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Analysis of , , and mRNA as Key Molecular Mechanisms in the Damage of Aortic Aneurysm and Dissection in Marfan Syndrome.

作者信息

Soto María Elena, Rodríguez-Brito Myrlene, Pérez-Torres Israel, Herrera-Alarcon Valentín, Martínez-Hernández Humberto, Hernández Iván, Castrejón-Téllez Vicente, Peña-Ocaña Betsy Anaid, Alvarez-Leon Edith, Manzano-Pech Linaloe, Gamboa Ricardo, Fuentevilla-Alvarez Giovanny, Huesca-Gómez Claudia

机构信息

Research Direction, Instituto Nacional de Cardiología Ignacio Chávez, Juan Badiano No. 1, Col. Sección XVI, Mexico City 14080, Mexico.

Cardiovascular Line in American British Cowdray (ABC) Medical Center, PAI ABC Sur 136 No. 16, Col. Las Américas, Mexico City 01120, Mexico.

出版信息

Int J Mol Sci. 2025 Mar 27;26(7):3067. doi: 10.3390/ijms26073067.


DOI:10.3390/ijms26073067
PMID:40243722
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11989073/
Abstract

Marfan syndrome (MFS) is an inherited connective tissue disorder, with aortic root aneurysm and/or dissection being the most severe and life-threatening complication. These conditions have been linked to pathogenic variants in the gene and dysregulated signaling. Our objective was to evaluate the mRNA expression of , , , and in aortic tissue from MFS patients undergoing surgery for aortic dilation. This prospective study (2014-2023) included 20 MFS patients diagnosed according to the 2010 Ghent criteria, who underwent surgery for aneurysm or dissection based on Heart Team recommendations, along with 20 non-MFS controls. RNA was extracted, and mRNA levels were quantified using RT-qPCR. Patients with dissection showed significantly higher mRNA levels [79 (48.1-110.1)] compared to controls [37.2 (25.1-79)] ( = 0.03). Conversely, expression was significantly lower in MFS patients [12.17 (6.54-24.70)] than in controls [44.29 (25.85-85.36)] ( = 0.029). A positive correlation was observed between higher expression and a larger sinotubular junction diameter (r = 0.42, = 0.07), while increased expression was particularly evident in MFS patients with dissection. Additionally, expression showed an inverse correlation with ascending aortic diameter (r = 0.53, = 0.01). In aortic tissue, we found decreased and receptor levels alongside increased mRNA levels. These molecular alterations may reflect compensatory mechanisms in response to tissue damage caused by mechanical stress, leading to dysregulation of physiological signaling pathways and ultimately contributing to aortic dilation in MFS.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6644/11989073/9081d3359964/ijms-26-03067-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6644/11989073/4c852ae52da1/ijms-26-03067-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6644/11989073/9081d3359964/ijms-26-03067-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6644/11989073/4c852ae52da1/ijms-26-03067-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6644/11989073/9081d3359964/ijms-26-03067-g002.jpg

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Analysis of , , and mRNA as Key Molecular Mechanisms in the Damage of Aortic Aneurysm and Dissection in Marfan Syndrome.

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[1]
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[2]
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Front Cell Dev Biol. 2024-1-10

[3]
Animal Models, Pathogenesis, and Potential Treatment of Thoracic Aortic Aneurysm.

Int J Mol Sci. 2024-1-11

[4]
The usefulness of the genetic panel in the classification and refinement of diagnostic accuracy of Mexican patients with Marfan syndrome and other connective tissue disorders.

Biomol Biomed. 2024-3-11

[5]
Markers of extracellular matrix remodeling and systemic inflammation in patients with heritable thoracic aortic diseases.

Front Cardiovasc Med. 2022-12-20

[6]
Pathophysiology and Therapeutics of Thoracic Aortic Aneurysm in Marfan Syndrome.

Biomolecules. 2022-1-14

[7]
Neutrophils as Regulators and Biomarkers of Cardiovascular Inflammation in the Context of Abdominal Aortic Aneurysms.

Biomedicines. 2021-9-16

[8]
Novel contributions of neutrophils in the pathogenesis of abdominal aortic aneurysm, the role of neutrophil extracellular traps: A systematic review.

Thromb Res. 2020-10

[9]
Predictors of Abdominal Aortic Aneurysm Risks.

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[10]
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