Cardiovascular calcification (CVC) is a progressive complication of chronic kidney disease and a predictor of CV events and mortality. The use of biomarkers to predict CV risk and activities of potential or current treatment drugs in these patients could have a crucial impact on therapeutic approaches. Our aim was to develop a novel assay for measurement of the rate of calcium phosphate crystallization in human plasma and provide a tool to evaluate the effects of crystallization inhibitors. The efficacy of inhibitors was determined by adding inhibitory compounds (polyphosphates, fetuin-A, sodium thiosulfate or citrate) to control samples. The assay was additionally validated for SNF472, an experimental formulation of phytate being developed for the treatment of calciphylaxis and CVC in patients with end-stage renal disease (ESRD) undergoing hemodialysis (HD). The method was repeatable and reproducible. The plasma crystallization rate was reduced up to 80% in a concentration-dependent manner following treatment with inhibitors in vitro, among which SNF472 was the most potent. This method appears beneficial in evaluating and discriminating between inhibitory activities of compounds such as polyphosphates on calcium phosphate crystallization, which present a novel therapeutic approach to treat CVC in ESRD patients.
Calcification is the normal process of calcium salt deposition in body tissues occurring due to the presence of supersaturated or metastable salt solutions in biological fluids1, 2. This process is usually represented by calcium phosphate mineralization in the form of hydroxyapatite (HAP), Ca10(PO4)6(OH)2, and controlled by thermodynamic conditions as well as the local concentrations of proteins in biological fluids. This inorganic mineralization mainly occurs in bones and teeth under physiological conditions. However, pathologic ectopic formations, such as calcification in soft tissue and cardiovascular calcification (CVC), are common in calcium-related disorders. CVC is recently described to be not only a passive physicochemical process, as explained above, but also an active cell-mediated process of artery calcification including both atherosclerotic (intimal artery layer) and medial calcification that involves multiple factors and mechanisms with a final common step of ectopic HAP accumulation.
Chronic kidney disease (CKD) and calciphylaxis are disorders that develop as a consequence of disturbances in calcium and phosphate metabolism, and involve inflammatory processes in which levels of circulating calcification inhibitors, such as fetuin-A3, matrix-Gla protein4, 5, pyrophosphate and osteopontin, are reduced while promoters of calcification are increased. This imbalance between circulating levels of promoters and inhibitors of calcification results in osteogenic transformation and HAP precipitation. In patients with advanced and end-stage renal disease (ESRD), CVC is a normal progressive complication and a predictor of cardiovascular events and mortality6, 7. These patients can also suffer from calciphylaxis, resulting in accelerated medial calcification of cutaneous arteries and arterioles8,9,10,11 and associated with high mortality rates12, 13.
Although no approved therapies are currently available for the treatment or reduction of HAP accumulation in CVC, there are evidences from randomized clinical trials of decreasing the progression of CVC in ESRD. These treatments include non-calcium-based phosphate binders to reduce hyperphosphatemia14, as well as calcimimetics to treat sHPT15. Moreover, other studies demonstrated the efficacy of physicochemical inhibitors of HAP crystal formation, such as bisphosphonates16, 17 in the reduction of CVC progression. Therapeutic agents for calciphylaxis additionally include bisphosphonates owing to their anti-inflammatory properties18, non-calcium phosphate binders19 and sodium thiosulfate (STS), an antioxidant and vasodilator agent8, 20, 21. However, none of these compounds have been approved for calciphylaxis and their use is off-label. Several studies have presented evidence supporting the utility of phytate in calcification-related diseases, such as renal calculi22,23,24, osteoporosis25, 26 and CVC in animal models27,28,29,30. SNF472, an intravenous (i.v.) formulation of myo-inositol hexaphosphate (phytate) that binds to the growing sites of HAP crystal, is currently being developed for the treatment of calciphylaxis and CVC in patients with ESRD undergoing HD.
Since calcification is a slow process and no specific biomarkers have been defined to date, evaluation of new therapeutic interventions in clinical trials is an arduous and challenging task. The search for novel biomarkers for effectively assessing the risk of CVC progression has been the major focus of scientific interest in recent years. Assessment of blood crystallization potential in patients with calcium-related disorders may be a relevant parameter to estimate the risk of CVC. Originally, a nanoparticle-based test was developed to measure the propensity for calcification in serum31. Subsequent clinical studies demonstrated associations of this nanoparticle marker with CVC and mortality, graft failure after renal transplantation and aortic stiffness32,33,34. However, this method lacked the ability to evaluate the effectiveness of potential therapeutic agents, such as polyphosphates (pyrophosphate, bisphosphonates or phytate). No assays are currently available to assess blood crystallization tendency in the presence of calcification inhibitors. Since polyphosphates protect against crystallization and are the mainstay of CVC treatments27, 29, 35,36,37, the key objective of this study was to develop a novel and rapid in vitro/ex vivo method to evaluate of calcium phosphate crystallization in plasma samples containing calcification inhibitors and validate its potential as a pharmacodynamic assay for use in both non-clinical and clinical settings.
Validation of the spectrophotometric PD assay in human plasma
Intra-day and Inter-day precision were evaluated by calculating %CV and presented as the average of three determinations (Table 1). For both parameters, CV was below 15%, signifying that the assay is both repeatable and reproducible with human plasma samples.
Reduction in the crystallization rate in human plasma samples was tested by spiking different concentrations of seven calcification inhibitors into blank plasma samples. As observed in Fig. 1, SNF472 showed the highest potency in inhibiting calcium phosphate crystallization with an IC50 value of 2.12 µM. Ibandronate (IC50 = 5.13 µM) and pamidronate (IC50 = 6.42 µM) were additionally very effective but not as potent as SNF472 (data for pamidronate not shown in Fig. 1 for clarity purposes). Pyrophosphate showed lower inhibitory potency (IC50 = 25.97 µM) as well as fetuin (IC50 = 545.80 µM). IC50 values of citrate and STS were 17.5 mM and >500 mM, respectively.
To validate the PD assay, the method was applied to evaluate the crystallization inhibition potential in rat and human plasma samples containing SNF472. Linearity, inter-day and intra-day precision, integrity of dilution and stability of phytate spiked in plasma were analyzed. The data obtained for these parameters are presented in Figs 2 and 3 and Table 2.
A dose-response curve in the defined range (0–30 μM) of SNF472 was obtained, as shown in Fig. 2a. A directly proportional relationship between inhibition of crystallization and concentration of SNF472 was observed within the interval of 1–4 µM (dashed lines) with a correlation coefficient (R2) of 0.98. Figure 2b presents the precision profile (CV versus concentration on the log scale) of the method in the calibration range. The dotted line represents the initial working range established by a threshold of 20% CV. A LLOQ value of 0.77 μM was obtained with Eq. (2) applied to the lower portion of the curve defined between 0 and 4 μM SNF472, R2 = 0.99 (Fig. 2c). The theoretical concentrations to attain 30%, 50%, 80% and 95% inhibition were calculated via nonlinear regression analysis of the dose-response curve as 1.17 μM, 2.12 μM, 5.59 μM and 16.65 μM, respectively.
The intra-day and inter-day precision of the spectrophotometric assay data used to determine the efficacy of crystallization inhibition in human plasma samples spiked with five different concentrations of SNF472 (LLOQ, IC30, IC50, IC80 and IC95) are presented in Table 2. Intra-day precision was low at LLOQ with CV of 61.9%, whereas within-day precision (CV < 20%) was acceptable at concentrations of SNF472 in plasma from IC30 onwards, with values between 17.4% and 3.0%. Inter-day results showed low precision at LLOQ and IC30 levels (108.8% and 38.3%, respectively), but CV of <20% from IC50 onwards.
The ability to dilute samples with concentrations above the upper limit of the calibration curve was assessed (Fig. 3a). Samples diluted 1/10 and 1/100 in blank plasma displayed similar activity values as control non-diluted samples with the same final concentration, with acceptable precision. Data on the stability of SNF472 in plasma samples after storage for different periods of time and under varying temperature conditions are presented in Fig. 3b–f. Samples containing higher concentrations of SNF472 (IC80 and IC95) were stable after three freeze/thaw cycles. However, significantly lower activities were observed at the IC30 concentration in samples exposed to two and three freeze/thaw cycles (Fig. 3b). PD activity did not change in samples maintained for up to 2 h at room temperature, compared to fresh samples as the control (Fig. 3c). Samples were stable for 4 h at 4 °C at all SNF472 concentrations, as shown in Fig. 3d. In addition, samples with SNF472 concentrations around the IC50 level or above were stable for up to 8 h at 4 °C while only those with concentrations at the IC80 level or above were stable for 24 h under these conditions. Stability of SNF472 spiked in human plasma samples after storage at −20 °C or −80 °C was the last parameter evaluated for assay validation. As shown in Fig. 3e, after four weeks of storage at −20 °C, SNF472 spiked in human plasma remained stable at IC30 or higher. Results obtained with samples stored at −80 °C for up to 48 weeks are shown in Fig. 3f. We observed no significant influence of the time of storage at this low temperature on efficacy values.
Preclinical revalidation of the PD assay in rat plasma
The dose-response curve for SNF472 in rat plasma is shown in Fig. 4a. The linear response of inhibition of calcium phosphate crystals is presented as dashed lines, and observed from 1 up to 10 µM SNF472 (R2 = 0.96). As observed in Fig. 4b, total levels of SNF472 in plasma samples obtained 20 min after s.c. injection and analyzed via UPLC®-MS were proportional to the administered dose and ranged between a mean of 13.6 μM in rats treated with 20 mg/kg SNF472 and 176 μM in rats treated with 100 mg/kg SNF472. Consequently, rat plasma samples were diluted 1/10 with blank plasma prior to the PD assay to fall within or near the linearity range obtained in the dose-response curve (Fig. 4a). PD results in Fig. 4c showed that s.c. administration of SNF472 to rats effectively reduces crystallization potential in plasma. In addition, inhibition of crystallization was increased in proportion to the SNF472 concentration found in plasma. Table 3 presents the mean SNF472 levels and mean inhibition of crystallization values obtained from the PD assay for each dose administered to rats. Good correlation was observed among doses, plasma levels and crystallization inhibition.
Implementation of the PD assay in HD patients
As shown in Fig. 5a, plasma obtained from non-dialyzed healthy volunteers and HD patients (pre- and post-dialysis) did not present significant differences in crystallization rate. Data obtained on inhibition of crystallization after in vitro addition of SNF472 at final concentrations of 0.77, 1.17, 2.12, 5.59 and 16.65 μM into plasma samples are presented in Fig. 5b. Addition of SNF472 to plasma obtained from non-dialyzed volunteers as well as pre-dialysis and post-dialysis patients reduced the crystallization rate in a concentration-dependent manner (maximum inhibition of 85%, 88% and 78%, respectively). SNF472 suppressed plasma crystallization to a higher extent in healthy volunteers than HD patients at concentrations lower than 5 µM. At higher SNF472 concentrations, similar maximum inhibition rates were estimated in plasma samples from non-dialyzed volunteers and pre-dialysis patients while inhibition in samples from post-dialysis patients was significantly lower.
CVC, a prevalent problem in CKD, is associated with high risk of adverse cardiovascular events and death38. Determination of a combination of biomarkers that can be clinically used as a predictor of cardiovascular risk and concomitant therapy for CKD patients is therefore a topic of significant research interest. However, clinical implementation of these markers is limited in some cases, given the need to standardize and validate assay reproducibility. Moreover, clinical applicability of the current cardiovascular biomarkers is more focused on risk of calcification than used as a guide to therapy39. Here, we have presented a rapid, repeatable and reproducible in vitro/ex vivo spectrophotometric assay that facilitates evaluation of the activities of potential calcification inhibitors of calcium phosphate crystallization in human plasma samples. Our results confirmed the effectiveness of physicochemical inhibitors that target the crystal formation process, such as bisphosphonates40, 41, pyrophosphate42 and phytate27,28,29 as potential treatments to prevent soft tissue calcification. These are compounds with structural similarities (polyphosphates) that impede further progression of crystallization by binding to HAP crystals and inhibiting vascular calcification. Among the inhibitors tested, SNF472 (an i.v. formulation of phytate) showed the highest potency in inhibiting formation of calcium phosphate crystals in plasma samples (IC50 = 2.12 µM). Bisphosphonates and pyrophosphate exhibited IC50 values that were in the micromolar range (5.13 and 25.97 µM, respectively), but higher than phytate. These results are consistent with previous studies in which bisphosphonates (non-hydrolysable analogs of pyrophosphate) showed higher efficiency in inhibiting crystallization than pyrophosphate43. Moreover, the different crystallization inhibition rates between polyphosphates may be related to the number of phosphates in the chemical structure. While phytate contains six phosphate groups, both bisphosphonates and pyrophosphate contain two groups. Fetuin-A, a well-known circulating serum glycoprotein and potent systemic calcification inhibitor, exhibited lower potency in inhibiting calcium phosphate crystals in the in vitro assay (IC50 of 545.80 µM). The different inhibitory activities obtained with polyphosphates and fetuin-A may be explained by the fact that polyphosphates present higher binding affinity in the first steps of calcium phosphate formation, while fetuin-A interferes with later steps of the process, including the formation of colloidal (calciprotein) particles, CPP44, 45. Citrate does not significantly bind the HAP crystals, but rather chelates calcium. Therefore, greater amounts of this compound are required to start inhibiting crystal formation (IC50 8.000–fold higher than phytate) under these in vitro supersaturated calcium conditions. The fact that the calcium concentration is almost 10-fold that of phosphate might explain this lower efficacy shown by citrate. However, it must be noted that the assay is performed in plasma obtained with EDTA, which in fact is chelating part of the added calcium and this might be the reason why calcium concentration had to be pushed so high in order to induce crystallization. Although STS also has the ability to bind free calcium, it is not a strong calcium chelator. In accordance with previously reported in vitro observations, we confirm that free calcium is only slightly affected by STS suggesting that STS inhibits vascular calcification at the millimolar range through different mechanisms from both calcium complexation and calcium phosphate crystallization inhibition46,47,48. These collective findings support the utility of our assay as a novel and rapid predictor of crystallization inhibitor activity. This is an important achievement because currently available assays31 are not appropriate for use with anionic crystallization inhibitors, such as polyphosphates, since cationic buffers (HEPES) interact with the negative charges of the inhibitors and impede their normal action. Our assay has been optimized for use with NaCl as the matrix and relies on the plasma and phosphate solution to maintain pH near 7.40, facilitating anionic inhibitor activity. Table 4 compares this novel method to those previously developed and that were properly reviewed by Pasch32.
In view of the efficacy shown by SNF472 and its current development for treatment of CVC and calciphylaxis in ESRD patients, we validated the utility of our assay in obtaining PD clinical measurements for this compound. The linear portion of the calibration curve nearly corresponded to the correct working range (SNF472 > 1.5 μM) at low inhibitor concentrations while at concentrations higher than 4 μM, efficacy reached a plateau and coefficient of variation (CV) was still lower than 20%. Similarly, intra-day precision experiments showed that this in vitro/ex vivo assay is repeatable with SNF472 concentrations at the IC30 value (1.17 μM) or above. In contrast, analysis of inter-day precision indicated that the PD assay is reproducible when inhibitor concentrations are nearly at IC50 or higher (2.12 µM). The high variability at low SNF472 concentrations can be explained by the steep response generated by the compound (Hill slope > 1), which makes assessment of its activity below IC50 difficult. This is not expected to be a problem, as the final therapeutic levels in humans are expected to be around 14 µM (at Tmax after intravenous infusion), and therefore PD activity is within the plateau interval where the assay is highly reproducible. If required, SNF472-containing plasma samples can be diluted up to 100-fold in blank plasma to obtain values in the linear range of the assay. In terms of the stability, plasma samples containing SNF472 could be maintained at 4 °C between blood collection and plasma separation. Plasma samples could be successfully frozen at −80 °C over a long storage period (up to one year) and thawed samples maintained at 4 °C for a maximum of 4 h before analysis. The parameters obtained for samples containing SNF472 may be extrapolated to samples containing other polyphosphates.
The validity of the test was confirmed in rat plasma, both in vitro and ex vivo, as well as in human plasma ex vivo. The addition of SNF472 to rat plasma samples reduced the HAP crystallization rate in a concentration-dependent manner up to 80%. Moreover, SNF472 administered subcutaneously to rats suppressed the ex vivo HAP crystallization potential of plasma up to 70%. This reduction was dose- and concentration-dependent. Therefore, the plasma concentration of SNF472 reached following s.c. administration has the same maximum efficacy as that in vitro, highlighting the utility of our novel PD assay in human studies. Additional non-clinical studies linking the PD assay results with inhibition of cardiovascular tissue calcification should confirm this potential association in vivo.
On the other hand, application of the assay to plasma samples obtained from healthy, non-dialyzed volunteers and HD patients revealed no significant differences between the basal plasma crystallization potential of patient and volunteer groups, suggesting that in vitro supersaturated conditions lead to loss in sensitivity of the method. This is a significant difference between our new method and the assay previously developed by Pasch et al.31, 32, which could differentiate the calcification propensity between HD patients and controls. The reason for this discrepancy may lie in the supersaturated calcium and phosphate concentrations used in the current assay. In these conditions, the calcium phosphate crystallization is forced to an extent that higher endogenous calcium or phosphate concentrations might not interfere. Thus, the novelty of our assay relies on its utility in testing the effects of inhibitors on crystallization and comparing their potencies. In this instance, after in vitro addition of SNF472 to blood of controls and HD patients, the in vitro concentrations required to normalize crystallization potential were higher in HD patients than healthy volunteers, highlighting slight resistance of the blood of HD patients to the inhibitory effects of SNF472, especially at low concentrations. However, maximum inhibition of crystallization (70-80%) could also be achieved in these patients.
In conclusion, we have developed a novel and rapid (30 min) assay to determine the in vitro/ex vivo inhibition potential of calcium phosphate crystallization inhibitors and validated its efficacy in rat and human plasma samples. Since evaluation of the impact of drug candidates on vascular calcification progression requires long-term clinical trials with hundreds of patients49, leading to high research costs, this assay may be effectively employed as a screening tool for rapid evaluation of potential efficacy in suppression of vascular calcification progression. Among the inhibitors tested in the current study, SNF472 (or phytate) was the most powerful, showing 2- and 12-fold higher potency than bisphosphonates and pyrophosphate, respectively. Further validation of results obtained with SNF472 in human samples highlights the potential utility of this assay as a PD measurement tool in the clinical setting.
Materials and Methods
A spectrophotometric pharmacodynamics (PD) assay for in vitro/ex vivo determination of crystallization potential in plasma
The spectrophotometric assay was performed in 96-well plates. Plasma (80 µL) was centrifuged at 10,000 g for 30 min at room temperature and subsequently mixed with 60 µL of 5 mM hydrogen phosphate and 60 µL of 41.67 mM calcium to attain final concentrations of 1.5 mM phosphate and 12.5 mM calcium, respectively. All reagent solutions were filtered and pH adjusted to 7.4. Crystallization of calcium phosphate was monitored spectrophotometrically for 30 min at room temperature via increase in absorbance at 550 nm using the Biotek Powerwave XS Microplate spectrophotometer. The plate was incubated at room temperature in an orbital shaker (750 rpm) and absorbance measured every 3 min. Plasma crystallization potential was assessed based on slope measurement in the linear range between 6 and 24 min from plots of increase in absorbance versus logarithm of time.
Validation of the spectrophotometric PD assay in human plasma
This study was conducted according to the guidelines of the Declaration of Helsinki. All procedures involving human subjects/patients were approved by the Ethical Committee of Clinical Investigation of the Balearic Islands (IB 2245/14 PI). Participants were informed of the purpose and characteristics of the study before providing written consent.
Venous blood samples were obtained from the antecubital vein of healthy volunteers under fasting conditions and collected in tubes with K2EDTA as anticoagulant. Plasma was obtained after centrifugation of blood at 3,500 rpm at 4 °C for 10 min and mixed to form a pool.
Intra-day and inter-day precision under repeatability and reproducibility conditions
The spectrophotometric PD assay was repeated with three runs in the same day (intra-day precision) and three consecutive days (inter-day precision) in a 96-well plate (12 replicates per run). Intra-day precision refers to the repeatability of the assay while inter-day precision indicates between-day precision (reproducibility). Both parameters were evaluated by determining the within-day and between-day average coefficients of variation (CV) of the slopes obtained.
Inhibition of HAP crystallization in plasma samples
The efficacy of different calcification inhibitors in preventing in vitro formation of calcium phosphate crystals was assessed in human plasma samples using the spectrophotometric PD assay. Inhibition of crystallization was measured by comparing the slopes of the control sample (blank) with those of samples containing the crystallization inhibitor as shown below:
Human plasma was spiked with increasing concentrations of inhibitors. Solutions of inhibitors were prepared by dilution in 0.15 M NaCl and pH adjusted to 7.40. The inhibitors and final concentration ranges tested in plasma were as follows: SNF472 (0–30 μM), pyrophosphate (PPi, 0–200 μM), ibandronate (0–50 μM), pamidronate (0–50 μM), STS (0–100000 μM), citrate (0–25000 μM) and fetuin-A (0–208 μM). To compare the potency of inhibition, half-maximal inhibition concentrations (IC50) were calculated using GraphPad Prism 5.0 software.
Validation of the spectrophotometric PD assay in determining the efficacy of SNF472 on inhibition of crystallization in human plasma
The spectrophotometric method was validated through evaluation of linearity, intra- and inter-day precision, integrity of dilution and stability of plasma samples spiked with SNF472 under long-term (−20 and −80 °C) and benchtop (room temperature and 4 °C) conditions and following freeze/thaw cycles.
Linearity was evaluated using solutions of SNF472 to attain final concentrations of 0.5, 1.0, 1.25, 1.5, 2.0, 3.0, 4.0, 5.0, 7.0, 10 and 30 µM in plasma. The calibration curve generated in the linearity assay was applied to calculate the lower limit of quantification (LLOQ), IC30, IC50, IC80 and IC95 values. LLOQ was determined using Eq. (2) and IC30, IC50, IC80 and IC95 values calculated with GraphPad Prism 5.0 software.
The assay was repeated with three runs per day for three consecutive days (12 replicates for LLOQ, EC30, EC50, EC80 and EC95 of SNF472 in plasma per run) to assess intra-day and inter-day precision, respectively, under repeatability and reproducibility conditions. Repeatability and reproducibility of the PD assay were evaluated by determining intra- and inter-day CV.
The ability to dilute samples that were originally above the upper limit of the calibration curve was studied by diluting SNF472-concentrated samples in blank plasma. LLOQ, EC30, EC50, EC80 and EC95 values of SNF472 in plasma per dilution factor (10x and 100x) were assayed in one run with six replicates.
The stability of SNF472 in plasma samples was evaluated at final LLOQ, IC30, IC50, IC80 and IC95 concentrations in plasma. Plasma samples were immediately assayed in one run with six replicates before and after storage for different time-periods and temperature conditions. For long-term storage, plasma samples were frozen at −20 or −80 °C after SNF472 spiking and stored between 2 weeks and 12 months. In terms of benchtop stability, plasma samples were stored on the bench at room temperature between 1 and 8 h or at 4 °C between 2 and 24 h. For freeze/thaw cycles, plasma samples were frozen at −80 °C, thawed and refrozen up to three times in consecutive days. Once completely thawed, plasma samples were used for assay or refrozen for a further freeze/thaw cycle.
Preclinical revalidation of the PD assay in rat plasma samples
A preliminary assay was performed in vitro by adding increasing concentrations of SNF472 to blank rat plasma to obtain the linear range for inhibition of crystallization and calculate LLOQ and IC50 values. Blood from three Sprague-Dawley male rats (282 ± 4 g, Charles River Laboratories, France) was collected in tubes with K2EDTA as anticoagulant. Plasma was obtained after centrifugation at 3,500 rpm for 10 min at 4 °C and mixed to obtain a pool. Nine SNF472 concentrations were prepared within a range of 0.5 to 10 µM.
In the second assay, five groups of three male Sprague-Dawley rats (314 ± 4 g, Charles River Laboratories, France) were subcutaneously administered 0 (saline), 20, 40, 60 or 100 mg/kg SNF472. Blood was collected after 20 min in tubes with K2EDTA, and plasma separated via centrifugation at 3,500 rpm for 10 min at 4 °C. The crystallization potential of plasma samples was measured using the spectrophotometric PD assay.
In parallel, SNF472 levels in the same rat plasma samples were determined by means of phytic acid quantification. Phytic acid was quantified via LC-MS using a method previously described by Tur et al.50.
Implementation of the PD assay in HD patients
Experiments were conducted according to the guidelines of the Declaration of Helsinki. All procedures involving human subjects/patients were approved by the Ethical Committee of Clinical Investigation of the Balearic Islands (IB 2245/14 PI). All participants were informed of the purpose and characteristics of the study before providing written consent.
A total of 13 healthy volunteers and 12 ESRD patients undergoing HD treatment in Hospital Son Llàtzer (Palma, Spain) participated in the study. One (volunteers) or two (HD patients) venous blood samples were obtained from the antecubital vein (volunteers) or the afferent line (using the sample port in HD patients), and collected in tubes with K2EDTA as anticoagulant. Two blood samples were obtained from HD patients before and after dialysis treatment. Blood was centrifuged at 3,500 rpm at 4 °C for 10 min to separate plasma.
Assessment of crystallization potential in plasma samples obtained from healthy volunteers and HD patients
The PD assay was performed on blank plasma samples and after in vitro addition of variable concentrations of SNF472 to attain LLOQ, IC30, IC50, IC80 and IC95 values of SNF472 in plasma.
Results are expressed as means ± SEM. Analyses were performed using the statistical software package GraphPad Prism 5.0. Statistical significance of data was analyzed using two-way ANOVA. In cases where significant effects were observed, a post-hoc Bonferroni test was applied. P-values < 0.05 were considered statistically significant.
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Jahnen-Dechent, W., Heiss, A., Schafer, C. & Ketteler, M. Fetuin-A regulation of calcified matrix metabolism. Circ Res 108, 1494–1509, doi:10.1161/circresaha.110.234260 (2011).
Sandin, K., Hegbrant, J. & Kloo, L. A theoretical investigation of the supersaturation of basic calcium phosphate in serum of dialysis patients. Journal of applied biomaterials & biomechanics: JABB 4, 80–86 (2006).
Ketteler, M. et al. Association of low fetuin-A (AHSG) concentrations in serum with cardiovascular mortality in patients on dialysis: a cross-sectional study. Lancet 361, 827–833, doi:10.1016/S0140-6736(03)12710-9 (2003).
Rennenberg, R. J. et al. Calcium scores and matrix Gla protein levels: association with vitamin K status. Eur J Clin Invest 40, 344–349, doi:10.1111/j.1365-2362.2010.02275.x (2010).
Schurgers, L. J. et al. The circulating inactive form of matrix gla protein is a surrogate marker for vascular calcification in chronic kidney disease: a preliminary report. Clin J Am Soc Nephrol 5, 568–575, doi:10.2215/cjn.07081009 (2010).
Mizobuchi, M., Towler, D. & Slatopolsky, E. Vascular calcification: the killer of patients with chronic kidney disease. J Am Soc Nephrol 20, 1453–1464, doi:10.1681/asn.2008070692 (2009).
London, G. M. et al. Arterial media calcification in end-stage renal disease: impact on all-cause and cardiovascular mortality. Nephrol. Dial. Transplant. 18, 1731–1740, doi:10.1093/ndt/gfg414 (2003).
Araya, C. E., Fennell, R. S., Neiberger, R. E. & Dharnidharka, V. R. Sodium thiosulfate treatment for calcific uremic arteriolopathy in children and young adults. Clin J Am Soc Nephrol 1, 1161–1166, doi:10.2215/CJN.01520506 (2006).
Adrogue, H. J., Frazier, M. R., Zeluff, B. & Suki, W. N. Systemic calciphylaxis revisited. Am J Nephrol 1, 177–183 (1981).
Kent, R. B. 3rd & Lyerly, R. T. Systemic calciphylaxis. South Med J 87, 278–281 (1994).
Janigan, D. T., Hirsch, D. J., Klassen, G. A. & MacDonald, A. S. Calcified subcutaneous arterioles with infarcts of the subcutis and skin (“calciphylaxis”) in chronic renal failure. Am J Kidney Dis 35, 588–597, doi:10.1016/S0272-6386(00)70003-5 (2000).
Sowers, K. M. & Hayden, M. R. Calcific uremic arteriolopathy: pathophysiology, reactive oxygen species and therapeutic approaches. Oxid Med Cell Longev 3, 109–121, doi:10.4161/oxim.3.2.11354 (2010).
Mazhar, A. R. et al. Risk factors and mortality associated with calciphylaxis in end-stage renal disease. Kidney Int 60, 324–332, doi:10.1046/j.1523-1755.2001.00803.x (2001).
Chertow, G. M., Burke, S. K. & Raggi, P. Sevelamer attenuates the progression of coronary and aortic calcification in hemodialysis patients. Kidney Int. 62, 245–252, doi:10.1046/j.1523-1755.2002.00434.x (2002).
Raggi, P. et al. The ADVANCE study: a randomized study to evaluate the effects of cinacalcet plus low-dose vitamin D on vascular calcification in patients on hemodialysis. Nephrol. Dial. Transplant. 26, 1327–1339, doi:10.1093/ndt/gfq725 (2011).
Ariyoshi, T., Eishi, K., Sakamoto, I., Matsukuma, S. & Odate, T. Effect of etidronic acid on arterial calcification in dialysis patients. Clin Drug Investig 26, 215–222, doi:10.2165/00044011-200626040-00006 (2006).
Hashiba, H., Aizawa, S., Tamura, K. & Kogo, H. Inhibition of the progression of aortic calcification by etidronate treatment in hemodialysis patients: long-term effects. Ther Apher Dial 10, 59–64, doi:10.1111/j.1744-9987.2006.00345.x (2006).
Torregrosa, J. V. et al. Successful treatment of calcific uraemic arteriolopathy with bisphosphonates. Nefrologia: publicacion oficial de la Sociedad Espanola Nefrologia 32, 329–334, doi:10.3265/Nefrologia.pre2012.Jan.11137 (2012).
Chan, M. R., Yevzlin, A. S., Hinshaw, M. & Jaffery, J. B. Calciphylaxis responsive to lanthanum carbonate (FOSRENOL) therapy. WMJ 107, 335–338, doi:10.1053/j.ajkd.2008.02.049 (2008).
Brucculeri, M., Cheigh, J., Bauer, G. & Serur, D. Long-term intravenous sodium thiosulfate in the treatment of a patient with calciphylaxis. Semin Dial 18, 431–434, doi:10.1111/j.1525-139X.2005.00082.x (2005).
Cicone, J. S., Petronis, J. B., Embert, C. D. & Spector, D. A. Successful treatment of calciphylaxis with intravenous sodium thiosulfate. Am. J. Kidney Dis. 43, 1104–1108, doi:10.1053/j.ajkd.2004.03.018 (2004).
Grases, F. et al. Urinary phytate in calcium oxalate stone formers and healthy people–dietary effects on phytate excretion. Scand. J. Urol. Nephrol. 34, 162–164, doi:10.1080/003655900750016526 (2000).
Curhan, G. C., Willett, W. C., Knight, E. L. & Stampfer, M. J. Dietary factors and the risk of incident kidney stones in younger women: Nurses’ Health Study II. Arch Intern Med 164, 885–891, doi:10.1001/archinte.164.8.885 (2004).
Conte, A. et al. Urinary lithogen risk test: usefulness in the evaluation of renal lithiasis treatment using crystallization inhibitors (citrate and phytate). Arch Esp Urol 52, 305–310 (1999).
Lopez-Gonzalez, A. A. et al. Phytate (myo-inositol hexaphosphate) and risk factors for osteoporosis. J Med Food 11, 747–752, doi:10.1089/jmf.2008.0087 (2008).
Lopez-Gonzalez, A. A. et al. Phytate levels and bone parameters: a retrospective pilot clinical trial. Front Biosci (Elite Ed) 2, 1093–1098, doi:10.2741/E167 (2010).
Grases, F. et al. Phytate (Myo-inositol hexakisphosphate) inhibits cardiovascular calcifications in rats. Front. Biosci. 11, 136–142, doi:10.2741/1786 (2006).
Grases, F. et al. Effect of crystallization inhibitors on vascular calcifications induced by vitamin D: a pilot study in Sprague-Dawley rats. Circulation journal: official journal of the Japanese Circulation Society 71, 1152–1156, doi:10.1253/circj.71.1152 (2007).
Van den Berg, C. J., Hill, L. F. & Stanbury, S. W. Inositol phosphates and phytic acid as inhibitors of biological calcification in the rat. Clin. Sci. 43, 377–383, doi:10.1042/cs0430377 (1972).
Grases, F. et al. Phytate reduces age-related cardiovascular calcification. Front. Biosci. 13, 7115–7122, doi:10.2741/3214 (2008).
Pasch, A. et al. Nanoparticle-based test measures overall propensity for calcification in serum. J. Am. Soc. Nephrol. 23, 1744–1752, doi:10.1681/ASN.2012030240 (2012).
Pasch, A. Novel assessments of systemic calcification propensity. Curr Opin Nephrol Hypertens 25, 278–284, doi:10.1097/mnh.0000000000000237 (2016).
Keyzer, C. A. et al. Calcification Propensity and Survival among Renal Transplant Recipients. J Am Soc Nephrol 27, 239–248, doi:10.1681/asn.2014070670 (2016).
Smith, E. R. et al. Serum calcification propensity predicts all-cause mortality in predialysis CKD. J Am Soc Nephrol 25, 339–348, doi:10.1681/asn.2013060635 (2014).
Riser, B. L. et al. Daily peritoneal administration of sodium pyrophosphate in a dialysis solution prevents the development of vascular calcification in a mouse model of uraemia. Nephrol Dial Transplant 26, 3349–3357, doi:10.1093/ndt/gfr039 (2011).
Tamura, K. et al. Prevention of aortic calcification by etidronate in the renal failure rat model. Eur. J. Pharmacol. 558, 159–166, doi:10.1016/j.ejphar.2006.12.006 (2007).
Hashiba, H., Aizawa, S., Tamura, K., Shigematsu, T. & Kogo, H. Inhibitory effects of etidronate on the progression of vascular calcification in hemodialysis patients. Ther Apher Dial 8, 241–247, doi:10.1111/j.1526-0968.2004.00136.x (2004).
Schiffrin, E. L., Lipman, M. L. & Mann, J. F. Chronic kidney disease: effects on the cardiovascular system. Circulation 116, 85–97, doi:10.1161/circulationaha.106.678342 (2007).
D’Marco, L., Bellasi, A. & Raggi, P. Cardiovascular biomarkers in chronic kidney disease: state of current research and clinical applicability. Dis Markers 2015, 586569, doi:10.1155/2015/586569 (2015).
Lomashvili, K. A., Monier-Faugere, M. C., Wang, X., Malluche, H. H. & O’Neill, W. C. Effect of bisphosphonates on vascular calcification and bone metabolism in experimental renal failure. Kidney Int 75, 617–625, doi:10.1038/ki.2008.646 (2009).
Price, P. A., Faus, S. A. & Williamson, M. K. Bisphosphonates alendronate and ibandronate inhibit artery calcification at doses comparable to those that inhibit bone resorption. Arterioscler. Thromb. Vasc. Biol. 21, 817–824, doi:10.1161/01.ATV.21.5.817 (2001).
Lomashvili, K. A., Cobbs, S., Hennigar, R. A., Hardcastle, K. I. & O’Neill, W. C. Phosphate-induced vascular calcification: role of pyrophosphate and osteopontin. J Am Soc Nephrol 15, 1392–1401, doi:10.1097/01.ASN.0000128955.83129.9C (2004).
Villa-Bellosta, R. & Sorribas, V. Prevention of vascular calcification by polyphosphates and nucleotides- role of ATP. Circulation journal: official journal of the Japanese Circulation Society 77, 2145–2151, doi:10.1253/circj.CJ-13-0016 (2013).
Heiss, A. et al. Structural basis of calcification inhibition by alpha 2-HS glycoprotein/fetuin-A. Formation of colloidal calciprotein particles. J Biol Chem 278, 13333–13341, doi:10.1074/jbc.M210868200 (2003).
Westenfeld, R., Jahnen-Dechent, W. & Ketteler, M. Vascular Calcification and Fetuin-A Deficiency in Chronic Kidney Disease. Trends in Cardiovascular Medicine 17, 124–128, doi:10.1016/j.tcm.2007.02.005 (2007).
O’Neill, W. C. & Hardcastle, K. I. The chemistry of thiosulfate and vascular calcification. Nephrol. Dial. Transplant. 27, 521–526, doi:10.1093/ndt/gfr375 (2012).
Pasch, A. et al. Sodium thiosulfate prevents vascular calcifications in uremic rats. Kidney Int. 74, 1444–1453, doi:10.1038/ki.2008.455 (2008).
Asplin, J. R. et al. Thiosulfate reduces calcium phosphate nephrolithiasis. J. Am. Soc. Nephrol. 20, 1246–1253, doi:10.1681/ASN.2008070754 (2009).
Chertow, G. M. et al. Effect of cinacalcet on cardiovascular disease in patients undergoing dialysis. N. Engl. J. Med. 367, 2482–2494, doi:10.1056/NEJMoa1205624 (2012).
Tur, F. et al. Validation of an LC-MS bioanalytical method for quantification of phytate levels in rat, dog and human plasma. J Chromatogr B Analyt Technol Biomed Life Sci 928, 146–154, doi:10.1016/j.jchromb.2013.03.023 (2013).
This work was supported by RETOS COLABORACIÓN RTC-2014-2460-1 from the Spanish Ministry of Economy and Competitiveness and a grant from CDTI IDI-20150233 co-founded by “Programa Operativo Plurirregional de Crecimiento Inteligente 2014-2020” from “Fondo Europeo de Desarrollo Regional” (FEDER).
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Novel bisphosphonate compound FYB-931 preferentially inhibits aortic calcification in vitamin D3-treated rats
Journal of Bone and Mineral Metabolism (2019)