Background
Ehlers-Danlos Syndrome (EDS) represents a heterogeneous group of heritable connective tissue disorders characterized by joint hypermobility, connective tissue friability, as well as skin and vascular fragility. The combined prevalence of all EDS subtypes appears to be nearly 1 to 5000 individuals world- wide [
1]. The current international classification of EDS distinguishes 13 clinical subtypes, for which molecular mutations have been identified in 19 different genes [
2].
Vascular fragility with easy bruising is common in all patients with EDS, but its severity varies between EDS subgroups [
3]. An increased bleeding tendency including menometrorrhagia, gum bleeding, and peri-operative hemorrhage has been described in many EDS-patients of varying EDS subtypes [
3]. Spontaneous aneurysms, dissections and ruptures of medium to large sized arteries, caused by defects in type III collagen, are a clinical hallmark of the vascular type of EDS (vEDS). These life-threatening complications result in a reduced life span with a median age of approximately 51 years [
4]. Major vascular events have also been described in EDS subtypes with other molecular defects, including defects of collagen I and V or molecules involved in collagen folding (FKBP22), processing (ADAMTS-2) or modification (LH1) [
3].
Recent advances in surgical and endovascular management of progressive arterial disease in EDS patients have been associated with good clinical outcomes [
5‐
8]. Nevertheless, due to the difficult handling of fragile tissue and vessels during the operation, a sufficient risk-benefit assessment becomes crucial. Given that spontaneous arterial rupture can also occur in non-dilated arteries, prognostic factors for identification of vascular high-risk patients are indispensable, yet undetermined to date [
9].
Arterial tonometry derived augmentation index (AIx) is measured by pulse wave analysis, and is an indirect surrogate measure of arterial stiffness [
10]. It has been shown to be an independent predictor of mortality and cardiovascular events in patients with hypertensive, cardiovascular and renal disease [
11]. Furthermore, recent findings suggest that the AIx is elevated in patients with Marfan syndrome and correlates with progression of aortic disease [
12,
13]. Therefore, in a first step, the AIx of EDS patients was compared to age-, gender-, weight-, and height-matched healthy controls and possible predicting factors were assessed.
Discussion
This study investigated the applanation tonometry derived augmentation index (AIx) in a well characterized cohort of EDS patients. EDS patients showed a significantly, independently increased AIx compared to matched healthy controls, suggesting increased arterial stiffness in EDS patients despite the known influencing factors such as age, sex, BP and smoking history. Although vascular EDS patients showed the highest AIx (31.2 ± 14.1%), no significant overall differences of the AIx could be observed between the different types of EDS.
The aortic AIx is used as an indirect index of vascular stiffness derived from aortic pressure waveform analysis [
25,
26]. It represents the ratio of the ejection pressure from the heart and the reflection pressure from the arterial system. In this study, the primary wave pressure (P1), which represents the primary left ventricular ejection pressure, showed no difference between EDS patients and healthy controls, leading to the conclusion, that the observed difference in AIx results from the arterial reflection wave. These findings suggest that the increased AIx might represent increased arterial stiffness in EDS patients. This hypothesis is supported by the fact that the time of the second aortic peak (T2) was significantly shorter in the EDS cohort, while the time for the first peak (T1) was comparable. The finding of an increased AIx in EDS patients cannot be compared to other studies yet due to missing literature on this topic. However, since the AIx of our healthy controls (14.8 ± 14.0%) are comparable to expected reference values obtained from larger unselected population-based studies the findings in EDS seems to be plausible [
27]. Furthermore, AIx was positively correlated to female gender, age, diastolic BP, and pack years of smoking, and was also negatively correlated to height and weight as reported in previous studies [
27‐
30].
Literature about arterial stiffness and cardiovascular risk in EDS patients is rare and the existing results are incongruent due to inhomogeneous study populations and different methods used to determine arterial stiffness [
31‐
35]. Population inhomogeneity is mainly based on the fact that EDS is an umbrella term for clinically diverse connective tissue disorders based on different genetic defects [
36].
Our results contradict in particular a recently published study by Miller et al., reporting increased arterial elasticity in patients with EDS measured by pulse wave velocity (PWV) [
35]. Nevertheless, this study only retrospectively analyzed a subset of EDS patients from the Clinical and Molecular Manifestations of HDCT study who had both orthostatic BP recordings and PWV measurements [
37]. There might be a selection bias, because the authors focused especially on the connection between orthostatic intolerance (OI) and EDS patients. The comparison of these results with our study has to be done with caution, as only few information on study population is available and the EDS patients were not matched to a healthy control group. Nevertheless, we have to point out that AIx is a measure of pressure wave reflection, while PWV is the most commonly and universally acceptable measure of arterial stiffness. The assessment of central/aortic pressures, PWR and AIx in this specific population compared to healthy controls are of great interest and should be the focus of future research.
Vascular complications in patients with EDS are historically attributed to impaired synthesis and processing of diverse collagen types, leading to fragility of blood vessel walls and perivascular connective tissue, thus a decreased arterial stiffness would be suspected. However, molecular pathomechanisms underlying development of arterial aneurysms, dissections, rupture and bleeding are poorly understood [
3]. It is to mention that arterial stiffness is not only determined by the arterial wall’s composition of elastin and collagen. For example, smooth muscle cells behave as a stiff material linking fibrous component and contribute to arterial stiffness especially when contracted [
38‐
40]. Furthermore, animal studies suggest that effective arterial stiffness results from complex interactions between smooth muscle cells and extracellular matrix. For instance, increased fibronectin, an extracellular protein, is associated with a cell dedifferentiation process leading to increased production of extracellular matrix proteins by smooth muscle cells [
41]. Stewart et al. [
42] found that the aortic AIx and carotid-femoral pulse wave velocity increases after the application of a nitric oxide synthase inhibitor, thus pointing out the importance of basal nitric oxide on functional regulation of central arteries in humans. Nitric oxide synthesis could be altered in EDS patients given the recent finding that markers of endothelial dysfunction such as VCAM-1, ICAM-1 and MCP-1 are increased in vEDS patients [
43].
Our EDS patients showed increased resting heart rate and BP compared to healthy controls. Increased resting sympathetic activity has already been described as part of autonomic dysregulation in EDS patients [
44]. The connection between elevated BP, increased arterial stiffness and vascular disease has been extensively reviewed in the general literature about cardiovascular pathology. Chronic elevated BP leads to decreased vascular distensability that, in turn, increases pulsatile shear stress and pressure leading to endothelial dysfunction and vascular disease [
45,
46]. Increased arterial wall stress in EDS patients compared to healthy controls has been reported by Boutouyrie et al. [
47] using high-resolution echo-tracking systems.
Shingu et al. [
48] found an elevated carotid AIx in patients with aortic aneurysm and dissection, which the authors attributed to increased left ventricular afterload. Whether an increased prevalence of aortic aneurysms and dissections could be a reason for the increased AIx in our EDS cohort remains unknown because study subjects did not undergo vasculopathy evaluation. Depending on EDS subtypes, EDS patients suffer joint pain, joint dislocation, muscle cramps and fatigue leading to significantly reduced physical activity [
49]. There are several studies suggesting a link between decreased physical activity and increased arterial stiffness [
50,
51]. Even when only considering the number of reported joint luxation in our EDS cohort (22% of all EDS patients), reduced daily activity as a cause for increase arterial stiffness should be considered. In this study, EDS patients used more NSAIDs and antihypertensive medication compared to healthy controls. The influence of several medications, including antihypertensive and anti-inflammatory drugs on arterial stiffness has been described in literature [
41], but no independent pharmacological influence on the AIx was observed in our study. Furthermore, it is to mention that no EDS patient was treated with Celiprolol, a cardioselective β-blocker that has recently been shown to increase stiffness of the common carotid artery in vEDS patients [
52].
Since medical and interventional management advances lead to improved survival and quality of life in EDS patients, the role of early identification of vascular high-risk patients gains importance. To date, little is known about prognostic factors that could predict the chance of developing fatal cardiovascular events in patients with EDS. Pepin et al. [
4] recently showed that the natural course of vEDS varies with gender and type of mutation in COL3A1. This group showed a 5-year survival difference between males and females which was primarily based on a higher death rate before age of 20 due to vascular rupture. Vascular inflammation marker has been shown to be significantly elevated in vascular EDS patients compared to matched controls [
53]. However, their potential to predict vascular complications in EDS patients are still subject of ongoing investigation [
43].
Increased applanation tonometry derived AIx has been reported in patients with Marfan syndrom [
13], a genetic connective tissue disorder due to mutation in the fibrillin 1 gene [
54]. These patients also suffer from fatal vascular events like aortic dissection and rupture [
55]. Mortensen et al. [
13] conducted a longitudinal observational study to follow-up cardiovascular disease progression in 50 adult patients with Marfan syndrome for almost 2 years. Beside baseline aortic root diameter, only aortic AIx showed an independent association to aortic disease progression. Furthermore, Kaplan-Meier curve analysis presented a significantly lower rate of aortic root disease in patients with lower AIx [
12]. EDS and Marfan syndrome are multisystemic disorders that primarily affect the soft connective tissues. Even if these disorders differ in genetic and molecular pathogenesis, there are at least some clinical overlaps [
36] suggesting that the increased AIx might predict vascular disease progression in EDS patients as reported in Marfan syndrome patients. In addition, the fact that the other “non-vascular” EDS subtypes showed increased AIx as well, could point out an increased risk for cardiovascular events beside the vEDS-typical vascular complications. However, data about the general cardiovascular risk in EDS patients compared to the general population are lacking.
There are some limitations to our study. The patient numbers of EDS subtypes, especially of vEDS, were relatively small to allow statistical comparison of different AIx values between different subtypes. Nonetheless, related to EDS incidence, the number of acquired patients was considerable. Arterial stiffness was not the primary outcome of this study, hence no specific power calculation for pulse wave analysis measurement were done. However, the AIx difference measured in EDS patients and healthy controls was considerably. In addition, our study design did not allow a longitudinal follow-up of cardiovascular events in EDS patients. Further longitudinal studies assessing AIx and cardiovascular events in EDS patients would be needed to show the clinical relevance of increased AIx as a prognostic factor for cardiovascular risk in these patients. Nevertheless, since vEDS patients harbor the highest risk for fatal vascular events and this subgroup presented the highest AIx in our study, AIx already indicate potential as a possible predictor for vascular high-risk patients.
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