Sexual dimorphism in SMAD3 pathogenic variant-harbouring individuals.

IF 3.5 2区 医学 Q2 GENETICS & HEREDITY
Julie Richer, Joe Davis Velchev, Sharan Goobie, Christie A Boswell-Patterson, Ingrid M B H van de Laar, Judith M A Verhagen, Marja W Wessels, Jolien W Roos-Hesselink, Ilse Luyckx, Hussein Al-Amodi, Michael W A Chu, Anne-Marie Laberge, Bekim Sadikovic, Tugce Balci, Aline Verstraeten, Bart Loeys
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引用次数: 0

Abstract

Background: Individuals harbouring SMAD3 pathogenic variants are at risk for aneurysms/dissections throughout the arterial tree. Based on prior reports of sex differences in thoracic aortic aneurysm/dissection, we investigated the sexual dimorphism for vascular events in SMAD3-variant-harbouring patients.

Methods: We analysed two large pedigrees comprising 84 individuals segregating pathogenic missense variants affecting the same p.Arg287 residue in SMAD3. We excluded individuals<40 years without vascular involvement, as they were too young to be classified. Individuals were subcategorised according to sex, the presence or absence and localisation (aneurysm/dissection with or without involvement of the aortic root/ascending aorta) of vascular lesions. We complemented our familial patient cohort with 178 SMAD3 patients reported in the literature between 2011 and 2023.

Results: In our two pedigrees, 11/30 (37%) variant-harbouring females had no vascular involvement, whereas none of the variant-harboring males (n=23) had no vascular involvement (p=0.001). While the two groups did not differ by age, males were at higher risk of vascular complications (p=0.037), there was no age difference between sexes. Of the 19 females with vascular involvement, six (32%) had vascular involvment sparing the aortic root/ascending aorta, whereas of the 23 males with vascular invovlement, only one (4%) had vascular involvement sparing the aortic root/ascending aorta (p=0.034). In the literature, we identified 116 male and 62 female additional patients. In the combined cohort of 220 patients, we demonstrated an over-representation of males (p<0.001) and non-penetrance in females for vascular pathology involving the aortic root/ascending aorta (p=0.028).

Conclusions: Non-penetrance is more common in women, and normal echocardiography in at-risk females is not as reassuring for risk of vasculopathy in other locations. The higher non-penetrance in women creates an ascertainment bias and results in an over-representation of male patients in the literature.

携带SMAD3致病变异个体的两性二态性。
背景:携带SMAD3致病变异的个体在整个动脉树中都有动脉瘤/夹层的风险。基于先前关于胸主动脉瘤/夹层性别差异的报道,我们研究了smad3变异患者血管事件的性别二态性。方法:我们分析了两个包含84个个体的大型家系,分离了影响SMAD3中相同p.a g287残基的致病性错义变异体。我们排除了2011年至2023年文献中报道的smad3患者。结果:在我们的两个家系中,11/30(37%)携带变异的雌性没有血管受累,而携带变异的雄性(n=23)没有血管受累(p=0.001)。虽然两组没有年龄差异,男性血管并发症的风险更高(p=0.037),但性别之间没有年龄差异。19例血管受累的女性中,6例(32%)血管受累保留了主动脉根/升主动脉,而23例男性中,只有1例(4%)血管受累保留了主动脉根/升主动脉(p=0.034)。在文献中,我们确定了116名男性和62名女性患者。在220例患者的联合队列中,我们证明了男性的过度代表性(p结论:非外显性在女性中更常见,并且在高危女性中正常的超声心动图并不能保证其他部位的血管病变风险。女性较高的非外显率产生了一种确定偏差,导致男性患者在文献中的过度代表。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Medical Genetics
Journal of Medical Genetics 医学-遗传学
CiteScore
7.60
自引率
2.50%
发文量
92
审稿时长
4-8 weeks
期刊介绍: Journal of Medical Genetics is a leading international peer-reviewed journal covering original research in human genetics, including reviews of and opinion on the latest developments. Articles cover the molecular basis of human disease including germline cancer genetics, clinical manifestations of genetic disorders, applications of molecular genetics to medical practice and the systematic evaluation of such applications worldwide.
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