Vascular Calcification: an Update on Mechanisms and Challenges in Treatment

Abstract

Vascular calcification is highly associated with cardiovascular disease mortality, particularly in high risk patients with diabetes and chronic kidney diseases (CKD). In blood vessels, intimal calcification is associated with atherosclerosis, whereas medial calcification is a non-occlusive process which leads to increased vascular stiffness and reduced vascular compliance. In the valves, calcification of the leaflets can change the mechanical properties of the tissue and result in stenosis. For many decades, vascular calcification has been noted as a consequence of aging. Studies now confirm that vascular calcification is an actively regulated process and shares many features with bone development and metabolism. This review provides an update on the mechanisms of vascular calcification including the emerging roles of the RANK/RANKL/OPG triad, osteoclasts and microRNAs. Potential treatments adapted from osteoporosis and CKD treatments that are under investigation for preventing and/or regressing vascular calcification will also be reviewed.

Vascular Calcification

Vascular calcification is the pathological deposition of mineral in the vascular system. It has a variety of forms, including intimal calcification and medial calcification, but can also be found in the valves of the heart. Vascular calcification is associated with atherosclerosis, diabetes, certain heredity conditions, and kidney disease, especially CKD. Patients with vascular calcification are at higher risk for adverse cardiovascular events. Vascular calcification affects a wide variety of patients. Idiopathic infantile arterial calcification is a rare form of vascular calcification where the arteries of neonates calcify. It is associated with certain genetic mutations and often results in death. In patients with renal failure undergoing hemodialysis, vascular calcification is a frequent complication, with time on hemodialysis associated with more severe calcification. Calcific uremic arteriolopathy (CUA) or calciphylaxis is another complication of hemodialysis, where arterioles calcify, leading to necrosis of the skin and ulceration and has a mortality rate of over 50% at 2 years (reviewed in [1]).

Intimal Calcification vs. Medial Calcification

Calcification of the vessel wall occurs in the intimal and medial layers. The intimal layer of the vessel wall is normally composed of endothelial cells and a small amount of subendothelial connective tissue. In atherosclerosis, the intima becomes greatly inflamed and thickened and calcification occurs. Calcification of coronary arteries is an excellent predictor of atherosclerotic plaque burden and may contribute to atherosclerotic plaque rupture, though the connection between atherosclerotic plaque calcification plaque rupture is heavily debated. Several studies show a link between high coronary artery calcium (CAC) and risk of cardiac events and mortality, yet some studies have suggested that the most calcified plaques may be more stable, and that the plaques most vulnerable to rupture may be those which have a mixed composition of calcified and uncalcified tissue [2].

The medial layer of the vessel wall is composed of smooth muscle cells and elastin rich extracellular matrix. Calcification of the media occurs preferentially along the elastic lamina, as opposed to the diffuse localization seen in intimal calcification, and is associated with diabetes, kidney disease, hypertension, and osteoporosis. The result of medial calcification is a stiffening of the artery wall, with the associated rise in blood pressure, and a higher risk of cardiovascular mortality [1].

Valves: native and bioprosthetic valves

Vascular calcification can also lead to the dysfunction of heart valves, both native valves and bioprosthetic valves. In the valves, calcification of the leaflets can change the mechanical properties of the tissue and result in stenosis. Calcification of the valves is commonly associated with aging, and is the most common pathology seen in excised native valves [3]. Diseased native valves are often treated by valve replacement surgery, with either mechanical or bioprosthetic valves. Bioprosthetic valves have excellent hemodynamic properties and do not require long-term administration of anticoagulants. However, bioprosthetic valves are prone to calcification and may require replacement after 5–10 years. In fact, calcification and its contribution to tissue deterioration is the major mode of failure of bioprosthetic valves. Calcification of both native and bioprosthetic valves impairs cardiac function due to the valves inability to properly regulate flow. Valve calcification is also linked to increased risk of cardiac events and mortality even if the patient is asymptomatic [4].

Mechanisms of Vascular Calcification

Vascular calcification has been noted as a consequence of aging for many decades. Growing evidence now suggests that vascular calcification, similar to bone remodeling, is an actively regulated process, including both inductive and inhibitory processes [5]. Bone-related proteins, such as alkaline phosphatase, osteocalcin, osteopontin, Runx2, and matrix vesicles, which nucleate hydroxyapatite mineral crystals, have all been observed in calcified valvular lesions. In addition, outright cartilage and bone formation have been identified [6, 7]. The identification of genes that cause ectopic calcification disorders in human and/or mice has contributed to our knowledge about the regulation of vascular calcification. Remarkably, single-gene mutations in type II TGFβ receptor and Notch 1 are associated with bicuspid aortic valve and valve disease [8]. Additionally, in vivo and in vitro models have been developed to mimic important aspects of vascular and valvular calcification and have identified new pathways important for this process. The current major mechanisms of vascular calcification based on these studies are summarized in Figure 1, including (1) failed anticalcific processes (2) induction of osteochondrogenesis (3) cell death (4) abnormal Ca/Pi homeostasis (5) circulating calciprotein particles and (6) matrix degradation/modification. The studies supporting these mechanisms have been reviewed in detail in recent articles [9–12]. In this article, we will focus on recent evidence for new mechanisms regulating vascular calcification, including the potential role of the RANK/RANKL/OPG axis and osteoclasts, and microRNAs. Finally, we review potential treatments that are under investigation for preventing and/or regressing vascular calcification.

Figure 1.

Major Mechanisms and Mediators of Vascular Calcification.

Potential role of the RANK/RANKL/OPG axis and osteoclasts

Most of the regulatory factors identified to date are thought to contribute to ectopic calcification either by promoting or inhibiting crystal nucleation or growth, cell death or osteogenic differentiation of mesenchymal cells, rather than affecting resorption, or removal, of the mineral after it has been formed. Osteoclasts are multinucleated, bone resorptive cells derived from bone marrow that play an important role in skeletal mass regulation. In bones, over active osteoclastic activity leads to bone loss (osteoporosis), and osteoclast deficiency leads to bone overgrowth (osteopetrosis). RANK is a type I membrane protein expressed on the surface of osteoclasts and is involved in their activation upon ligand (RANKL) binding. OPG produced by osteoblasts is a potent inhibitor of osteoclast differentiation and survival by acting as a decoy receptor for RANKL leading to decreased signaling through it membrane receptor, RANK [13].

Growing evidence suggests that the triad of RANK/RANKL/OPG, key proteins involved in bone metabolism, may be important players in vascular calcification. OPG, RANKL and RANK are present in atherosclerotic plaques and valve disease, and their relative expression levels are different depending on the stage of the disease [14, 15]. OPG appears to be protective against vascular calcification, since OPG^−/− mice developed spontaneous arterial calcification [16], and depleting OPG in ApoE−/− mice increased atherosclerotic lesion progression and calcification [17]. Likewise, evidence that RANKL stimulates vascular calcification is growing. In one study, RANKL increased vascular smooth muscle cell calcification directly by binding to RANK and increasing BMP4 production through the alternative NF-κB pathway [18]. In another study, RANKL indirectly promoted smooth muscle cell calcification by enhancing macrophage paracrine pro-calcific activity through release of Il-6 and TNFa [19]. These studies suggest that RANK/RANKL may be important in promoting vascular calcification, while OPG inhibits vascular calcification.

Whether or not osteoclasts or osteoclast deficiency might play a role in vascular calcification is less clear. Osteoclast-like cells that express tartrate resistant acid phosphatase (TRAP) can be found in calcified vascular lesions in people, but were typically present at very low levels and only at advanced stages of disease [6, 20]. Since osteoclasts typically function to resorb bone, a deficiency of osteoclast-like cells as observed in human calcified lesions might be expected to facilitate vascular calcium accrual. However, in ApoE−/− mice, osteoclast-like cells were observed in atherosclerotic lesions, and selective knockdown of Runx2 in smooth muscle cells led to decreased RANKL expression, osteoclast-like cell number, and lesion calcification, suggesting that osteoclasts might actually promote vascular calcification [21]. Clearly, further studies to determine the role of osteoclasts in vascular calcification are needed to distinguish between these possibilities.

microRNAs: new players in vascular calcification

MicroRNAs (miRNA) are noncoding single stranded RNAs of ~22 nucleotides that are recognized as a novel class of gene regulators. miRNAs bind to complementary sequences on target mRNAs, usually resulting in translational repression or target degradation. One single miRNA may target multiple genes providing extensive translational regulation and multiple miRNAs may work together promoting combinatorial regulation by individually targeting many components of a pathway. The role of microRNAs in cardiovascular biology is currently under intense investigation, and specific miRNAs have been associated with various cardiovascular disorders, including vascular remodeling, cardiac hypertrophy, heart failure and post-myocardial infarction remodeling [22]. Increasing evidence shows that miRNAs may play a pivotal role in regulating vascular cell functions and contribute to vascular calcification. For example, miR-125b, previously found to be involved in osteoblast differentiation, was found to be involved in the osteogenic transdifferentiation of VSMCs by targeting SP7 in vivo and in vitro [23]. miR-204 was identified as an important regulator of VSMC functions by down-regulating its target gene Runx2 and inhibiting medial artery calcification in vivo [24]. Using kl/kl mouse model and specific miRNA inhibitors, miR-135a*, miR-762, miR-714 and miR-712* were shown to target Ca²⁺ transporters that are involved in vascular smooth muscle cell calcification [25]. These studies implicate miRNAs as a novel link in the mechanisms of vascular calcification.

Potential Treatments of Vascular Calcification

To date, a variety of therapies have been tested to try and prevent or regress vascular calcification. Preventative therapies must be given to at-risk populations prior to the formation or progression of vascular calcification, whereas a therapy capable of eliminating or reducing vascular calcification has the advantage of treating patients who have already developed vascular calcification. The available therapies are often existing treatments for related conditions and can be categorized as osteoporosis therapies, CKD therapies, and cardiovascular disease therapies. There are also experimental therapies at various research stages. These therapies are outlined in Table 1, which describes the therapies and their mechanism of action, as well as any evidence of efficacy.

Table 1.

Therapies for Treating Vascular Calcification Under Investigation.

Treatment	Mechanism of Action	Proposed Effect on Vascular Calcification	Evidence	References
Osteoporosis Therapies for Treating Vascular Calcification
Bisphosphonates	Inhibitor of osteoclast formation & survival; calcium phosphate crystal poison	Reduces release of Ca2+ and blocks hydroxyapatite nucleation and growth	Human Trials - Slowed vascular calcification with some bisphosphonates; resolution of calciphylaxis	[26–30]
Denosumab	Binds RANKL & inhibits binding to RANK	Reduces release of Ca2+; blocks RANKL mediated SMC calcification	Animal Studies - Reduced vascular calcification in mouse model of glucocorticoid-induced calcification	[18, 21, 31]
Osteoprotegerin	Binds RANKL & inhibits binding to RANK	Reduces release of Ca2+; blocks RANKL mediated SMC calcification	Animal Studies - Prevented mineralization of atherosclerotic lesions in LDLR −/− mice	[16, 32, 33]
Teriparatide	Stimulates bone formation	Increases levels of circulating osteopontin, an inhibitor of calcification	Animal Studies - Decreased valve calcification in a diabetic LDLR −/− mice	[34, 35]
Chronic Kidney Disease Therapies for Treating Vascular calcification
Phosphate Binder	Bind to dietary phosphate & prevent absorption by digestive system	Reduces serum levels of phosphate to help slow mineralization of soft tissue	Human Trials - Phosphate binders without Ca may slow progression of vascular calcification	[36, 37]
Vitamin D Receptor Agonists	Treat secondary hyperparathyroidism and Vitamin D deficiency associated with CKD	Increases levels of osteopontin and klotho, preventing calcification	Human Trials - Survival benefit with VDRA therapy	[38, 39]
Calcimimetics	Bind to calcium-sensing receptors to treat secondary hyperparathyroidism	Lowers circulating calcium levels	Human Trials - Randomized study found calcimimetics slowed progression of calcification	[40, 41]
Vitamin K	CKD patients often deficient for vitamin K, a cofactor in various metabolic pathways	Increases activation of circulating MGP, an inhibitor of calcification	Human Trials - Supplementation increased levels of active MGP	[42–44]
Sodium Thiosulfate	A vasodilator, antioxidant, and a calcium chelator	Improves local circulation, and reduces inflammation and calcification	Human Trials - Established treatment for calciphylaxis; possible treatment for other forms of vascular calcification	[45–47]
Cardiovascular Disease Therapies for Treating Vascular calcification
Endothelin Receptor Antagonists	Blocks endothelin receptor signaling and reduces blood pressure	Reduced blood pressure may result in decreased calcification	Animal Studies - Vascular calcification halted or reversed in mouse models	[48, 49]
Statins	HMG CoA reductase inhibitors; Reduce cholesterol production by liver	Prevents lipid deposition on heart valves and reduce inflammation	Human Trials–Benefit for valve calcification not seen in randomized controlled studies	[50, 51]
Experimental Therapies for Treating Vascular calcification
EDTA Chelation Therapy	Binds free calcium	Lowers serum calcium levels to reduce calcification	Human Trials - Small pilot suggested benefit to less than half of patients	[52]
Metabolic Acidosis	Side-effect of certain diseases; decreased pH of bodily fluids	Dissolution of mineral in calcified vessels	Animal Studies - Prevented vascular calcification in uremic rat model	[53, 54]
Autologous Osteoclasts	Main mineral-resorbing cells in the body	Resorb abnormal mineral in vascular calcification	Animal Studies–Limited calcification of elastin implanted subdermally in rats	[55, 56]

Osteoporosis Therapies

Bisphosphonates (Pyrophosphate Analogs)

Bisphosphonates have been used as an effective therapy for osteoporosis for almost 40 years. They inhibit bone resorption by binding to hydroxyapatite where they are ingested by osteoclasts. The uptake of these pyrophosphate analogs interferes with normal osteoclast functions, and reduces bone resorption. Pyrophosphate analogues are also extremely potent inhibitor of hydroxyapatite nucleation and crystal growth [26]. Due to the high association of osteoporosis and vascular calcification, bisphosphonates were viewed as a potential therapy for vascular calcification. Pyrophosphate and bisphosphonates have been found to inhibit both vascular calcification and calciphylaxis in a several animal studies [27]. It has been hypothesized that this effect is due to lowered serum levels of calcium and phosphate, and/or reduced nucleation and growth of calcium phosphate crystals that lead to vascular calcification. Bisphosphonates may be useful for treating calciphylaxis, with a small prospective study suggesting that intravenous ibandronate halted progression and improved healing in 8 patients with calciphylaxis [28]. For vascular calcification, even though bisphosphonate therapy has shown effectiveness in animal models, there is still some debate over its efficacy for preventing vascular calcification in humans, and the results differ by the specific bisphosphonate in question. In studies of patients with ESRD undergoing dialysis, etidronate has been found to limit the further progression of vascular calcification [29]. On the other hand, alendronate and ibandronate have had mixed results at limiting the progression of vascular calcification, with animal studies suggesting alendronate and ibandronate limit vascular calcification, while randomized controlled trials found no effect of alendronate or ibandronate therapy in humans [30]. The pros of bisphosphonate therapy need to be weighed with the cons, and bisphosphonates are not advisable for CKD patients due to side effects.

Denosumab

Denosumab is a human monoclonal antibody targeting RANKL. RANKL is required for osteoclast differentiation and survival, so denosumab inhibits bone resorption and is one of the newest therapies for osteoporosis. As described above, RANKL also has direct effects to promote vascular smooth muscle cell calcification [18] and TRAP+ osteoclast like cell formation [21]. Because of these activities, denosumab has also been studied for its ability to prevent vascular calcification. In a mouse model of glucocorticoid-induced osteoporosis, denosumab reduced the amount of calcium that was found to deposit in the aorta [31]. Study in humans is needed to determine if denosumab is able to prevent vascular calcification.

Osteoprotegerin

Osteoprotegerin (OPG) is a protein that inhibits bone resorption. It is a decoy receptor that binds and inhibits RANKL, and like denosumab, prevents osteoclastogenesis. OPG is likely involved in vascular calcification, and it inhibits calcification in vitro; it is thought that this activity comes from OPG increasing expression of insulin-like growth factor-1 receptor on smooth muscle cells [32]. One study of OPG knock-out mice found that the mice developed extensive vascular calcification in addition to the expected result of osteoporosis [16]. Treatment with a recombinant fusion protein, Fc-OPG, has been shown to inhibit vascular calcification in animal studies [33].

Teriparatide (Human Parathyroid Hormone 1–34)

Teriparatide is a recombinant protein representing a portion of human parathyroid hormone (hPTH), specifically amino acids 1-34. It has been used clinically to increase bone mineral density in patients with osteoporosis, with some studies showing greater efficacy than bisphosphonates [34]. Due to the role of PTH in regulating calcium and phosphate levels, it has been studied as a method to prevent vascular calcification. One study in diabetic low density lipoprotein receptor deficient mice found that daily subcutaneous administration of teriparatide greatly reduced the extent of both aortic and cardiac valve calcification [35]. It was also found to increase expression of osteopontin, a potent circulating inhibitor of calcification.

Chronic Kidney Disease Therapies

Phosphate Binders

Phosphate binders are a class of drugs that bind phosphate and form an insoluble complex in the digestive system. This prevents the phosphate from ever being absorbed, which is beneficial for patients with ESRD on dialysis whose kidneys are unable to maintain proper phosphate homeostasis [36]. There are two main types of phosphate binders: calcium-containing binders, such as calcium acetate, and calcium-free binders, such as lanthanum carbonate and sevelamer carbonate. Although both types are effective at regulating phosphate levels, they differ in their effect on vascular calcification, with the calcium-containing phosphate binders being thought to contribute to the development and progression of vascular calcification, and the calcium-free phosphate binders being thought to slow progression. This hypothesis is supported by several studies in human CKD patients [37]. Most patients on dialysis are currently taking some form of phosphate binder, but the data suggests that non-calcium containing phosphate binders should be used in patients with high risk for vascular calcification.

Vitamin D Receptor Agonists

Vitamin D is a vitamin that plays a role in multiple metabolic pathways, including regulation of mineral metabolism. Vitamin D receptor agonists (VDRAs) are given to patients with CKD to ameliorate the effects of hyperparathyroidism and vitamin D deficiency. Vitamin D deficiency is associated with early mortality CKD patients and VDRA therapy prolongs survival in hemodialysis patients, but their mechanism was not fully understood [38]. In a mouse model of chronic kidney disease, VDRA therapy significantly reduced aortic calcification [39]. In this study, the effect of VDRA therapy was associated with increased expression of serum klotho, a phosphaturic hormone, and vascular medial osteopontin, an inhibitor of vascular calcification.

Calcimimetics

Calcimimetics are compounds that mimic the effects of calcium in vivo. They have been used to treat hyperparathyroidism by binding to calcium sensing receptor (CaR) in the parathyroid glands. Calcimimetics are allosteric modulators of CaR which make the CaR more sensitive to existing levels of circulating calcium, which in turn, suppress secretion of PTH. Calcimimetics have been shown to reduce vascular calcification in a variety of uremic rat models [40]. There is also evidence of efficacy in humans. The ADVANCE study found that calcimimetics with VDRA therapy slowed progression of vascular calcification over VDRA therapy alone in hemodialysis [41]. Calcimimetics may be an important tool to treat vascular calcification, but it is unclear if it will work in non-CKD patients.

Vitamin K

Vitamin K is a group of cofactor vitamins involved in coagulation and various metabolic pathways. It is required by the enzyme gamma-glutamate carboxylase to modify Matrix Gla protein (MGP), into its active carboxylated form [42]. Active MGP inhibits calcification, and the exact mechanism is still being elucidated. Possibilities include binding to crystals and halting further growth, or by binding to bone morphogenic protein (BMP) and preventing osteogenic differentiation of cells. Vitamin K was found to inhibit vascular calcification in warfarin-treated rats [43]. In humans, increased expression of under carboxylated MGP is associated with vascular calcification and increased risk of cardiovascular mortality, and supplementation with vitamin K2 was found to increase levels of carboxylated MGP in dialysis patients [44]. Further study is necessary to determine if the increased levels of active MGP will lead to prevention of vascular calcification in humans.

Sodium Thiosulfate

Sodium thiosulfate is a small molecule that acts as a vasodilator, antioxidant, and a calcium chelator in vivo. It has been used successfully to treat calciphylaxis, where it reduces calcification and improves local circulation. It binds to calcium to form calcium thiosulfate which can be excreted from the body [45]. Due to its success in treating calciphylaxis, it has been studied for treatment of other forms of vascular calcification. In a uremic rat model of vascular calcification, treatment with sodium thiosulfate completely prevented aortic calcification; however, this was associated with lowered bone strength in the treated animals [46]. One pilot study of sodium thiosulfate treatment in patients undergoing hemodialysis suggested that sodium thiosulfate maybe be safe to use, with few side effects seen after 5 months of treatment; larger studies are needed to confirm efficacy [47].

Cardiovascular Disease Therapies

Endothelin Receptor Antagonists

The endothelin receptor is involved with regulating blood pressure; when endothelins bind to this receptor blood pressure increases due to vasoconstriction. For this reason, endothelin receptor antagonists (ERAs), that block the binding of endothelins, are popular therapies for hypertension. The receptor is also important in vascular calcification, with one study showing an increase in levels of endothelin in vitro and in vivo vascular calcification; this calcification could be ameliorated by ERAs [48]. Studies in rat models of hypertension found that darusentan reduced aortic calcification [49]. Study in humans is needed before the effect of ERA therapy on vascular calcification can be ascertained, but this method shows promise.

Statins

Statins are a group of drugs that help lower serum cholesterol by inhibiting HMG CoA reductase in the liver, to help prevent the formation of atherosclerotic lesions. Valve stenosis and calcification has some similarities to atherosclerosis, including inflammation and lipid deposition, and both atherosclerosis and valve calcification often appear in the same patients [50]. For these reasons, statin therapy was investigated as a potential treatment to prevent calcific valve stenosis. Early retrospective studies suggested a benefit of statins, with treated patients exhibiting reduced progression of calcific aortic stenosis [51]. However, when controlled randomized trials were conducted, there was no benefit seen. It is now generally accepted that statin therapy does not impact calcific aortic stenosis [50].

Experimental Therapies

EDTA Chelation Therapy

Ethylenediaminetetraacetic acid (EDTA) is a synthetic amino acid which is capable of binding free calcium. It is has various commercial and scientific applications, but its usefulness in medicine is unclear. Because it can bind calcium, it has been proposed as a therapy for vascular calcification. One small human trial has shown a regression of vascular calcification in some patients as measured by computed tomography [52]. However, this study lacked a control group for comparison and less than half of the patients responded to the therapy, so further study is needed.

Metabolic Acidosis

Metabolic acidosis is the condition where the pH of the blood and bodily fluids is abnormally low. It is commonly seen in patients with CKD, and can result in a plethora of negative side effects including bone disease, muscle degradation, inflammation, and cardiovascular disease. It has been suggested that metabolic acidosis may have a beneficial effect on preventing calcification in the vasculature through the same chemical and cellular mechanisms that result in bone dissolution. Specifically, metabolic acidosis is known to result in the physicochemical dissolution of bone mineral, as well as the activation of osteoclasts through signaling pathways such as RANKL [53]. A study of calcitriol-induced calcification in uremic rats found that metabolic acidosis helped prevent calcification in vitro and in vivo [54]. It is unclear if the beneficial effects of metabolic acidosis can be separated from the negative effects.

Autologous Osteoclasts

Osteoclasts are the main mineral resorbing cells in the body. They are formed from fusing mononuclear precursor cells of the myeloid lineage and differentiate in response to cytokines including macrophage colony-stimulating factor (M-CSF) and RANKL [55]. A landmark study found that osteoclasts derived from rat bone marrow were capable of removing mineral from calcified elastin in vitro; additionally, when the cells were co-implanted with elastin subdermally in rats, calcification was limited [56]. These studies were the first to suggest that autologous osteoclasts might be utilized as a therapy for vascular calcification. Methods for local delivery and activation of osteoclasts at sites of vascular calcification in vivo would aid in the development of this type of cell therapy. In our lab, we have engineered monocytic precursors to differentiate into osteoclasts under the control of a small molecule. This differentiation is independent of RANKL and MCSF, and is resistant to inhibition by OPG. When combined with autologous precursors, this system could be used to develop a local cell-based therapy to treat or prevent ectopic calcification (Wu et al, submitted).

Future challenges

Vascular calcification was first recognized more than a century ago. In the last few decades, the advances in this field have improved our understanding of the molecular mechanisms that contribute to vascular calcification. Most recently, several lines of evidence have inversely correlated vascular calcification with bone formation, and several potential treatments under investigation are related to osteoporosis therapies. However, the efficacy of these drugs in inhibiting vascular calcification was discovered from either the studies of several animal models or a relatively small set of human trials, and may be more based on their efficacy at blocking calcium phosphate crystal growth, rather than their inhibition of osteoclast function. Further studies using larger numbers of patients are needed to reveal the action of these drugs. In addition, therapeutic strategies used in CKD patients to reduce phosphate burden or block calcium channels, while showing promise in preventing progression of vascular calcification, may have potential risks for bone health. Thus, for the development of new treatments specifically targeting vascular calcification, serious consideration of the implications for bone metabolism must be taken into account to avoid potentially harmful effects to bone health.