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We are analyzing https://link.springer.com/article/10.1007/s00392-019-01512-z.

Title:
Myeloperoxidase in atrial fibrillation: association with progression, origin and influence of renin–angiotensin system antagonists | Clinical Research in Cardiology
Description:
Background Myeloperoxidase (MPO), secreted by neutrophils under inflammatory conditions, is elevated in atrial fibrillation (AF). MPO may be involved in atrial remodeling that underpins AF progression characterized by a switch from paroxysmal to persistent AF and the formation of low-voltage areas (LVA). MPO levels are modulated by renin–angiotensin system antagonists (RAS-A), commonly used to treat AF comorbidities, and are associated with reduced AF incidence, implicating a potential link. Objective We investigated MPO levels in progressing AF in peripheral and left atrial (LA) blood and analyzed a potential effect of RAS-A. Methods Samples of AF patients were collected from the femoral vein and the LA during catheter ablation (n = 121) and at follow-up (n = 23). No-AF probands (n = 37) served as controls. MPO was determined using commercial ELISA. Results MPO levels were significantly increased in AF patients compared to controls (median, 27.7 ng/ml (IQR 14.3–66.6) versus 12.6 (IQR 9.9–17.7), p < 0.001), without differences between clinical AF progression phenotypes. MPO concentration was tenfold higher in LA than periphery (279.2 ng/ml (IQR 202.2–342.9) versus 27.7 ng/ml (IQR 14.3–65.9), p < 0.001). MPO remained increased at midterm follow-up irrespective of rhythm outcome. RAS-A was associated with significantly lower peripheral (22.2 ng/ml (IQR 12.7–48.2) versus 37.1 ng/ml (IQR 18.2–85.2), p < 0.05) MPO levels in AF patients. Conclusion The pro-fibrotic enzyme MPO is generally elevated in AF patients irrespective of AF type, the presence of LVA or midterm rhythm outcome. Our data suggest that MPO may directly originate from the LA. RAS-A decrease peripheral MPO levels in AF patients. Graphic abstract
Website Age:
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🌠 Phenomenal Traffic: 5M - 10M visitors per month


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Keywords {🔍}

article, atrial, pubmed, fibrillation, google, scholar, cas, mpo, myeloperoxidase, patients, central, progression, levels, iqr, angiotensin, leipzig, privacy, cookies, content, research, system, kornej, ngml, access, cardiac, heart, data, publish, search, clinical, cardiology, reninangiotensin, antagonists, june, holzwirth, hindricks, büttner, rasa, peripheral, left, ablation, author, information, log, journal, association, erik, jelena, erbs, bollmann,

Topics {✒️}

renin–angiotensin system antagonists month download article/chapter renin angiotensin system pro-fibrotic enzyme mpo mitogen-activated protein kinase transcription factor nf-kappab article clinical research chronic kidney disease related subjects full article pdf obstructive pulmonary disease article holzwirth angiotensin ii stimulates angiotensin ii receptors angiotensin ii signal privacy choices/manage cookies atrial fibrillation prophylaxis atrial fibrillation developed author correspondence petra büttner andreas bollmann & gerhard hindricks atrial fibrillation pathophysiology catheter ablation atrial fibrillation—role european economic area low-voltage areas late gadolinium enhancement low voltage zones von leitner e updated systematic review randomized controlled trials clinically stable periods normal reference values glomerular filtration rate check access instant access van wagoner dr van gelder ic treat af comorbidities reduced af incidence midterm rhythm outcome framingham heart study article log conditions privacy policy accepting optional cookies ethics declarations conflict investigated mpo levels significantly lower peripheral article cite nt-proanp levels

Questions {❓}

  • Delanaye P, Schaeffner E, Ebert N, Cavalier E, Mariat C, Krzesinski J-M, Moranne O (2012) Normal reference values for glomerular filtration rate: what do we really know?
  • D’Ascenzo F, Corleto A, Biondi-Zoccai G, Anselmino M, Ferraris F, Di Biase L, Natale A, Hunter RJ, Schilling RJ, Miyazaki S, Tada H, Aonuma K, Yenn-Jiang L, Tao H, Ma C, Packer D, Hammill S, Gaita F (2013) Which are the most reliable predictors of recurrence of atrial fibrillation after transcatheter ablation?

Schema {🗺️}

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         description:Myeloperoxidase (MPO), secreted by neutrophils under inflammatory conditions, is elevated in atrial fibrillation (AF). MPO may be involved in atrial remodeling that underpins AF progression characterized by a switch from paroxysmal to persistent AF and the formation of low-voltage areas (LVA). MPO levels are modulated by renin–angiotensin system antagonists (RAS-A), commonly used to treat AF comorbidities, and are associated with reduced AF incidence, implicating a potential link. We investigated MPO levels in progressing AF in peripheral and left atrial (LA) blood and analyzed a potential effect of RAS-A. Samples of AF patients were collected from the femoral vein and the LA during catheter ablation (n = 121) and at follow-up (n = 23). No-AF probands (n = 37) served as controls. MPO was determined using commercial ELISA. MPO levels were significantly increased in AF patients compared to controls (median, 27.7 ng/ml (IQR 14.3–66.6) versus 12.6 (IQR 9.9–17.7), p &lt; 0.001), without differences between clinical AF progression phenotypes. MPO concentration was tenfold higher in LA than periphery (279.2 ng/ml (IQR 202.2–342.9) versus 27.7 ng/ml (IQR 14.3–65.9), p &lt; 0.001). MPO remained increased at midterm follow-up irrespective of rhythm outcome. RAS-A was associated with significantly lower peripheral (22.2 ng/ml (IQR 12.7–48.2) versus 37.1 ng/ml (IQR 18.2–85.2), p &lt; 0.05) MPO levels in AF patients. The pro-fibrotic enzyme MPO is generally elevated in AF patients irrespective of AF type, the presence of LVA or midterm rhythm outcome. Our data suggest that MPO may directly originate from the LA. RAS-A decrease peripheral MPO levels in AF patients.
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      description:Myeloperoxidase (MPO), secreted by neutrophils under inflammatory conditions, is elevated in atrial fibrillation (AF). MPO may be involved in atrial remodeling that underpins AF progression characterized by a switch from paroxysmal to persistent AF and the formation of low-voltage areas (LVA). MPO levels are modulated by renin–angiotensin system antagonists (RAS-A), commonly used to treat AF comorbidities, and are associated with reduced AF incidence, implicating a potential link. We investigated MPO levels in progressing AF in peripheral and left atrial (LA) blood and analyzed a potential effect of RAS-A. Samples of AF patients were collected from the femoral vein and the LA during catheter ablation (n = 121) and at follow-up (n = 23). No-AF probands (n = 37) served as controls. MPO was determined using commercial ELISA. MPO levels were significantly increased in AF patients compared to controls (median, 27.7 ng/ml (IQR 14.3–66.6) versus 12.6 (IQR 9.9–17.7), p &lt; 0.001), without differences between clinical AF progression phenotypes. MPO concentration was tenfold higher in LA than periphery (279.2 ng/ml (IQR 202.2–342.9) versus 27.7 ng/ml (IQR 14.3–65.9), p &lt; 0.001). MPO remained increased at midterm follow-up irrespective of rhythm outcome. RAS-A was associated with significantly lower peripheral (22.2 ng/ml (IQR 12.7–48.2) versus 37.1 ng/ml (IQR 18.2–85.2), p &lt; 0.05) MPO levels in AF patients. The pro-fibrotic enzyme MPO is generally elevated in AF patients irrespective of AF type, the presence of LVA or midterm rhythm outcome. Our data suggest that MPO may directly originate from the LA. RAS-A decrease peripheral MPO levels in AF patients.
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