# Comparative Analysis of Perivascular Adipose Tissue Attenuation on Chest Computed Tomography Angiography in Patients with Marfan Syndrome: A Case–Control Study

**Authors:** Domenico Tuttolomondo, Francesco Secchi, Nicola Gaibazzi, Nathasha Samali Udugampolage, Alessandro Pini, Massimo De Filippo, Pietro Spagnolo, Rosario Caruso, Jacopo Taurino

PMC · DOI: 10.3390/diagnostics15060673 · Diagnostics · 2025-03-10

## TL;DR

This study compares fat tissue changes around blood vessels in people with Marfan syndrome and healthy individuals using CT scans.

## Contribution

The study identifies perivascular adipose tissue attenuation as a potential early marker for vascular changes in Marfan syndrome.

## Key findings

- PVAT values were significantly lower in Marfan syndrome patients compared to controls (p = 0.002).
- The results suggest PVAT could indicate early vascular changes in MFS patients with normal aortic diameter.

## Abstract

Background: Marfan syndrome (MFS) is a rare autosomal dominant disorder affecting connective tissues due to mutations in the fibrillin-1 gene. These genetic changes often result in severe cardiovascular conditions, including asymptomatic thoracic aortic dilation potentially leading to dissection or rupture. Perivascular adipose tissue attenuation (PVAT) observed on computed tomography may serve as a marker of localized inflammation and indicate early histopathological changes in the vascular walls of MFS patients compared to healthy individuals. Objective: This study aimed to compare PVAT values between patients with MFS and healthy controls in order to explore whether MFS patients show higher PVAT secondary to these histopathological abnormalities. Methods: This case–control study assessed PVAT on ascending aorta through computed tomography angiography (CTA) in 54 genetically confirmed MFS patients and 43 controls with low ischemic risk, excluding those with known aortic aneurysms. Results: PVAT analysis revealed significant differences between the MFS patients and healthy controls (−70.6 HU [−72.6 HU to −68.5 HU] versus −75.1 HU [−77.1 HU to −73.1 HU], p = 0.002), suggesting potential early vascular changes in the MFS group. Conclusions: The findings underscore the potential diagnostic role of PVAT in patients with genetically confirmed MFS but normal ascending aorta diameter.

## Linked entities

- **Genes:** FBN1 (fibrillin 1) [NCBI Gene 373992]
- **Diseases:** Marfan syndrome (MONDO:0007947)

## Full-text entities

- **Genes:** FBN1 (fibrillin 1) [NCBI Gene 2200] {aka ACMICD, ECTOL1, FBN, GPHYSD2, MASS, MFLS}
- **Diseases:** dissection (MESH:D000784), autosomal dominant disorder (MESH:D030342), histopathological abnormalities (MESH:D000014), MFS (MESH:D008382), aortic aneurysms (MESH:D001014), rupture (MESH:D012421), thoracic aortic dilation (MESH:D002311), ischemic (MESH:D002545), inflammation (MESH:D007249)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11941396/full.md

## References

37 references — full list in the complete paper: https://tomesphere.com/paper/PMC11941396/full.md

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Source: https://tomesphere.com/paper/PMC11941396