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1.
Kardiologiia ; 58(4): 96-100, 2018 Nov 18.
Article in English | MEDLINE | ID: mdl-30704391

ABSTRACT

We present here a case of successful staged treatment of a patient with para-aortic abscess that arose 5 years after thoracic endovascular aortic repair because of thoracic aortic aneurysm. After stabilization of the patient's condition by intensive antibiotic therapy we performed left-subclavian extra-thoracic debranching as the first stage of the surgical treatment. In 2 weeks via median sternotomy and on-pump we removed the infected endograft and performed extraanatomical ascending-to-descending aortic bypass with good postoperative result.


Subject(s)
Aortic Aneurysm, Thoracic , Blood Vessel Prosthesis Implantation , Endovascular Procedures , Aorta, Thoracic , Blood Vessel Prosthesis , Humans , Stents , Tomography, X-Ray Computed , Treatment Outcome
2.
PLoS One ; 10(4): e0122601, 2015.
Article in English | MEDLINE | ID: mdl-25856389

ABSTRACT

Epigenetic mechanisms of gene regulation in context of cardiovascular diseases are of considerable interest. So far, our current knowledge of the DNA methylation profiles for atherosclerosis affected and healthy human vascular tissues is still limited. Using the Illumina Infinium Human Methylation27 BeadChip, we performed a genome-wide analysis of DNA methylation in right coronary artery in the area of advanced atherosclerotic plaques, atherosclerotic-resistant internal mammary arteries, and great saphenous veins obtained from same patients with coronary heart disease. The resulting DNA methylation patterns were markedly different between all the vascular tissues. The genes hypomethylated in athero-prone arteries to compare with atherosclerotic-resistant arteries were predominately involved in regulation of inflammation and immune processes, as well as development. The great saphenous veins exhibited an increase of the DNA methylation age in comparison to the internal mammary arteries. Gene ontology analysis for genes harboring hypermethylated CpG-sites in veins revealed the enrichment for biological processes associated with the development. Four CpG-sites located within the MIR10B gene sequence and about 1 kb upstream of the HOXD4 gene were also confirmed as hypomethylated in the independent dataset of the right coronary arteries in the area of advanced atherosclerotic plaques in comparison with the other vascular tissues. The DNA methylation differences observed in vascular tissues of patients with coronary heart disease can provide new insights into the mechanisms underlying the development of pathology and explanation for the difference in graft patency after coronary artery bypass grafting surgery.


Subject(s)
Atherosclerosis/genetics , Coronary Disease/genetics , Coronary Vessels/metabolism , Epigenesis, Genetic , Mammary Arteries/metabolism , Plaque, Atherosclerotic/genetics , Saphenous Vein/metabolism , Aged , Atherosclerosis/metabolism , Atherosclerosis/pathology , Coronary Disease/metabolism , Coronary Disease/pathology , Coronary Vessels/pathology , CpG Islands , DNA Methylation , Female , Genome-Wide Association Study , Homeodomain Proteins/genetics , Homeodomain Proteins/metabolism , Humans , Male , Mammary Arteries/pathology , MicroRNAs/genetics , MicroRNAs/metabolism , Middle Aged , Molecular Sequence Annotation , Organ Specificity , Plaque, Atherosclerotic/metabolism , Plaque, Atherosclerotic/pathology , Saphenous Vein/pathology
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