Literature DB >> 22655494

One-year observation of inflammatory markers in patients with aortic valve stenosis.

Jolanta Swierszcz1, Jacek S Dubiel, Jozef Krzysiek, Krystyna Sztefko.   

Abstract

BACKGROUND AND AIM OF THE STUDY: The study aim was to conduct an annual evaluation of plasma levels of C-reactive protein (CRP), tumor necrosis factor-alpha (TNF-alpha), interleukin-6 (IL-6) and antibodies against Chlamydia pneumoniae during a 12-month period following the natural course of aortic valve stenosis (AVS).
METHODS: A total of 60 patients with AVS and 14 control subjects underwent echocardiographic examinations at the start of the study period, and again after a 12-month follow up period. Subsequently, the AVS patients were allocated retrospectively to two groups (n = 30 in each) according to their echocardiographic parameters: patients who showed a progressive deterioration of valvular function (PAVS group); and those who showed a lack of such progression (LPAVS group). Plasma concentrations of CRP, TNF-alpha, IL-6, and antichlamydial IgA, IgG, and IgM antibodies were evaluated at the start of the study, and again during the 12th month.
RESULTS: During the study, CRP levels were increased only in the AVS group. TNF-alpha and IgM levels were higher in the AVS group compared to controls, at both the initial visit and the final observation. During the 12-month observation period the TNF-alpha level was increased in the PAVS group, whereas CRP levels in the LPAVS group were decreased. TNF-alpha levels were higher in the PAVS group than the LPAVS group, at both the initial visit and after 12 months; CRP levels did not differ between these groups. In the PAVS group, the IL-6 level was higher after 12 months, but the IgM level was higher at the initial visit. The results of a factorial analysis identified the main factors responsible for the decrease in aortic valve area to be TNF-alpha and CRP.
CONCLUSION: TNF-alpha, CRP, and IgM antichlamydial antibodies should be further investigated as potential predictive factors for the progression of AVS.

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Year:  2011        PMID: 22655494

Source DB:  PubMed          Journal:  J Heart Valve Dis        ISSN: 0966-8519


  5 in total

1.  Inflammation Drives Retraction, Stiffening, and Nodule Formation via Cytoskeletal Machinery in a Three-Dimensional Culture Model of Aortic Stenosis.

Authors:  Jina Lim; Arshia Ehsanipour; Jeffrey J Hsu; Jinxiu Lu; Taylor Pedego; Alexander Wu; Chris M Walthers; Linda L Demer; Stephanie K Seidlits; Yin Tintut
Journal:  Am J Pathol       Date:  2016-07-05       Impact factor: 4.307

Review 2.  Cell-matrix mechanics and pattern formation in inflammatory cardiovascular calcification.

Authors:  Jeffrey J Hsu; Jina Lim; Yin Tintut; Linda L Demer
Journal:  Heart       Date:  2016-07-12       Impact factor: 5.994

3.  Protective Role of Smad6 in Inflammation-Induced Valvular Cell Calcification.

Authors:  Xin Li; Jina Lim; Jinxiu Lu; Taylor M Pedego; Linda Demer; Yin Tintut
Journal:  J Cell Biochem       Date:  2015-10       Impact factor: 4.429

4.  Serotonin receptor type 2B activation augments TNF-α-induced matrix mineralization in murine valvular interstitial cells.

Authors:  Felicia Fong; Joshua Xian; Linda L Demer; Yin Tintut
Journal:  J Cell Biochem       Date:  2020-09-09       Impact factor: 4.429

5.  C-Reactive Protein to Albumin Ratio as A Novel Inflammatory-Based Marker for 30-Day Mortality in Patients Undergoing Transcatheter Aortic Valve Replacement.

Authors:  Fahrettin Katkat; Muhsin Kalyoncuoglu; Sevgi Ozcan; Sevil Tugrul; Hanife Abanus; Orhan Ince; Mehmet Balli; Irfan Sahin; Ertugrul Okuyan
Journal:  Braz J Cardiovasc Surg       Date:  2022-05-23
  5 in total

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