C-Myc over-expression significantly associated with high sVEGF and normal sFlt-1 level in DLBCL patients, suggesting a complex interrelationship between c-Myc oncogene expression and angiogenic regulators. C-Myc over-expression, high sVEGF and normal sFLt-1 levels at diagnosis had an independent adverse influence on survival in DLBCL patients and considered bad prognostic markers.
our data support the hypothesis that angiogenic factors play a functional role in blast cell movement from the bone marrow to peripheral tissues. Assessment of sHGF at AML diagnosis is likely to be helpful in predicting patient outcome and selecting optimal therapeutic regimen.
MRI is an established and accurate method of measuring left and right ventricular volumes by summing chamber areas in multiple contiguous slices. Acquisition time may be up to 45 min. We have estimated volumes with gradient echo imaging to test the accuracy of a more rapid method (total acquisition time 15 min) using a recognized echocardiographic algorithm. The results were compared with the spin echo method. We studied 20 patients (mean age 52 years, 15 male) within 6 months of anterior myocardial infarction and 20 normal subjects (mean age 40 years, 19 males). For the rapid method, cine acquisitions were made in the horizontal long axis plane and in two short axis planes which divided the long axis into three equal parts. Volume was calculated assuming the ventricle to be composed of a cylinder, a truncated cone and a cone. There was good agreement between the two methods at end diastole with a mean difference (+/- standard error, +/- 95% confidence interval for limits of agreement) of -3 ml (+/- 8.3, +/- 37%) for normal subjects and 1.5 ml (+/- 4.2, +/- 25%) for patients. Agreement was less good at end systole with mean difference of 12.1 (+/- 3.5, +/- 41%) for normal subjects and 25.7 (+/- 3.7, +/- 47%) for patients. The rapid method, therefore, significantly underestimated end systolic volume compared with the previous method. Rapid measurements of end diastolic volume are more accurate than those of end systolic volume and hence ejection fraction. Provided the potential error is recognized, the rapid technique can be used in routine clinical practice in both normal and abnormal ventricles.
Plasma levels of soluble P-selectin were increased in patients with AMI, and UA compared to patients with SA and normal controls. Measurement of soluble P-selectin may be helpful marker of impending coronary artery insult in diabetic patients.
Neutropenia in patients with hepatosplenic (HS) schistosomiasis may stem from enhanced neutrophil apoptosis. However, the molecular mechanism of neutrophil apoptosis has not been clearly defined. Neutrophils harvested from neutropenic patients with HS schistosomiasis (n = 25), non-neutropenic patients with hepatointestinal (HI) schistosomiasis (n = 10), and age- and sex-matched healthy control subjects (n = 10) were examined for the degree of apoptosis after incubation with autologous sera. Neutrophil apoptosis was quantified by flow cytometry through determination of propidium iodide nuclear staining and confirmed by DNA gel electrophoresis at 0 time (fresh neutrophil), 4 and 24 h culture. Neutrophils from healthy subjects were also incubated with either 10% heterologous normal or neutropenic serum, with and without anti-Fas ligand antibody. Serum Fas ligand levels were assessed in sera of patient groups and healthy controls by ELISA. Compared with normal controls and HI, HS group demonstrated greater neutrophil apoptosis in the presence of autologous serum (P < 0.01, < 0.05, respectively). Furthermore, compared with normal neutrophils exposed to heterologous normal serum, those exposed to heterologous neutropenic serum exhibited higher apoptosis rates (P < 0.01). The apoptotic effect of neutropenic sera is attenuated by anti-Fas ligand. Fas expression was significantly higher in HS group as compared to both HI and normal healthy controls (P < 0.05). Serum Fas ligand levels were significantly higher among HS group as compared to both HI and control groups (P < 0.01 for both). Neutrophil apoptosis was not correlated to the size of spleen in HS group. In conclusion, the rate of neutrophil apoptosis is accelerated in neutropenic HS schistosomiasis. These findings suggest that enhanced neutrophil apoptosis demonstrated in HS patients is triggered by soluble Fas ligand, which is mostly derived from spleen.
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