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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Perivascular Adipose Tissue Inflammation and Coronary Artery Disease: An Autopsy Study Protocol

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Farias-Itao, Daniela Souza ; Pasqualucci, Carlos Augusto ; Nishizawa, Aline ; Ferraz Silva, Luiz Fernando ; Campos, Fernanda Marinho ; Souza da Silva, Karen Cristina ; Paraizo Leite, Renata Elaine ; Grinberg, Lea Tenenholz ; Lucena Ferretti-Rebustini, Renata Eloah ; Jacob Filho, Wilson ; Suemoto, Claudia Kimie
Total Authors: 11
Document type: Journal article
Source: JMIR RESEARCH PROTOCOLS; v. 5, n. 4 OCT-DEC 2016.
Web of Science Citations: 2
Abstract

Background: Perivascular adipose tissue (PAT) inflammation may have a role in coronary artery disease (CAD) pathophysiology. However, most evidence has come from samples obtained during surgical procedures that may imply in some limitations. Moreover, the role of B lymphocytes and inflammation in PAT that is adjacent to unstable atheroma plaques has not been investigated in humans using morphometric measurements. Objective: The objective of this study is to investigate the inflammation in PAT, subcutaneous, and perirenal adipose tissues (SAT and PrAT) among chronic CAD, acute CAD, and control groups in an autopsy study. Methods: Heart, SAT, and PrAT samples are collected from autopsied subjects in a general autopsy service, with the written informed consent of the next-of-kin (NOK). Sociodemographic and clinical data are obtained from a semistructure interview with the NOK. Coronary arteries are dissected and PAT are removed. Sections with the greatest arterial obstruction or unstable plaques, and the local with absence of atherosclerosis in all coronary arteries are sampled. PAT are represented adjacent to these fragments. Adipose tissues are fixed in 4% buffered paraformaldehyde solution and analyzed immunohistochemically for macrophages (CD68), macrophage polarization (CD11c for proinflammatory and CD206 for anti-inflammatory), B lymphocytes (CD20), and T lymphocytes (CD3). Slides will be scanned, and inflammatory cells will be quantified in 20 random fields. Participants will be categorized in CAD groups, after morphometric measurement of arterial obstruction and plaque composition analysis in accordance with American Heart Association classification. Three study groups will be investigated: acute CAD (at least one unstable plaque); chronic CAD (>= 50% arterial obstruction); and controls (< 50% arterial obstruction). Inflammatory cells in PAT, SAT, and PrAT will be counted and compared between groups using multivariate linear regression, adjusted for age, body mass index, hypertension, diabetes, alcohol use, and smoking. Results: We present the methods of our study that was developed from 2 pilots. Currently, data collection and tissue processing are ongoing. Data collection, histology and immunochemistry procedures, and quantification of all inflammatory cells are expected to be concluded within 1 year. Conclusions: This study will contribute for the understanding of the mechanisms of CAD pathophysiology because it will help to clarify the role of inflammation both in chronic and acute CAD. (AU)

FAPESP's process: 13/00335-2 - Association between epicardial adipose tissue inflammation and coronary artery disease: a clinicopathological study
Grantee:Claudia Kimie Suemoto
Support Opportunities: Regular Research Grants