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18F-FDG PET scanning of abdominal aortic aneurysms and correlation with molecular characteristics: a systematic review



The purpose of this study is to give an overview of studies investigating the role of fludeoxyglucose F18 (18F-FDG) positron emission tomography (PET) scanning in patients with aortic aneurysms with a focus on molecular characteristics of the aneurysm wall.


MEDLINE, EMBASE, and the Cochrane database were searched for relevant articles. After inclusion and exclusion, we selected 18 relevant articles reporting on 18F-FDG PET scanning of aortic aneurysms.


The sample size of studies is limited, and there are no standardized imaging protocols and quantification methods. 18F-FDG PET scanning was shown to display molecular characteristics of the aortic wall. Different studies showed contradictory findings of aortic 18F-FDG uptake in aneurysm patients compared to controls.


Non-invasively determining molecular characteristics of aortic wall weakening might lead to better rupture and growth prediction. This might influence the decision of the surgeon between conservative and surgical treatment of aneurysms. To date, there is conflicted evidence regarding the use of 18F-FDG PET scanning to predict aneurysm rupture and growth. The role of 18F-FDG PET scanning in rupture risk prediction needs to be further investigated, and standardized imaging protocols and quantification methods need to be implemented.



Abdominal aortic aneurysm (AAA) is an abnormal focal dilation of the aortic wall and the most accepted definition for it is a diameter of 3.0 cm or more. Ruptured AAA is a serious complication with an overall mortality rate of 90 %, making it essential to develop strategies to predict rupture. Currently, the decision between conservative versus surgical treatment involves weighing the risk of aneurysm rupture versus the risks of a surgical procedure. This calculation of aneurysm rupture risk is based on assumptions of population-averaged properties for the aneurysm wall based on maximum aneurysm diameter. Anatomic characteristics like aortic tortuosity and diameter asymmetry have also been described as reflectors for rupture risk [1]. However, not only large aneurysms but also small aneurysms can rupture, making the diameter of AAA alone not the ideal determinant in risk stratification [2, 3].

The etiology of AAA is multifactorial including genetic factors. AAA rupture represents a mechanical failure [4], attributable to alterations in extracellular matrix components of the aortic wall. Increased activity of the so-called matrix metalloproteinases, enzymes with proteolytic activity that also play a role in other degenerative diseases like osteoarthritis, has been demonstrated [58]. Production of these enzymes by inflammatory cells such as macrophages, B- and T-lymphocytes, and mast cells has been shown [6, 9]. Fludeoxyglucose F18 (18F-FDG) is a positron emission tomography (PET) tracer, which is believed to reflect glucose accumulation by inflammatory cells, and thus, it could be useful in non-invasively displaying inflammatory characteristics of the aneurysm wall. It would be of great importance, both from the patient’s perspective and as from a health-care economical point of view, to predict aneurysm rupture by non-invasively detecting inflammatory activity in the aortic aneurismal wall. We therefore conducted a systematic review of human studies in which 18F-FDG PET scanning is performed on patients with aortic aneurysms and correlation between 18F-FDG PET scanning and clinical events or histology/molecular characteristics is addressed.


Search strategy

MEDLINE and EMBASE databases were systematically searched on all studies relating abdominal or thoracic aortic aneurysm, 18F-FDG PET scanning, and surgically derived aortic wall material (Fig. 1). The search was conducted in September 2015 according to the search strategy and data collection guidelines of the Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) statement [10]. A manual search of the Cochrane Library yielded no relevant articles.

Fig. 1
figure 1

Flowchart of the systematic review

Data collection and extraction

After disregarding duplicates, the title and the abstract of 271 articles were independently screened by two observers (U.T. and D.M) according to predefined criteria. The search query can be found in Additional file 1. Inclusion criteria were as follows: (1) presenting data about patients with thoracic or abdominal aortic aneurysm and (2) 18F-FDG PET scanning with or without reporting data on correlation between 18F-FDG PET scanning and molecular characteristics. Letters, comments, abstracts for conferences, case reports <10, and animal studies were eliminated. We excluded studies with acute aortic syndromes, as these are generally considered as a separate pathology.

Nineteen articles of studies that matched the inclusion criteria were obtained. Articles were excluded if one of the following criteria were applicable: (1) ex vivo imaging and (2) not written in English. After reading the full text of the articles, we excluded one article because of not focusing on PET of the aortic wall. Reference lists of the included articles were searched manually and yielded no new articles. Disagreements between the reviewers were resolved by consensus.


Our search resulted in 18 articles in which 18F-FDG PET scanning is reported on patients with aortic aneurysms. PET scanning protocols were specified in all studies. QPCR, histology, and immunohistochemistry protocols were described in all studies. PET scanning was either performed in asymptomatic patients or in symptomatic patients, which is in some studies defined by abdominal or lower back pain and in other studies by accelerated growth, leaking, or rupture of the aneurysm. An overview of AAA patients investigated with 18F-FDG PET scanning is given in Table 1.

Table 1 An overview of studies in patients with AAAs which are investigated with 18F-FDG PET scanning

Articles correlating 18F-FDG uptake in AAA patients to clinical events

In 2002, Sakalihasan et al. were the first to report the correlation of 18F-FDG uptake in AAA patients to clinical events. In this study, 26 patients with AAA were included and visual uptake of 18F-FDG was seen in ten patients [11]. Patients with asymptomatic AAA but also patients presenting with lower back pain and AAA (symptomatic AAA) were analyzed. While patients with negative 18F-FDG uptake required no urgent surgery, five of the ten patients with positive uptake required urgent surgery within 2 to 30 days. However, not all symptomatic AAAs showed 18F-FDG uptake. Next to the study performed by Sakalihasan et al., another study correlated 18F-FDG uptake to clinical events in AAA patients. Nchimi et al. studied 53 patients with aortic aneurysms, of which 6 are with thoracic aortic aneurysms [12]. More clinical events (rupture, dissection, or growth >1 cm) occurred in patients with visually increased 18F-FDG uptake. Quantitatively, 18F-FDG positron emission tomographic uptake correlated positively with both wall stress and stress/strength index.

Articles comparing 18F-FDG uptake between AAA patients and controls without AAA disease

Findings published by Sakalihasan et al. in 2002 prompted further research to investigate the role of 18F-FDG PET scanning in rupture risk prediction. Several studies have been performed in which 18F-FDG uptake of AAA patients is compared to 18F-FDG uptake in controls without AAA disease. In a study published in 2008 by Truijers et al., 17 patients with asymptomatic AAA were investigated retrospectively and maximum standardized uptake values (SUVmax) were compared to age-matched controls. 18F-FDG PET scanning in both the patient and control groups was performed for staging of primary lung cancer [13]. Patients had significantly higher SUVmax values than controls. Accordingly, Reeps et al. report increased SUVmax values in 12 patients with asymptomatic AAA compared to an age-matched control group without aortic aneurysm disease [14]. In 2012, Tegler et al. [15] examined seven asymptomatic men with large AAA (range, 52–66 mm) and five asymptomatic men with small AAA (range 34–40 mm) with 18F-FDG PET scanning. Consistent with the findings of Truijers et al. and Reeps et al., a significant increase in SUVmax was found in asymptomatic patients with AAAs compared to controls without aneurysm [14].

Nonetheless, studies have been published reporting no difference or even decreased 18F-FDG uptake in AAA patients compared to controls without AAA disease. In a case-control study conducted in 2012, Palombo et al. compared 18F-FDG uptake in aortic walls of 40 male patients with asymptomatic AAA disease to controls (with neoplastic disease) without any clinical evidence for atherosclerotic disease [16]. Patients with AAAs both had lower mean SUV and maximum SUV compared to adjacent non-aneurysmal segments within the same patient but also compared to controls. Consistent with the findings of Palombo et al. [16], another study published by Marini et al. in the same year reports decreased SUVmax in the aneurismal walls of 12 patients with asymptomatic AAA, compared to 12 age- and sex-matched controls (with neoplastic disease) [17]. Morbelli et al. confirmed findings of Palombo et al. [16] and Marini et al. [17]. In this study, 18F-FDG uptake in 30 AAA patients was compared to 30 controls. Decreased 18F-FDG uptake was seen in the aneurysms of AAA patients in comparison to the corresponding arterial segment of the control group but also in comparison to the non-aneurysmal segment of the same patient [18]. Another case-control study is published by Barwick et al. in 2014 [19]. They searched a PET/CT database of predominantly oncological patients and matched 151 aneurysm patients to 159 non-aneurysmal controls and do not report significant differences in visual 18F-FDG uptake or SUVmax between patients and controls. Moreover, no significant differences were found in SUVmax between patients who underwent surgery, had AAA rupture, or did not have rupture or surgery.

Articles correlating 18F-FDG uptake to aneurysm expansion

Since AAA has an inflammatory component, increased inflammatory activity in the aortic wall could potentially indicate recent growth of an aneurysm and thus help in rupture risk prediction. Two studies investigated the correlation between 18F-FDG uptake and recent AAA growth [14, 20], yet no correlations were found. In addition, 18F-FDG uptake in the aortic aneurismal walls may indicate future aneurysm expansion. Three studies investigated the relationship between 18F-FDG uptake and future expansion [21-23]. Kotze et al. investigated 18F-FDG uptake in 25 AAA patients with small aortic abdominal aneurysms and measured aneurysm expansion rate 6 months and 1 year later with ultrasound. Of the 25 patients included, three patients had lower back or abdominal pain. A significant inverse correlation was found between whole-vessel SUVmax and ultrasound expansion at 1 year after scanning [22]. This research group again reported the same findings in 40 AAA patients, of which 2 presented with lower back pain [20]. SUVmax again correlated inversely with further aortic expansion at 1 year measured by ultrasound.

Recently, an article reported about the potential of 18F-FDG in risk stratification of AAA [21]. In this study, patients with AAA <55 mm underwent 18F-FDG PET scanning at baseline and 9 months later. Patients with an increase in AAA size after 9 months had significantly lower 18F-FDG uptake at baseline compared to patients without significant increase in AAA size. Moreover, the increase in 18F-FDG uptake throughout time was higher in patients displaying a significant increase in AAA size.

Correlation of 18F-FDG uptake to histology of the aortic wall in AAA

The ability of 18F-FDG PET scanning to non-invasively detect histopathological characteristics of the aneurismal wall was investigated in six studies (Table 1).

Reeps et al. [14] studied 12 asymptomatic and 3 patients presenting with aneurysm-specific abdominal pain: symptomatic AAA. All patients underwent 18F-FDG PET/CT, followed by open AAA repair. Analysis by immunohistology was done from areas with maximum 18F-FDG uptake. Immunohistological analysis showed that increasing SUVmax levels were significantly associated with increasing medial inflammatory cell infiltrates, higher densities of CD68-positive macrophages, and with CD3-positive T-lymphocytes. Moreover, increased 18F-FDG uptake was significantly associated with increased MMP-9 expression. Furthermore, significant negative correlation of collagen fiber and vascular smooth muscle cells (VSMC) content compared with increasing SUVmax was found. Five years later, the same research group also investigated the role of partial volume correction in accurate quantitative assessment of 18F-FDG uptake in the same patient group [24]. Partial volume corrected mean SUV (PVC-SUVmean) and maximum SUV (PVC-SUVmax) were determined. Both PVC-SUVmean and PVC-SUVmax were significantly higher than the uncorrected SUVmean and SUVmax. Previously demonstrated significance correlation of 18F-FDG uptake with macrophage infiltration and increased MMP-9 expression did not change by applying partial volume correction nor improved correlation coefficients.

In 2012, Tegler et al. [15] investigated seven patients with large AAAs (size 52–66 mm) and five patients with small AAAs (size 30–40 mm). No visual uptake of 18F-FDG was seen, while histological analysis of specimens taken from the aneurismal wall of the seven patients with large AAAs all showed high inflammatory cell infiltration with B-lymphocytes, T-lymphocytes, and macrophages.

Marini et al. report a decrease in cell density in aneurysmal wall biopsies of AAA patients. They concluded that, because a significant relation was found between cell density and 18F-FDG uptake, reduced cell density in these patients account for the low prevalence of positive findings of AAA patients at PET imaging [17].

In a study published in 2013 by Courtois et al. [25], PET/CT imaging in 18 patients with symptomatic or asymptomatic AAA was performed. Eight of the patients showed 18F-FDG uptake (PET+), while ten showed no 18F-FDG uptake (PET−). A comparison was made in immunohistology, mRNA, and protein levels of PET+ and PET− patients. Moreover, biopsies of the AAA wall in regions with maximum 18F-FDG uptake were also compared to biopsies in the same patient where no uptake of 18F-FDG was seen. No significant correlation was found between AAA diameter and 18F-FDG uptake. Significantly higher levels of circulating C-reactive protein (CRP) were found preoperative in PET+ patients. Inflammatory infiltrate in the adventitia was significantly higher in the PET+ group compared to the PET− group or the biopsy taken from the negative site. The density of smooth muscle cells in the media was significantly reduced in the positive 18F-FDG uptake sites as compared with their respective negative counterparts and with the PET− patients. The mRNA and protein levels of extracellular matrix degrading enzymes (MMPs) in the media but also adventitia significantly increased in 18F-FDG positive sites, compared to negative sites in the same patients.

A similar approach was used again by the same research group very recently, in which 12 AAA patients were included, with six of the patients showing 18F-FDG uptake and six showing no uptake. Regions with 18F-FDG uptake showed increased gene expression levels of markers involved in inflammatory processes and extracellular matrix remodeling. Moreover, increased levels of a chemokine, CCL18, were found in the adventitia of patients with 18F-FDG uptake [26].

Articles reporting solely PET scanning in AAA patients without correlations

Some studies solely investigated 18F-FDG PET scanning without correlating it to clinical events, aneurismal growth, or histological characteristics. In a study, performed in 2009 by Kotze et al., 14 patients with AAA were investigated of which one presented with lower back pain [20]. Twelve of these patients showed increased 18F-FDG uptake, defined by this group by a SUVmax >2.5 but not correlations were made.

Menezes et al. examined 17 patients with asymptomatic AAA and performed PET scans at several time points after 18F-FDG injection [27]. They conclude that there is no significant advantage in imaging 3 h over 1 h after 18F-FDG injection. In this study, no correlation of PET scanning to clinical characteristics is reported. In 2011, Muzaffar et al. reviewed 18F-FDG PET/CT scans from 926 patients with cancer and found AAA in 15 patients [28]. This study solely reports a SUVmax, without correlating it to clinical characteristics.


In this article, we give an overview of what is known about 18F-FDG PET scanning in patients with aortic aneurysms. Only one study reports inclusion of patients with thoracic aneurysms [12]. Imaging modalities as MRI and CT scanning were excluded, because an earlier search yielded no useful articles to discuss in this review.

18F-FDG PET scanning is an evolving imaging tool in the evaluation of inflammatory disorders and might thus be useful in predicting rupture risk. Indeed, Xu et al. [29] showed that high wall stress regions, calculated using the finite element method, colocalize with areas of positive 18F-FDG uptake. These results are consistent with the findings of Nchimi et al. [12].

Contradictory reports on 18F-FDG uptake in AAA patients compared to controls can be found in this review. Patient selection is a possible explanation for these contradictions. For instance, Sakalihasan et al. scanned large, rapidly expanding or symptomatic AAAs [11]. In addition, some studies scanned patients prior to surgery [1417, 25, 26], while other studies analyzed 18F-FDG PET scans of AAA patients under routine surveillance, either prospectively [12, 2123] or retrospectively [13, 19]. Furthermore, studies investigated both patients and controls with a neoplastic disease [13, 19], but studies also report on 18F-FDG PET scanning in AAA patients without neoplastic disease and compare this to a control group with neoplastic disease [16, 17]. As neoplasms display increased 18F-FDG uptake, this might lead to false positive readings. Moreover, two studies did not specify the reason of 18F-FDG PET scanning in their control group [14, 15].

18F-FDG uptake in AAA patients should be compared to a control group without atherosclerosis: patients without hypertension, hyperlipidemia, and non-smokers. Atherosclerosis is a systemic disease, and results in the control group might be influenced by calcification. While several studies described their control group [13, 16, 17, 19], others did not [14, 15]. Currently, not much is known about calcification and 18F-FDG uptake. There are some reports in the literature suggesting that 18F-FDG uptake precedes calcification [30, 31]. A study reported congruent 18F-FDG uptake with calcification spots on CT in 7 % of calcifications [32], while there is also a study reporting 18F-FDG uptake in the thoracic aortic wall, distinct from calcification sites at CT [33]. Rominger et al. retrospectively evaluated 932 patients with 18F-FDG PET/CT and show significant correlation between 18F-FDG uptake and calcifications in the abdominal aorta [34]. Moreover, increased 18F-FDG uptake and increased calcifications in the arterial system were both established as independent predictors for future vascular events, while both increased 18F-FDG uptake and calcification were identified as being at the highest risk for a vascular event. Four studies in this review investigated whether there was a difference in calcification between AAA patients and controls. While Kotze et al. [20] and Marini et al. [17] find no significant differences, Palombo et al. [16] and Morbelli et al. [18] report increased arterial calcium load in AAA patients compared to controls. Moreover, an inverse correlation between arterial calcium load and arterial wall metabolism was found.

In addition to patient selection, and incorrect control groups, timing of PET imaging and quantification methods is a possible explanation to contradictory reports in literature. Considerable differences exist in timing of imaging and quantification methodology as reported in studies. Only seven studies specified whether visual uptake of 18F-FDG was seen [11, 12, 15, 16, 19, 25, 26]. Some studies describe the use of SUVmax or SUVmean divided by blood pool or liver activity [12, 1619, 2123, 2527], while others only use SUVmax or SUVmean without blood pool correction [1315, 20, 24, 28]. This makes it difficult to compare results in literature, highlighting the importance of standardized techniques and quantification methods. Six studies scanned 60 min after 18F-FDG injection [1113, 15, 25, 26, 28], four other studies 90 min [14, 18, 21, 24], and three others [20, 22, 23] 180 min after 18F-FDG administration. Blomberg et al. showed improvement in atherosclerotic plaque quantification in the carotid arteries and thoracic aorta scanning 180 min after 18F-FDG administration compared to 90 min [35]. However, Menezes et al. [21] show that there is no significant difference in SUVmax uptake at 60 min compared to scanning at 180 min.

Correlations between 18F-FDG uptake and pathological weakening of the wall can aid in investigating how effective this imaging tool will be in rupture prediction. Correlation between 18F-FDG PET and histology was first shown in a case report [36], where 18F-FDG uptake corresponded to an inflammatory infiltrate in the aortic wall. In this review, several studies show correlation between 18F-FDG uptake and histological aneurysm characteristics. Reeps et al. [14] showed that there is a significant correlation between total inflammatory infiltrate and MMP-9. MMP-9 already has been shown to be significantly upregulated in ruptured sites of AAAs compared to non-ruptured sites [37]. Moreover, its expression is shown to be decreased in non-ruptured abdominal aneurysms compared to ruptured abdominal aneurysms [38]. It remains the question whether the inflammatory infiltrate in the AAA wall is an etiological factor responsible for the increase in MMP or merely a reaction to an unknown etiological factor causing this increase in MMP expression.

Remarkably, Truijers et al. [13], showed the highest 18F-FDG uptake in patients with relatively small AAAs, while the patient with the largest AAA showed very low 18F-FDG uptake. Moreover, studies that compared 18F-FDG uptake in AAA compared to a matched control group reported lower 18F-FDG uptake [1618]. These observations are most likely the result of a reduction in cell density occurring in large AAAs as documented by Marini et al. [17]. In contrast to the aneurysmal segment, the arterial tree of patients with AAA display higher 18F-FDG uptake [18]. The dispersed nature of inflammatory cell islands in larger AAAs causes an underestimation of radioactivity concentration whenever the thickness of the source is less than twice the system spatial resolution. PET scanning has limited spatial resolution, and therefore, it remains a challenge to investigate the arterial wall. While findings of Marini et al. do not label 18F-FDG PET scanning as an inadequate tool for risk stratification in AAA, it is essential to realize that currently, a patient with a negative PET scan should not be considered as low risk for rupture.

Courtois et al. [25, 26] compared patients with and without 18F-FDG uptake as assessed visually. Interesting results are shown that give insight into the pathophysiology of abdominal aortic aneurysms. The significant reduction in expression of MMP-12 and MMP-15 from regions with no 18F-FDG uptake in PET+ patients may be indicative of a final attempt in the tissue to restore extracellular matrix. This response might be a futile attempt to protect from a yet unknown etiologic factor, leading to more inflammation and thus to a PET+ patient. However, when analyzing remodeling of ECM, it is important to take into account substrates of proteolytic enzymes [39] and the contribution of the structural protein to tensile strength of the aortic wall.

In humans, 18F-FDG is the most frequently used PET tracer in nuclear investigations of aortic aneurysms and was also shown to have the highest sensitivity in a rat experimental AAA model, compared to two other PET tracers involved in leukocyte activation [40]. Tegler et al. investigated two other PET tracers targeting proteins involved in chronic inflammation but were not able to show differences in uptake between AAA patients and controls [41].

Developing effective PET tracers to improve AAA rupture risk stratification should focus on pathophysiological processes in AAA. As AAA walls display a large infiltration of immune cells such as macrophages, PET tracers targeting receptors on macrophages such as integrin αvβ3 might be useful [42]. The search for novel PET tracers that can be useful in predicting AAA rupture is ongoing. Animal studies are helpful in investigating novel molecular probes that might be useful in predicting AAA rupture. English et al. used a novel abdominal aortic aneurysm model in rats and showed that increased 18F-FDG uptake is predictive of rupture [43]. Nahrendorf et al. [44] show, by using macrophage-targeted nanoparticles labeled with fluorine-18 in PET/CT scanning, that macrophages localized in the aneurysmal wall can be visualized. Recently, Shi et al. showed angiogenesis in AAA experimental mice by PET scanning with a (64)Cu-labeled anti-CD105 antibody [45]. Also, other imaging techniques are being used for rupture prediction in animal models such as non-invasive MR imaging and near-infrared fluorescence [46, 47]. Future experiments need to prove the ability to use these techniques for rupture risk stratification in AAA patients.

In addition to the aneurysmal wall, improved molecular imaging of the intraluminal thrombus (ILT) not only qualitatively but also quantitatively might provide valuable information helpful in predicting rupture risk. Koole et al. [48] showed that ILT thickness is associated with higher MMP levels and lower vascular smooth cell numbers, which might implicate that AAA wall adjacent to a thick layer of ILT is significantly weaker than wall in the same AAA adjacent to a thinner or no ILT. Moreover, Nchimi et al. showed that the occurrence of ILT precedes AAA peak growth [49].

Symptoms in AAA patients point out to an increased rupture risk, but these indicators of increased risk for AAA rupture are not available in asymptomatic AAA patients. In this patient group, there is a need to establish risk percentages for AAA rupture. Studies report subtle differences in 18F-FDG uptake between patients and controls [14, 15, 18, 50]. As definition of quantitative cutoff values is essential in establishing risk percentages for aneurysm rupture and keeping this little difference in SUVmax in mind between AAA patients and controls, it is essential to correct for partial volume effects observed in the thin aortic wall [24]. However, in the end, it is unlikely that one single PET scan with a random PET tracer will lead to a reliable single quantitative cutoff value for rupture risk prediction. Serial imaging of AAAs will increase the chance to detect inflammatory activity in the aortic aneurismal wall. Investigating the aneurysm wall metabolism at more than a single time point will give valuable information as formation and expansion of aortic aneurysms takes many years. It is currently unknown whether inflammatory processes lead to expansion of aneurysms. No significant correlation was found between the degree of 18F-FDG uptake and recent AAA growth rate or maximum infrarenal AAA diameter in four studies [13, 14, 16, 22]. This supports the hypothesis that inflammation precedes expansion instead of expansion preceding inflammation. However, in contradiction with this hypothesis, Kotze et al. report inverse correlation between whole-vessel 18F-FDG uptake and aneurysm expansion at ultrasound after 1 year, indicating that aortic aneurysms with lower metabolic activity may be more likely to expand [22]. AAA formation and progression is a dynamic process, with repetitive sequences of inflammatory damage and repair. Periods of rapid expansion are followed by periods of quiescence [51]. It is likely that this dynamic process causes a cyclic variation in 18F-FDG uptake. Indeed, findings published by Morel et al. support evidence of cyclic changes in the metabolism of AAA during growth phases [21]. Consistent with findings published by Kotze et al. [22], AAAs with lower 18F-FDG uptake were more likely to expand in this study. It is likely that aneurysms with lower 18F-FDG are at the end of their “period of stasis” and will start with their “period of expansion.” Next to the study published by Morel et al. [21], solely one case study reports a correlation between aneurysm wall glucose metabolism and inflammatory changes with an increase in SUVmax and aneurysm size over time [52]. Following AAA patients with repeated PET/CT scans might be useful, but this approach needs to be weighed against higher radiation exposure.


Currently, a limited number of studies have investigated the role of 18F-FDG PET scanning in patients with AAAs and the correlation between 18F-FDG PET scanning of AAAs and molecular characteristics (Table 2). Therefore, we included also studies without molecular characteristics available. While there are studies showing increased 18F-FDG uptake in patients with AAAs correlated with clinical events, there are also studies reporting decreased 18F-FDG uptake in AAA patients compared to controls. Literature suggests that 18F-FDG PET scanning might be useful in displaying molecular alterations characteristic of the weakening of the AAA wall. However, it still remains a question whether these molecular characteristics of aortic wall weakening might lead to better rupture and growth prediction. Moreover, most studies are limited by a very small patient population. Larger patient populations are warranted. Standardized imaging protocols and quantification methods are essential to compare patient populations. However, given the conflicting evidence to date with 18F-FDG PET scanning, it is unlikely that a reliable quantitative cutoff value to predict rupture risk may be established. The potential of change in quantitative measure on serial 18F-FDG PET scanning may be helpful. Moreover, animal studies in which non-invasively detection of inflammation or proteolysis in AAA wall by means of in vivo molecular imaging is investigated and needs to be implemented in humans in order to improve rupture risk stratification.

Table 2 Main findings of the systematic review



fludeoxyglucose F18


abdominal aortic aneurysm


C-reactive protein


computed tomography


extracellular matrix


magnetic resonance imaging


positron emission tomography


  1. Fillinger MF, Racusin J, Baker RK, Cronenwett JL, Teutelink A, Schermerhorn ML, et al. Anatomic characteristics of ruptured abdominal aortic aneurysm on conventional CT scans: Implications for rupture risk. J Vasc Surg. 2004;39(6):1243–52. doi:10.1016/j.jvs.2004.02.025.

    Article  PubMed  Google Scholar 

  2. Powell JT, Gotensparre SM, Sweeting MJ, Brown LC, Fowkes FG, Thompson SG. Rupture rates of small abdominal aortic aneurysms: a systematic review of the literature. Eur J Vasc Endovasc Surg. 2011;41(1):2–10. doi:10.1016/j.ejvs.2010.09.005.

    Article  PubMed  CAS  Google Scholar 

  3. Georgakarakos E, Ioannou CV. Geometrical factors as predictors of increased growth rate or increased rupture risk in small aortic aneurysms. Med Hypotheses. 2012;79(1):71–3. doi:10.1016/j.mehy.2012.04.003.

    Article  PubMed  Google Scholar 

  4. Vorp DA, Vande Geest JP. Biomechanical determinants of abdominal aortic aneurysm rupture. Arterioscler Thromb Vasc Biol. 2005;25(8):1558–66. doi:10.1161/01.ATV.0000174129.77391.55.

    Article  PubMed  CAS  Google Scholar 

  5. Ailawadi G, Eliason JL, Upchurch Jr GR. Current concepts in the pathogenesis of abdominal aortic aneurysm. J Vasc Surg. 2003;38(3):584–8.

    Article  PubMed  Google Scholar 

  6. Kadoglou NP, Liapis CD. Matrix metalloproteinases: contribution to pathogenesis, diagnosis, surveillance and treatment of abdominal aortic aneurysms. Curr Med Res Opin. 2004;20(4):419–32. doi:10.1185/030079904125003143.

    Article  PubMed  CAS  Google Scholar 

  7. Tamarina NA, McMillan WD, Shively VP, Pearce WH. Expression of matrix metalloproteinases and their inhibitors in aneurysms and normal aorta. Surgery. 1997;122(2):264–71. discussion 71–2.

    Article  PubMed  CAS  Google Scholar 

  8. Choke E, Cockerill G, Wilson WR, Sayed S, Dawson J, Loftus I, et al. A review of biological factors implicated in abdominal aortic aneurysm rupture. Eur J Vasc Endovasc Surg. 2005;30(3):227–44. doi:10.1016/j.ejvs.2005.03.009.

    Article  PubMed  CAS  Google Scholar 

  9. Jacob T, Ascher E, Hingorani A, Gunduz Y, Kallakuri S. Initial steps in the unifying theory of the pathogenesis of artery aneurysms. J Surg Res. 2001;101(1):37–43. doi:10.1006/jsre.2001.6193.

    Article  PubMed  CAS  Google Scholar 

  10. Moher D, Liberati A, Tetzlaff J, Altman DG. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. J Clin Epidemiol. 2009;62(10):1006–12. doi:10.1016/j.jclinepi.2009.06.005.

    Article  PubMed  Google Scholar 

  11. Sakalihasan N, Van Damme H, Gomez P, Rigo P, Lapiere CM, Nusgens B, et al. Positron emission tomography (PET) evaluation of abdominal aortic aneurysm (AAA). Eur J Vasc Endovasc Surg. 2002;23(5):431–6. doi:10.1053/ejvs.2002.1646.

    Article  PubMed  CAS  Google Scholar 

  12. Nchimi A, Cheramy-Bien JP, Gasser TC, Namur G, Gomez P, Seidel L, et al. Multifactorial relationship between 18F-fluoro-deoxy-glucose positron emission tomography signaling and biomechanical properties in unruptured aortic aneurysms. Circ Cardiovasc Imaging. 2014;7(1):82–91. doi:10.1161/CIRCIMAGING.112.000415.

    Article  PubMed  Google Scholar 

  13. Truijers M, Kurvers HA, Bredie SJ, Oyen WJ, Blankensteijn JD. In vivo imaging of abdominal aortic aneurysms: increased FDG uptake suggests inflammation in the aneurysm wall. J Endovasc Ther. 2008;15(4):462–7. doi:10.1583/08-2447.1.

    Article  PubMed  Google Scholar 

  14. Reeps C, Essler M, Pelisek J, Seidl S, Eckstein HH, Krause BJ. Increased 18F-fluorodeoxyglucose uptake in abdominal aortic aneurysms in positron emission/computed tomography is associated with inflammation, aortic wall instability, and acute symptoms. J Vasc Surg. 2008;48(2):417–23. doi:10.1016/j.jvs.2008.03.059. discussion 24.

    Article  PubMed  Google Scholar 

  15. Tegler G, Ericson K, Sorensen J, Bjorck M, Wanhainen A. Inflammation in the walls of asymptomatic abdominal aortic aneurysms is not associated with increased metabolic activity detectable by 18-fluorodeoxglucose positron-emission tomography. J Vasc Surg. 2012;56(3):802–7. doi:10.1016/j.jvs.2012.02.024.

    Article  PubMed  Google Scholar 

  16. Palombo D, Morbelli S, Spinella G, Pane B, Marini C, Rousas N, et al. A positron emission tomography/computed tomography (PET/CT) evaluation of asymptomatic abdominal aortic aneurysms: another point of view. Ann Vasc Surg. 2012;26(4):491–9. doi:10.1016/j.avsg.2011.05.038.

    Article  PubMed  Google Scholar 

  17. Marini C, Morbelli S, Armonino R, Spinella G, Riondato M, Massollo M, et al. Direct relationship between cell density and FDG uptake in asymptomatic aortic aneurysm close to surgical threshold: an in vivo and in vitro study. Eur J Nucl Med Mol Imaging. 2012;39(1):91–101. doi:10.1007/s00259-011-1955-1.

    Article  PubMed  Google Scholar 

  18. Morbelli S, Ghigliotti G, Spinella G, Marini C, Bossert I, Cimmino M, et al. Systemic vascular inflammation in abdominal aortic aneurysm patients: a contrast-enhanced PET/CT study. Q J Nucl Med Mol Imaging. 2014;58(3):299–309.

    PubMed  CAS  Google Scholar 

  19. Barwick TD, Lyons OT, Mikhaeel NG, Waltham M, O'Doherty MJ. 18F-FDG PET-CT uptake is a feature of both normal diameter and aneurysmal aortic wall and is not related to aneurysm size. Eur J Nucl Med Mol Imaging. 2014;41(12):2310–8. doi:10.1007/s00259-014-2865-9.

    Article  PubMed  CAS  Google Scholar 

  20. Kotze CW, Menezes LJ, Endozo R, Groves AM, Ell PJ, Yusuf SW. Increased metabolic activity in abdominal aortic aneurysm detected by 18F-fluorodeoxyglucose (18F-FDG) positron emission tomography/computed tomography (PET/CT). Eur J Vasc Endovasc Surg. 2009;38(1):93–9. doi:10.1016/j.ejvs.2008.12.016.

    Article  PubMed  CAS  Google Scholar 

  21. Morel O, Mandry D, Micard E, Kauffmann C, Lamiral Z, Verger A, et al. Evidence of Cyclic Changes in the Metabolism of Abdominal Aortic Aneurysms During Growth Phases: (1)(8)F-FDG PET Sequential Observational Study. J Nucl Med. 2015;56(7):1030–5. doi:10.2967/jnumed.114.146415.

    Article  PubMed  CAS  Google Scholar 

  22. Kotze CW, Groves AM, Menezes LJ, Harvey R, Endozo R, Kayani IA, et al. What is the relationship between (1)(8)F-FDG aortic aneurysm uptake on PET/CT and future growth rate? Eur J Nucl Med Mol Imaging. 2011;38(8):1493–9. doi:10.1007/s00259-011-1799-8.

    Article  PubMed  Google Scholar 

  23. Kotze CW, Rudd JH, Ganeshan B, Menezes LJ, Brookes J, Agu O, et al. CT signal heterogeneity of abdominal aortic aneurysm as a possible predictive biomarker for expansion. Atherosclerosis. 2014;233(2):510–7. doi:10.1016/j.atherosclerosis.2014.01.001.

    Article  PubMed  CAS  Google Scholar 

  24. Reeps C, Bundschuh RA, Pellisek J, Herz M, van Marwick S, Schwaiger M, et al. Quantitative assessment of glucose metabolism in the vessel wall of abdominal aortic aneurysms: correlation with histology and role of partial volume correction. Int J Cardiovasc Imaging. 2013;29(2):505–12. doi:10.1007/s10554-012-0090-9.

    Article  PubMed  Google Scholar 

  25. Courtois A, Nusgens BV, Hustinx R, Namur G, Gomez P, Somja J, et al. 18F-FDG uptake assessed by PET/CT in abdominal aortic aneurysms is associated with cellular and molecular alterations prefacing wall deterioration and rupture. J Nucl Med. 2013;54(10):1740–7. doi:10.2967/jnumed.112.115873.

    Article  PubMed  CAS  Google Scholar 

  26. Courtois A, Nusgens BV, Hustinx R, Namur G, Gomez P, Kuivaniemi H, et al. Gene expression study in positron emission tomography-positive abdominal aortic aneurysms identifies CCL18 as a potential biomarker for rupture risk. Mol Med. 2014;20:697–706. doi:10.2119/molmed.2014.00065.

    PubMed Central  Google Scholar 

  27. Menezes LJ, Kotze CW, Hutton BF, Endozo R, Dickson JC, Cullum I, et al. Vascular inflammation imaging with 18F-FDG PET/CT: when to image? J Nucl Med. 2009;50(6):854–7. doi:10.2967/jnumed.108.061432.

    Article  PubMed  Google Scholar 

  28. Muzaffar R, Kudva G, Nguyen NC, Osman MM. Incidental diagnosis of thrombus within an aneurysm on 18F-FDG PET/CT: frequency in 926 patients. J Nucl Med. 2011;52(9):1408–11. doi:10.2967/jnumed.111.091264.

    Article  PubMed  Google Scholar 

  29. Xu XY, Borghi A, Nchimi A, Leung J, Gomez P, Cheng Z, et al. High levels of 18F-FDG uptake in aortic aneurysm wall are associated with high wall stress. Eur J Vasc Endovasc Surg. 2010;39(3):295–301. doi:10.1016/j.ejvs.2009.10.016.

    Article  PubMed  CAS  Google Scholar 

  30. Abdelbaky A, Corsini E, Figueroa AL, Fontanez S, Subramanian S, Ferencik M, et al. Focal arterial inflammation precedes subsequent calcification in the same location: a longitudinal FDG-PET/CT study. Circ Cardiovasc Imaging. 2013;6(5):747–54. doi:10.1161/CIRCIMAGING.113.000382.

    Article  PubMed  Google Scholar 

  31. Rudd JH, Myers KS, Bansilal S, Machac J, Woodward M, Fuster V, et al. Relationships among regional arterial inflammation, calcification, risk factors, and biomarkers: a prospective fluorodeoxyglucose positron-emission tomography/computed tomography imaging study. Circ Cardiovasc Imaging. 2009;2(2):107–15. doi:10.1161/CIRCIMAGING.108.811752.

    Article  PubMed  PubMed Central  Google Scholar 

  32. Ben-Haim S, Kupzov E, Tamir A, Israel O. Evaluation of 18F-FDG uptake and arterial wall calcifications using 18F-FDG PET/CT. J Nucl Med. 2004;45(11):1816–21.

    PubMed  Google Scholar 

  33. Tatsumi M, Cohade C, Nakamoto Y, Wahl RL. Fluorodeoxyglucose uptake in the aortic wall at PET/CT: possible finding for active atherosclerosis. Radiology. 2003;229(3):831–7. doi:10.1148/radiol.2293021168.

    Article  PubMed  Google Scholar 

  34. Rominger A, Saam T, Wolpers S, Cyran CC, Schmidt M, Foerster S, et al. 18F-FDG PET/CT identifies patients at risk for future vascular events in an otherwise asymptomatic cohort with neoplastic disease. J Nucl Med. 2009;50(10):1611–20. doi:10.2967/jnumed.109.065151.

    Article  PubMed  Google Scholar 

  35. Blomberg BA, Thomassen A, Takx RA, Hildebrandt MG, Simonsen JA, Buch-Olsen KM, et al. Delayed (1)(8)F-fluorodeoxyglucose PET/CT imaging improves quantitation of atherosclerotic plaque inflammation: results from the CAMONA study. J Nucl Cardiol. 2014;21(3):588–97. doi:10.1007/s12350-014-9884-6.

    Article  PubMed  Google Scholar 

  36. Defawe OD, Hustinx R, Defraigne JO, Limet R, Sakalihasan N. Distribution of F-18Fluorodeoxyglucose (F-18FDG) in abdominal aortic aneurysm: high accumulation in macrophages seen on PET imaging and immunohistology. Clin Nucl Med. 2005;30(5):340–1.

    Article  PubMed  Google Scholar 

  37. Wilson WR, Anderton M, Schwalbe EC, Jones JL, Furness PN, Bell PR, et al. Matrix metalloproteinase-8 and -9 are increased at the site of abdominal aortic aneurysm rupture. Circulation. 2006;113(3):438–45. doi:10.1161/CIRCULATIONAHA.105.551572.

    Article  PubMed  CAS  Google Scholar 

  38. Petersen E, Gineitis A, Wagberg F, Angquist KA. Activity of matrix metalloproteinase-2 and -9 in abdominal aortic aneurysms. Relation to size and rupture. Eur J Vasc Endovasc Surg. 2000;20(5):457–61. doi:10.1053/ejvs.2000.1211.

    Article  PubMed  CAS  Google Scholar 

  39. Snoek-van Beurden PA, Von den Hoff JW. Zymographic techniques for the analysis of matrix metalloproteinases and their inhibitors. Biotechniques. 2005;38(1):73–83.

    Article  PubMed  CAS  Google Scholar 

  40. Sarda-Mantel L, Alsac JM, Boisgard R, Hervatin F, Montravers F, Tavitian B, et al. Comparison of 18F-fluoro-deoxy-glucose, 18F-fluoro-methyl-choline, and 18F-DPA714 for positron-emission tomography imaging of leukocyte accumulation in the aortical wall of experimental abdominal aneurysms. J Vasc Surg. 2012;56(3):765–73. doi:10.1016/j.jvs.2012.01.069.

    Article  PubMed  Google Scholar 

  41. Tegler G, Sorensen J, Ericson K, Bjorck M, Wanhainen A. 4D-PET/CT with [(11)C]-PK11195 and [(11)C]-(D)-deprenyl does not identify the chronic inflammation in asymptomatic abdominal aortic aneurysms. Eur J Vasc Endovasc Surg. 2013;45(4):351–6. doi:10.1016/j.ejvs.2013.01.011.

    Article  PubMed  CAS  Google Scholar 

  42. Kitagawa T, Kosuge H, Chang E, James M, Tomoaki Y, Shen B, et al. Integrin-Targeted Molecular Imaging of Experimental Abdominal Aortic Aneurysms by 18F-FPPRGD2 Positron Emission Tomography. Circ Cardiovasc Imaging. 2013;6(6):950–6. doi:10.1161/CIRCIMAGING.113.00234.

    Article  PubMed  PubMed Central  Google Scholar 

  43. English SJ, Piert MR, Diaz JA, Gordon D, Ghosh A, D'Alecy LG, et al. Increased 18F-FDG uptake is predictive of rupture in a novel rat abdominal aortic aneurysm rupture model. Ann Surg. 2015;261(2):395–404. doi:10.1097/SLA.0000000000000602.

    Article  PubMed  PubMed Central  Google Scholar 

  44. Nahrendorf M, Keliher E, Marinelli B, Leuschner F, Robbins CS, Gerszten RE, et al. Detection of macrophages in aortic aneurysms by nanoparticle positron emission tomography-computed tomography. Arterioscler Thromb Vasc Biol. 2011;31(4):750–7. doi:10.1161/ATVBAHA.110.221499.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  45. Shi S, Orbay H, Yang Y, Graves SA, Nayak TR, Hong H, et al. PET Imaging of Abdominal Aortic Aneurysm with 64Cu-Labeled Anti-CD105 Antibody Fab Fragment. J Nucl Med. 2015;56(6):927–32. doi:10.2967/jnumed.114.153098.

    Article  PubMed  CAS  Google Scholar 

  46. Klink A, Heynens J, Herranz B, Lobatto ME, Arias T, Sanders HM, et al. In vivo characterization of a new abdominal aortic aneurysm mouse model with conventional and molecular magnetic resonance imaging. J Am Coll Cardiol. 2011;58(24):2522–30. doi:10.1016/j.jacc.2011.09.017.

    Article  PubMed  PubMed Central  Google Scholar 

  47. Lancelot E, Amirbekian V, Brigger I, Raynaud JS, Ballet S, David C, et al. Evaluation of matrix metalloproteinases in atherosclerosis using a novel noninvasive imaging approach. Arterioscler Thromb Vasc Biol. 2008;28(3):425–32. doi:10.1161/ATVBAHA.107.149666.

    Article  PubMed  CAS  Google Scholar 

  48. Koole D, Zandvoort HJ, Schoneveld A, Vink A, Vos JA, van den Hoogen LL, et al. Intraluminal abdominal aortic aneurysm thrombus is associated with disruption of wall integrity. J Vasc Surg. 2013;57(1):77–83. doi:10.1016/j.jvs.2012.07.003.

    Article  PubMed  Google Scholar 

  49. Nchimi A, Courtois A, El Hachemi M, Touat Z, Drion P, Withofs N, et al. Multimodality imaging assessment of the deleterious role of the intraluminal thrombus on the growth of abdominal aortic aneurysm in a rat model. Eur Radiol. 2015.

  50. Truijers M, Fillinger MF, Renema KW, Marra SP, Oostveen LJ, Kurvers HA, et al. In-vivo imaging of changes in abdominal aortic aneurysm thrombus volume during the cardiac cycle. J Endovasc Ther. 2009;16(3):314–9. doi:10.1583/08-2625.1.

    Article  PubMed  Google Scholar 

  51. Brady AR, Thompson SG, Fowkes FG, Greenhalgh RM, Powell JT. Abdominal aortic aneurysm axpansion: risk factors and time Intervals for surveillance. Circulation. 2004;110(1):16–21.

    Article  PubMed  Google Scholar 

  52. Reeps C, Gee MW, Maier A, Pelisek J, Gurdan M, Wall W, et al. Glucose metabolism in the vessel wall correlates with mechanical instability and inflammatory changes in a patient with a growing aneurysm of the abdominal aorta. Circ Cardiovasc Imaging. 2009;2(6):507–9. doi:10.1161/CIRCIMAGING.109.858712.

    Article  PubMed  Google Scholar 

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Correspondence to U. T. Timur.

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Competing interests

The authors declare that they have no conflict of interest.

Authors’ contributions

UT and DM performed the literature search. UT wrote the manuscript. JH, PJ, FM, and WM helped to analyze data and draft the manuscript. All authors read and approved the final manuscript.

Additional file

Additional file 1:

The search query used in this study. Medline, EMBASE and the Cochrane database were searched in september 2015 for relevant articles. After inclusion and exclusion, 18 relevant articles reporting on PET scanning of aortic aneurysms were included. (DOCX 20 kb)

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Timur, U.T., van Herwaarden, J.A., Mihajlovic, D. et al. 18F-FDG PET scanning of abdominal aortic aneurysms and correlation with molecular characteristics: a systematic review. EJNMMI Res 5, 76 (2015).

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  • Aortic aneurysm
  • AAA
  • 18F-FDG
  • PET scanning
  • Rupture risk prediction
  • Molecular characteristics