9 research outputs found

    Baseline characteristics of the study patients.

    No full text
    *<p>By Fisher exact test.</p>§<p>by Wilcoxon Rank Sum Test.</p><p>ACE = angiotensin-converting enzyme; ARB = angiotensin II receptor blocker; CABG = coronary artery bypass graft surgery; CKD = chronic kidney disease; CRP = C-reactive protein; eGFR = estimated glomerular filtration rate; NA = not applicable; PCI = percutaneous coronary intervention.</p

    Kaplan-Meier survival analyses during follow-up.

    No full text
    <p>Composite outcomes of cardiac death and myocardial infarction according to concentrations of plasma arginine (panel A), asymmetric dimethylarginine (ADMA; panel B), and symmetric dimethylarginine (SDMA; panel C), divided by median levels. P values by log-rank test are shown.</p

    Relationships between NO synthesis inhibitors and renal function.

    No full text
    <p>Relationship between asymmetric (ADMA; upper panel) and symmetric (SDMA; lower panel) dimethylarginine plasma levels and estimated glomerular filtration rate (eGFR) in the study population.</p

    Arginine, ADMA and SDMA plasma levels.

    No full text
    <p>Arginine (panel A), asymmetric dimethylarginine (ADMA; panel B), and symmetric dimethylarginine (SDMA; panel C) plasma levels (mean±SD values) in healthy subjects (n = 20), in controls with chronic kidney disease (CKD; n = 10), and in NSTEMI patients without (n = 71) and with (n = 33) CKD.</p

    Cox regression analysis for the primary end point of the study (composite outcome of cardiac death and myocardial infarction).

    No full text
    <p>Hazard ratios (HR) in models 1–4 are adjusted for age, hemoglobin and left ventricular ejection fraction; HRs in models 5–7 are also mutually adjusted.</p><p>HRs for CKD are vs. no-CKD; for all other variables, HRs are for values above vs. below median.</p><p>ADMA = asymmetric dimethylarginine; CKD = chronic kidney disease; CI = confidence intervals; SDMA = symmetric dimethylarginine.</p

    miRNA clusters efficiently differentiate SA and UA patients from Controls.

    No full text
    <p>Hierarchical clustering demonstrated that different miRNA “signatures” efficiently classify between matched controls (CTRLS) and CAD patients. The cluster composed by miR-1 and miR-126 and miR-485-3p can be used to correctly classify SA patients from controls with 90.2% (yellow bar) efficiency. Similarly the miR-1, miR-126 and miR-133a cluster can be used to correctly classify UA patients from controls with 87.2% (red bar) efficiency. No signatures of miRNAs could be found to efficiently discriminate SA from UA patients with an accuracy > 66% (miR-126 and miR-337-5p cluster, blue bar). </p
    corecore