CHARACTERIZATION OF THE INFLAMMATORY RESPONSE PROFILE IN THE PERIVASCULAR ADIPOSE TISSUE ASSOCIATED WITH CORONARY ARTERY DISEASE: AN AUTOPSY STUDY

• Grant number: 17/11313-0
• Support Opportunities: Regular Research Grants
• Start date: December 01, 2017
• End date: May 31, 2020
• Field of knowledge: Health Sciences - Medicine
• Principal Investigator: Claudia Kimie Suemoto
• Grantee: Claudia Kimie Suemoto
• Host Institution: Faculdade de Medicina (FM). Universidade de São Paulo (USP). São Paulo , SP, Brazil
• Associated researchers: Carlos Augusto Gonçalves Pasqualucci ; Daniela Souza Farias Itao ; Luiz Fernando Ferraz da Silva

Abstract

Introduction: Coronary artery disease (CAD) is the main cause of morbimortality in the world. In a previous study, we found a positive correlation between the number of macrophages in the perivascular adipose tissue (PAT) and the percentage of obstruction of the atherosclerotic plaque,and an association between B-lymphocytes and unstable lesions. However, it is necessary toelucidate the inflammatory response profile in the PAT associated with CAD. The analysis of the macrophage polarization was performed in few studies with surgical samples, which could initiate an inflammatory process. Moreover, the main lineages of the T and B-lymphocytes in human PAT have not been research yet. Aim: To investigate the association between the inflammation response profile in periplaque PAT adjacent to the atherosclerosis plaque in coronary arteries, and to compare this inflammatory response profile with PAT adjacent to the coronary artery without atherosclerosis(distal PAT), using autopsy material. Methods: This cross-sectional study will be conducted in 82 samples of participants previously collected in São Paulo Autopsy Service of the University of São Paulo. The coronary arteries were dissected, fixed in 4% paraformaldehyde, andmicroscopically evaluated using morphometric measures. The atherosclerotic plaques wereclassified in terms of instability according to the American Heart Association criteria. Thesamples of periplaque and distal PAT will be submitted to immunohistochemistry technique toidentify macrophage polarization M1 (CD11c+) e M2 (CD206+), and double-marking to identifyTh1 lymphocytes (CD4+CD183+), Tregs (CD4+FoxP3+), B1 (CD20+CD43+) and B2(CD20+CD43-). The slides will be scanned and the inflammatory cells will be counted in 20 random fields systematically distributed. The inflammatory cells will be compared using linear regression models adjusted to possible confusing factors. (AU)

Scientific publications

(References retrieved automatically from Web of Science and SciELO through information on FAPESP grants and their corresponding numbers as mentioned in the publications by the authors)

YAHAGI-ESTEVAM, MARISTELLA; FARIAS-ITAO, DANIELA SOUZA; PARAIZO LEIT, RENATA ELAINE; RODRIGUEZ, ROBERTA DIEHL; PASQUALUCCI, CARLOS AUGUSTO; NITRINI, RICARDO; JACOB-FILHO, WILSON; POWER, MELINDA C.; SUEMOTO, CLAUDIA KIMIE. The Potential Role of Selection Bias in the Association Between Coronary Atherosclerosis and Cognitive Impairment. JOURNAL OF ALZHEIMER'S DISEASE, v. 93, n. 4, p. 10-pg., 2023-01-01. (17/11313-0, 13/12290-3, 17/24066-1, 13/00335-2)

FARIAS-ITAO, DANIELA SOUZA; PASQUALUCCI, CARLOS AUGUSTO; DE ANDRADE, RENATO ARAUJO; FERRAZ DA SILVA, LUIZ FERNANDO; YAHAGI-ESTEVAM, MARISTELLA; GELAS LAGE, SILVIA HELENA; PARAIZO LEITE, RENATA ELAINE; CAMPO, ALEXANDRE BRINCALEPE; SUEMOTO, CLAUDIA KIMIE. Macrophage Polarization in the Perivascular Fat Was Associated With Coronary Atherosclerosis. JOURNAL OF THE AMERICAN HEART ASSOCIATION, v. 11, n. 6, p. 30-pg., 2022-03-15. (13/12290-3, 17/11313-0, 13/00335-2, 17/24066-1)

NISHIZAWA, ALINE; CUELHO, ANDERSON; DE FARIAS-ITAO, DANIELA S.; CAMPOS, FERNANDA M.; LEITE, RENATA E. P.; FERRETTI-REBUSTINI, RENATA E. L.; GRINBERG, LEA T.; NITRINI, RICARDO; JACOB-FILHO, WILSON; PASQUALUCCI, CARLOS A.; et al. Direct Measurements of Abdominal Visceral Fat and Cognitive Impairment in Late Life: Findings From an Autopsy Study. FRONTIERS IN AGING NEUROSCIENCE, v. 11, MAY 7 2019. (12/25337-5, 13/12290-3, 17/11313-0)