Inflammatory Cells in Adipose Tissue and Skeletal Muscle of Patients with Peripheral Arterial Disease or Chronic Venous Disease: A Prospective, Observational, and Histological Study

Author:

Ferreira Joana1234ORCID,Longatto-Filho Adhemar2456,Afonso Julieta24ORCID,Roque Susana24ORCID,Carneiro Alexandre Lima7,Vila Isabel389,Silva Cristina389ORCID,Cunha Cristina389,Mesquita Amílcar10,Cotter Jorge23489,Correia-Neves Margarida24,Mansilha Armando1,Cunha Pedro23489

Affiliation:

1. Vascular Surgery Department–Fisiologia e Cirurgia, Centro Hospitalar Universitário de São João, 4200-319 Porto, Portugal

2. Life and Health Science Research Institute (ICVS), School of Medicine, University of Minho, 4710-057 Braga, Portugal

3. Centro Académico Hospital da Senhora da Oliveira, 4835-044 Guimarães, Portugal

4. ICVS/3B’s–PT Government Associated Laboratory, 4710-057 Braga, Portugal

5. Department of Pathology (LIM-14), University of São Paulo School of Medicine, São Paulo 01246-903, SP, Brazil

6. Molecular Oncology Research Center, Barretos Cancer Hospital, Barretos 14784-400, SP, Brazil

7. Radiology Department, ULSAM—Hospital de Santa Luzia, 4904-858 Viana do Castelo, Portugal

8. Medicine Department, Hospital da Senhora da Oliveira, 4835-044 Guimarães, Portugal

9. Center for the Research and Treatment of Arterial Hypertension and Cardiovascular Risk, Internal Medicine Department, Hospital da Senhora da Oliveira, 4835-044 Guimarães, Portugal

10. Vascular Surgery Department, Hospital da Senhora da Oliveira, 4835-044 Guimarães, Portugal

Abstract

The main goal of this study was to assess whether the presence of peripheral arterial disease (PAD) correlates with increased inflammatory cell infiltration. An observational, single-centre, and prospective study was conducted from January 2018 to July 2022. Clinical characteristics and anthropometric measures were registered. Consecutive PAD patients with surgical indications for a common femoral artery approach and patients with varicose veins with an indication for surgical ligation of the saphenofemoral junction were included. In both groups, samples of sartorius skeletal muscle, subcutaneous adipose tissue (SAT), and perivascular adipose tissue (PVAT) were collected from the femoral region. We analysed the characteristics of adipocytes and the presence of haemorrhage and inflammatory cells in the samples of PVAT and SAT via haematoxylin–eosin staining. We found that patients with PAD had significantly more inflammatory cells in PVAT [16 (43.24%) vs. 0 (0%) p = 0.008]. Analysing SAT histology, we observed that patients with PAD had significantly more CD45+ leucocytes upon immunohistochemical staining [32 (72.73%) vs. 3 (27.27%) p = 0.005]. Upon analysing skeletal muscle histology with haematoxylin–eosin staining, we evaluated skeletal fibre preservation, as well as the presence of trauma, haemorrhage, and inflammatory cells. We registered a significantly higher number of inflammatory cells in patients with PAD [well-preserved skeletal fibres: PAD = 26 (63.41%) vs. varicose veins = 3 (37.50%) p = 0.173; trauma: PAD = 4 (9.76%) vs. varicose veins = 2 (25.00%) p = 0.229; haemorrhage: PAD = 6 (14.63%) vs. varicose veins = 0 (0%) p = 0.248; inflammatory cells: PAD = 18 (43.90%) vs. varicose veins = 0 (0%) p = 0.018]. Patients with PAD had a higher number of inflammatory cells in skeletal muscle and adipose tissue (PVAT and SAT) when compared with those with varicose veins, emphasizing the role of inflammation in this group of patients.

Funder

Portuguese Society of Vascular Surgery

Northern Portugal Regional Operational Programme

National funds

Publisher

MDPI AG

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