Calcium oxalate dihydrate renal calculi constitute the most prevalent and recurrent type of renal lithiasis [1,2]. They are usually associated with hypercalciuria, and on occasions with urinary pH values above 6.0 [3-7]. The use of extracorporeal shock wave lithotripsy (ESWL) to treat these renal calculi commonly gives excellent fragmentation results due to their fragility [8]. Nevertheless, the retention of post-ESWL fragments within the kidney is an important health problem, and a study of calcium stone patients found only 32% were stone-free 12 months after ESWL [9]. It appears that persistence and growth of fragments is common following ESWL [10-14]. In vitro [15-17] and in vivo [9] studies suggest that citrate [9,15,16] and phytate [17] can reduce residual post-ESWL calculi fragment growth or agglomeration. Despite those findings, however, there is a need for better understanding of the factors that contribute to stone growth following ESWL. Such knowledge will assist in designing methods for preventing such growth.

The present study belongs to a series examining the regrowth of residual post-ESWL calculi fragments in terms of calculi type, urinary conditions and presence of crystallization inhibitors. While a previous study examined regrowth of calcium oxalate monohydrate (COM) residual post-ESWL calculi fragments [17], the present study examined calcium oxalate dihydrate (COD) calculi fragments.

The study used 48 spontaneously-passed post-ESWL fragments of COD calculi collected on the day of the ESWL procedure. Fragment selection proceeded according to the general protocol applied by our laboratory in the study of all renal stones. This methodology is based on a combination of optical stereomicroscopy, infrared spectrometry and scanning electron microscopy (SEM) equipped with an energy dispersive X-ray analyzer (EDS) [18]. All selected fragments had a very similar morphology which was representative of that observed in the majority of spontaneously-passed post-ESWL COD calculi fragments. Fragment sizes varied from 2 to 4 mm.

Fragments were not pre-treated, and were placed into four hermetic flow chambers (3 cm diameter and 4 cm high), with each chamber containing 12 fragments. These chambers were then placed into a larger temperature-controlled (37[deg]C) chamber. Each chamber was used to test a different incubation condition: pH = 5.5 and normocalciuria ([Ca total] = 3.75 mM), pH = 5.5 and hypercalciuria ([Ca total] = 6.25 mM), pH = 6.5 and normocalciuria ([Ca total] = 3.75 mM) and pH = 6.5 and hypercalciuria ([Ca total] = 6.25 mM). The duration of all incubations was 192 h, except for those under pH = 6.5 hypercalciuric conditions, which were for 48 h due to the high rate of fragment mass increase. The methodology used was similar to that previously described by Chow et al. [16,19]. Freshly prepared synthetic urine was introduced into the flow chambers using a multichannel peristaltic pump at a rate of 750 mL/day through the bottom of the flasks. The calculi fragments were placed on the porous flask bottom, allowing the entire fragment surface to be exposed to the artificial urine (see Figure 1). This system allows growth of new crystals on the fragments. Fragment growth was evaluated by measuring the difference in weight between the dried fragments before and after the experiment. The weight of the fragments was measured using a precision balance after the fragments had been kept in a desiccator until their weight became constant, indicating complete dryness. The mean growth rate of the 12 fragments under each condition was calculated. The growth of the different renal calculi fragments was standardized by calculating the relative mass increase in order to avoid the effects that different surface areas may have on growth rate measurements.

The effects of the crystallization inhibitors phytate, pyrophosphate and citrate were evaluated. The concentrations used corresponded to the physiological concentrations in urine.

The experimental research has been performed with the approval of the Bioethics Committee of the University of Balearic Islands and the research was carried out in compliance with the Helsinki Declaration.

Under all four incubation conditions, COM crystals were found to form on COD calculi fragments (Figures 2, 3, 4, 5). New COD crystal formation represented the minority (less than 50%) of crystal formation under pH = 5.5 hypercalciuric (Figure 3) and pH = 6.5 normocalciuric (Figure 4) conditions. In contrast, large amounts of COD crystals formed under pH = 6.5 hypercalciuric conditions (Fig 5a,c). Significant amounts of hydroxyapatite (HAP) and brushite (BRU) crystals formed under pH = 6.5 hypercalciuria conditions (Figure 5a,b), but not under other conditions.

The mean growth rates of COD calculi fragments under the four incubation conditions are summarized in Table 2. While growth rates of 0.22 --0.35 [mu]g/mg[center dot]h were observed under the majority of conditions, the rate was approximately ten times greater (3.87 [plus minus] 0.43 [mu]g/mg[center dot]h) under pH = 6.5 hypercalciuria conditions.

The effects of three known crystallization inhibitors (phytate, pyrophosphate and citrate) were investigated (Figures 6 and 7). We found that addition of 2.27 [mu]M phytate to the pH = 5.5 hypercalciuria incubation, and the addition of 4.55 [mu]M phytate to the pH = 6.5 hypercalciuria incubation completely inhibited the COD calculi fragment mass increase. Addition of lower phytate concentrations (less than 2.27 [mu]M), mainly inhibited COM crystal formation. The addition of 69.0 [mu]M pyrophosphate to the pH = 6.5 hypercalciuria incubation resulted in an 87% reduction of calculi fragment mass increase. The addition of 5.29 mM citrate to the pH = 6.5 hypercalciuria incubation had no effect on the COD calculi fragment mass increase.

The present study found that in normocalciuric/normooxaluric urine at pH = 5.5, only new COM crystals formed on COD calculi fragments. At the same pH, new COD crystals only formed under hypercalciuric conditions, in addition to COM crystals (Figure 3). Low phytate concentrations (less than 2.27 [mu]M), inhibited this COM crystal formation. At pH = 6.5, COD crystals formed under normocalciuric conditions (Figure 4), while under hypercalciuria conditions the calcium phosphates HAP and BRU also formed with the COD crystals. These findings are consistent with several clinical observations showing that COM calculi are generally associated with a lack of crystallization inhibitors and COD calculi with hypercalciuria and high urinary pH values [3-6]. It is important to emphasize that the growth rate of COD calculi fragments was similar under all conditions except under pH = 6.5 hypercalciuria, conditions under which the growth rate was approximately ten times that observed under other conditions (see Table 2). These findings suggest that the presence of COD calculi fragments in the kidneys together with hypercalciuria and high urinary pH values (around 6.5) are a high risk factor for stone development. These data suggest that a COD calculus fragment of only 5 mg could become a 45 mg fragment in just 3 months under these conditions.

Crystallization inhibitors can notably retard calculi fragment development. The present study found that phytate at concentrations found in normal human urine [20] totally prevented COD calculi fragment growth. In addition, pyrophosphate also reduced the COD calculi fragment mass increase. In contrast, citrate did not show any significant crystallization inhibitory capacity under the conditions investigated. This finding appears to be in disagreement with previous reports showing that high citrate concentrations reduced the growth rate of stones by more than 50% [16]. However, this apparent discordance may be because the stated growth rate reduction must be assigned to citrate complexation with calcium, which results in an important reduction in the relative calcium oxalate supersaturation. Thus, it must be considered that in the present study a calcium supplement was added to obtain the same calcium oxalate supersaturation value found in the absence of citrate. Interestingly, while citrate did not inhibit calcium salt crystallization on COD crystals in the present study, it was shown to inhibit calcium salt crystallization on glycoproteins and organic matter [21,22]. These observations again highlight the specificity of crystallization inhibitors.

The growth rate of COD calculi fragments under pH = 6.5 hypercalciuria conditions was approximately ten times that observed under other conditions. This observation suggests COD calculi residual fragments in the kidneys together with hypercalciuria and high urinary pH values may represent an important risk factor for stone development. In addition, the study found that specific crystallization inhibitors can effectively reduce calculi fragment growth.

The author(s) declare that they have no competing interests.

AC conceived the study and participated in the search and selection of COD calculi fragments. JP performed the crystallization studies under hypercalciuria conditions. BI performed the crystallization studies under normocalciuria conditions and pH = 5.5. PS performed the crystallization studies under normocalciuria conditions and pH = 6.5. FG participated in the study design and coordination, and assisted in preparation of the manuscript. All authors read and approved the final manuscript.

The pre-publication history for this paper can be accessed here:

http://www.pubmedcentral.nih.gov/redirect3.cgi?&&reftype=extlink&artid=1526447&iid=127656&jid=67&&http://www.biomedcentral.com/1471-2490/6/16/prepub

P.S. is grateful to the Spanish Ministry of Education, Culture and Sport for an FPU program fellowship. B.I. is grateful to the Conselleria d'Innovacio i Energia del Govern de les Illes Balears for a fellowship. Financial support from the Conselleria d'Innovacio i Energia, Govern Balear (Grant PROIB-2002GC1-04) and from the Spanish Ministry of Science and Technology (project BQU 2003-01659) is gratefully acknowledged.