Distinct patterns of vascular failure in COL1A1-associated osteogenesis imperfecta and FBN1-associated Marfan syndrome

Introduction Heritable connective tissue disorders are an important cause of aortic disease; however, the mechanisms of vascular failure in genetically defined aortopathies remain incompletely understood. Methods We analyzed the clinical course, imaging findings, and histopathologic features of two patients with clinically and genetically characterized connective tissue disorders: COL1A1-associated osteogenesis imperfecta and FBN1-associated Marfan syndrome. Results The COL1A1-associated patient developed multilevel arterial complications, including aortic regurgitation requiring aortic valve replacement at age 36, rupture of a dissected right common iliac artery in the same year, chronic type A aortic dissection requiring root, ascending, and arch replacement at age 54, and rupture of the infrarenal abdominal aorta at a diameter of only 30 mm. The FBN1-associated patient presented with type B aortic dissection at age 34 and subsequently developed progressive aneurysmal disease requiring staged thoracoabdominal replacement, total arch replacement for acute type A dissection, and aortic root replacement, followed by multiple peripheral vascular reconstructions. Histopathologic examination demonstrated valvular myxomatous degeneration in both cases. The aortic wall in both patients showed medial degeneration with fragmentation of elastic fibers. In addition, the COL1A1-associated patient demonstrated abdominal aortic wall thinning, with a minimum thickness of 1.25 mm. Conclusions These two patients exhibited contrasting longitudinal vascular courses despite some overlapping histopathologic findings. The COL1A1-associated OI patient experienced rupture of a dissected infrarenal aortic segment, whereas the FBN1-associated Marfan patient experienced repeated dissections followed by progressive vascular dilatation and multiple surgical reconstructions. These observations are descriptive and do not establish genotype-specific patterns or mechanisms of vascular failure.

Authors

Institutions

Publication Details

Journal
Frontiers in Cardiovascular Medicine
Published
2026-10-27
DOI
https://doi.org/10.3389/fcvm.2026.1922704
Primary Topic
Connective tissue disorders research
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Distinct patterns of vascular failure in COL1A1-associated osteogenesis imperfecta and FBN1-associated Marfan syndrome

Toru Ikezoe, Sachito Minegishi, Hidehito Endo, Tomohiro Iwakura et al.
Frontiers in Cardiovascular Medicine
Connective tissue disorders research
article

Distinct patterns of vascular failure in COL1A1-associated osteogenesis imperfecta and FBN1-associated Marfan syndrome

Toru Ikezoe, Sachito Minegishi, Hidehito Endo, Tomohiro Iwakura, Hiroshi Kubota, Yusuke Inaba, Masaru Kimura, Yaeko Ichikawa, Toshihiko Isaji, Hiroshi Tsuchiya, Yu Takahashi, Yutaka Hosoi, Masao Nunokawa, Kouta Kogure
article en

Abstract

Introduction Heritable connective tissue disorders are an important cause of aortic disease; however, the mechanisms of vascular failure in genetically defined aortopathies remain incompletely understood. Methods We analyzed the clinical course, imaging findings, and histopathologic features of two patients with clinically and genetically characterized connective tissue disorders: COL1A1-associated osteogenesis imperfecta and FBN1-associated Marfan syndrome. Results The COL1A1-associated patient developed multilevel arterial complications, including aortic regurgitation requiring aortic valve replacement at age 36, rupture of a dissected right common iliac artery in the same year, chronic type A aortic dissection requiring root, ascending, and arch replacement at age 54, and rupture of the infrarenal abdominal aorta at a diameter of only 30 mm. The FBN1-associated patient presented with type B aortic dissection at age 34 and subsequently developed progressive aneurysmal disease requiring staged thoracoabdominal replacement, total arch replacement for acute type A dissection, and aortic root replacement, followed by multiple peripheral vascular reconstructions. Histopathologic examination demonstrated valvular myxomatous degeneration in both cases. The aortic wall in both patients showed medial degeneration with fragmentation of elastic fibers. In addition, the COL1A1-associated patient demonstrated abdominal aortic wall thinning, with a minimum thickness of 1.25 mm. Conclusions These two patients exhibited contrasting longitudinal vascular courses despite some overlapping histopathologic findings. The COL1A1-associated OI patient experienced rupture of a dissected infrarenal aortic segment, whereas the FBN1-associated Marfan patient experienced repeated dissections followed by progressive vascular dilatation and multiple surgical reconstructions. These observations are descriptive and do not establish genotype-specific patterns or mechanisms of vascular failure.

Frontiers in Cardiovascular MedicineVol. 13
Kyorin University (JP), Sakakibara Hospital (JP)
Good health and well-being
Openalex Percentile: Top 15%
Connective tissue disorders research
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Laika access coming soon