Marvin Ernesto García Reyes

Dr. Marvin Ernesto García Reyes


Research Focus & Metrics

Academic Career Length

13Years (2014-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
1 January 2017 in Annals of Vascular Surgery
Verified
Journal Article
Closed access
GMGaspar Mestres
Gaspar Mestres
MRMarvin Ernesto García Reyes
Marvin Ernesto García Reyes
XYXavier Yugueros
Xavier Yugueros
RURodrigo Urrea
Rodrigo Urrea
PTPaolo Tripodi
Paolo Tripodi
VRVincent Riambau
Vincent Riambau

29 February 2024 in European Journal of Vascular and Endovascular Surgery
Verified
Journal Article
Closed access
XCXavier Faner Capó
Xavier Faner Capó
MRMarvin Ernesto García Reyes
Marvin Ernesto García Reyes
ÁCÁlvaro Salinas Cánovas
Álvaro Salinas Cánovas
LBLluís Sánchez Besalduch
Lluís Sánchez Besalduch
DRDavid Flota Ruiz
David Flota Ruiz
CGCristina Casanovas Guitart
Cristina Casanovas Guitart

1 September 2025 in European Journal of Vascular and Endovascular Surgery
Verified
Journal Article
Closed access
XFXavier Faner-Capó
Xavier Faner-Capó
MRMarvin Ernesto García Reyes
Marvin Ernesto García Reyes
ÁSÁlvaro Salinas-Cánovas
Álvaro Salinas-Cánovas
DJDiego Juárez-Enríquez
Diego Juárez-Enríquez
DFDavid Flota-Ruiz
David Flota-Ruiz
MCMontserrat Yeste Campos
Montserrat Yeste Campos

1 July 2026 in Arteriosclerosis, Thrombosis, and Vascular Biology
Verified
Journal Article
Closed access
MBMireia Bragulat-Arévalo
Mireia Bragulat-Arévalo
AGAndrea Guala
Andrea Guala
MCMarta Ferrer Cornet
Marta Ferrer Cornet
MRMarvin Ernesto García Reyes
Marvin Ernesto García Reyes
JGJuan Garrido-Oliver
Juan Garrido-Oliver
LDLydia Dux-Santoy
Lydia Dux-Santoy
BACKGROUND: Most abdominal aortic aneurysms (AAA) present intraluminal thrombus (ILT). Whether its role is detrimental or protective for AAA evolution and patients outcomes is debated. 18 F-fluorodeoxyglucose positron emission tomography analysis in patients with AAA has shown contradictory results and has not widely explored ILT. The aim of this cross-sectional study was to investigate the colocalized association between 18 F-fluorodeoxyglucose and ILT presence and characteristics in AAA. METHODS: Consecutive patients with infrarenal AAA were prospectively enrolled and underwent positron emission tomography/magnetic resonance imaging. From the abdominal aorta segmentation, an aortic wall volume was defined and discretized into 28 standardized aortic patches, permitting colocalized interpatient and intrapatient analyses. The target-to-background ratio (TBR) was extracted in each patch, and extremely low (coldspots) and high (hotspots) absorption areas were computed. Local AAA diameters and ILT characteristics were computed in each patch. Linear mixed-effect models were used to test the association between AAA and ILT characteristics and 18 F-fluorodeoxyglucose uptake. RESULTS: Thirty-six patients (median age, 73 [interquartile range, 68–77] years, 31 [86.1%] men) completed the protocol. The AAA maximum diameter was 49.6 (45.0–56.2) mm, and most patients (28 [77.8%]) presented ILT. Patients with thrombus presented higher coldspot area and lower hotspot area ( P <0.001). Patches in nondilated regions presented higher TBR compared with AAA patches ( P <0.001), which showed a negative association of TBR with local diameter ( β =−0.006) and thrombus presence ( β =−0.003). TBR decreased with increased ILT coverage ( β =−0.002), while coldspot area increased ( β =0.046). In both the ILT and thrombus-covered wall, TBR decreased with increasing ILT thickness. CONCLUSIONS: Decreased metabolic activity as per 18-fluorodeoxyglucose positron emission tomography is observed in the AAA wall compared with the nondilated abdominal region. This effect is exacerbated by local thrombus presence and thickness, suggesting that ILT contributes to the further degradation of the aortic wall in the diseased region.

1 July 2017 in Revista Española de Cardiología (English Edition)
Verified
Journal Article
Closed access
JRJulián Rodríguez-García
Julián Rodríguez-García
MRMarvin Ernesto García Reyes
Marvin Ernesto García Reyes
ASAntonia Sambola
Antonia Sambola
ESEdgar Cortés Sánchez
Edgar Cortés Sánchez
VFValentín Fernández-Valenzuela
Valentín Fernández-Valenzuela
DGDavid García-Dorado
David García-Dorado

3 October 2025 in Applied Sciences
Verified
Journal Article
Open access
PDF file
MBMireia Bragulat-Arévalo
Mireia Bragulat-Arévalo
MCMarta Ferrer Cornet
Marta Ferrer Cornet
LDLydia Dux-Santoy
Lydia Dux-Santoy
RORuperto Oliveró
Ruperto Oliveró
MRMarvin Ernesto García Reyes
Marvin Ernesto García Reyes
AGAndrea Guala
Andrea Guala
18F-fluorodeoxyglucose (18F-FDG) positron emission tomography (PET) could be useful to assess inflammation of the aortic wall, a potential early indicator of aneurysm formation. Nonetheless, its current clinical assessment presents several limitations. The study aimed to develop and validate an innovative technique to obtain thoraco-abdominal aortic wall PET uptake maps. PET/magnetic resonance (MR) was acquired in 82 patients with aortic aneurysms. The thoraco-abdominal aorta was segmented and expanded inward and outward (by 1 to 5 mm) and discretized into 80 standardized wall patches. Standard uptake values (SUV) were calculated for each patch and the thrombus. For inter-observer reproducibility, a second blinded observer analyzed 26 random patients. Validation against manual expert measurements was performed. The feasibility of the patch-wise PET analysis was 98.4%. Inter-observer Dice scores were 0.89 for lumen and 0.82 for thrombus segmentations. SUV mapping presented excellent reproducibility, modestly improving with wall thickness (ICC 0.950 to 0.966), while its agreement with expert measurements improved with thinner walls (ICC 0.848 to 0.755). An optimal balance between reproducibility and accuracy was obtained at 6 mm wall thickness. Reproducible and accurate thoraco-abdominal aortic wall 18F-FDG uptake maps can be obtained from PET/MR, potentially facilitating the exploration of local factors associated with vascular inflammation.