 1.31 +/- 0.23 mg/l, respectively. There was a significant difference in Zn/Cu ratio among patients based on the NYHA classification of heart failure (P = 0.003). Age was negatively correlated with Zn levels in IDCMP group (P = 0.037) and positively with Cu levels in healthy volunteers (P = 0.012). A lower Zn level in IDCMP patients compared to healthy volunteers and specially a significant difference in Zn/Cu ratio of patients based on their NYHA classification would suggest a critical role of zinc and Cu imbalance in development of IDCMP.

PMID: 18716717 [PubMed - as supplied by publisher]

(Source: Biological Trace Element Research)...
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POSTED 08/21/2008 at 11:00 PM --


The longitudinal course of cardiomyopathy in friedreich’s ataxia during childhood
Abstract   Background Clinical heart disease was recognized in the first descriptions of Friedreich’s ataxia (FA). Cardiac manifestations reported for this progressive neurologic disease include hypertrophic cardiomyopathy, dilated cardiomyopathy, and electrophysiologic disturbances. Longitudinal data for childhood cases are limited. This study aimed to define the longitudinal course of the cardiac abnormalities with FA diagnosed during childhood and to correlate the presence of cardiomyopathy with clinical and genetic factors. Methods A retrospective chart review was conducted, with prospective, blinded interpretation of echocardiograms and electrocardiograms. All the patients with a diagnosis of FA referred to the cardiology department of a single institution from 1974 to 2004 were included in the study. Results This study investigated a total of 113 echocardiograms for 28 patients. Overall, the group had left ventricular hypertrophy and normal systolic function, with a median mass z-score of 2.48 (range, −3.8 to 35.6) and a median ejection fraction (EF) of 61% (range, 23–81%). Of the 28 patients, 23 (82%) had two or more echocardiograms. The median follow-up time to the most recent echocardiogram was 5.1 years (range, 0.4–16.5 years). Many in this longitudinal follow-up cohort (57%) showed hypertrophic cardiomyopathy on at least one echocardiogram, with the last follow-up assessment showing systolic dysfunction for 38% of these patients. There was a slow nonlinear decline in systolic function over time, with the mean EF decreasing more rapidly as age increased (p = 0.02) and maintenance of EF in the normal range until the age of 22 years. Of the 12 patients with systolic dysfunction and follow-up echocardiograms, 10 showed improvement to the normal EF range on at least one echocardiogram, and 5 remained normal through the last study. None of the trends in cardiac function and morphology correlated with frataxin GAA repeat length (the primary genetic defect in FA) or ambulatory status. One patient required an implantable defibrillator. There were no deaths or heart transplantations. Conclusions Overall, patients with FA have preserved cardiac function with increased mass throughout childhood. Because many patients who experience depressed systolic function show improvement in subsequent studies, evaluation for potentially reversible causes of heart failure should be conducted. Relative clinical stability during childhood and maintenance of normal systolic function into the second decade may be helpful for parent and patient education. Content Type Journal ArticleCategory Original ArticleDOI 10.1007/s00246-008-9305-1Authors Alaina Kipps, Department of Cardiology 300 Longwood Avenue Boston MA 02115 USAMark Alexander, Department of Cardiology 300 Longwood Avenue Boston MA 02115 USASteven D. Colan, Department of Cardiology 300 Longwood Avenue Boston MA 02115 USAKimberlee Gauvreau, Department of Cardiology 300 Longwood Avenue Boston MA 02115 USALeslie Smoot, Department of Cardiology 300 Longwood Avenue Boston MA 02115 USALisa Crawford, Department of Cardiology 300 Longwood Avenue Boston MA 02115 USABasil T. Darras, Children’s Hospital, Boston Department of Neurology 300 Longwood Avenue Boston MA 02115 USAElizabeth D. Blume, Department of Cardiology 300 Longwood Avenue Boston MA 02115 USA Journal Pediatric CardiologyOnline ISSN 1432-1971Print ISSN 0172-0643 (Source: Pediatric Cardiology)... MORE...
POSTED 08/21/2008 at 04:23 AM --


Recombinant adeno-associated virus-mediated gene delivery of long chain acyl coenzyme a dehydrogenase (lcad) into lcad-deficient mice
Very long chain acyl coenzyme A (CoA) dehydrogenase (VLCAD) deficiency is a relatively common mitochondrial [beta]-oxidation disorder. The most severe form of VLCAD deficiency presents with neonatal cardiomyopathy and hepatic failure and is generally fatal within the first year of life. Mice deficient for long chain acyl CoA dehydrogenase (LCAD) closely resemble the clinical syndrome observed in VLCAD-deficient humans. Recombinant adeno-associated viral (rAAV) vectors with pseudotype capsids were investigated for their potential towards correcting the phenotype observed in mice heterozygous (+/-) for LCAD (i.e. liver and muscle steatosis).rAAV containing the mouse LCAD cDNA (mLCAD) under the transcriptional control of the CMV/chicken [beta]-actin hybrid promoter were injected intramuscularly into the tibialis anterior (TA) muscle of LCAD+/- mice or injected into the portal vein to transduce hepatocytes.Ten weeks post-injection of rAAV1-mLCAD into the TA muscle, significantly increased levels of mLCAD within mitochondria were demonstrated by immunostaining of TA sections, immunoblotting of mitochondrial isolates and by the electron transfer flavoprotein (ETF) fluorescence reduction enzyme activity assay. Magnetic resonance spectroscopy of vector-injected TA muscle demonstrated a reduction in the lipid content compared to phosphate-buffered saline-injected mice, whereas a systemic effect was observed as a reduction in liver macrosteatosis. Eight weeks after portal vein injection of rAAV8-mLCAD into LCAD+/- mice, increased levels of mLCAD within hepatocyte mitochondria were demonstrated by immunostaining and also by the ETF assay. Scoring of the hepatosteatosis observed in partially deficient LCAD mice indicated a reduction in the lipid content within livers of vector-treated mice.These studies show that rAAV-mediated delivery of mLCAD was efficient and led to an amelioration of local and systemic pathologies observed in partially deficient LCAD mice. Copyright © 2008 John Wiley & Sons, Ltd. (Source: The Journal of Gene Medicine)... MORE...
POSTED 08/20/2008 at 11:00 PM --


Current status and future prospects for cell transplantation to prevent congestive heart failure.
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Current status and future prospects for cell transplantation to prevent congestive heart failure.

Semin Thorac Cardiovasc Surg. 2008;20(2):131-7

Authors: Menasché P

Although most cardiac cell therapy trials have focused on patients with acute myocardial infarction, attempts at "regenerating" chronically failing hearts have also been performed. These studies have entailed use of skeletal myoblasts and bone marrow-derived cells. In the case of skeletal myoblasts, the randomized placebo-controlled myoblast autologous grafting in ischemic cardiomyopathy (MAGIC) trial has failed to show that myoblast injections increased ejection fraction beyond that seen in controls but the finding that the highest dose of myoblasts resulted in a significant antiremodeling effect compared with the placebo group provides an encouraging signal. In the case of bone marrow cells, surgical injections of the mononuclear fraction combined with coronary artery bypass surgery have not shown a substantial benefit but positive results have been reported with intraoperative epicardial injections of CD133(+) progenitors. There are three possible reasons for these mixed results. The first is the marked heterogeneity of cell functionality (particularly in the case of bone marrow), which would expectedly translate into variable clinical outcomes. The second reason is the low rate of sustained engraftment. The third possible explanation is a mismatch between the choice of end points and the presumed mechanism of action of the cells. The initial assumption that adult stem cells could effect myocardial tissue regeneration has led to usual focus on ejection fraction as the major surrogate endpoint. It is now increasingly recognized that adult stem cells, in contrast to their embryonic counterparts, have little if any regenerative capacity and that their presumed beneficial effects more likely involve paracrine signaling, in which case infarct size, perfusion, or left ventricular volumes might be more appropriate markers. Altogether, these observations provide a framework for future research, the results of which will then have to be integrated in the protocol design of second-generation clinical trials.

PMID: 18707646 [PubMed - in process]

(Source: Seminars in Thoracic and Cardiovascular Surgery)...
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POSTED 08/20/2008 at 04:02 AM --


A-wave acceleration: a new doppler echocardiographic index for evaluation of left ventricular diastolic dysfunction in elderly patients
Age alters Doppler indexes of left ventricular diastolic performance. Thus, the Doppler detection of left ventricular diastolic dysfunction in the elderly is difficult. The reliability of Doppler indexes in detecting left ventricular diastolic dysfunction in the elderly patients with cardiac diseases known to affect diastolic function were evaluated. Diastolic function using pulsed Doppler in 6 groups of 10 subjects each: elderly normal, young normal, and elderly with hypertrophic cardiomyopathy, aortic stenosis, coronary artery disease, and dilated cardiomyopathy was tested. The comparison of elderly normal with young normal showed that A-wave acceleration did not change significantly. Comparing elderly normal to elderly with diseases showed that all tested indexes except A-wave acceleration failed to separate normal elderly from diseased elderly. A-wave acceleration appears to be a useful index that can help in diagnosis of left ventricular diastolic dysfunction in elderly patients independent of age effects. (Source: Angiology)... MORE...
POSTED 08/19/2008 at 11:00 PM --


Duloxetine: apical ballooning cardiomyopathy: case report
(Source: Reactions)... MORE...
POSTED 08/18/2008 at 05:15 AM --


Predictor factors for the development of arterial hypertension following heart transplantation
Sánchez-Lázaro IJ, Martínez-Dolz L, Almenar-Bonet L, Moro-López JA, Agüero J, Ortiz-Martínez V, Izquierdo MT, Salvador A. Predictor factors for the development of arterial hypertension following heart transplantation.Clin Transplant 2008 DOI: 10.1111/j.1399-0012.2008.00875.x© 2008 Wiley Periodicals, Inc.Abstract: Introduction: Up to 95% of the patients with heart transplantation (HT) suffer from arterial hypertension (AHT). The development of de novo AHT after HT has not been greatly studied.Aim: To identify the predictor variables for the development of de novo AHT after HT.Materials and methods: We retrospectively studied 253 patients with HT and who did not previously have AHT. We excluded cases of early mortality, re-transplants and combined transplants. We considered AHT as the constant need to take anti-hypertensive drugs to maintain blood pressure < 140/90 mmHg. We studied all the variables relating to recipient, donor, surgical procedure, immunosuppression and follow-up. The statistics used were the Student's t-test, chi-square statistic and a logistic regression analysis.Results: Of the 253 patients, 109 (43%) developed AHT. The variables associated with more prevalent AHT were male recipient/donor, idiopathic dilated cardiomyopathy (IDCM) as cause of HT, having been a smoker as well as renal deterioration (RD) and hypercholesterolemia after HT. The multivariate analysis found smoking prior to the HT and hypercholesterolemia during follow-up as independent risk factors and urgent HT as a protective variable.Conclusions: AHT after HT is frequent. The variables associated in our population were smoking before HT, male recipient/donor, IDCM prior to HT and hypercholesterolemia and RD after HT. (Source: Clinical Transplantation)... MORE...
POSTED 08/17/2008 at 11:00 PM --


Ventricular repolarization gradients in a patient with takotsubo cardiomyopathy
A 61-year-old woman had recurrent syncopal attacks caused by torsades de pointes associated with remarkable QT prolongation (QTc = 740 ms). Left ventriculography showed apical akinesis (ballooning) and basal hyperkinesis, but coronary angiography was normal. This was compatible with takotsubo cardiomyopathy. The wall motion of the left ventricle (LV) normalized within 2 months, and the remarkable QT prolongation and negative T-waves gradually normalized. However, polymorphic ventricular tachycardia recurred at 2.5 months after its initial onset, and we measured repolarization gradients using activation recovery intervals (ARIs) in an electrophysiological study. During atrial pacing at a cycle length of 1000 ms, the negative T-waves were observed in leads II, III, aVF, and V2–6 with QT prolongation, and the ARIs in both the epicardium and the endocardium increased from the basal site to the apical site. Moreover, the ARI tended to be longer in the epicardium than the endocardium at each level of the LV. In contrast, atrial extrastimulation changed the T-wave morphology (from negative to biphasic) in leads II, III, aVF, and V2–6 and changed the ARI gradients both from the LV basal site to the apical site and from the epicardium to the endocardium. These results suggest that the T-wave abnormalities seen in takotsubo cardiomyopathy during sinus rhythm are due to abnormal LV repolarization gradients. (Source: Europace)... MORE...
POSTED 08/17/2008 at 11:00 PM --


Dual-chamber implantable cardioverter defibrillator implantation guided by non-fluoroscopic electro-anatomical navigation
A dual-chamber implantable cardioverter defibrillator was implanted in a 37-year-old pregnant woman with dilated cardiomyopathy, symptomatic sinus bradycardia, and a family history of sudden death. Two leads were connected to a three-dimensional navigation system and placed at the right atrium and right ventricle, respectively, without fluoroscopy. (Source: Europace)... MORE...
POSTED 08/17/2008 at 11:00 PM --


Hypertrophic cardiomyopathy and athlete's heart: a tale of two entities.
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Hypertrophic cardiomyopathy and athlete's heart: a tale of two entities.

Eur J Echocardiogr. 2008 Aug 18;

Authors: Martín M, Reguero JJ, Castro MG, Coto E, Hernández E, Carro A, Calvo D, Morí de la Tassa C

Sudden death during sports activities, although unfrequent, is a tragic event with great impact on both the general and medical communities. The two commonest conditions leading to sudden cardiac death in young athletes are hyperthrophic cardiomyopathy (HCM), the main cause in the USA, and arrythmogenic right ventricular cardiomyopathy, which is the leading cause in Europe. We report the case of a 17-year-old football player with a pathological electrocardiography (ECG) in the pre-participation screening programme, highly suggestive of HCM, in which ECG study showed a septum thickness of 28 mm. Genetic analysis revealed R 495 W mutation in the 18 exon of the MyBPC3 (myosin-binding protein C) and sports activities were contraindicated. Two years later, septum thickness was 19.5 mm. Usefulness of 12-lead ECG, differential diagnosis between athlete's heart and HCM, and the stratification in patients with HCM are discussed.

PMID: 18713777 [PubMed - as supplied by publisher]

(Source: European Journal of Echocardiography)...
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POSTED 08/17/2008 at 11:00 PM --


Cardiac retransplantation in adults: an evidence-based systematic review.

Cardiac retransplantation in adults: an evidence-based systematic review.

Thorac Cardiovasc Surg. 2008 Sep;56(6):323-7

Authors: Tjang YS, Tenderich G, Hornik L, Körfer R

BACKGROUND: It remains a matter of dispute whether cardiac retransplantation should be performed. We aimed to systematically review the available evidence regarding cardiac retransplantation in adults. MATERIAL AND METHODS: In PubMed, we searched for original reports on cardiac retransplantation in adults. The evidence level of individual studies was assessed. RESULTS: Twenty-two studies met our selection criteria. The cumulative incidence was 3 % (range: 1 % to 15 %). The incidence rate was 164/10 000 person-years (range: 145 to 318/10 000 person-years). The main indications for retransplantation were cardiac allograft vasculopathy (55 %), acute rejection (19 %), and primary graft failure (17 %). The early mortality rate was 16 % (range: 5 % to 38 %). Refractory acute rejection and primary graft failure, female donor, shorter transplant interval, initial diagnosis of ischemic cardiomyopathy, need for mechanical circulatory support, a center volume of less than 9 transplantations/year, older recipient age, requirement of pretransplant ventilator and intensive care, and ischemic time were associated with poorer outcomes, while cardiac allograft vasculopathy as the cause of allograft failure, employment, and later transplant period were associated with improved survival. CONCLUSION: This systematic review shows that the results of cardiac retransplantation in adults are inconclusive. Retransplantation for cardiac allograft vasculopathy is associated with satisfactory outcomes.

PMID: 18704853 [PubMed - in process]

(Source: The Thoracic and Cardiovascular Surgeon)...
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POSTED 08/17/2008 at 06:26 AM --


[therapy-induced effects in normal tissue.]
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[Therapy-induced effects in normal tissue.]

Radiologe. 2008 Aug 17;

Authors: van Kaick G, Delorme S

More than 50% of cancer patients survive for more than 5 years, owing to modern and effective treatment. Therefore, long-term sequelae of treatment are more frequently seen than in the past. Such effects on normal tissue may both mimic and obscure tumor recurrences. Besides the direct consequences of surgery, tissue damage due to radiation or chemotherapy frequently cause problems in differential diagnosis. Among the numerous sequelae of radiotherapy, the most prominent are disturbance of the blood-brain barrier, radiation pneumonitis, osteodystrophy and osteoradionecrosis, fatty changes of bone marrow, or increased radiodensity of breast parenchyma. Chemotherapy may cause, e.g., diffuse abnormalities of white matter, pneumonitis and lung fibrosis, cardiomyopathy, or diffuse and patchy changes in bone marrow signals in MRI. The most devastating long-term complications are secondary cancers and leukemia induced by both radiotherapy and chemotherapy.

PMID: 18709346 [PubMed - as supplied by publisher]

(Source: Der Radiologe)...
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POSTED 08/16/2008 at 11:00 PM --


Cardiovascular magnetic resonance imaging for intensive care infants: safe and effective?
Abstract   Background Cardiac magnetic resonance imaging (MRI) is an important diagnostic tool for congenital heart disease (CHD), as reflected by class 1 recommendations for the use of cardiac MRI by various consensus panels. However, little is known about the safety and clinical utility of cardiac MRI for these critically ill infants with CHD, whose further management cannot be directed by echocardiography. This study aimed to assess the safety, the potential hemodynamic side effects, and the clinical benefits of cardiac MRI for infants with complex CHD during their intensive care unit stay. Methods Infants referred from the pediatric cardiac intensive care unit (PCICU) to the authors’ cardiac MRI program in the past 2 years were retrospectively analyzed using the electronic chart system available at their institution. Data collected included age, diagnosis, inotropic support, urine output, diuretic medication, body temperature and lactate levels, length of MRI examination, adverse effects during and after the procedure, clinical implications of MRI, length of stay in the PCICU, and mean blood pressure and heart rate before, during, and after MRI. Results Among 592 patients in the past 2 years, 20 (3.4%) were referred for MRI testing during their stay in the PCICU. The mean age of the infants was 4.8 ± 3.2 months. Four of the patients were neonates, and eight were postoperative patients. Intracardiac malformations were present in 16 of the infants, vascular rings causing tracheal stenosis in 3 patients, and cardiomyopathy in 1 patient. The mean stay in the PCICU was 28 ± 43 days. Eight of the infants were ventilated, with a mean fraction of inspired oxygen (FiO2) of 0.30 ± 0.15. Four were receiving inotropic support. All the nonventilated children were intubated for the MRI and extubated in the MRI laboratory. The mean duration of the MRI (door-to-door time) was 110 ± 27 min. All except one patient were hemodynamically stable, and no increase in catecholamine support was necessary during or after the scans. A 10-month-old girl receiving inotropic support needed a single dose of epinephrine due to a short episode of bradycardia after a breathhold for a contrast agent MRI angiography. Mean body core temperature at arrival to the PCICU was 36.8 ± 0.7°C. The mean serum lactate level after the MRI was 1.2 ± 0.4 mmol/l. The mean blood pressure and heart rate before, during, and after MRI were unchanged. The mean diuresis on examination day was insignificantly lower (2.4%) than the day before with unchanged medication (5.09 ± 1.58 vs 5.53 ± 1.77 ml/kg/h). For 14 (70%) of the 20 patients, surgical or catheter interventional procedures were initiated based on novel MRI information. Conclusion Cardiac MRI can be performed safely with low risk and limited hemodynamic changes for infants during their stay in the PCICU. Cardiac MRI provides key information for invasive management decisions in this subset of patients. Content Type Journal ArticleCategory Original ArticleDOI 10.1007/s00246-008-9295-zAuthors Samir Sarikouch, Heart and Diabetes Center Northrhine-Westfalia Department of Congenital Heart Disease Georgstraße 11 32545 Bad Oeynhausen GermanyRainer Schaeffler, Heart and Diabetes Center Northrhine-Westfalia Department of Congenital Heart Disease Georgstraße 11 32545 Bad Oeynhausen GermanyHermann Körperich, Heart and Diabetes Center Northrhine-Westfalia Institute for Radiology, Nuclear Medicine, and Molecular Imaging Georgstraße 11 32545 Bad Oeynhausen GermanyAristidis Dongas, Heart and Diabetes Center Northrhine-Westfalia Institute for Anaesthesiology Georgstraße 11 32545 Bad Oeynhausen GermanyNikolaus A. Haas, Heart and Diabetes Center Northrhine-Westfalia Department of Congenital Heart Disease Georgstraße 11 32545 Bad Oeynhausen GermanyPhilipp Beerbaum, Guy’s & St. Thomas Hospital, King`s College Division of Imaging Sciences London UK Journal Pediatric CardiologyOnline ISSN 1432-1971Print ISSN 0172-0643 (Source: Pediatric Cardiology)... MORE...
POSTED 08/16/2008 at 02:59 AM --


Analysis of specific th1/th2 helper cell responses and igg subtype antibodies in anti-cd4 monoclonal antibody treated mice with autoimmune cardiomyopathy
Summary  The cytokine repertoire of ADP/ATP carrier-specific humoral immune responses and the cytokine-dependent anti-ADP/ATP carrier antibody IgG subclasses were examined in a cohort of ADP/ATP carrier-immunized BALB/c mice treated with anti-CD4 monoclonal antibody. Eighteen male BALB/c mice (6–8 weeks old) were randomized into 3 groups: dilated cardiomyopathy (DCM) group, DCM-tolerance (Tol) group and control group. The mice in DCM group were immunized with the peptides derived from human ADP/ATP carrier protein for 6 months and mice in the control group were sham-immunized, while the mice in DCM-Tol group were immunized with ADP/ATP carrier protein and anti-CD4 McAb simultaneously. Serum autoantibody against ADP/ATP carrier and IgG subclasses were measured by ELISA, intracellular cytokines IFN-γ and IL-4 of Th cells were monitored with flow cytometry, and splenic T cell cytokines IFN-γ, IL-2, IL-4 and IL-6 were detected by using real-time fluorescent quantitative PCR. The results showed that the autoantibody against ADP/ATP carrier was found in all mice in DCM group, and the antibody level, serum IgG1 and IgG2a subclasses, cytokines in T cells and Th cells were all elevated in DCM group, as compared with those in control group (P<0.01). On the other hand, in DCM-Tol group, the autoantibody level and contents of all the cytokines were significantly different from those in DCM group (P<0.01), and were close to those in control group. And the levels of IgG1, IgG2a, IgG2b and IgG3 were influenced, to varying degrees, by anti-CD4 McAb as compared with those in DCM group. All these four types of IgG subclasses were substantially decreased in DCM-Tol group as compared with DCM group. It is concluded that the treatment with anti-CD4 McAb could prevent the activation of T cells, reverse the abnormal secretion of cytokines and the imbalance between Th1/Th2 cell subsets and abnormal production of autoantibody against ADP/ATP carrier, and eventually avoid myocardial injuries. Content Type Journal ArticleDOI 10.1007/s11596-008-0408-yAuthors Zhaohui Wang, Huazhong University of Science and Technology Laboratory of Cardiovascular Immunology, Institute of Cardiology, Union Hospital, Tongji Medical College Wuhan 430022 ChinaYuhua Liao, Huazhong University of Science and Technology Laboratory of Cardiovascular Immunology, Institute of Cardiology, Union Hospital, Tongji Medical College Wuhan 430022 ChinaJing Yuan, Huazhong University of Science and Technology Laboratory of Cardiovascular Immunology, Institute of Cardiology, Union Hospital, Tongji Medical College Wuhan 430022 ChinaJinghui Zhang, Huazhong University of Science and Technology Laboratory of General Surgery, Union Hospital, Tongji Medical College Wuhan 430022 ChinaJihua Dong, Huazhong University of Science and Technology Institute of Virology, Union Hospital, Tongji Medical College Wuhan 430022 ChinaJinping Wang, Huazhong University of Science and Technology Institute of Virology, Union Hospital, Tongji Medical College Wuhan 430022 China Journal Journal of Huazhong University of Science and Technology -- Medical Sciences --Online ISSN 1993-1352Print ISSN 1672-0733 Journal Volume Volume 28 Journal Issue Volume 28, Number 4 / August, 2008 (Source: Journal of Huazhong University of Science and Technology -- Medical Sciences --)... MORE...
POSTED 08/15/2008 at 05:20 AM --


Nesiritide improves hemodynamics in children with dilated cardiomyopathy: a pilot study
Abstract   Background This study aimed to obtain hemodynamic measurements of nesiritide in children with dilated cardiomyopathy. Methods A prospective, randomized, double-blinded, placebo-controlled pilot study was conducted in the pediatric intensive care unit at the University of California, Los Angeles. All subjects younger than 21 years admitted to the pediatric intensive care unit with a diagnosis of dilated cardiomyopathy and submitted to cardiac catheterization were randomized to receive either nesiritide or placebo. Right heart catheterization with Swan-Ganz catheter placement was performed. Nesiritide was infused over 24 h. Hemodynamic data were obtained before, during, and after the 24-h nesiritide infusion. The measures obtained included pulmonary capillary wedge pressure (PCWP), central venous pressure, mean pulmonary arterial pressure (MPAP), systolic arterial blood pressure (SBP), cardiac index, and systemic vascular resistance. Results The study included 20 children: 9 randomized to nesiritide and 11 to placebo. At 24 h, the mean decreases in PCWP, MPAP, and SBP were significantly greater for nesiritide than for placebo: PCWP (–5.3 vs. 1.2 mmHg; p = 0.02), MPAP (–8.0 vs. 0.4 mmHg; p = 0.006), SBP (–7.9 vs. 2.6 mmHg; p = 0.04). Conclusions Nesiritide significantly decreases PCWP, MPAP, and SBP in children with dilated cardiomyopathy. Content Type Journal ArticleCategory Original ArticleDOI 10.1007/s00246-008-9272-6Authors Sarina K. Behera, University of California Department of Pediatrics Los Angeles CA USAJennifer C. Zuccaro, University of California Department of Pediatrics Los Angeles CA USAGlenn T. Wetzel, University of Tennessee Health Science Center Department of Pediatrics Memphis TN USAJuan C. Alejos, University of California Department of Pediatrics Los Angeles CA USA Journal Pediatric CardiologyOnline ISSN 1432-1971Print ISSN 0172-0643 (Source: Pediatric Cardiology)... MORE...
POSTED 08/15/2008 at 01:23 AM --


Microrna and cardiac pathologies
MicroRNA has been shown to be essential for correct cardiovascular development and physiology in a number of recent reports. Studies have also started to characterize the link between specific microRNAs and aspects of pathogenesis—such as chamber morphogenesis, conduction, and contraction—and between microRNA expression signatures and pathological cardiac phenotypes—such as hypertrophy, ischemic cardiomyopathy, dilated cardiomyopathy, and aortic stenosis. Congenital anomalies of the heart may also be associated with the dysregulation of specific microRNAs. Here we report on the latest findings. (Source: Physiological Genomics)... MORE...
POSTED 08/14/2008 at 11:00 PM --


Absence of auto-antibodies against cardiac troponin i predicts improvement of left ventricular function after acute myocardial infarction
Aims Application of antibodies against cardiac troponin I (cTnI-Ab) can induce dilation and dysfunction of the heart in mice. Recently, we demonstrated that immunization with cTnI induces inflammation and fibrosis in myocardium of mice. Others have shown that auto-antibodies to cTnI are present in patients with acute coronary syndrome, but little is known about the clinical relevance of detected cTnI-Ab. Methods and results First, anti-cTnI and anti-cTnT antibody titres were measured in sera from 272 patients with dilated- (DCM) and 185 with ischaemic- (ICM) cardiomyopathy. Secondly, 108 patients with acute myocardial infarction (AMI) were included for a follow-up study. Heart characteristics were determined by magnetic resonance imaging 4 days and 6–9 months after AMI. Altogether in 7.0% of patients with DCM and in 9.2% with ICM, an anti-cTnI IgG antibody titre ≥1:160 was measured. In contrast, only in 1.7% of patients with DCM and in 0.5% with ICM, an anti-cTnT IgG antibody titre ≥1:160 was detected. Ten out of 108 patients included in the follow-up study were tested positive for cTnI-Ab with IgG Ab titres ≥1:160. TnI-Ab negative patients showed a significant increase in left ventricular ejection fraction (LVEF) and stroke volume 6–9 months after AMI. In contrast, there was no significant increase in LVEF and stroke volume in TnI-Ab positive patients. Conclusion We demonstrate for the first time that the prevalence of cTnI-Abs in patients with AMI has an impact on the improvement of the LVEF over a study period of 6–9 months. (Source: European Heart Journal)... MORE...
POSTED 08/13/2008 at 11:00 PM --


A smoker's paradox in patients hospitalized for heart failure: findings from optimize-hf
Aims Cigarette smoking is a well-established risk factor for cardiovascular disease yet several studies have shown lower mortality after acute coronary syndromes in smokers compared with non-smokers, the so called ‘smoker’s paradox’. This study aimed to ascertain the relationship between smoking and clinical outcomes in patients hospitalized with heart failure (HF). Methods and results OPTIMIZE-HF (Organized Program to Initiate Lifesaving Treatment in Hospitalized Patients with Heart Failure) collected data on 48 612 patients from 259 hospitals. Characteristics, treatments, and outcomes were compared for current/recent smokers vs. those without current/recent smoking, and multivariable regression analyses with adjustment for hospital clustering were performed. There were 7743 (15.9%) smokers, 39 126 (80.5%) non-smokers, and 1743 (3.6%) missing. Smokers were younger, had similar renal function, but lower ejection fraction. The risk of in-hospital mortality was less in smokers (2.3 vs. 3.9%, P < 0.001). After extensive covariate adjustment, smokers still had lower in-hospital mortality risk OR (odds ratio) 0.70, 95% CI (confidence interval) 0.56–0.88, P = 0.002. Post-discharge, smokers (n = 998) had similar mortality risk (6.7 vs. 8.4%, P = 0.29) compared with those without current/recent smoking. Conclusion Smokers hospitalized with HF had lower risk adjusted in-hospital mortality and similar early post-discharge mortality compared with non-smokers. The residual association of smoking and better prognosis, the ‘smoker’s paradox’, was not fully explained by measured covariates. (Source: European Heart Journal)... MORE...
POSTED 08/13/2008 at 11:00 PM --


The effect of ageing on cardiac remodelling and hospitalization for heart failure after an inaugural anterior myocardial infarction
Aims Following myocardial infarction (MI), both age and left ventricular (LV) remodelling are associated with an increased risk of adverse events. We tested the hypothesis that the increased incidence of heart failure following MI in elderly patients is associated with a greater propensity for LV remodelling. Methods and results We monitored 266 patients with anterior MI. Echocardiographic studies were performed at hospital discharge, at 3 months, and at 1 year following hospitalization for MI. A clinical follow-up examination was performed after 3 years. Left ventricular remodelling was documented by an increase in LV end-diastolic volume after 1 year. Left ventricular end-diastolic and end-systolic volumes did not differ with age for all time points studied. Left ventricular remodelling was observed in 31, 26, 34, and 34% of patients <48, 48–57, 58–71, and >71 years of age, respectively. The 3 year heart-failure hospitalization rates were 1.9, 1.5, 11.0, and 20.3% for patients <48, 48–57, 58–71, and >71 years of age, respectively. Hospitalization for heart failure was more frequent in older patients. Conclusion We found that age was a major determinant of subsequent re-hospitalization for heart failure. However, we found no significant association between age and the LV remodelling process. (Source: European Heart Journal)... MORE...
POSTED 08/13/2008 at 11:00 PM --


 

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Men's Plus

"The restoration and maintenance of normal organ and brain function, a strong immune system, and the balancing of hormones is the key to vibrant health and in avoiding premature-aging!"

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