Plasma levels of tumor necrosis factor-α and its receptors in patients with mitral stenosis and sinus rhythm undergoing percutaneous balloon valvuloplasty
This study aimed to determine whether plasma levels of tumor necrosis factor-alpha (TNF-alpha) and soluble TNF receptor (sTNF-R) increases in rheumatic mitral stenosis (MS) patients with sinus rhythm and to examine the effect of percutaneous mitral balloon valvuloplasty (PMBV) on these parameters. Twenty-six patients with MS and sinus rhythm (study group, 20 female, mean age 33 +/- 8 years), who were scheduled for PMBV, and a well-matched control group consisting of 21 healthy volunteers (15 female, mean age 35 +/- 6 years) were enrolled in the study. Tumor necrosis factor-alpha and sTNF-R levels were compared between study patients and controls, and between peripheral and left atrium (LA) blood. Changes in TNF alpha and sTNF-R levels 24 h and 4 weeks after PMBV were analyzed. Significantly higher baseline TNF-alpha and sTNF-R levels were noted in the study group. In the study group, TNF-alpha and its receptors were also found to be higher in LA blood than in baseline peripheral blood. After PMBV, mitral valve area (MVA) increased and transmitral pressure gradient decreased significantly. At the 24th hour after PMBV, the TNF-alpha level decreased from 29.61 +/- 12.22 pg/ml to 22.42 +/- 8.81 pg/ml (P < 0.0001) and at the 4th week, from 22.42 +/- 8.81 pg/ml to 18.92 +/- 7.37 pg/ml (P < 0.0001). Similar reductions were observed in the sTNF-R level. Regression analysis between the difference in sTNF-R level measured 24 h after and before PMBV and the difference in MVA measured 24 h after and before PMBV showed a significant direct relationship between these variables. This study suggests that isolated rheumatic MS without atrial fibrillation is accompanied by increased TNF-alpha and sTNF-R level. The successful PMBV establishes a significant reduction in TNF-alpha and its receptors, probably due to improved postprocedural hemodynamic parameters.
机构:
Univ Calif San Diego, Sch Med, Salk Program Mol Med, La Jolla, CA 92093 USAUniv Calif San Diego, Sch Med, Salk Program Mol Med, La Jolla, CA 92093 USA
机构:Hop Henri Mondor, INSERM, Unite 841, Inst Mondor Rech Biomed,Equipe 19, F-94010 Creteil, France
Defer, Nicole
;
Azroyan, Anie
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机构:Hop Henri Mondor, INSERM, Unite 841, Inst Mondor Rech Biomed,Equipe 19, F-94010 Creteil, France
Azroyan, Anie
;
Pecker, Francoise
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机构:Hop Henri Mondor, INSERM, Unite 841, Inst Mondor Rech Biomed,Equipe 19, F-94010 Creteil, France
Pecker, Francoise
;
Pavoine, Catherine
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机构:
Hop Henri Mondor, INSERM, Unite 841, Inst Mondor Rech Biomed,Equipe 19, F-94010 Creteil, FranceHop Henri Mondor, INSERM, Unite 841, Inst Mondor Rech Biomed,Equipe 19, F-94010 Creteil, France
机构:
Univ Calif San Diego, Sch Med, Salk Program Mol Med, La Jolla, CA 92093 USAUniv Calif San Diego, Sch Med, Salk Program Mol Med, La Jolla, CA 92093 USA
机构:Hop Henri Mondor, INSERM, Unite 841, Inst Mondor Rech Biomed,Equipe 19, F-94010 Creteil, France
Defer, Nicole
;
Azroyan, Anie
论文数: 0引用数: 0
h-index: 0
机构:Hop Henri Mondor, INSERM, Unite 841, Inst Mondor Rech Biomed,Equipe 19, F-94010 Creteil, France
Azroyan, Anie
;
Pecker, Francoise
论文数: 0引用数: 0
h-index: 0
机构:Hop Henri Mondor, INSERM, Unite 841, Inst Mondor Rech Biomed,Equipe 19, F-94010 Creteil, France
Pecker, Francoise
;
Pavoine, Catherine
论文数: 0引用数: 0
h-index: 0
机构:
Hop Henri Mondor, INSERM, Unite 841, Inst Mondor Rech Biomed,Equipe 19, F-94010 Creteil, FranceHop Henri Mondor, INSERM, Unite 841, Inst Mondor Rech Biomed,Equipe 19, F-94010 Creteil, France