Sex-related differences in histopathology and hormonal associations in ascending aortic aneurysms.

IF 4.3
European heart journal open Pub Date : 2026-06-26 eCollection Date: 2026-07-01 DOI:10.1093/ehjopen/oeag084
Tamara C Borsboom, Maximiliaan L Notenboom, Lambertus J Wisse, Kevin M Veen, Jonathan R G Etnel, Jolien W Roos-Hesselink, Johanna J M Takkenberg, Marie José T H Goumans, Marco C DeRuiter
{"title":"Sex-related differences in histopathology and hormonal associations in ascending aortic aneurysms.","authors":"Tamara C Borsboom, Maximiliaan L Notenboom, Lambertus J Wisse, Kevin M Veen, Jonathan R G Etnel, Jolien W Roos-Hesselink, Johanna J M Takkenberg, Marie José T H Goumans, Marco C DeRuiter","doi":"10.1093/ehjopen/oeag084","DOIUrl":null,"url":null,"abstract":"<p><strong>Aims: </strong>Sex-related differences in ascending aorta aneurysm (AscAA) pathology and the underlying mechanisms remain incompletely understood. In this study, sex-specific patterns of aortic media degeneration (MD) in idiopathic AscAA were investigated.</p><p><strong>Methods and results: </strong>Aortic tissue and blood samples were obtained from 32 patients undergoing elective AscAA resection (mean age 65.6 years, 25% women). Two donor aortas served as healthy controls. Tissues were evaluated using a modified consensus scoring system assessing elastin integrity, mucoid extracellular matrix accumulation (MEMA), smooth muscle cell organization, and collagen remodelling. Immunohistochemistry was used to quantify extracellular matrix and remodelling markers. Outcome parameters included aortic diameter, immunohistochemical profiling, MD scores, and sex hormone profiling. Absolute ascending aortic diameters did not differ between sexes. Women exhibited significantly more advanced and diffuse MD across all sampled locations, with higher total MD scores before and after adjustment for aortic size. This was attributed to increased elastin degradation, MEMA, and elevated local MMP2 expression, consistent with a degradative remodelling profile. In contrast, men displayed a more focal and inflammatory phenotype, characterized by increased MMP9, cKIT, and CD68 expression, and relatively thicker media. Circulating hormone levels were reduced in both sexes but were not directly associated with MD severity. However, female-specific decreases in DHEA and male-specific decreases in testosterone, AMH, and androstenedione were observed.</p><p><strong>Conclusion: </strong>This study reveals pronounced sex-specific differences in AscAA wall degeneration. Women demonstrate a structurally more vulnerable aortic wall at comparable dilatation, fuelling discussion for revision of female treatment plans.</p>","PeriodicalId":93995,"journal":{"name":"European heart journal open","volume":"6 4","pages":"oeag084"},"PeriodicalIF":4.3000,"publicationDate":"2026-06-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13373786/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"European heart journal open","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1093/ehjopen/oeag084","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/7/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Aims: Sex-related differences in ascending aorta aneurysm (AscAA) pathology and the underlying mechanisms remain incompletely understood. In this study, sex-specific patterns of aortic media degeneration (MD) in idiopathic AscAA were investigated.

Methods and results: Aortic tissue and blood samples were obtained from 32 patients undergoing elective AscAA resection (mean age 65.6 years, 25% women). Two donor aortas served as healthy controls. Tissues were evaluated using a modified consensus scoring system assessing elastin integrity, mucoid extracellular matrix accumulation (MEMA), smooth muscle cell organization, and collagen remodelling. Immunohistochemistry was used to quantify extracellular matrix and remodelling markers. Outcome parameters included aortic diameter, immunohistochemical profiling, MD scores, and sex hormone profiling. Absolute ascending aortic diameters did not differ between sexes. Women exhibited significantly more advanced and diffuse MD across all sampled locations, with higher total MD scores before and after adjustment for aortic size. This was attributed to increased elastin degradation, MEMA, and elevated local MMP2 expression, consistent with a degradative remodelling profile. In contrast, men displayed a more focal and inflammatory phenotype, characterized by increased MMP9, cKIT, and CD68 expression, and relatively thicker media. Circulating hormone levels were reduced in both sexes but were not directly associated with MD severity. However, female-specific decreases in DHEA and male-specific decreases in testosterone, AMH, and androstenedione were observed.

Conclusion: This study reveals pronounced sex-specific differences in AscAA wall degeneration. Women demonstrate a structurally more vulnerable aortic wall at comparable dilatation, fuelling discussion for revision of female treatment plans.

升主动脉瘤组织病理学和激素相关性的性别差异。
目的:升主动脉动脉瘤(AscAA)病理的性别相关差异及其潜在机制尚不完全清楚。在这项研究中,研究了特发性AscAA中主动脉介质变性(MD)的性别特异性模式。方法和结果:32例择期AscAA切除术患者的主动脉组织和血液样本(平均年龄65.6岁,25%为女性)。两条供体主动脉作为健康对照。使用改进的共识评分系统评估组织,评估弹性蛋白完整性、黏液细胞外基质积累(MEMA)、平滑肌细胞组织和胶原蛋白重塑。免疫组织化学用于量化细胞外基质和重塑标志物。结局参数包括主动脉直径、免疫组织化学谱、MD评分和性激素谱。升主动脉绝对直径在两性之间没有差异。女性在所有取样部位都表现出更严重的弥漫性MD,在主动脉尺寸调整前后的MD总分更高。这归因于弹性蛋白降解、MEMA和局部MMP2表达升高,与降解性重构特征一致。相比之下,男性表现出更多的局灶性和炎性表型,其特征是MMP9、cKIT和CD68表达增加,介质相对较厚。循环激素水平在两性中均有所降低,但与MD严重程度无直接关系。然而,观察到女性特异性的DHEA减少和男性特异性的睾酮,AMH和雄烯二酮减少。结论:本研究揭示了AscAA壁变性的显著性别差异。在类似的扩张下,女性表现出结构上更脆弱的主动脉壁,这引发了对女性治疗方案修订的讨论。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
2.80
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书