CORRELATION BETWEEN ASCENDING AORTA, PULMONARY TRUNK, AND BRACHIOCEPHALIC TRUNK DIAMETERS DURING FETAL DEVELOPMENT
DOI:
https://doi.org/10.36557/2674-8169.2026v8n2p146-165Keywords:
Vascular Biometry, Fetal development, Aortic Arch, Innominate Artery, Neonatal Diseases and Abnormalities, Ascending Aorta, Brachiocephalic Trunk, External DiameterAbstract
Introduction: Vascular morphometry plays a key role in diagnosing congenital pathologies and supporting clinical management. Although the diameters of great vessels in adults are well-established, with influences from factors such as age and sex, there remains a gap in the literature regarding their development in fetuses. In particular, the relationship between the diameters of the ascending aorta (AA), pulmonary trunk (PT), and brachiocephalic trunk (BCT) with gestational age and sex, as well as the onset of sexual dimorphism throughout development, remains underexplored. Objective: To investigate the correlation between the diameters of the AA, PT, and BCT with gestational age and sex in human fetuses. Methodology: Thirty-five fetal cadavers (18 male, 17 female), collected between 2012 and 2020 at the Human Anatomy Laboratory of UFS, were analyzed following ethical approval and exclusion of cardiovascular malformations. Gestational age was determined using the hallux-to-calcaneus length method. External diameters of the AA, PT, and BCT were measured with a digital caliper. Data were analyzed using Spearman’s correlation coefficient to assess associations with gestational age and Student’s t test to compare differences between sexes. Results: Strong positive correlations were found between gestational age and the diameters of the AA (ρ = 0.710), PT (ρ = 0.701), and BCT (ρ = 0.828) (p < 0.001 for all), confirming consistent growth throughout fetal development. No significant differences were found between males and females (p > 0.05). Conclusion: This study provides normative fetal data for the AA, PT, and BCT, demonstrating that vessel diameters increase proportionally with gestational age. The absence of sexual dimorphism in the fetal period suggests that postnatal hormonal and environmental factors may contribute to vascular size differences observed later in life. These findings provide clinically relevant reference values for prenatal diagnosis of vascular abnormalities. In addition, enhance understanding of vascular development.
Downloads
References
Ilbawi AM, Spicer DE, Bharati S, Cook A, Anderson RH. Morphologic study of the ascending aorta and aortic arch in hypoplastic left hearts: surgical implications. J Thorac Cardiovasc Surg. 2007 Jul;134(1):99-105. doi: 10.1016/j.jtcvs.2007.01.070.
Sievers HH, Charitos EI. Ascending Aorta Diameters: Normal, Abnormal, or Pathologic? Ann Thorac Surg. 2016 Jun;101(6):2430-1. doi: 10.1016/j.athoracsur.2015.12.021.
Jappar IA, Koh AS, Gao F, Tan RS, Teo LLY, Tan YH, Koh WP, Ewe SH. Distribution and Determinants of Proximal Ascending Aorta Dimensions Among Asian Adults. JACC Asia. 2022 Feb 15;2(1):116-118. doi: 10.1016/j.jacasi.2021.11.012.
Rogers IS, Massaro JM, Truong QA, Mahabadi AA, Kriegel MF, Fox CS, Thanassoulis G, Isselbacher EM, Hoffmann U, O'Donnell CJ. Distribution, determinants, and normal reference values of thoracic and abdominal aortic diameters by computed tomography (from the Framingham Heart Study). Am J Cardiol. 2013 May 15;111(10):1510-6. doi: 10.1016/j.amjcard.2013.01.306.
Kaplan S, Aronow WS, Ahn C, Lai H, DeLuca AJ, Weiss MB, Dilmanian H, Spielvogel D, Lansman SL, Belkin RN. Prevalence of an increased ascending thoracic aorta diameter diagnosed by two-dimensional echocardiography versus 64-multislice cardiac computed tomography. Am J Cardiol. 2008 Jan 1;101(1):119-21. doi: 10.1016/j.amjcard.2007.07.081.
Shen Y, Wan C, Tian P, Wu Y, Li X, Yang T, An J, Wang T, Chen L, Wen F. CT-base pulmonary artery measurement in the detection of pulmonary hypertension: a meta-analysis and systematic review. Medicine (Baltimore). 2014 Dec;93(27):e256. doi: 10.1097/MD.0000000000000256.
Edwards PD, Bull RK, Coulden R. CT measurement of main pulmonary artery diameter. Br J Radiol. 1998 Oct;71(850):1018-20. doi: 10.1259/bjr.71.850.10211060.
Ring NJ, Marshall AJ. Idiopathic dilatation of the pulmonary artery. Br J Radiol. 2002 Jun;75(894):532-5. doi: 10.1259/bjr.75.894.750532.
Wittram C. The normal main pulmonary artery diameter. Br J Radiol. 2003 Jan;76(901):79; author reply 79. doi: 10.1259/bjr/53914377.
Sarıkaya Y, Arslan S, Taydaş O, Erarslan Y, Arıyürek OM. Axial pulmonary trunk diameter variations during the cardiac cycle. Surg Radiol Anat. 2020 Nov;42(11):1279-1285. doi: 10.1007/s00276-020-02493-9.
Xiao F, Liang CY, Chen WH, Li M, Tao XC, Chen H, Chen JY. Pulmonary arterial stent for pulmonary trunk stenosis after size-mismatched lung transplantation. Chin Med J (Engl). 2019 May 20;132(10):1247-1249. doi: 10.1097/CM9.0000000000000209.
Thijssen CGE, Mutluer FO, van der Toorn JE, Bons LR, Gökalp AL, Takkenberg JJ, Mokhles MM, van Kimmenade RRJ, Vernooij MW, van der Lugt A, Budde RPJ, Roos-Hesselink JW, Kavousi M, Bos D. Longitudinal changes of thoracic aortic diameters in the general population aged 55 years or older. Heart. 2022 Apr 28:heartjnl-2021-320574. doi: 10.1136/heartjnl-2021-320574.
Williams MC. Sex-based Differences in Outcomes Related to Thoracic Aorta Dimensions. Radiology. 2022 Jul;304(1):216-217. doi: 10.1148/radiol.220402.
Szpinda M. Morphometric study of the ascending aorta in human fetuses. Ann Anat. 2007a;189(5):465-72. doi: 10.1016/j.aanat.2007.01.007.
Szpinda M. The normal growth of the pulmonary trunk in human foetuses. Folia Morphol (Warsz). 2007b May;66(2):126-30.
Szpinda M. External diameters of the pulmonary arteries in human foetuses: an anatomical, digital and statistical study. Folia Morphol (Warsz). 2008 Nov;67(4):240-4.
Aragão JA, et al. Morphometric Analysis of Brachiocephalic Trunk in Brazilian Cadavers of Human Foetuses. Int J Anat Radiol Surg. 2022 Apr, Vol-11(2): AO15-AO17
Goldstein I, Reece EA, Hobbins JC. Sonographic appearance of the fetal heel ossification centers and foot length measurements provide independent markers for gestational age estimation. Am J Obstet Gynecol. 1988;159(4):923-26. doi: 10.1016/s0002-9378(88)80172-8.
Royston JP. Some techniques for assessing multivariate normality based on the Shapiro-Wilk W. J R Stat Soc C Appl Stat. 1983;32(2):121–33.
Alsaqr AM. Remarks on the use of Pearson’s and Spearman’s correlation coefficients in assessing relationships in ophthalmic data. Afr Vis Eye Health. 2021;80(1):10.
Kim TK. T test as a parametric statistic. Korean J Anesthesiol. 2015 Dec;68(6):540-6. doi: 10.4097/kjae.2015.68.6.540.
The jamovi project. jamovi (Version 2.6) [Computer Software]. 2025. Available from: https://www.jamovi.org
Szpinda M. The normal growth of the thoracic aorta in human foetuses. Folia Morphol (Warsz). 2007c May;66(2):131-7.
Smolich JJ, Mynard JP, Penny DJ. Pulmonary trunk, ductus arteriosus, and pulmonary arterial phasic blood flow interactions during systole and diastole in the fetus. J Appl Physiol (1985). 2011 May;110(5):1362-73. doi: 10.1152/japplphysiol.00038.2011.
Downloads
Published
How to Cite
Issue
Section
License
Copyright (c) 2026 José Aderval Aragão, Felipe Matheus Sant’Anna Aragão, Iapunira Catarina Sant’Anna Aragão, Marcelo Lucas de Lima Prado, Bárbara Costa Lourenço, Vera Lúcia Correa Feitosa, Francisco Prado Reis, Deise Maria Furtado de Mendonça, Danilo Ribeiro Guerra

This work is licensed under a Creative Commons Attribution 4.0 International License.
Authors are copyright holders under a CCBY 4.0 license.



