Vascular calcification is heterogeneous and triggered by multiple mechanisms. It has been implicated in the development of heart failure with preserved ejection fraction (HFpEF) and cognitive function impairment. Understanding the pathophysiology of vascular calcification may help us improve the management of HFpEF, atherosclerosis, accelerated arterial stiffness, hypertension, and cognitive dysfunction. Currently, there are no effective strategies for treating accelerated arterial stiffness. This may indicate that once arterial stiffness or vascular calcification has developed, it may be less likely to stop the ongoing pathophysiology. Therefore, earlier intervention targeting the probable pathways of vascular calcification may benefit the patients with vascular calcification and related pathological conditions. In this review, we briefly discuss the proposed pathophysiological roles of vascular calcification in the development of heart failure and cognitive decline, the animal models used to study the link between vascular calcification and cardiovascular diseases, and the possible corresponding management strategies.

Vascular calcification is a prevalent finding in the elderly population, associated with the process of vascular aging which is commonly conceptualized as arterial stiffness [1], and usually recognized as a disease marker and prognostic factor for cardiovascular diseases [2,3,4]. However, given that arterial stiffness has been increasingly implicated in the pathophysiology of heart failure and cognitive decline, vascular calcification, with its inevitable consequence of stiffening arteries, may also play a significant role and serve as a potential intervention target [5].

Atherosclerosis has been considered as the most important hallmark of vascular pathology. In contrast, arteriosclerosis or arterial stiffness is a vascular aging process [1], which leads to end-organ damage because of the reduced compliance and the arterial reservoir function of the arterial system [6] and the resultant increasing transmitting energy of arterial pulse waves [7]. Vascular calcification, a pathophysiological consequence of atherosclerosis, is associated with an inevitably more stiffened arterial system, and as a result, may serve as a connecting bridge between these two important pathways linked to the development of cardiovascular diseases. Ample evidence shown in animal data and studies of diabetes and end-stage renal disease has demonstrated that calcification of elastic fibers contributes to increased arterial stiffness [8,9].

Henry et al. [10] conducted a large-scale prospective population-based study and found that renal function is inversely associated with cardiovascular and all-cause mortality, in which vascular calcification is the major cause of cardiovascular disease in patients with chronic kidney disease (CKD) as it is associated with myocardial ischemia, impaired myocardial function, valvular insufficiency, arrhythmias and stroke, and appears to be a strong independent predictor of mortality [10]. Besides, patients with atherosclerotic plaque in the intimal layer often have more severely calcified aortae compared to those of the normal population. The prognostic role of calcification of abdominal aorta and coronary arteries in the prediction of incident cardiovascular events has been demonstrated in general population and diabetes patients [11]. Therefore, a deeper comprehension of the pathophysiology of vascular calcification could shed light on the identification of the possible intervention strategies for atherosclerosis and arteriosclerosis.

It has been reported that more than half of the general population with heart failure have preserved ejection fraction (HFpEF) [12]. Observational studies have concluded that the morbidity of HFpEF is similar to that of systolic heart failure [13]. Interestingly, among elderly women living in the community, HFpEF comprises nearly 90% of incident heart failure cases [14], in whom vascular calcification and osteoporosis are also common findings. Currently, the treatment of HFpEF is still empirical and there are no evidence-based therapeutic recommendations for this disease [15].

The mechanism underlying HFpEF is complicated. Abnormal matrix dynamics, altered myocyte cytoskeleton, impaired active relaxation, chronotropic incompetence, reduced left atrial strain, and cardiac inflammation on extracellular matrix remodeling are all implicated in the development of HFpEF [16]. Vascular calcification is common in elderly subjects and can lead to increased arterial stiffness. As shown in Figure 1, vascular calcification may play a significant role in the development of HFpEF. Except for the conventional understanding that vascular calcification is closely associated with atherosclerosis and precipitate the ischemic events, vascular calcification may also enhance arterial stiffness and render arterial stiffness less reversible. Subsequently, the reduced aortic reservoir function, which can be conceptualized as the second pump of the circulatory system, can also contribute to the reduced coronary diastolic flow and myocardial ischemia. Moreover, the vascular calcification and related arterial stiffness are associated with increased pulse pressure and consequent elevated left ventricular (LV) afterload. The process that the impaired vascular function can lead to the worsened LV function is usually coined as ventricular-arterial coupling. As such, targeting ventriculo-arterial coupling, the adverse consequence of vascular calcification, may be helpful to improve the prognosis of HFpEF [17].

To quantify the interplay between arteries and heart, an index of ventriculo-arterial coupling has been mathematically modeled [18]. Most LV performance indices, including ejection fraction, stroke volume, and cardiac output, are load-dependent and are influenced by the functional coupling of LV with arteries [19]. The ventriculo-arterial coupling is related to the efficiency of mechanical energetic transfer from the heart to arteries [20]. The physiological significance has been experimentally studied using the framework of the ratio of effective arterial elastance (Ea) to end-systolic elastance (Ees), which is relatively independent of the loading conditions [21]. The normal LV operates efficiently with an Ea/Ees ratio of about 0.6 [22]. The ratio increases as the pump function deteriorates with concomitant peripheral vasoconstriction resulting partly from enhanced sympathetic stimulation and altered baroreceptor gain. The increased Ea/Ees can be significantly reduced by vasodilator therapy which may optimize mechanoenergetic performance of LV in heart failure subjects through lowering peripheral vessel resistance [23]. The utilization of this ventriculo-arterial coupling index, Ea/Ees, could assist us in understanding the impact of vascular calcification on cardiac performance [24].

It has been well recognized that cardiovascular morbidity and mortality of patients undergoing dialysis is disproportionally elevated and cannot be fully explained by the high prevalence of established cardiovascular risk factors such as aging, inflammation, hypertension, diabetes mellitus, dyslipidemia, obesity, and smoking [25]. However, these conditions are all closely associated with arterial stiffness and vascular calcification, and are also prevalent in HFpEF. Targeting vascular calcification may help develop effective treatment strategies to reduce arterial stiffness and improve the ventriculo-arterial coupling, the mechanical efficiency of cardiac pump.

The brain is one of the organs that receive abundant blood supply, constituted by as much as 20% of cardiac output, and accounts for 20% of the total body oxygen consumption at rest [26]. High ambient flow and low impedance are thought to sensitize the cerebral microcirculation to harmful effects of excessive pressure and flow pulsatility [27]. Increased carotid-femoral pulse wave velocity (cf-PWV) was modestly associated with cognitive decline and impairment, as assessed using the Modified Mini-Mental State examination [28]. In 167 hypertensive patients without a history of cardiovascular or cerebrovascular disease, a higher cf-PWV was significantly associated with a greater volume of white matter hyperintensities and the presence of lacunar infarcts [29]. Thus, systemic large artery disease is linked to cerebral small-artery disease in hypertensive patients [29]. Furthermore, in the community-based Age, Gene/Environment Susceptibility - Reykjavik study, cf-PWV was associated with higher white matter hyperintensity volume [27]. Carotid pulsatility index was associated with lower whole brain, grey matter, and white matter volumes [27]. cf-PWV and carotid pulse pressure were associated with lower memory scores [27]. These results support that marked stiffening of the aorta is associated with transmission of excessive flow pulsatility into the brain, microvascular structural brain damage, and lower scores in various cognitive domains [27].

How a stiff aorta facilitates the transmission of high pulsatility of blood flow to the cerebral circulation remains to be clarified. Compared to the carotid arteries, the aorta is highly compliant in young and healthy subjects. Such impedance mismatch constitutes barriers of wave reflections; when a traveling pressure wave from ascending aorta encounters the first-generation arteries, the pulsatile energy would not be fully transmitted into the distal vasculature [27]. Pulse wave encephalopathy has been coined to describe such a hypothetical pathophysiology.

Recently, it has been proposed that arterial stiffness may contribute to the development of symptomatic dementia through a “double hit” mechanism [30]. In this brain MRI and PET imaging study, arterial stiffness was highest in individuals with both high beta-amyloid deposition, a hallmark of Alzheimer disease, and white-matter hyperintensity. Whether or not arterial stiffness is involved in the pathophysiology of Alzheimer disease should be further explored. If there is a true pathophysiological linkage between arterial stiffness and Alzheimer disease, the clarification of the underlying mechanism can provide novel therapeutic targets for these patients. As shown in Figure 2, given that vascular calcification is closely associated with atherosclerosis, cerebral ischemia and cognitive function decline can be anticipated. In addition, vascular calcification and the related increased arterial stiffness can also result in decreased cognitive function through the reduced arterial reservoir function and enhanced transmitting pulsatility of arterial pressure and flow into brain, which altogether cause cerebral damage and cognitive function decline. Therefore, therapeutic strategies to reduce the progression of vascular calcification may be effective to slow down the arterial stiffening and the associated cognitive decline in the aging process.

It is well established that heart failure subjects have worsening cognitive function [31,32,33]. Interestingly, heart failure subjects with hypertension seem to be more likely to develop cognitive dysfunction than those without [34,35]. This observation highlights that sustained hypertension related to vascular calcification in this population may compromise cerebral autoregulatory mechanisms and produce brain damage and exacerbate cognitive impairment [30].

Numerous efforts have been made to understand the arterial hemodynamics and its impact on target organ damage and dysfunction. Future research including basic, clinical, and epidemiological studies will be needed to clarify the possible mechanisms depicted as above.

Animal models allow us to study in detail the progression of a pathological process in a time course of disease development and to have new insights into the cellular mechanism and molecular pathways responsible for these processes. Thus far, there are two categories of animal models for aortic calcification associated with chronic renal failure: (1) calcification in both intimal and medial layer, and (2) calcification mainly in medial layer.

Animal Model of Vascular Calcification in Chronic Renal Failure

The 5/6th nephrectomy rat model has been used to evaluate uremia-related vascular calcifications. Bro et al. [36] and Buzello et al. [37] induced aortic calcification in both intimal and medial layers in 6 weeks, with no apparent atherosclerosis in tunica media, by inducing a chronic renal failure (5/6th nephrectomy) in apolipoprotein E (apoE) knockout mice. Nasrallah et al. [38] developed a model by inducing CKD, through electrocautery of one kidney followed by nephrectomy of the other, in calcification-prone DBA/2 knockout mice and fed with a 0.9% high phosphate diet, which led to widespread medial calcification in the vascular tree in 14-15 weeks; they found that the levels of calcification were similar to those observed in humans, without interference of atherosclerosis or inflammation.

Animal Model of Aortic Calcification in the Medial Layer without Chronic Renal Failure

Recently, Price et al. [39] developed a rat model for aortic calcification independent of kidney failure, by treating rats with sufficient warfarin and vitamin K antagonist that inhibits the formation of the calcium-binding amino acid, g-carboxyglutamic acid (a calcification inhibitor expressed by smooth muscle cells and macrophages in the artery wall in specific proteins), and induced spotty calcification in aortic trees. They also treated rats with vitamin K to counteract effects of warfarin on coagulation. In a previous cross-sectional human study, the prevalence of arterial calcification was increased in patients with current or past warfarin use independent of other risk factors [9], which suggests prolonged warfarin use is associated with the development of vascular calcification.

Animal Model of Heart Failure and Calcification

Currently, there is no animal model of vascular calcification directly associated with heart failure. The widely used heart failure rat model is the induced myocardial infarction by coronary artery ligation in Sprague-Dawley male rats. Our experience was that even when the left coronary artery was not completely ligated, heart failure could still develop, resulting from chronic myocardial ischemia. To investigate the interactions between vascular calcification, heart failure, and cognitive function, the combination of the above heart failure and vascular calcification models can be a useful tool for animal studies.

Many novel concepts have been proposed to ameliorate the progression of vascular calcification, which include targets in calcium homeostasis, endothelin receptor, statin, angiotensin receptor blockade, matrix metalloproteinases (MMPs), antidiabetic agents, and chelating agents [5]. Most of these agents remain in primitive stages and their effects on myocardial function are unclear. Figure 3 summarizes the potential strategies to target vascular calcification.

Many novel concepts have been proposed to target vascular calcification. The possible candidate strategies for reducing or even reverting the progression of vascular calcification are briefly introduced below.

• Phosphate binders: Elevated calcium and phosphate levels contribute to vascular calcification. Decreasing phosphate levels through diet restrictions or through the use of phosphate binders (including calcium-free phosphate binders) is associated with a decreased amount of vascular calcification. It has been shown that sevelamer treatment might contribute to the suppression of ectopic calcification in chronic renal failure [40].

• Vitamin D receptor agonists: In a mouse model of CKD, the administration of vitamin D receptor agonists calcitriol or paricalcitol significantly reduced aortic calcification [41].

• Calcimimetics: Substances that mimic the effects of calcium on the parathyroid gland and decrease the level of parathyroid hormones. Although results from in vitro and animal studies support the hypothesis that calcimimetics decrease vascular calcification [42], the effects are inconsistent [43].

• Bisphosphonates: Based on the assumption that an impaired “bone-vessel axis” is involved in the pathogenesis of vascular calcification, testing the influence of bisphosphonates on vascular calcification is a consequential step. However, the data concerning the impact of bisphosphonates on vascular calcification are inconsistent [44,45].

• Other substances for osteoporosis therapy: In a mouse osteoporosis model, denosumab reduced aortic calcification [46]. No human studies have been reported yet.

• Calcifying progenitor cells with decalcifying potential [47] has been shown to have the capability to reverse atherosclerotic vascular calcification. The progenitor cells isolated from the aortas of mice had bidirectional, osteoblastic and osteoclastic lineage. The bidirectional cells were demonstrated to increase the severity of calcium build-up and calcified plaques in arteries; however, this effect could be prevented by simultaneous treatment with the PPARγ-activating drug, which decreased the infiltration of osteoblasts into the plaques while increasing the infiltration of osteoclasts.

• HMG-CoA reductase inhibitors (statins) and angiotensin II type 1 receptor blockers (ARBs): Statins and ARBs are well-established therapeutic options in cardiovascular medicine and influence atherogenesis effectively. A combination of these substances reduces vascular calcification [48].

• MMPs are activated during vascular calcification and inhibition of MMPs in a CKD rat model has been shown to decrease vascular calcification [49].

• TRAM-34, an inhibitor of intermediate-conductance calcium-activated potassium channels (KCa3.1), inhibited the transition of VSMC into osteoblast-like cells, thus protecting the VSMC from calcification.

• Antidiabetic agent:

- Metformin is a mainstay medication in diabetes therapy and seems to reduce calcification in a rat model via the AMPK-eNOS-NO pathway by increasing NO production [50].

- Advanced glycation end product inhibitors limit vascular calcification in a rat model [51].

• Chelating agents were demonstrated to be effective in reducing vascular calcification in in vitro and animal studies [52]. Dietary L-lysine, vitamin E, and iron effectively reduce vascular calcification in animal models [53,54].

Vascular calcification is heterogeneous and triggered through multiple mechanisms. Few studies addressed the influence of vascular calcification on ventriculo-arterial coupling status and cognitive function. Understanding the pathophysiology consequence of vascular calcification may help us improve the management of patients with atherosclerosis, accelerated arterial stiffness, hypertension, HFpEF, and cognitive dysfunction. Currently, there have been no effective strategies to reduce the severity of arterial stiffness. This may indicate that once arterial stiffness or vascular calcification has developed, it may be less likely to stop the ongoing pathophysiology. Therefore, earlier intervention targeting the above probable pathways of vascular calcification may benefit the patients with heart failure and cognitive dysfunction. More efforts should be made to understand the mechanisms of this prevalent finding in the aging population and, more importantly, develop corresponding intervention strategies to diminish its adverse consequence. In addition, although the adverse impact of hypertension on cognitive function [55] and the favorable effects of antihypertensive agents on cognitive dysfunction [56] have been well delineated, the evidence supporting the effectiveness of anticalcification therapies on cardiovascular function and cognitive function is scarce [57]. More well-designed outcome research is needed.

Nothing to declare.

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