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Persistent Inflammatory Activity in Blood Cells and Artery Tissue from Patients with Previous Bare Metal Stent
Farsky, Pedro Silvio; Hirata, Mario H; Arnoni, Renato Tambellini; Almeida, Antonio Flavio Sanches; Issa, Mario; Lima, Paula Helena Ortiz; Higuchi, Maria de Lourdes; Lin-Wang, Hui T.
Affiliation
  • Farsky, Pedro Silvio; Instituto Dante Pazzanese de Cardiologia. São Paulo. BR
  • Hirata, Mario H; Laboratório de Investigação Molecular em Cardiologia, Instituto Dante Pazzanese de Cardiologia. São Paulo. BR
  • Arnoni, Renato Tambellini; Instituto Dante Pazzanese de Cardiologia. São Paulo. BR
  • Almeida, Antonio Flavio Sanches; Instituto Dante Pazzanese de Cardiologia. São Paulo. BR
  • Issa, Mario; Instituto Dante Pazzanese de Cardiologia. São Paulo. BR
  • Lima, Paula Helena Ortiz; Instituto Dante Pazzanese de Cardiologia. São Paulo. BR
  • Higuchi, Maria de Lourdes; Instituto do Coração (InCor) do Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo. São Paulo. BR
  • Lin-Wang, Hui T; Laboratório de Investigação Molecular em Cardiologia, Instituto Dante Pazzanese de Cardiologia. São Paulo. BR
Arq. bras. cardiol ; 111(2): 134-141, Aug. 2018. tab, graf, ilus
Article in English | Sec. Est. Saúde SP, CONASS, SESSP-IDPCPROD, Sec. Est. Saúde SP | ID: biblio-1223515
Responsible library: BR79.1
ABSTRACT

BACKGROUND:

Studies have pointed out a higher mortality after coronary artery bypass surgery (CABG) in patients with stent.

OBJECTIVE:

To evaluate inflammatory markers in peripheral blood cells and in coronary artery tissue samples obtained during CABG in patients with stent compared to controls.

METHODS:

The case series consisted of two groups, one with previous stent implantation (n = 41) and one control (n = 26). The expression of the LIGHT, IL-6, ICAM, VCAM, CD40, NFKB, TNF, IFNG genes was analyzed in peripheral blood cells collected preoperatively. The coronary artery was evaluated for interleukin-6, ICAM, VCAM, CD40, NFKB, TNF-alpha and IFN-gamma by immunohistochemistry. A total of 176 tissue samples were grouped for analysis in A1- arteries with stent (n = 38); A2- native arteries from patients with stent in another artery (n = 68); and A3- arteries without stent from controls undergoing routinely CABG surgery (n = 70). A significance level of 0.05 was adopted.

RESULTS:

Patients with stent showed higher TNF (p = 0.03) and lower CD40 gene expression (p = 0.01) in peripheral blood cells than controls without stent. In coronary artery samples, the TNF-alpha protein staining was higher in the group A1, not only in the intima-media layer (5.16 ± 5.05 vs 1.90 ± 2.27; p = 0.02), but also in the adipose tissue (6.69 ± 3.87 vs 2.27 ± 4.00; p < 0.001). Furthermore, group A1 had a higher interleukin-6 protein staining in adipose tissue than group A3 (p = 0.04).

CONCLUSION:

We observed a persistently higher systemic TNF expression associated with exacerbated TNF-alpha and interleukin-6 local production in patients with stents. This finding may contribute to a worse clinical outcome.
Subject(s)

Full text: Available Collection: National databases / Brazil Database: CONASS / Sec. Est. Saúde SP / SESSP-IDPCPROD Main subject: Blood Cells / Stents / Percutaneous Coronary Intervention / Inflammation Language: English Journal: Arq. bras. cardiol Year: 2018 Document type: Article Institution/Affiliation country: Instituto Dante Pazzanese de Cardiologia/BR / Instituto do Coração (InCor) do Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo/BR / Laboratório de Investigação Molecular em Cardiologia, Instituto Dante Pazzanese de Cardiologia/BR

Full text: Available Collection: National databases / Brazil Database: CONASS / Sec. Est. Saúde SP / SESSP-IDPCPROD Main subject: Blood Cells / Stents / Percutaneous Coronary Intervention / Inflammation Language: English Journal: Arq. bras. cardiol Year: 2018 Document type: Article Institution/Affiliation country: Instituto Dante Pazzanese de Cardiologia/BR / Instituto do Coração (InCor) do Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo/BR / Laboratório de Investigação Molecular em Cardiologia, Instituto Dante Pazzanese de Cardiologia/BR
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