Introduction

The traditional concept for the renal arterial blood supply describes one renal artery originating from the abdominal aorta at the level of L1–L2 vertebrae and entering the kidney at the hilum where it divides into presegmental and segmental branches [25]. However, kidneys are well known to show a diverse spectrum of variations in their vascular system. The variations in the renal arterial vasculature are attributed to the failure of one or several of the multiple renal arteries present during the embryologic development of the kidney to regress [1].

Renal vasculature variants have long captivated the interest of anatomists. Knowledge of these variations is essential in the modern era of medicine with the advances of minimally invasive surgery, renal transplantation and endovascular procedures. Therefore, careful evaluation is crucial before initiating treatment. Multidetector computed tomography angiography (MDCTA) is non-invasive, quick, widely available and less expensive compared to magnetic resonance angiography and replaces digital subtraction angiography. A retrospective comparative study of 2,144 living kidney donors found that the sensitivity, specificity and diagnostic accuracy of CTA to detect renal arterial variations is 100%, 97.48% and 97.9%, respectively, compared to intraoperative findings [23].

Renal arterial vascular variations have been studied among diverse population groups. There are great discrepancies in the literature with respect to the prevalence of renal artery variants with frequencies ranging between 4 and 61.5% [12, 21]. The differences vary among nationalities and within the same population groups [4, 20]. However, data on their prevalence in the Bulgarian population is currently lacking. Therefore, the purpose of this study was to conduct a comprehensive analysis of normal renal arterial vasculature and the prevalence of different anatomic variations.

Material and methods

This is a retrospective study with an initial cohort consisting of 610 patients who underwent CTA of the abdomen for various indications for the period January 2016–December 2021 in Prof. Dr. Alexander Chirkov University Hospital in Sofia, Bulgaria. The hospital is a major referral center for cardio-vascular diseases in Bulgaria, and therefore, the results should serve as an adequate representation of the vasculature variations in the general Bulgarian population. Informed consent and ethical approval were waived by local ethics due to the retrospective nature of the study.

The CT protocol included multiphase imaging or angiography phase only based on the study requirements. The scans were performed on a 320-slice Aquilion One CT scanner (Cannon Medical Systems). The scanning parameters were as follows: tube voltage: 100–120 kV, automatic milliamperage setting, slice thickness: 0.5 mm, tube rotation time 0.5 s. A volume of 90-110 ml non-ionic iodine contrast medium was administered with an automatic injector in an antecubital vein at a rate of 4–4.5 mL/s, followed by 30 ml saline. Bolus tracking technique was employed to determine the scan start time. Region of interest was placed in the descending thoracic aorta. Image acquisition in the arterial phase began after a 10–15 s delay when the enhancement at the region of interest reached 180 HU. The image analysis was performed on dedicated Vitrea workstations (Cannon Medical Systems). Interpretation included primary axial images followed by multiplanar (MPR), maximum intensity projection (MIP) and volume rendering (VR) reconstruction techniques.

The following exclusion criteria were applied to the initial cohort: (1) surgical interventions, or pathologic conditions that distorted the normal renal vascular anatomy, (2) CT studies done in other hospitals, and (3) studies with technically insufficient quality of the arterial phase scans. In addition, duplicate studies of patients with multiple exams were also excluded. Finally, after excluding the aforementioned groups, the remaining 561 patients were included in the study.

Classification

Normal anatomy was present when each kidney was supplied by one renal artery, originating from the aorta and dividing into segmental branches at the hilum. In the case of multiple renal arteries, the vessel with the biggest diameter was considered as main and the rest as “accessory.” Accessory renal arteries were further categorized on the basis of their point of entry into the kidney. Arteries with an entry point in the hilum were classified as “hilar.” Arteries entering the kidney parenchyma at the superior and inferior pole were described as superior and inferior polar arteries, respectively. To evaluate the level of origin of main renal arteries and ARA from the aorta, the place of each artery`s ostium was noted according to the vertebral body or intervertebral disk level. In case an artery originated from another vessel, the specific origin artery was reported. Any vessel that branched within 2 cm from the origin was classified as having “early division.” Data were categorized based on laterality, gender and symmetry. The final criterion of classification was based on the retro- or precaval course observed in both the right main renal artery and ARA.

Statistical analysis

The occurrence of each of the previously classified variables was recorded in a Microsoft Excel spreadsheet. Descriptive and comparative statistical analyses were performed on the data using SPSS, Version 20.0 software pack. The mean, standard deviation, minimum, maximum and percentage occurrence of the above categories was recorded. Comparisons between variations on the basis of laterality, gender and symmetry were carried out using chi-square test. Statistical significance was reached when p < 0.05.

Results

The mean age of the patients was 63.7 ± 16.2 years, range 19–90 years and the majority were male (58.6%). Only 260 patients (46.3%) had one renal artery with hilar bifurcation on both sides (Fig. 1). Anatomic variations in renal arterial vasculature were found in the remaining 301 patients (53.7%). The most common variation was the presence of ARA, discovered in 41.2% of the subjects (n = 231). Findings for laterality revealed that 24.2% (n = 136) of the right-sided kidneys and 25.5% (n = 143) of the left-sided kidneys were supplied by more than one renal artery. Statistical significance between these rates was not established (p = 0.684). The distribution in the number of ARA on both sides is presented on Table 1. Bilateral ARA were discovered in 8.55% of the patients (n = 48), the most common pattern was one 1 ARA on both sides- in 6.24% (n = 35) (Fig. 2). Two ARA on both sides were present in 1 patient (0.18%) who had a horseshoe kidney as a concomitant congenital kidney anomaly (Fig. 3). Seven renal arteries were discovered in one patient (0.2% of the cohort)—the patient had three ARA on the right side and two on the left side (Fig. 4). The difference in the number of ARA according to gender did not reach statistical significance on either side (p = 0.138). In males ARA was found in 25.5% on the right side and in 28.1% on the left side while the occurrence in females was, respectively, 22.4% on the right side and 22.0% on the left side.

Fig. 1
figure 1

MDCTA VR reconstruction shows normal renal anatomy- each kidney is supplied by one renal artery, originating from the aorta and dividing into segmental branches at the hilum

Table 1 Distribution of accessory renal arteries according to laterality
Fig. 2
figure 2

a MDCTA VR reconstruction shows the right main renal artery originating from the aorta at the level of L1-L2 intervertebral disk. The ostium of the left main renal artery is located at the level of the superior third of L2 vertebral body. There is one inferior polar accessory renal artery on each side, originating at the level of L3. b Axial MIP reconstruction shows precaval course of the right accessory renal artery

Fig. 3
figure 3

a MDCTA VR reconstruction shows a patient with an abdominal aortic aneurysm. Horseshoe kidney was discovered on the CTA as an incidental finding. The right and left main renal arteries originate below and at the level of the aneurysm, respectively. The patient has two accessory renal artery on each side. b Axial CTA image presents the position of the horseshoe kidney in front of the infrarenal aortic aneurysm

Fig. 4
figure 4

MDCTA VR reconstruction of a patient with seven renal arteries- four on the right side and three on the left side

In regard to the entry point in the kidney, hilar ARA were significantly more common than both superior and inferior polar ARA on either side (p < 0.001) (Figs. 2, 5, 6). Table 2 depicts the distribution of ARA according to their entry point.

Fig. 5
figure 5

MDCTA VR reconstruction shows the presence of a superior polar accessory renal artery on the left side, originating above the left main renal artery

Fig. 6
figure 6

MDCTA VR reconstruction shows two hilar accessory renal artery on the right side. One hilar accessory renal artery and early division of the main renal artery on the left side (asterisk)

Table 2 Distribution of accessory renal arteries according to the entry point in the kidney

The level of origin of the main renal arteries and ARA from the aorta ranged between Th12-L1 intervertebral disk and L5 vertebral body. The right main renal artery originated between the upper margin of the L1 vertebral body and the lower margin of L2 vertebral body in 97% of the patients and the left one- in 96.8% of the patients, with the most common levels being the L1 and L2 vertebral bodies, respectively (35.1% and 38.3%). The right main renal artery showed a higher ostium position in comparison to the left. ARA exhibited greater variability of origin location with 71.8% of right-sided ARA and 74.6% of left-sided ARA arising between the upper margin of L1 and the lower margin of L2. Three main renal arteries and eleven ARA arose from an aortic branch vessel- the common iliac arteries, internal iliac artery and from a common trunk with the median sacral artery. The distribution of the origin level of the main renal arteries and ARA is presented in Table 3.

Table 3 Distribution of origin levels of main and accessory renal arteries

Early branching was described in 21.7% (n = 122) of the patients. ED was noted in 72 (12.8%) of the right-sided kidneys and 50 (8.9%) of the left-sided kidneys and a significant difference was determined (p = 0.035) (Fig. 6). Bilateral ED occurred in 11 patients (1.9%). The rates of ED were similar between males (21.3%) and females (21.5%) and statistical significance was not established (p = 0.292).

One right main renal artery and seven right ARA originated from the common iliac arteries and did not cross the inferior vena cava. The remaining 560 right main renal arteries and 149 right ARA had a retro- or precaval course. In total 49 (6.9%) of all right renal arteries had a precaval disposition. Three main renal arteries (0.5% of all right main renal vessels) and 46 ARA (30.8% of right ARA) had a precaval course. This anatomic variant was significantly more common in ARA in comparison to the main vessels (p < 0.001) (Fig. 2).

Discussion

The clinical importance of arterial variations is both medical and surgical. Renal arteries are end arteries without anastomotic connections, therefore their involvement by different pathological conditions such as atherosclerosis, fibromuscular dysplasia, dissection may lead to ischemic nephropathy and functional deterioration. There is no consensus among practitioners on the role of ARA in the pathogenesis of arterial hypertension... Due to their small caliber, lower perfusion pressure and atherosclerotic changes, there is an association between the activation of the renin-angiotensin system and hypertension [15, 17]. Some researchers consider them a factor for diminished response in radiofrequency renal denervation [30].

From a surgical perspective, it is well known that crossing inferior polar ARA is an etiological factor for extrinsic ureteropelvic junction compression and hydronephrosis in children with a reported incidence of 11–25% [5, 13]. With the advances in laparoscopic and robot-assisted surgery, vascular preoperative evaluation is essential for the planning of a number of abdominal and pelvic surgical interventions, thus, lowering the risk of iatrogenic injury [31]. Although ARA are an undesirable factor in transplantation and are associated with a higher rate of complications, recent studies report similar short and long-term outcomes in multiple and single renal artery grafts [9, 33]. Furthermore, it is important to report ED because sufficient arterial length is needed to ensure safe vascular anastomosis.

Presence of ARA and their origin location is also important during surgical or endovascular treatment of abdominal aortic aneurysms. Although data is inconsistent, some researchers report a higher incidence of acute kidney injury and long-term worsening of renal function after the sealing of ARA [28].

There are big differences in the occurrence of anatomic variations among different populations. Our study shows a higher number of anatomic renal arterial variations compared to most previously published results. Only 46.3% of the patients exhibited classic renal arterial anatomy. Similar to other studies, the most common variation was the presence of ARA, discovered in 41.2% of our subjects (n = 231) [11, 14, 22]. These results are higher than the average reported frequency of 10–30% in other studies [3, 10, 20]. Possible reasons for this variability of the results could be the size of the study group and adopted classification, which also varies greatly among researchers. Another reason could be attributed to the type of study- cadaveric, radiologic or surgical. According to laterality, published results are inconsistent. Some researchers report higher prevalence on the right side [26] and others on the left [14] but without significant differences. Our results demonstrated that ARA are more common on the left side in comparison to the right side (25.5 vs. 24.3%, respectively) without reaching statistical significance. In our study, similar to most researchers greater proportion of males exhibited the presence of ARA [18]. However, a statistically significant difference between genders was not observed. Contrary to our results Sośnik stated a significantly greater occurrence of ARA in males [24].

The occurrence frequency of hilar ARA (72.6%) in our study was remarkably higher compared to polar ARA (15.2% superior polar ARA and 12.2% inferior polar ARA). Similar to our results Çınar et al. described a greater frequency of hilar ARA (84.5%) compared to polar ARA (15.5%) and a greater proportion of superior than inferior polar ARA [7]. One study by Johnson et al. also report a higher prevalence of hilar ARA compared to polar ARA. However, ARA entering the kidney through the lower pole were more common in comparison to superior polar ARA [14].

In our study, the most common site of both main and accessory renal arteries origin was the abdominal aorta between the level of L1 and L2 vertebrae. These findings are consistent with the classical teaching and previously published data reporting that 94–95% of the main renal arteries and 78–80% of ARA arise from the aorta at the L1-L2 level [11, 20]. Similar to our results Natsis states that the majority of right main renal arteries originate at the level of L1 and the majority of left main renal arteries- at the level of L2, while the most common level described by Palmieri is the L1-L2 intervertebral disk on both sides [20, 21]. ARA exhibits a bigger range and more inferior ostium location compared to the main renal arteries. In the current study, both the main and accessory renal arteries on the left showed a lower ostium position compared to the contralateral side, coinciding with previous literature reports [11, 20]. Three main renal arteries (0.3%) and eleven ARA (3.4%) did not arise from the aorta. The most common origin arteries were the common iliac arteries. One left main renal artery showed a very rare variant and originated from a common trunk with the median sacral artery. One left ARA arose from the left internal iliac artery. The renal arteries are known to originate from the iliac arteries, superior and inferior mesenteric arteries, contralateral renal artery, lumbar artery or the thoracic aorta. Kim et al. described a case in which the main renal artery supplying the right kidney originated from the left proximal common iliac artery. In our cohort, such variation was not observed. However, in one patient an accessory renal artery to the right kidney arose from the contralateral left common iliac artery [16]. The variations in the ostium location and number of renal arteries are commonly encountered together with other concomitant genitourinary anomalies such as horseshoe or ectopic kidney [10]. This data is confirmed in a study by Majos et al. published in 2018. The authors describe a significantly greater number of arteries in horseshoe kidneys compared to separate kidneys (p < 0.0001) as well as greater variability in arterial origin location in the horseshoe kidney group (p = 0.0001). The arteries supplying the horseshoe kidneys originated from the common iliac arteries in 14.78% of the cases and below them in less than 1% whereas such variations were not described in the separate kidney group [19]. Moreover, apart from originating from a different vessel than the aorta, the renal arteries give rise to different vessels which also exhibit multiple variations. A recently published case report by Vas et al. describes an extremely rare variant in which a replaced right hepatic artery originated from the right distal renal artery and exhibited a cranial course to the porta hepatis [29]. Such variation was not observed in our large cohort.

The prevalence of ED in the literature ranged between 4 and 35.9% [8, 27]. The frequency of 21.7% in our study could be considered moderate and aligns with previously published data. The majority of the studies do not establish a significant association between ED and laterality, although it was more prevalent on the right side [6, 18, 27]. However, according to our findings, ED is significantly more common on the right- 12.8 vs. 8.9%, p = 0.035. With respect to gender, two studies report significantly higher ED occurrence in males [6, 11]. On the other hand, Kumaresan et al. report a higher prevalence in females but without statistical significance [18]. However, in our study the rates of early bifurcation were similar between genders- 21.3% in males and 21.5% in females. Discrepancies in branching pattern could be attributed to the methodology of data sampling and the adopted definition of ED in each study, which often varies between studies.

Traditionally, right-sided renal arteries pass behind the IVC. The reported prevalence of the precaval course of the renal arteries is 4.5–9.17% [2, 8]. It is important to acknowledge precaval renal arteries because their presence has been associated with asymmetrical obstruction of the renal collecting system although the incidence of symptomatic hydroneprhosis is still unknown [32]. In the present study, 6.9% of the right renal arteries had a precaval course which is in agreement with other studies. Similar to the studies of Yeh et al. and Bouali et al. the overwhelming majority of the precaval renal arteries were accessory [2, 32]. Precaval course was noted in only 0.5% of the main renal arteries and in 30% of ARA and a significant difference was determined (p < 0.001). Precaval course of a single and main artery was found in one patient which is a very rare variant, and only a few cases are described in the literature [32].

Conclusion

The renal arterial vasculature exhibits complex anatomy and a large number of variations. The interdisciplinary significance of these variations is undisputed. The present study provides novel data on the prevalence of renal arterial variations in the Bulgarian population. Anatomic renal arterial vasculature variants are common and the most frequently encountered variation was an accessory renal artery. Therefore awareness and thorough preoperative radiological assessment are essential for the success and safety of surgical and endovascular interventions.