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1.
Gen Thorac Cardiovasc Surg ; 70(6): 547-552, 2022 Jun.
Article in English | MEDLINE | ID: mdl-34797477

ABSTRACT

OBJECTIVES: The number of hemodialysis patients requiring aortic valve replacement (AVR) is increasing. Although bioprosthetic valves are increasingly popular, they are associated with a risk of structural valve deterioration (SVD). The aim of this study is to examine the outcomes of bioprosthetic valves in hemodialysis patients undergoing AVR and to identify treatment strategies that can decrease the risk of SVD. METHODS: Between February 2010 and November 2019, 61 patients on hemodialysis underwent AVR using bioprosthetic valves at our hospital. Five patients died while still in the hospital. Kaplan-Meier estimates of overall survival and univariate Cox proportional hazards regression analyses were performed for the remaining 56 patients. RESULTS: During follow-up, there were six SVD events (10.7%) related to the bioprosthetic valves. The survival rate was 67.9% at 3 years and 39.5% at 5 years. In all SVD cases, SVD was caused by aortic stenosis. The mean interval between AVR and the discovery of SVD was 41.5 months. The SVD-free rate was 88.6% at 3 years and 65.3% at 5 years. Preoperative phosphorus levels are associated with SVD risk. High preoperative phosphorus concentration is associated with elevated SVD risk. CONCLUSIONS: In this study, we determined that the risk of SVD can be influenced by preoperative phosphorus level. Strict control of the phosphorus concentration of hemodialysis patients may decrease structural valve deterioration after aortic valve replacement.


Subject(s)
Aortic Valve Stenosis , Bioprosthesis , Heart Valve Prosthesis Implantation , Heart Valve Prosthesis , Aortic Valve/surgery , Aortic Valve Stenosis/surgery , Heart Valve Prosthesis Implantation/adverse effects , Humans , Phosphorus , Prosthesis Design , Prosthesis Failure , Renal Dialysis/adverse effects , Retrospective Studies , Treatment Outcome
2.
Biochem Biophys Res Commun ; 394(3): 721-7, 2010 Apr 09.
Article in English | MEDLINE | ID: mdl-20230782

ABSTRACT

The nucleoprotein (NP) of the influenza virus is expressed in the early stage of infection and plays important roles in numerous steps of viral replication. NP is relatively well conserved compared with viral surface spike proteins. This study experimentally demonstrates that NP is a novel target for the development of new antiviral drugs against the influenza virus. First, artificial analogs of mycalamide A in a chemical array bound specifically with high affinity to NP. Second, the compounds inhibited multiplication of the influenza virus. Furthermore, surface plasmon resonance imaging experiments demonstrated that the binding activity of each compound to NP correlated with its antiviral activity. Finally, it was shown that these compounds bound NP within the N-terminal 110-amino acid region but their binding abilities were dramatically reduced when the N-terminal 13-amino acid tail was deleted, suggesting that the compounds might bind to this region, which mediates the nuclear transport of NP and its binding to viral RNA. These data suggest that compound binding to the N-terminal 13-amino acid tail region may inhibit viral replication by inhibiting the functions of NP. Collectively, these results strongly suggest that chemical arrays are convenient tools for the screening of viral product inhibitors.


Subject(s)
Antiviral Agents/isolation & purification , Drug Discovery/methods , Pyrans/chemistry , RNA-Binding Proteins/antagonists & inhibitors , Viral Core Proteins/antagonists & inhibitors , Amino Acid Sequence , Animals , Antiviral Agents/chemistry , Antiviral Agents/pharmacology , COS Cells , Chlorocebus aethiops , Drug Evaluation, Preclinical/methods , Humans , Influenza A virus , Nucleocapsid Proteins , Photochemical Processes , Pyrans/pharmacology , RNA-Binding Proteins/chemistry , Viral Core Proteins/chemistry , Virus Replication/drug effects
4.
J Clin Endocrinol Metab ; 89(4): 1833-7, 2004 Apr.
Article in English | MEDLINE | ID: mdl-15070952

ABSTRACT

To study the role of adiponectin, a novel adipocyte-specific secreted protein, on the pathophysiology of eating disorders, circulating levels of fasting adiponectin, leptin, insulin, and glucose were measured in 31 female patients with anorexia nervosa (AN) and in 11 with bulimia nervosa. Hormone levels were compared with 16 age-matched, normal body weight controls, six healthy constitutionally thin subjects, and nine obese subjects. Moreover, changes in levels were reevaluated after nutritional treatment and weight gain in 13 patients with AN. Serum adiponectin concentrations in AN and bulimia nervosa were significantly lower than those in normal-weight controls. These results were unexpected because the levels were high in constitutionally thin subjects and low in obese subjects, which provide a negative correlation with body mass index (BMI) and body fat mass. In contrast, serum leptin levels correlated very well with BMI and fat mass among all the patients and controls. The insulin resistance was significantly low in AN and high in obese subjects. The concentrations of adiponectin after weight recovery increased to the normal level despite a relatively small increase in BMI. These findings suggest that abnormal feeding behavior in the patients with eating disorders may reduce circulating adiponectin level, and weight recovery can restore it.


Subject(s)
Anorexia Nervosa/physiopathology , Bulimia/physiopathology , Intercellular Signaling Peptides and Proteins , Proteins/metabolism , Adiponectin , Adipose Tissue/pathology , Adult , Anorexia Nervosa/blood , Anorexia Nervosa/pathology , Anorexia Nervosa/therapy , Body Composition , Body Mass Index , Bulimia/blood , Bulimia/pathology , Case-Control Studies , Female , Humans , Insulin Resistance , Leptin/blood , Middle Aged , Nutrition Therapy , Obesity/blood , Obesity/pathology , Obesity/physiopathology , Osmolar Concentration , Thinness/blood , Thinness/pathology , Thinness/physiopathology , Weight Gain
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