01 October 2012: Basic Research
Quantitative anatomy of the growing abdominal aorta in human fetuses: An anatomical, digital and statistical study
Michał Szpinda ABCDE , Anna Szpinda CDE , Alina Woźniak CD , Celestyna Mila-Kierzenkowska DF , Adam Kosiński D , Marek Grzybiak D
DOI: 10.12659/MSM.883483
Med Sci Monit 2012; 18(10): BR419-426
Background
The abdominal aorta (Figure 1), the continuation of the thoracic aorta, begins at the aortic hiatus of the diaphragm at the level of T12, descends within the retroperitoneal space, and terminates as the aortic bifurcation by dividing into the right and left common iliac arteries [1]. From a strictly anatomical point of view, an appropriate terminal branch of the aorta is the median sacral artery – more developed in mammals than in man, but more conspicuous in fetuses than in adults [2]. The aortic bifurcation most commonly occurs at the level of L4, and only rarely at the levels of L5, S1, or L2 [2, 3]. However, a low aortic bifurcation is much more common than a high division, in which case the abdominal aorta tends to be longer or shorter, respectively [4].
Advances in perinatal medicine require an extensive knowledge of fetal aorto-iliac morphological data [5,10]. The normative morphometric data of the abdominal aorta in human fetuses may be helpful as a reference for future Doppler studies in the prenatal diagnosis and monitoring of congenital aortic abnormalities (eg, aneurysms, hypoplasia, atresia, agenesis, and idiopathic infantile arterial calcification) that include discordant diameters of the aorta and its great branches [11–17]. Thus, it is important to define the normal growth patterns for the abdominal aorta as early as possible, especially if the existing data on this subject are limited. Theoretical models of aortic quantitative anatomy have meticulously focused only on the length and the external diameter of the abdominal aorta [18]. To date however, the abdominal aorta volume has not been reported in human fetuses or in adults.
In order to improve the knowledge of aortic morphometric parameters, our objectives for the present study were to determine:
Material and Methods
The examinations were carried out on 124 human fetuses of both sexes (60 males, 64 females), which had been derived in the years 1989–2001 from spontaneous abortions or stillbirths, as a result of placental insufficiency. The sample collection was terminated in 2001 because of the legal restriction on obtaining human fetuses that was introduced in Poland at that time. All the fetuses collected in our Department were Caucasian. Legal and ethical considerations were approved by the University Research Ethics Committee (KB/217/2006). On macroscopic examination, both internal and external anatomical malformations were ruled out in all included specimens, which were diagnosed as normal. The gestational age of the fetuses collected varied from 15 to 34 weeks (Table 1). We did not have fetuses at the age of 35–39 weeks of gestation at our disposal. The fetal ages of the specimens were calculated on the basis of 2 criteria: 1) gestational age based on measurements of the crown-rump length [19], and 2) known date of the beginning of the last maternal menstrual period. The correlation between the gestational age based on the crown-rump length and that calculated by the last menstruation attained the value R=0.98 (p<0.001) for the whole sample. For statistical analysis, the fetuses were divided into 6 monthly groups, related to the 4th–9th months of gestation.
The arterial bed was filled with white latex LBS 3060 through a Steri-Cath catheter (diameter of 0.5–1 mm), which was introduced by lumbar access into the abdominal aorta. The fetal arteries were filled under an automatically controlled pressure of 50–60 mm Hg, using a SEP 11S syringe infusion pump (Ascor S.A., Medical Equipment, Warsaw 2001). All specimens were immersed in 10% neutral buffered formalin solution for 4–24 months for preservation, and then dissected under 10-power magnification using a stereoscope with Huygens ocular. Each fetus was dissected to expose its abdominal aorta. The optical axis of the objective lens was oriented vertically to the abdominal aorta
For each fetus the following 4 parameters of the abdominal aorta were assessed:
In a continuous effort to minimize measurement and observer bias, all the measurements were performed by 1 researcher (M. Sz.). Each measurement was repeated 3 times under the same conditions but at a different time, and then averaged. The differences between the repeated measurements, as the intra-observer variation, were evaluated by the Wilcoxon signed-rank test. The length, proximal and distal external diameters, and volume of the abdominal aorta were correlated to fetal age in order to establish their growth patterns. The relative growth of the abdominal aorta was expressed as the length-to-proximal external diameter ratio. As the first step in the statistical analysis, Student’s t-test was used to examine the influence of sex on the values of the parameters studied. To test whether the different variables significantly changed with age, the one-way ANOVA test for unpaired data and post-hoc RIR Tukey test were used.
Linear and nonlinear regression analysis was used to derive the line of best fit for each morphometric feature of the abdominal aorta and gestational age. Coefficients of determination (R2) between the parameters and fetal age were estimated. Differences were considered significant at p<0.05.
Results
No significant differences were found in the evaluation of intra-observer reproducibility of the abdominal aorta measurements.
There were no significant differences in the 4 studied parameters of the abdominal aorta according to sex. Therefore, the statistical analysis of morphometric values has been summarized in Table 2, irrespective of sex. On the contrary, the growth curves of best fit for the plot for each parameter studied against gestational age were statistically significant (p<0.0001).
The values of the abdominal aorta length increased from 9.35±1.24 mm for the 4-month group to 36.29±4.98 mm for the 9-month group. With regard to fetal age in weeks, the length of the abdominal aorta (Figure 2) followed the first-degree polynomial (linear) function y=−14.596+1.519 × Age ±2.639 (R2=0.92).
The statistical analysis revealed significant differences between the proximal and distal external diameters of the abdominal aorta; the former was found to be greater than the latter (p<0.01). The proximal external diameter of the abdominal aorta varied from 1.18±0.25 to 5.19±0.49 mm for the groups of 4 and 9 months, respectively. The proximal external diameter was dependent on fetal age (Figure 3), given by the first-degree polynomial (linear) function y=−2.065+0.212 × Age ±0.348 (R2=0.92). The values for distal external diameter of the abdominal aorta increased from 1.03±0.23 to 4.92±0.46 mm for groups of fetuses at 4 and 9 months of gestation, respectively. The numerical data show that the distal external diameter of the abdominal aorta as a function of fetal age in weeks (Figure 4) was expressed by the first-degree polynomial (linear) regression y=−2.097+0.203 × Age ±0.351 (R2=0.92).
Both length and external diameters of the abdominal aorta were found to rise proportionately, because they had the same growth rate through the analyzed fetal ages. This fact is illustrated in Figure 5, in which the length-to-proximal external diameter ratio of the abdominal aorta, plotted against gestational age, was relatively stable according to the linear function y=7.724–0.017 × Age ±0.925.
The present study revealed that the volume of the abdominal aorta ranged from 9.6±4.5 to 740.5±201.8 mm3 for fetuses aged 4 and 9 months, respectively. The volumetric growth of the abdominal aorta (Figure 6) modeled the second-degree polynomial (quadratic) function y=911–101 × Age +2.838 × Age2 ±78 (R2=0.89).
Discussion
The present study constitutes the continuation of our previous morphometric studies on the normal evolution of the ascending aorta [22], aortic arch [23], and thoracic aorta [24], which provided both detailed normative ranges and growth patterns for these aortic segments during gestation. Because the existing data on the abdominal aorta have been precisely focused on its length and diameters only [18], the present study provides reference values and growth patterns for length, external diameters and volume of the abdominal aorta in human fetuses. The fetal sample could be considered as normal, because the aortas were not affected by:
In fact, the subjects might potentially have smaller aortic size due to placental insufficiency. However, they could not suffer from intrauterine growth retardation, because the correlation between the gestational age based on the crown-rump length and that calculated by the last menstruation reached the value R=0.98 (p<0.001) for the whole sample. The aortic root diameter was reported to remain normal in most cases of intra-uterine growth retardation [25]. The lack of such quantitative information in the medical literature concerning the abdominal aorta has limited discussion on this subject. Furthermore, neither tissue shrinkage related to neutral buffered formalin fixation nor the 50–60 mm Hg filling pressure significantly influenced the measurements of the abdominal aorta
All the parameters measured could be considered as exact and clearly definable. The aortic hiatus of the diaphragm is an oblique structure, dividing the aorta in an oblique manner, as it passed from the mediastinum into the retroperitoneal space. Consequently, the length on its anterior aspect was different from the length as measured on its posterior aspect. For this reason, the length was always measured on the anterior aspect of the abdominal aorta.
No significant male-female differences for any of the abdominal aorta parameters were revealed in our series, in keeping with previous studies concerning the remaining aortic segments in fetuses [21–24] and children [26]. In contrast to our study, in adolescents and adults, both the aortic length and diameters were found to be greater in males than females of the same age, and these differences even increased with advanced age [27]. On the other hand, according to Yahel and Arensburg [28], the abdominal aorta length was reported to be similar in both sexes, and constituted about 32.4–43.2% of the descending aorta length. According to the medical literature [29,30], the abdominal aorta length closely correlates with body length and stature.
Of note, in the present study several transformations were computed concerning either aortic length or diameter
Our findings indicate that during the study period the abdominal aorta length varied from 9.35±1.24 to 36.29±4.98 mm, given by the linear model y=−14.596+1.519 × Age ±2.639. Also, Özgüner and Sulak [18] reported the values of aortic length, showing a proportionate evolution with gestational age. According to these authors, the abdominal aorta length varied from 10.42±1.09 mm in the first trimester (9–12 weeks), through 17.55±3.8 mm in the second trimester (13–25 weeks), and 32.73±4.3 mm in the third trimester (26–37 weeks) to 42.91±1.9 mm in full-term fetuses (38–40 weeks). Thus, the regression equation for the abdominal aorta length, modeled as a linear function of gestational age in terms of weeks, was y=−5.254+1.207 × Age ±1.273. When comparing the 2 linear models, the expected growth velocity for length, expressed by the age coefficient, was more dynamic in the material under examination (1.519 mm per week) than in Özgüner and Sulak’s autopsy study (1.207 mm per week). Furthermore, Hirata [33] proved that during a 6–7-month period, the growth of the abdominal aorta length was more intensive than that of the ascending and thoracic aortas, whereas during a 7–8-month period proportions of each subdivision were stable.
In our sample, external diameter of the abdominal aorta decreased regularly from proximal to distal along its length, attributed to a decrease in flow volume as blood was supplied to abdominal organs [34,35]. In the material under examination, the proximal and distal external diameters of the abdominal aorta increased proportionately from 1.18±0.25 to 5.19±0.49 mm, and from 1.03±0.23 to 4.92±0.46 mm, respectively, with the lines of best fit as follows: y=−2.065+0.212 × Age ±0.348 and y=−2.097+0.203 × Age ±0.351. According to these models, external diameters of the abdominal aorta increased every week by 0.212 mm at its origin, and by 0.203 mm at its bifurcation. Özgüner and Sulak [18] reported that external diameters at the origin of the abdominal aorta in the following trimesters reached the following values: 1.20±0.2 mm, 2.85±0.7 mm and 5.77±0.8 mm, and in full-terms fetuses as much as 8.28±0.7 mm, being described by the linear regression y=−1.816+0.246 × Age ±0.306 (R=0.98). Furthermore, external diameters at the aortic bifurcation attained the following values: 1.12±0.2 mm, 2.37±0.6 mm, 4.50±0.4 mm and 6.26±0.66 mm, respectively, according to the linear model y=−1.026+0.179 × Age ±0.244 (R=0.97). Having compared regression coefficients, the growth dynamics presented by these authors were found to be faster in relation to the proximal external diameter (0.246 mm per week), and slower in relation to the distal external diameter (0.179 mm per week), than results obtained in the present study (ie, 0.212 and 0.203 mm per week, respectively).
In the material under examination, the distal external diameter of the abdominal aorta turned out to be very interesting when correlated with those of the common, external and internal iliac arteries, which had previously been studied in the same fetuses [4,36,37]. Although no laterality differences for external diameters within the whole group were observed, a strong trend towards greater external diameters was found on the right side: for the common (63.7%), external (71%), and internal (65.3%) iliac arteries. The external diameters of the internal iliac arteries were found to be nearly 50% greater than external diameters of the external iliac arteries. As predominant vessels, the internal iliac arteries supply pelvic organs, and then continue as the umbilical arteries to reach the placenta. Because fetal pelvic organs need more blood supply than the lower limbs, and the umbilical arteries are the direct continuation of the internal iliac arteries, the diameters of the internal iliac arteries are greater than those of the external iliac arteries [2,18,38,39].
As indicated in Figure 5, having correlated length of the abdominal aorta with its proximal external diameter, we found a proportionate evolution. Because these 2 parameters grew all the time at the same rhythm, the abdominal aorta length-to-proximal external diameter ratio was relatively stable, according to the linear function y=7.724–0.017 × Age ±0.925.
To date, data concerning the abdominal aorta volume during gestation has been scant in the quantitative anatomical medical literature. The abdominal aorta volume calculated from 2-D measurements using digital analysis is considered as precise and objective [21]. Of note, our results showed that the best fit correlation between the abdominal aorta volume and gestational age was the second-degree polynomial (quadratic) function y=911–101 × Age+2.838 × Age2 ±78. In our series, the abdominal aorta volume increased 77-fold from 9.6±4.5 to 740.5±201.8 mm3. To date however, there have been no comparative data in the medical literature concerning volume of the abdominal aorta.
Basing on our previous findings [22–24], we indicated that there was also observed a proportionate growth of the abdominal aorta in relation to the remaining aortic segments, as length and volume of the abdominal aorta were correlated to those of the ascending aorta, aortic arch, and thoracic aorta. The 4 following aortic segments (ie, the ascending aorta, aortic arch, thoracic aorta and abdominal aorta) increased in a proportionate fashion in relation to each other, being expressed as 5:7:22:16 for their lengths, and 4.8:6:15:9.6 for their volumes, respectively. The abdominal aorta length was responsible for 42.6–42.8% of the descending aorta length, closely corresponding with results obtained by Yahel and Arensburg [28]. The proportionate evolution of each aortic subdivision throughout gestation appeared to remain different from fetuses aged 6–7 months from Hirata’s autopsy study [33], the abdominal aortas of which grew more intensively.
Having presented the normal growth of the abdominal aorta during gestation, we would like to stress the importance of the measurements, because the reader should be provided with relevant data, so as to distinguish abnormal from normal fetal development. Nowadays, the advancing resolution capabilities of ultrasound devices lead to an increase in
To summarize, using the normograms, especially for external diameters, constructed in the present study, the severe congenital anomalies of the abdominal aorta can be detected, monitored and treated in the intrauterine or newborn periods. Although the volumetric growth is considered to be the most characteristic and valuable parameter of every dimensional arrangement of structures [21,41], abdominal aortic volume determination is not relevant in clinical and echographic settings, because echographists need to determine only the length and diameters of the abdominal aorta.
References
1. Standring S: Gray’s Anatomy The Anatomical Basis of Clinical Practice, 2008; 1086-89, Elsevier, Edinburgh
2. Gościcka D, Szpinda M, Stankiewicz W, Die Verzweigung der Aorta abdominalis bei menschlichen Feten: Ann Anat, 1995; 177; 549-52 [in German]
3. Kornreich L, Hadar H, Sulkes J, Effect of normal ageing on the sites of aortic bifurcation and inferior vena cava confluence: a CT study: Surg Radiol Anat, 1997; 20; 63-68, pmid: 9574492
4. Szpinda M, Szpinda A, WoŸniak A, The normal growth of the common iliac arteries in human fetuses – an anatomical, digital and statistical study: Med Sci Monit, 2012; 18(3); BR109-16, pmid: 22367120
5. Wojcicki P, Drozdowski P, In utero surgery – current state of the art: Part I: Med Sci Monit, 2010; 16(11); RA237-44, pmid: 20980970
6. Wójcicki P, Drozdowski P, Wójcicka K, In utero surgery – current state of the art: Part II: Med Sci Monit, 2011; 17(12); RA262-70, pmid: 22129913
7. Duczkowski M, Duczkowska A, Bekiesinska-Figatowska M, The imaging features of selected congenital tumors – own material and literature review: Med Sci Monit, 2010; 16(Suppl 1); 52-59
8. Niedzielski J, Congenital anomalies associated with anorectal malformations -16-year experience of one surgeon: Arch Med Sci, 2009; 5(4); 596-601
9. Koplay M, Kantarci M, Common hepatic artery arising from the aorta – demonstration with multidetector CT angiography and its clinical importance: Arch Med Sci, 2011; 7(1); 176-77, pmid: 22291754
10. Achiron R, Zimand S, Hegesh J, Fetal aortic arch measurements between 14 and 38 weeks’ gestation: in utero ultrasonographic study: Ultrasound Obstet Gynecol, 2000; 15; 226-30, pmid: 10846779
11. Stanley JC, Graham LM, Abdominal aortic coarctation and hypoplasia: Surgery of the aorta and its branches, 2000; 11-16, Philadelphia, Saunders
12. de Albuquerque FJ, Coutinho C, Castro Netto EC, Infra-renal abdominal aorta agenesis: a case report with emphasis on MR angiography findings: BJR, 2008; 81; 179-83
13. Kim JI, Lee W, Kim SJ, Primary congenital abdominal aortic aneurysm: a case report with perinatal serial follow-up imaging: Pediatr Radiol, 2008; 38; 1249-52, pmid: 18679609
14. Nasrallah FK, Baho H, Sallout A, Prenatal diagnosis of idiopathic infantile arterial calcification with hydrops fetalis: Ultrasound Obstet Gynecol, 2009; 34; 601-4, pmid: 19813208
15. Kimura-Hayama ET, Meléndez G, Mendizábal AL, Uncommon Congenital and Acquired Aortic Diseases: Role of Multidetector CT Angiography: RadioGraphics, 2010; 30; 79-98, pmid: 20083587
16. Brown J, Shehata BM, Campbell R, Atresia of abdominal aorta in neonate with recanalization and development of normal aortic architecture: case report and review of literature: Congenit Heart Dis, 2011; 6(3); 280-83, pmid: 21410650
17. Orun U, Bilici M, Yilmaz O, Aortic Coarctation with Down syndrome: Med Sci Monit, 2011; 17(1); LE1, pmid: 21169915
18. Özgüner G, Sulak O, Development of the abdominal aorta and iliac arteries during the fetal period: a morphometric study: Surg Radiol Anat, 2011; 33; 35-43, pmid: 20623285
19. Iffy L, Jakobovits A, Westlake W: Pediatrics, 1975; 56; 173-86, pmid: 1161367
20. Szpinda M, Szwesta A, Szpinda E, Morphometric study of the ductus arteriosus during human development: Ann Anat, 2007; 189; 47-52, pmid: 17319608
21. Szpinda M, Morphometric study of the great arteries of the thorax in human fetuses (in Polish): Habilitation thesis, 2006; 1-143, Bydgoszcz, CM UMK
22. Szpinda M, Morphometric study of the ascending aorta in human fetuses: Ann Anat, 2007; 189; 465-72, pmid: 17910400
23. Szpinda M, Daroszewski M, Quantitative analysis of the aortic arch in human fetuses: Medical and Biological Sciences, 2009; 23; 97-102
24. Szpinda M, The normal growth of the thoracic aorta in human foetuses: Folia Morphol, 2007; 66; 131-37
25. Cartier MS, Doubilet PM, Fetal aortic and pulmonary artery diameters: sonographic measurements in growth-retarded fetuses: Am J Roentgenol, 1988; 151; 991-93, pmid: 3051966
26. Poutanen T, Tikanoja T, Sairanen H, Normal aortic dimensions and flow in 168 children and young adults: Clin Physiol Funct Imaging, 2003; 23; 224-29, pmid: 12914562
27. Dixon AK, Lawrence JP, Mitchell JRA, Age-related changes in the abdominal aorta shown by CT: Clin Radiol, 1984; 35; 33-37, pmid: 6690178
28. Yahel J, Arensburg B, The topographic relationships of the unpaired visceral branches of the aorta: Clin Anat, 1998; 11; 304-09, pmid: 9725573
29. Pennington N, Soames RW, The anterior visceral branches of the abdominal aorta and their relationship to the renal arteries: Surg Radiol Anat, 2005; 27; 395-403, pmid: 16177834
30. Panagouli E, Lolis E, Venieratos D, A morphometric study concerning the branching points of the main arteries in humans: relationships and correlations: Ann Anat, 2011; 193; 86-99, pmid: 21169000
31. Hyett J, Moscoso G, Nicolaides K, Morphometric analysis of the great vessels in early fetal life: Hum Reprod, 1995; 10; 3045-48, pmid: 8747069
32. van Meurs-van Woezik H, Krediet P, Measurements of the descending aorta in infants and children: comparison with other aortic dimensions: J Anat, 1982; 135; 273-79, pmid: 7174502
33. Hirata K, A metrical study of the aorta and main aortic branches in the human fetus: Nippon Ika Daigaku Zasshi, 1989; 56; 584-91, pmid: 2606949
34. Pearce WH, Slaughter MS, LeMaire S, Aortic diameter as a function of age, gender and body surface area: Surgery, 1993; 114; 691-97, pmid: 8211683
35. Fleischmann D, Hastie TJ, Danneger FC, Quantitative determination of age-related geometric changes in the normal abdominal aorta: J Vasc Surg, 2001; 33; 97-105, pmid: 11137929
36. Szpinda M, Szpinda A, Dombek M, External Diameters of the Abdominal Aorta and Iliac Arteries in Human Fetuses: Adv Clin Exp Med, 2011; 20(6); 691-98
37. Szpinda M, Szpinda A, Normative Growth Data for the External Diameters of the External and Internal Iliac Arteries in Human Fetuses – an Anatomical, Digital and Statistical Study: Adv Clin Exp Med, 2012; 21(2); 143-50, pmid: 23214278
38. Osada T, Nagata H, Murase N, Hemodynamic relationships among upper-abdominal aorta and femoral arteries: Basis for measurement of arterial blood flow to abdominal-pelvic organs: Med Sci Monit, 2009; 15(7); CR332-40, pmid: 19564822
39. Osada T, Nagata H, Murase N, Determination of comprehensive arterial blood inflow in abdominal-pelvic organs: Impact of respiration and posture on organ perfusion: Med Sci Monit, 2011; 17(2); CR57-66, pmid: 21278689
40. Mendeloff J, Stallion A, Hutton M, Aortic aneurysm resulting from umbilical artery catheterization: case report, literature review, and management algorithm: J Vasc Surg, 2001; 33; 419-24, pmid: 11174798
41. Gundersen HJ, Bendtsen TF, Korbo L, Some new, simple and efficient stereological methods and their use in pathological research and diagnosis: APMIS, 1988; 96; 379-94, pmid: 3288247
In Press
Clinical Research
Institutional and Regional Variations in Access to Clinical Trials and Next-Generation Sequencing in Turkis...Med Sci Monit In Press; DOI: 10.12659/MSM.951027
Clinical Research
Low-Intensity Blood Flow-Restricted Multi-Joint Exercise Improves Muscle Function in Patients With Patellof...Med Sci Monit In Press; DOI: 10.12659/MSM.950516
Review article
Musculoskeletal Ultrasound and MRI in the Evaluation of Chemotherapy-Induced Peripheral Neuropathy: A ReviewMed Sci Monit In Press; DOI: 10.12659/MSM.951283
Clinical Research
Sensory Processing, Dissociation, and Affective Symptoms in Misophonia: A Cross-Sectional Study of 35 AdultsMed Sci Monit In Press; DOI: 10.12659/MSM.950938
Most Viewed Current Articles
17 Jan 2024 : Review article 10,187,196
Vaccination Guidelines for Pregnant Women: Addressing COVID-19 and the Omicron VariantDOI :10.12659/MSM.942799
Med Sci Monit 2024; 30:e942799
13 Nov 2021 : Clinical Research 3,708,487
Acceptance of COVID-19 Vaccination and Its Associated Factors Among Cancer Patients Attending the Oncology ...DOI :10.12659/MSM.932788
Med Sci Monit 2021; 27:e932788
14 Dec 2022 : Clinical Research 2,341,643
Prevalence and Variability of Allergen-Specific Immunoglobulin E in Patients with Elevated Tryptase LevelsDOI :10.12659/MSM.937990
Med Sci Monit 2022; 28:e937990
16 May 2023 : Clinical Research 706,524
Electrophysiological Testing for an Auditory Processing Disorder and Reading Performance in 54 School Stude...DOI :10.12659/MSM.940387
Med Sci Monit 2023; 29:e940387






