Patent Application
20130131179
1. Field of the Invention
The present invention relates to iron metabolism-improving agents that improve iron metabolism in the living body, and more specifically, to the iron metabolism-improving agent that improves iron metabolism in a chronic renal failure patient who receives blood purification therapy such as hemodialysis, hemofiltration and hemodiafiltration.
Further, the present invention relates to methods for improving iron metabolism in a chronic renal failure patient who receives blood purification therapy such as hemodialysis, hemofiltration and hemodiafiltration, by administration of above iron metabolism-improving agents; and more specifically, to a method for improving iron metabolism employing a dialysate and/or a substitution fluid that contain above iron metabolism-improving agents.
Furthermore, the present invention relates to blood purification methods including hemodialysis and hemodiafiltration in a chronic renal failure patient employing dialysates containing above iron metabolism improving agents, and to blood purification methods including hemodiafiltration and hemofiltration in a chronic renal failure patient employing substitution fluids containing above iron metabolism-improving agents.
2. Discussion of the Background
Chronic renal failure patients who receive blood purification therapy, typically hemodialysis, suffer from lowered quality of life (QOL), hospitalization and high mortality rates induced by various complications. It is well known that causes of such complications include chronic inflammatory state, nutritional deficiencies, arteriosclerosis and erythropoietin (EPO) resistant renal anemia, and that interrelation among them deteriorates prognosis.
Although a comprehensive mechanism causing these pathologies is not known yet, a suspected cause is iron metabolic abnormality induced by renal failure, that is, cellular dysfunction induced by iron accumulation in various organs and tissues as well as increased oxidative stress due to iron-mediated Fenton reactions.
Renal anemia that occurs in chronic renal failure patients receiving blood purification therapy is the pathology of decreased hemopoiesis in the bone marrow resulting from relative underproduction of erythropoietin in renal tissues due to renal dysfunction. A treatment method for renal anemia is administration of recombinant human erythropoietin (rHuEPO) preparations. Recently, rHuEPO preparations are also used for renal failure patients during the conservative period before introduction of dialysis.
However, there are often cases where anemia is not improved despite administration of rHuEPO preparations because of reduced hematopoietic response to EPO—this is EPO-resistant renal anemia, mainly induced by iron deficiency in the bone marrow. It has been considered that, in chronic renal failure patients, increased demand for iron resulting from enhanced hematopoiesis due to rHuEPO treatments causes iron deficiency in the bone marrow. On the other hand, it is also known the state that anemia is improved by additional administration of iron notwithstanding presumable sufficient iron storage considering the serum ferritin concentration—the state of functional iron deficiency.
The present inventors have revealed the existence of iron metabolic abnormality in dialysis patients and a part of its mechanism (Non-patent literature 1). That is, while the serum iron levels of hemodialysis patients were lower than those of healthy subjects, the serum ferritin levels of hemodialysis patients were significantly higher than those of healthy subjects. In addition, the polymorphonuclear leukocyte iron levels of above hemodialysis patients were about 3 times higher and their ferritin levels were about 1.5 times higher than those of healthy subjects.
In evaluation only in patients with lower serum ferritin levels, similar elevations of intracellular iron concentrations were observed.
Hence, the present inventors observed that the polymorphonuclear leukocyte iron levels were enhanced notwithstanding serum ferritin levels in dialysis patients.
Iron transport proteins are considered to relate to intracellular iron metabolism. There have been new findings regarding iron transport proteins at the cellular level, especially in duodenal and reticuloendothelial cells. Well-known proteins that take up iron into cells are transferrin receptor (TfR), which takes up ferric (Fe3+)-binding transferrin, divalent metal transporter 1 (DMT1), which transports ferrous (Fe2+), and ferroportin 1 (FP1), which exports iron out of cells.
The present inventors have also revealed the relationship between increased intracellular iron concentrations and iron-transport proteins in polymorphonuclear leukocytes (Non-patent literature 1). That is, it was confirmed that TfR relates to the iron uptake into polymorphonuclear leukocytes and FP1 relates to the iron export out of polymorphonuclear leukocytes. In addition, the present inventors have revealed at the mRNA level as well as the protein level that the expression of TfR, an iron-uptake protein, is increased and, contrarily, the expression of FP1, an iron-exporting protein, is decreased in the polymorphonuclear leukocytes of hemodialysis patients compared to healthy subjects.
The above indicates that iron excessively accumulates in polymorphonuclear leukocytes in hemodialysis patients because of the abnormal regulation of above-mentioned iron-transport proteins, that is, an “iron enclosure”.
Since iron-transport proteins are expressed in the whole-body cells, presumably similar changes of iron-transport protein expression to the changes in polymorphonuclear leukocytes of dialysis patients may occur in the reticuloendothelial system.
The most important iron metabolism in the living body is the regenerating system where iron is recycled for hematopoiesis at the bone marrow by, first, engulfment of senescent erythrocytes in the reticuloendothelial system, followed by extraction of iron from hemoglobin. Under this system, approximately from 20 to 25 mg of iron is recycled per day. When the “iron enclosure” occurs in the hepatic or splenic reticuloendothelial systems or bone marrow macrophages, the regenerating system of iron metabolism is broken down, which leads to the state of functional iron deficiency where iron is deficient notwithstanding high serum ferritin concentration.
Meantime, many chronic renal failure patients are considered to be chronically in the inflammatory state because their levels of C-reactive protein, an indicator of acute inflammatory response, are high. Heretofore, chronic anemia induced by chronic inflammatory diseases have been reported to be caused by iron recycle disorder due to accumulation of iron in splenic and hepatic macrophages as well as due to the “iron enclosure” in the reticuloendothelial system (Non-patent literature 2).
Moreover, a relationship between a part of EPO-resistant renal anemia and chronic inflammatory state has been suggested (Non-patent literature 3).
Recently, given the reports pointing out a relationship between the pathology of anemia induced by chronic inflammatory diseases and inflammatory cytokines (Non-patent literature 4), inflammatory cytokines have received attention as a factor of iron transport protein dysregulation in dialysis patients.
The present inventors have investigated for the influence of inflammatory cytokines on iron transport proteins employing human-monocyte-derived cultured cells (Non-patent literature 5). As a result, increased expression of TfR and DMT1 as well as decreased expression of FP1 were observed at the mRNA and protein levels. In addition, it was observed that similar changes occurred by stimulation of cytokines in the iron-preloaded condition. Hence, it was indicated that cytokines induce iron transport protein dysregulation in the reticuloendothelial system notwithstanding the intracellular iron concentration.
Since conventional dialysis preparations on the market contain a slight amount (from 8 to 12 mEq/L) of acetic acid for the purpose of stabilization, it has been indicated that acetic acid can promote hypercytokinemia because of its stimulation to monocytes. In the meantime, aconitase, a citric acid-converting enzyme, has iron-sulfur complexes at the active center, and, when the intracellular iron concentration is low, the iron-sulfur complexes decompose to lower the enzyme activity. Also, it has been reported that, among iron-metabolism-controlling proteins (IRPs: iron regulatory proteins) existing in the cytoplasm, IRP1 binds IRE (iron responsive element) existing in the mRNAs of iron transport proteins under the iron deficient condition to inhibit decay of mRNAs of TfR and DMT1 as well as inhibit translation initiation of mRNAs of FP1 (Non-patent literature 6). Because IRP1 is known to activate aconitase when the intracellular iron concentration is high, citric acid can correct the iron transport protein abnormality through reduction of binding between IRP1 and IRE as a result of enhanced aconitase activity.
Summarizing the above, a presumable major cause of EPO-resistant renal anemia is the iron recycle disorder due to “iron enclosure” in the reticuloendothelial system resulting from iron transport protein dysregulation in the reticuloendothelial cultivated cells—like in polymorphonuclear leukocytes—induced by hypercytokinemia developed in dialysis patients. Moreover, this iron recycle disorder can be considered to play a key role in the onset and development of various complications which affect prognosis.
According to the above, it is contemplated that prevention of hypercytokinemia or correction of iron transport protein dysregulation can release “iron enclosure” in the reticuloendothelial system and enhance serum iron concentrations to improve iron recycle in chronic renal failure patients receiving blood purification therapy such as hemodialysis, hemofiltration and hemodiafiltration, and that eventually EPO-resistant renal anemia can be improved and risks of complications can be avoided to improve QOL as well as prognosis of patients.
Heretofore, however, there has been presented no specific method for improvement of iron metabolism abnormality, that is, excessive iron uptake into cells and suppressed iron export out of cells; or for transfer of iron accumulated in the reticuloendothelial system so as to be recycled in the hematopoietic system in chronic renal failure patients receiving blood purification therapy. Conventionally, add-on therapy of iron preparations to EPO preparations has been considered to be effective as a treatment method for chronic renal failure patients with EPO-resistant renal anemia. However, this is one of methods relying on experience of specialized physicians, and therefore, there is no specifically established treatment method at present.
In the view of the above problems, the present invention has as an object to provide iron metabolism-improving agents that improve iron metabolism in chronic renal failure patients, and more specially, in those who receive blood purification therapy such as hemodialysis, hemofiltration and hemodiafiltration.
The present invention also has as another object to provide methods for improving iron metabolism in a chronic renal failure patient who receives blood purification therapy such as hemodialysis, hemofiltration and hemodiafiltration, by administration of iron metabolism-improving agents provided by the present invention, and more specifically, to provide a method for improving iron metabolism employing a dialysate and/or a substitution fluid that contain above iron metabolism-improving agents.
Further, the present invention has as another object to provide methods for blood purification including hemodialysis and hemodiafiltration in a chronic renal failure patient employing dialysates that contain above-mentioned iron metabolism-improving agents, and to provide methods for blood purification including hemodiafiltration and hemofiltration in a chronic renal failure patient employing substitution fluids that contain above-mentioned iron metabolism-improving agents.
To solve problems in the conventional art, an embodiment of the present invention comprises:
(1) An iron metabolism-improving agent comprising citric acid and/or a citrate salt;
(2) The iron metabolism-improving agent of above (1) comprising citric acid and/or a citrate salt as electrolytes;
(3) The iron metabolism-improving agent of above (1) or (2) comprising no acetic acid and/or an acetate salt and comprising citric acid and/or a citrate salt as electrolytes; and,
(4) The iron metabolism-improving agent of above (1), (2) or (3) comprising citric acid and/or a citrate salt as electrolytes, and further comprising solely or in combination another/other electrolyte/electrolytes and glucose.
More specifically, an embodiment of the invention comprises:
(5) The iron metabolism-improving agent of any one of above (1) to (4) formulated into a dialysate; and
(6) The iron metabolism-improving agent of any one of above (1) to (4) formulated into a substitution fluid.
Another embodiment of the invention comprises:
(7) A method for improving iron metabolism in a chronic renal failure patient receiving blood purification therapy such as hemodialysis, hemofiltration and hemodiafiltration, by administration of the iron metabolism-improving agent of any one of above (1) to (4); and more specifically,
(8) An iron metabolism improving method in a chronic renal failure patient receiving blood purification therapy such as hemodialysis, hemofiltration and hemodiafiltration employing a dialysate and/or a substitution fluid that contain the iron metabolism-improving agent of above (5) or (6).
Another embodiment of the invention comprises:
(9) A blood purification method including hemodialysis and hemodiafiltration in a chronic renal failure patient employing a dialysate that contains the iron metabolism-improving agent of above (5); and
(10) A blood purification method including hemodiafiltration and hemofiltration in a chronic renal failure patient employing a substitution fluid that contains the iron metabolism-improving agent of above (6).
The iron metabolism-improving agent provided by the present invention contains citric acid and/or a citrate salt, and more specifically, contains citric acid and/or a citrate salt as electrolytes; and one of efficacies thereof is improvement of abnormal iron recycle induced by renal failure in a chronic renal failure patient receiving blood purification therapy.
Furthermore, the iron metabolism-improving agent provided by the present invention recovers the recycle system of iron metabolism to allow iron to be recycled and eventually prevents hypercytokinemia simultaneously correcting the internal iron transport protein dysregulation in the living body.
Hence, it is one of excellent advantages of the present invention that improvement of EPO-resistant renal anemia in chronic renal failure patients by the iron metabolism-improving agent provided by the invention reduces risks of onset of complications as well as improves QOL and prognosis of patients.
A more complete appreciation of the invention and many of the attendant advantages thereof will be readily obtained as the same become better understood by reference to the following detailed description when considered in connection with the accompanying drawings, wherein:
Other features of the invention will become apparent in the course of the following descriptions of exemplary embodiments which are given for illustration of the invention and are not intended to be limiting thereof.
As aforementioned, the iron metabolism-improving agent provided by the present invention contains citric acid and/or a citrate salt, and specifically, contains citric acid and/or a citrate salt as electrolytes.
More specifically, the iron metabolism-improving agent provided by the present invention is characterized in that it does not contain acetic acid and/or an acetate salt and contains citric acid and/or a citrate salt as electrolytes, and additionally, contains another/other electrolyte/electrolytes and glucose solely or in combination.
Hence, preferably, the iron metabolism-improving agent provided by the invention is administered in a formulation of a dialysate or a substitution fluid. A preferable embodiment of such a dialysate or a substitution fluid is a bicarbonate dialysate or a bicarbonate substitution fluid that contains sodium bicarbonate of bicarbonate ions as alkalizer.
In view of the above, a preferable embodiment of the iron metabolism-improving agent provided by the present invention is a dialysate so-called dialysis preparation “A” comprising electrolytes, pH adjusting agents and/or glucose; the dialysis preparation “A” is diluted, for administration, with a diluting water or, preferably, with so-called dialysis preparation “B” comprising sodium hydrogencarbonate of bicarbonate irons. Another preferable embodiment of the iron metabolism-improving agent provided by the present invention is a substitution fluid so-called dialysis preparation “B” comprising electrolytes, pH adjusting agents and/or glucose; the dialysis preparation “B” is mixed, for administration, with a dialysis preparation “A” comprising electrolytes, pH adjusting agent and sodium hydrogencarbonate.
Preferable electrolytes used in the iron metabolism-improving agent provided by the present invention in addition to citric acid and/or a citrate salt such as sodium citrate include, for example, sodium chloride, potassium chloride, magnesium chloride, calcium chloride, sodium lactate, potassium lactate and calcium lactate. Especially preferable electrolytes include sodium chloride, potassium chloride, calcium chloride, magnesium chloride and sodium citrate.
In addition to above-mentioned components, the iron metabolism-improving agent provided by the present invention contains glucose and pH adjusting agents to suitably control the pH of a dialysate and/or a substitution fluid after preparation.
Preferable pH adjusting agents include citric acid, lactic acid, hydrochloric acid, malic acid, ascorbic acid, tartaric acid and sodium hydroxide. Especially preferable pH adjusting agents include citric acid and hydrochloric acid.
Accordingly, the iron metabolism-improving agent provided by the present invention contains above-mentioned components preferably at the concentrations as described below when suitably diluted and mixed to be a bicarbonate dialysate or a bicarbonate substitution fluid.
When calcium ions are included as an electrolyte in the iron metabolism-improving agent provided by the present invention, insoluble compounds are produced because of the existence of citric acid and/or a citrate salt such as sodium citrate. However, production of such insoluble compounds is prevented by citric acid with controlling a pH at low level.
Furthermore, use of citric acid suppresses generation of precipitates. When electrolytes in a dialysis preparation “A” or a substitution fluid “B” are mixed with sodium bicarbonate of bicarbonate irons in a dialysis preparation “B” or a substitution fluid “A”, reaction between bicarbonate ions and calcium or magnesium ions produces insoluble metal carbonates. Therefore, these “A” and “B” are mixed and diluted just before use as a dialysate for artificial kidney. An advantage of the present invention is that citric acid's precipitate-suppressing effect prolongs the stability of dialysate.
According to the present invention, preferably citric acid and/or a citrate salt are contained in the iron metabolism-improving agent in the amount that allows a pH of prepared dialysate to range about between 2.2 and 2.9, and that allows a citrate ion concentration to usually range between 0.02 and 5 mEq/L as described above.
Moreover, against conventional dialysis preparation “A” and substitution fluid “B” containing acetic acid, the iron metabolism-improving agent provided by the present invention is characterized by acetic-acid free formulation. Hence, it is another advantage of the present invention that a dialysate and/or a substitution fluid formulated with the iron metabolism-improving agent provided by the present invention are physiologically more compatible because sodium bicarbonate is used as the only alkalizer.
The iron metabolism-improving agent provided by the present invention is capable of correcting iron transport protein dysregulation through reduction of IRP1-IRE binding as a result of enhanced aconitase activity owing to action of citric acid and/or a citrate salt contained therein. In addition, the iron metabolism-improving agent provided by the present invention is also capable of correcting iron transport protein dysregulation through prevention of hypercytokinemia in dialysis patients owing to acetic-acid free formulation thereof. Consequently, “iron enclosure” in the reticuloendothelial system is released, and then, serum iron concentration increases to improve iron metabolism abnormality, which, as a result, improves iron recycle contributing largely to improvement of EPO-resistant renal anemia.
The above-mentioned points are some of especially unique features of the iron metabolism-improving agent provided by the present invention.
In addition to formulations into dialysates and substitution fluids, other available formulations of the iron metabolism-improving agent provided by the invention include liquid, elixir, capsule, granule, pill, percutaneous absorption, suspension or emulsion, suppository, powder, alcoholic, tablet, syrup, injection, adhesive skin patch and lemonade; mixed with carriers, excipients, diluting agents and other agents acceptable for pharmaceutical products. Also, the iron metabolism-improving agent provided by the present invention can be taken orally (ingested) formulated with suitable excipients into, for example, powder, granule, tablet, liquid (including beverage, and jelly), candy and so on.
Having generally described this invention, a further understanding can be obtained by reference to certain specific examples which are provided herein for purposes of illustration only and are not intended to be limiting unless otherwise specified.
Renal failure dogs were dialyzed and effects on iron metabolism were evaluated.
After 18-hour fasting, male beagle dogs were anesthetized with pentobarbital sodium (30 mg/kg) via cephalic vein and underwent midline laparotomy followed by complete bilateral ureteral ligation.
Dialysis experiment was performed after 2 days of the operation. Pentobarbital sodium (30 mg/kg) was administered via cephalic vein for introduction. During the operation, pentobarbital sodium was appropriately administered intravenously with an infusion pump to maintain anesthesia.
Blood access was created by an 8 Fr catheter filled with physiological saline mixed with heparin (10 units/mL) implanted into femoral arteriovenous fistula. Then, endotracheal intubation was performed to set a ventilator for respiratory care.
A single-patient hemodiafiltration system, DBG-01 (by Nikkiso Co., Ltd.), was used for hemodialysis. For filter membrane and a blood tubing set, PS-0.6UW and a pediatric blood tubing set were used, respectively.
For a group, a dialysate provided by the present invention prepared in accordance with the prescription in the table 1 below was used. For the other group, commercial dialysate “AK-Solita™ •DL” was used. Both groups had three cases, respectively.
Hemodialysis was performed continuously for 4 hours at a blood flow rate of 100 mL/min and at a dialysate flow rate of 300 mL/min without body fluid removal.
For prevention of blood coagulation, 100 units/kg of heparin was administered intravenously in advance of dialysis initiation, and after that, additionally 50 units/kg of heparin was administered intravenously every 1 hour.
During dialysis, pentobarbital sodium was appropriately administered intravenously with an infusion pump to maintain anesthesia.
Blood was collected before bilateral ureteral ligation, before dialysis initiation, and at 2 and 4 hours after dialysis initiation. Collected blood was centrifuged in a refrigerated centrifuge to measure serum iron, unsaturated iron binding capacity (UIBC), plasma creatinine (Cre), blood urea nitrogen (BUN), citric acid and acetic acid.
Total iron binding capacity (TIBC) was calculated by adding serum iron to UIBC.
After termination of dialysis, blood was removed through blood access with physiological saline, and then after perfusion, splenic tissues were collected from the dissected animals. The collected tissues were stained with prussian blue stain for iron assessment, and the iron stain percentage was computed by image analysis. In addition, immunohistochemical staining of tissue ferritin was performed for macroscopic observation. For tissue analysis, a comparison was performed among two experimental groups consisting of one group administered with the dialysate provided by the present invention and the other group administered with the commercial dialysate, an untreated control group consisting of three healthy cases, and a renal failure control group consisting of three cases untreated with dialysis.
Results of citric acid concentration, serum iron concentration, UIBC and TIBC are shown in
The acetic acid concentration results after two hours of dialysis initiation are shown in Table 2.
The plasma Cre and BUN concentrations of dogs in the renal failure group markedly increased after two days of bilateral ureteral ligation before dialysis initiation. The onset of renal failure was confirmed.
The plasma Cre and BUN concentrations having increased due to renal failure decreased immediately after dialysis in both groups administered with the dialysate provided by the invention and the commercial dialysate. While the plasma citric acid concentrations of the group administered with dialysate provided by the invention changed at similar levels to before hemodialysis, the plasma citric acid concentrations of the group administered with the commercial dialysate decreased after dialysis (
With respect to iron, the serum iron concentrations having decreased due to renal failure significantly increased by dialysis with the dialysate provided by the invention compared to before dialysis (
UIBC values after dialysis were significantly lower in both groups administered with the dialysate provided by the invention and the commercial dialysate than before dialysis. By the two-way analysis of variance, significant differences of UIBC values were observed depending on duration of dialysis session as well as on type of dialysates (from before dialysis through 4 h after dialysis: time, F(2,12)=9.91, p<0.01; dialysate, F(1,12)=7.82, p<0.05, time× dialysate, F(2,12)=0.53, p>0.05:
Because practically no change was observed in TIBC values by dialysis and there was no significant difference between the type of dialysates (
The iron stain percentages in splenic tissues of renal failure groups were higher than those of untreated group. The increased iron stain percentages decreased by dialysis; iron staining was less intense in the group administered with the dialysate provided by the invention than iron staining in the group administered with the commercial dialysate (
The splenic tissue ferritin staining intensity decreased more, and fewer cells were stained in the group dialyzed with the dialysate provided by the invention than the group dialyzed with the commercial dialysate.
Above analyses of tissues indicate that iron is enclosed in organs under renal failure state and dialysis can release the iron enclosure, and that splenic iron enclosure is markedly released by the dialysate provided by the invention compared to the commercial dialysate.
Accordingly, it is indicated that dialysis with a dialysate provided by the invention can be effective in improvement of declined iron recycle rate due to renal failure.
Effects of citric acid administration on iron metabolism were evaluated in bilaterally nephrectomized rats.
Eight-week-old male CD(SD) rats (body weight: about 300 g) were used in the groups as shown in Table 3. After intra-peritoneal administration of pentobarbital sodium for anesthesia, bilateral total kidneys were extirpated from the back of rat (Rats in the first group in Table 3 were untreated.) and a central venous catheter (CVC) was placed.
At about 24 hours after the operation, 1 mL of blood was collected by CVC. Immediately after blood collection, physiological saline or a 4.5% (w/v) sodium citrate solution was administered by CVC at 0.25 mL/h for 4 hours in the second and third groups in Table 3, and 1 mL of blood was collected by CVC immediately after termination of administration.
Collected blood was centrifuged in a refrigerated centrifuge to measure plasma creatinine (Cre), blood urea nitrogen (BUN), iron and citric acid.
Plasma citric acid concentrations were 5.27±1.23 mg/dL in the first group but increased to 16.38±9.49 mg/dL and 17.11±18.64 mg/dL in the second and third groups respectively due to extirpation of bilateral kidneys (
Plasma iron concentrations were 112±14 μg/dL in the first group but were 61±17 μg/dL in the second group, indicating decreases due to renal failure state (
Effects of citric acid administration in a dialysis session dialysis on iron metabolism in rat at the second day after extirpation of bilateral kidneys were evaluated.
Examinations were performed in male CD(SD) rats in the groups in Table 4. After intra-peritoneal administration of pentobarbital sodium (50 mg/kg) for anesthesia, bilateral total kidneys were extirpated from the back of rat.
At the second day after operation, after intra-peritoneal administration of pentobarbital sodium (50 mg/kg) for anesthesia, catheters were placed in the left femoral artery and vein to create blood access, and a central venous catheter (CVC) was placed for citric acid administration as well as blood collection. After 1 mL of blood was collected by CVC, dialysis was performed for 4 hours with a commercial dialysate (AK-Solita •DL) under anesthesia. In the second and third groups of Table 4, physiological saline or a 4.5% (w/v) sodium citrate solution was administered by CVC at 1.0 mL/h continuously, and 1 mL of blood was collected by CVC immediately after termination of dialysis.
Collected blood was centrifuged in a refrigerated centrifuge to measure plasma creatinine (Cre), blood urea nitrogen (BUN), iron and citric acid.
Plasma Cre and BUN concentrations increased markedly at the second day after extirpation of bilateral kidneys before dialysis, and onset of renal failure was confirmed. Increased plasma Cre and BUN concentrations decreased immediately by dialysis.
Plasma citric acid concentrations were 5.33 mg/dL in the first group but increased to 9.87 mg/dL in the second group due to extirpation of bilateral kidneys, while plasma citric acid concentrations in the third group were 5.33 mg/dL at the same level as the first group (
Plasma iron concentrations were 59 μg/dL in the first group, 113 μg/dL in the second group and 83 μg/dL in the third group. Although there were slight differences among the groups, decreases of plasma iron concentrations due to renal failure state induced by extirpation of bilateral kidneys were observed (
Preparation A (component and amount per 10 L)
Preparation B (component and amount per 12.6 L)
Sodium hydrogencarbonate 1,030.0 g
Preparation A (component and amount per 1,010 mL)
Preparation B (component and amount per 1,010 mL)
As aforementioned, according to the present invention, an acetic acid- and/or acetate salt-free iron metabolism improving agent containing citric acid and/or a citrate salt prevents hypercytokinemia, corrects iron transport protein dysregulation and releases “iron enclosure” in the reticuloendothelial system, which leads to enhancement of serum iron concentrations and improvement in iron recycle in a chronic renal failure patient receiving blood purification therapy. As a result, EPO-resistant renal anemia of such a patient is improved, and complication occurrence risks are reduced. Hence, the present invention has great medical advantages and usefulness for its contribution to improvement of QOL and prognosis of patients.
Where a numerical limit or range is stated herein, the endpoints are included. Also, all values and subranges within a numerical limit or range are specifically included as if explicitly written out.
Obviously, numerous modifications and variations of the present invention are possible in light of the above teachings. It is therefore to be understood that, within the scope of the appended claims, the invention may be practiced otherwise than as specifically described herein.
All patents and other references mentioned above are incorporated in full herein by this reference, the same as if set forth at length.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2006-334294 | Dec 2006 | JP | national |
| 2007-079488 | Mar 2007 | JP | national |
The present application is a continuation of U.S. Ser. No. 12/482,723, filed Jun. 11, 2009, which is a continuation of International Patent Application No. PCT/JP2007/073766, filed on Dec. 10, 2007, and claims priority to Japanese Patent Application No. JP 2006-334294, filed on Dec. 12, 2006, and Japanese Patent Application No. JP 2007-079488, filed on Mar. 26, 2007, all of which are incorporated herein by reference in their entireties.
| Number | Date | Country | |
|---|---|---|---|
| Parent | 12482723 | Jun 2009 | US |
| Child | 13741721 | US | |
| Parent | PCT/JP2007/073766 | Dec 2007 | US |
| Child | 12482723 | US |
