Key result
Saphenous vein perivascular adipose tissue exhibits significantly less metaflammation and fibrosis than arterial tissue.
Why the study?
Long-term saphenous vein graft patency in CABG is a crucial issue, but whether perivascular adipose tissue surrounding the saphenous vein has distinct phenotypes compared with other vascular PVATs was unknown.
Does perivascular adipose tissue surrounding the saphenous vein have a distinct antiatherosclerotic phenotype compared to PVAT of other vessels in patients undergoing CABG?
Cross-Sectional (n=48)
Double-blind
Yes
Does perivascular adipose tissue surrounding the saphenous vein have a distinct antiatherosclerotic phenotype compared to PVAT of other vessels in patients undergoing CABG?
p-value: p=<0.05
The saphenous vein perivascular adipose tissue exhibits an antiatherosclerotic phenotype with less metaflammation and fibrosis, which may explain the high long-term patency of saphenous vein grafts harvested using the no-touch technique.
SV-PVAT's reduced metaflammation and fibrosis may reflect a protective phenotype; hypothesis-generating and should not yet alter graft practices.
Background Perivascular adipose tissue (PVAT) is associated with metabolically driven chronic inflammation called metaflammation, which contributes to vascular function and the pathogenesis of vascular disease. The saphenous vein (SV) is commonly used as an essential conduit in coronary artery bypass grafting, but the long-term patency of SV grafts is a crucial issue. The use of the novel "no-touch" technique of SV harvesting together with its surrounding tissue has been reported to result in good long‑term graft patency of SV grafts. Herein, we investigated whether PVAT surrounding the SV (SV-PVAT) has distinct phenotypes compared with other PVATs of vessels. Methods and Results Fat pads were sampled from 48 patients (male/female, 32/16; age, 72±8 years) with coronary artery disease who underwent elective coronary artery bypass grafting. Adipocyte size in SV-PVAT was significantly larger than the sizes in PVATs surrounding the internal thoracic artery, coronary artery, and aorta. SV-PVAT and PVAT surrounding the internal thoracic artery had smaller extents of fibrosis, decreased gene expression levels of fibrosis-related markers, and less metaflammation, as indicated by a significantly smaller extent of cluster of differentiation 11c-positive M1 macrophage infiltration, higher gene expression level of adiponectin, and lower gene expression levels of inflammatory cytokines, than did PVATs surrounding the coronary artery and aorta. Expression patterns of adipocyte developmental and pattern-forming genes were totally different among the PVATs of the vessels. Conclusions The phenotype of SV-PVAT, which may result from inherent differences in adipocytes, is closer to that of PVAT surrounding the internal thoracic artery than that of PVAT surrounding the coronary artery or that of PVAT surrounding the aorta. SV-PVAT has less metaflammation and consecutive adipose tissue remodeling, which may contribute to high long-term patency of grafting when the no-touch technique of SV harvesting is used.
No takes yet. Share an insight, caveat, or question.
Mikami et al. (2021) conducted a cross-sectional in Coronary artery disease (n=48). Perivascular adipose tissue surrounding the saphenous vein (SV-PVAT) vs. Perivascular adipose tissue surrounding the internal thoracic artery, coronary artery, and aorta was evaluated on Phenotype of SV-PVAT including adipocyte size, fibrosis, and metaflammation markers (p=<0.05). Perivascular adipose tissue surrounding the saphenous vein exhibited significantly less metaflammation and fibrosis compared to tissue surrounding the coronary artery and aorta.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: