Skip to main content
Download PDF
  • Research article
  • Open access
  • Published:

Association between serum phosphate levels and anemia in non-dialysis patients with chronic kidney disease: a retrospective cross-sectional study from the Fuji City CKD Network

BMC Nephrology volume 24, Article number: 244 (2023) Cite this article

Abstract

Background

Patients with chronic kidney disease (CKD) present high mortality and morbidity rates despite the availability of various therapies. Although CKD-mineral and bone disorder (MBD) and renal anemia are important factors in patients with CKD, only few studies have analyzed the relationship between them. Therefore, this study aimed to evaluate the relationship between CKD-MBD and anemia in patients with CKD who did not receive erythropoiesis-stimulating agent or iron therapies.

Methods

This retrospective cross-sectional study included patients with CKD aged ≥ 20 years with estimated glomerular filtration rate (eGFR) categories G2a to G5 who were referred to the Fuji City General Hospital between April 2018 and July 2019. The exclusion criterion was ongoing treatment for CKD-MBD and/or anemia.

Results

The data of 300 patients with CKD were analyzed in this study. The median age of patients was 71 (range, 56.5–79) years. The median eGFR was 34 (range, 20–48) mL/min/1.73 m2, and the mean hemoglobin (Hb) level was 12.7 g/dL (standard deviation, 2.3), which decreased as the CKD stage increased. In a multivariate linear regression analysis of anemia-related factors, including age, renal function (eGFR), nutritional status, inflammation, and iron dynamics (serum iron level, total iron-binding capacity, ferritin levels), the serum phosphate levels were significantly associated with the Hb levels (coefficient [95% confidence interval], -0.73 [-1.1, -0.35]; P < 0.001). Subgroup analysis revealed a robust association between serum phosphate levels and Hb levels in the low-ferritin (coefficient [95% confidence interval], -0.94 [-1.53, -0.35]; P = 0.002) and advanced CKD groups (coefficient [95% confidence interval], -0.89 [-1.37, -0.41]; P < 0.001).

Conclusions

We found an association between high serum phosphate levels and low Hb levels in patients with CKD not receiving treatment for anemia. These results underscore the possibility of a mechanistic overlap between CKD-MBD and anemia.

Peer Review reports

Background

Anemia is a common complication of chronic kidney disease (CKD) [1] and an established risk factor for congestive heart failure and cardiovascular disease (CVD) [2, 3]. Previous studies have found that improvement in anemia inhibits CKD progression [4] and helps prevent CVD [5]. Anemia in patients with CKD, known as “renal anemia,” is caused by erythropoietin (EPO) deficiency, and current treatment strategies focus on this condition [1]. Renal anemia is caused by reduced EPO production owing to renal dysfunction. Recently, even mild renal dysfunction was reported to cause renal anemia [6]. However, causes for anemia in patients with CKD are multifactorial, including EPO deficiency, iron deficiency, inflammation, and vitamin D insufficiency [1, 7, 8].

Recently, several studies have found an association between CKD-mineral and bone disorder (CKD-MBD) and anemia [9]. A study of 2,089 patients with CKD stages 1–5 showed a significant correlation between high serum phosphate levels and anemia after performing a cross-sectional analysis [10], whereas another study of 2,930 patients with CKD stages 3–5 showed an association between high serum phosphate levels and anemia [11].

Fibroblast growth factor-23 (FGF23), a hormone that regulates bone metabolism, is assumed to be the key factor linking CKD-MBD and anemia. Interestingly, several clinical studies involving patients with CKD stages 3–4 [12] and 2–4 [13], along with patients undergoing hemodialysis [14], have demonstrated an association between FGF23 and anemia. However, these results should be interpreted with caution, as many evaluated patients were receiving iron and erythropoiesis-stimulating agent (ESA) therapies. To the best of our knowledge, no studies have reported on patients with CKD not treated with iron or ESA therapy; therefore, this study aimed to evaluate the relationship between CKD-MBD and anemia after excluding these factors.

In this study, we investigated the association between high serum phosphate levels and anemia in patients referred through the Fuji City CKD Network to examine whether an overlap between CKD-MBD and anemia exists. The Fuji City CKD Network was launched in 2013, based on collaboration between family physicians and nephrologists, to provide treatment for CKD. It aimed to reduce the initiation of dialysis and incidence of CVD in patients with CKD by early identification and appropriate treatment through referrals from their physicians. Many patients referred through this network had not been treated for CKD-MBD or renal anemia. Therefore, this group of patients was well suited for investigating the association between CKD-MBD and anemia, and we conducted this cross-sectional study to investigate the association between the serum phosphate and hemoglobin (Hb) levels.

Methods

Study population

This retrospective cross-sectional study included patients with CKD at the Fuji City General Hospital between April 2018 and July 2019. The inclusion criteria were as follows: patients aged ≥ 20 years with estimated glomerular filtration rate (eGFR) categories ranging from G2a to G5, based on the CKD guidelines [15], with or without abnormal urinary findings or renal imaging findings. The exclusion criterion was ongoing treatment for CKD-MBD and/or anemia.

Clinical and laboratory data collection

We recorded the patients’ demographic data, comorbid conditions, and current medications at enrollment.

Different parameters, including the levels of blood creatinine (mg/dL), alkaline phosphatase (U/L), lactic acid dehydrogenase (U/L), total protein (g/dL), albumin (g/dL), sodium (mEq/L), potassium (mEq/L), urea nitrogen (mg/dL), calcium (mg/dL), phosphate (mg/dL), serum iron (µg/dL), total iron-binding capacity (µg/dL), ferritin (ng/mL), magnesium (mg/dL), and C-reactive protein (mg/dL), along with white blood cell count (× 103/µL), red blood cell count (× 106 /µL), Hb level (g/dL), hematocrit (%), mean corpuscular volume (fL), mean corpuscular hemoglobin concentration (g/dL), platelet count (× 103/µL), reticulocyte count (%), and hydrogen carbonate level (mmol/L) were tested using standard commercial assays. Spot urine samples were also obtained to determine the protein level. eGFR was calculated using the following formula for Japanese individuals:

eGFR (mL/min/1.73 m2) = 194 × (serum creatinine level [mg/dL])−1.094 × (age [years])−0.287 × (0.739 if female) [16].

Statistical analyses

To determine the between-group differences, the chi-square test was used for categorical data and the Mann–Whitney U test and Student’s t-test for continuous data. Subsequently, the Hb levels for each CKD stage were shown using a box-and-whisker diagram. A multivariate linear regression analysis was performed to examine the independent association between the phosphate and Hb levels. In this analysis, we considered the following as confounding factors, based on previous clinical studies [10,11,12,13,14]: age, sex, comorbidities, renal dysfunction, poor nutrition, iron dynamics, inflammation, and hematopoietic potential. The variables related to renal dysfunction were eGFR, urea nitrogen level, and urinary protein level, and those related to poor nutrition were albumin level and body mass index. The variables related to iron dynamics included the serum iron level, total iron-binding capacity, and ferritin level, whereas those related to inflammation were the C-reactive protein level and white blood cell count. The variables related to hematopoietic potential included reticulocyte count. Further, calcium level was used as a variable related to phosphate level. We also confirmed that these variables were not multicollinear. Moreover, Spearman’s rank correlation coefficients and regression coefficients from univariate linear regression analysis were determined for the association between variables used in multivariate analysis and the Hb levels. Moreover, the association was evaluated using a three-knot restricted cubic spline analysis using similar explanatory variables. Next, a multivariate linear regression analysis with similar variables was performed as a sensitivity analysis, excluding patients with extremely high or low eGFR. The sensitivity analysis included patients with an eGFR < 60 mL/min/1.73 m2, which is the criterion for a low eGFR [15] and an eGFR ≥ 8 mL/min/1.73 m2, which is the lower limit for considering conservative treatment, according to the Japanese maintenance dialysis guidelines [17]. Finally, as subgroup analysis, a multivariate linear regression analysis with similar variables was performed for two group sets, i.e., the CKD stage 2–3 and CKD stage 4–5 groups, and for two groups divided by the median ferritin and phosphate levels. The low-ferritin and low-phosphate groups comprised patients with ferritin and phosphate levels < 136 ng/mL and < 3.4 mg/dL, respectively. In this study, all tests were two-sided, and a P-value < 0.05 was considered statistically significant. Complete case analysis was used where any data were missing. All statistical analyses were performed using the statistical software for social sciences, Stata Version 15.1 (College Station, TX, USA).

Results

Between April 2018 and July 2019, 343 patients with CKD were referred to the Fuji City General Hospital through the Fuji City CKD Network. Of these, 326 patients were included in this study. Based on the exclusion criterion, we excluded 15 patients with medication related to CKD-MBD, such as vitamin D or phosphate binders, nine patients receiving treatment for anemia, including iron or ESA, and two patients receiving both treatments. Finally, a total of 300 patients with CKD were analyzed in the study.

Table 1 presents the patients’ background data based on the median phosphate level (3.4 mg/dL). The median age of patients was 71 (range, 56.5–79) years, including 92 (31%) patients with a history of diabetes. The median eGFR and calcium levels were 34 (range, 20–48) mL/min/1.73 m2 and 9.1 (range, 8.7–9.4) mg/dL, respectively. The median serum phosphate level was 3.3 (range, 3–3.8) mg/dL, and the mean Hb level was 12.7 g/dL (standard deviation, 2.3), which decreased as the CKD stage increased (Fig. 1).

Table 1 Characteristics of the 300 study patients based on their phosphate levels
Full size table
Fig. 1
figure 1

Hb levels classified by the CKD stage. Hb, hemoglobin; CKD, chronic kidney disease

Full size image

Table 2 lists the correlation and regression coefficients for the association between the variables used in the multivariate analysis and the Hb levels. In addition to known anemia-related variables, the serum phosphate levels were also negatively correlated with the Hb levels.

Table 2 Correlation coefficients and univariate linear regression analysis of each variable to the hemoglobin levels
Full size table

Table 3 shows the results of the multivariate linear regression analysis with Hb as an objective variable. In the unadjusted model, serum phosphate levels showed a significant negative correlation with the Hb levels (coefficient [95% confidence interval (CI)], -1.45 [-1.77, -1.13]; P < 0.001). In Model 3 analysis with the addition of anemia-related factors, such as age, renal function, nutritional status, inflammation, and iron dynamics, the serum phosphate levels showed a significant negative correlation with the Hb levels (coefficient [95% CI], -0.73 [-1.1, -0.35]; P < 0.001).

Table 3 Multivariate linear regression analysis of phosphate levels to the hemoglobin levels (all patients, n = 300)
Full size table

Figure 2 shows a restricted cubic spine curve showing the association between the serum phosphate and Hb levels. The Hb levels decreased as the phosphate levels increased.

Fig. 2
figure 2

Cubic spline curve showing the association between the serum phosphate and Hb levels. Hb, hemoglobin

Full size image

Sensitivity analysis in patients with an eGFR < 60 mL/min/1.73 m2 and ≥ 8 mL/min/1.73 m2 revealed a significant negative correlation between the serum phosphate levels and Hb levels, similar to the results of the primary analysis (Table 4). The subgroup analysis (Tables 5, 6 and 7) revealed a robust negative correlation between high serum phosphate levels and the Hb levels in the low-ferritin and CKD stage 4–5 groups.

Table 4 Multivariate linear regression analysis of phosphate levels to the hemoglobin levels (patients with an eGFR < 60 mL/min/1.73 m2 and ≥ 8 mL/min/1.73 m2, n = 245)
Full size table
Table 5 Subgroup analysis of the multivariate linear regression of phosphate levels to the hemoglobin levels based on CKD stage
Full size table
Table 6 Subgroup analysis of the multivariate linear regression of phosphate levels to the hemoglobin levels based on the ferritin levels
Full size table
Table 7 Subgroup analysis of the multivariate linear regression of phosphate levels to the hemoglobin levels based on phosphate levels
Full size table

Discussion

In this study, we performed a cross-sectional analysis in a group of patients with CKD stages 2–5 who were not receiving treatment for anemia and/or CKD-MBD. We found a significant correlation between high serum phosphate levels and anemia, even after adjusting the effects of factors already known to be involved in anemia, including renal function, nutritional status, and iron metabolism. This result suggests a factor-mediated overlap between CKD-MBD and anemia. The strength of this study was that it presented this association in patients who had not undergone ESA and iron therapy, considering the effect of iron dynamics.

Patients with exceedingly elevated eGFR or an eGFR low enough to necessitate dialysis might not be suitable for this analysis, which aimed to examine the association between serum phosphate levels and anemia in stable non-dialysis CKD patients. Consequently, a sensitivity analysis was performed to exclude these individuals, revealing a significant correlation and supporting the findings of the primary analysis.

Previous studies have reported that FGF23 is a factor possibly associated with the overlap between CKD-MBD and anemia. It is a polypeptide hormone secreted by osteoclasts and other organs that suppresses the renal reabsorption and intestinal absorption of phosphate [18] and suppresses renal vitamin D synthesis [19], thereby decreasing blood phosphate level. FGF23 is thought to be a sensitive marker for the onset and progression of CKD, as its level is elevated earlier than is the serum phosphate level in response to phosphate load [20]. It is also an independent risk factor for CKD development [21]. Recently, elevated FGF23 levels were found to be associated with adverse outcomes, such as vascular calcification [22], left ventricular hypertrophy [23], cardiovascular events [24], and increased mortality [25, 26].

A previous study showed that various physiological mechanisms are involved in FGF23 activity in anemia [27]. First, FGF23 inhibits proerythroblasts from maturing into erythrocytes. Second, it reduces EPO secretion from the kidney, thereby decreasing the differentiation of erythroid progenitors [28]. Third, it promotes excessive hepcidin expression, which affects the erythrocytes in the G2/M phase of their cell cycle and enhances erythrocyte apoptosis.

Clinical studies have shown an association between FGF23 and anemia. A cross-sectional study of 53 patients with CKD stages 3 and 4 showed a negative correlation between the serum FGF23 level and Hb level [12]. The findings of a prospective cohort study of 3,869 patients with non-dialysis CKD indicated significant associations between elevated FGF23 levels and anemia [13]. A retrospective cohort study of 2,089 patients with non-dialysis CKD published in 2018 reported that high FGF23 levels were associated with anemia in a cross-sectional analysis; moreover, it showed an association between high serum FGF23 levels and an increased risk of developing anemia in a longitudinal analysis [10]. In a prospective cohort study of 1,044 patients undergoing hemodialysis, higher and lower FGF23 levels were associated with higher odds of ESA-hyporesponsiveness, although the association did not reach statistical significance [14]. These study findings suggest a physiological overlap between CKD-MBD and anemia through factors, such as FGF23. However, these studies included patients who were already being treated for anemia and did not show a pure association that was unaffected by treatment. As FGF23 is associated with iron metabolism and inflammation [29], the administration of ESA [30] and iron preparations [31] can affect FGF23 levels; therefore, we sought to evaluate the relationship after excluding these effects.

In this study, we performed a multivariate linear regression analysis, including iron kinetics and inflammation in a group of patients without any treatment effect on anemia and CKD-MBD, to eliminate the impact of treatment as far as possible. Our results showed a significant correlation between high serum phosphate levels and anemia, even after adjusting the effects of factors already known to be involved in anemia, such as renal function, nutritional status, and iron metabolism. This finding underscores the possibility of mechanistic overlap between CKD-MBD and anemia.

The subgroup analysis showed a robust correlation between high serum phosphate levels and anemia in the low-ferritin and CKD stage 4–5 groups, indicating a possible interaction of association between high serum phosphate levels and anemia in these groups. Nevertheless, both eGFR and ferritin level were not significant in the test of interaction (P = 0.336 and P = 0.398, respectively). However, the sample size in this study was not adequately powerful for conclusive interaction test results; thus, these interactions cannot be ruled out. Concerning the physiological mechanism of the interaction between phosphate and ferritin, iron deficiency may strengthen the association between CKD-MBD and anemia through FGF23, whose level is elevated during iron deficiency [32]. Unfortunately, no subgroup analysis of iron kinetics was conducted in previous studies, making it difficult to compare the results. Nevertheless, our findings suggest that iron-deficient patients with CKD may benefit from appropriate iron supplementation and strict management of CKD-MBD to prevent the development and progression of renal anemia. In contrast, the possibility of an interaction between phosphate and renal function may indicate that it is difficult to generalize the present results to the entire non-dialysis CKD population.

The association between phosphate and anemia shown in this study may be mediated by factors other than FGF23. While anemia is a risk factor for the development of CVD, CVD may also, in turn, increase the risk of anemia via elevated levels of inflammatory cytokines and other factors [33]. Conversely, phosphate promotes vascular calcification and increases the risk of CVD. Therefore, the possibility of phosphate levels being associated with anemia through increased arteriosclerosis and cardiovascular risk cannot be ruled out. In addition, parathyroid hormone (PTH) inhibits erythropoiesis and promotes osmotic fragility of erythrocytes through calcium-ATPase stimulation [34]; thus, it is conceivable that high-phosphate levels may have promoted PTH secretion and affected anemia. However, we were unable to obtain PTH data and examine this effect in this study.

There were several other limitations to our study. First, because of the observational nature of the study design, causality cannot be inferred, and there may be unmeasured confounders. Moreover, this study was a cross-sectional analysis; therefore, we could not examine changes over time. Second, we have not examined factors that link CKD-MBD and anemia, such as FGF23 and hepcidin. Third, the present data are limited to a single center and are not representative of all CKD populations. Fourth, we did not measure nutritional status indicators other than albumin. Finally, vitamin D deficiency affects renal anemia; however, we could not obtain data on 25-hydroxy vitamin D and 1–25-dihydroxy vitamin D levels. Thus, the effect of vitamin D deficiency on the association between CKD-MBD and anemia could not be considered in this study.

Conclusions

A significant correlation was noted between high serum phosphate levels and anemia in patients with CKD who had not received treatment for anemia and CKD-MBD, even after excluding the effects of factors already known to be involved in anemia, such as renal function, nutritional status, and iron metabolism. This result underscores the possibility of a mechanistic overlap between CKD-MBD and anemia. Further prospective studies are required to elucidate the factors underlying this overlap in the same patient group.

Availability of data and materials

The datasets used during the current study are available from the corresponding author on reasonable request.

Abbreviations

CI:

Confidence interval

CKD:

Chronic kidney disease

CVD:

Cardiovascular disease

eGFR:

Estimated glomerular filtration rate

EPO:

Erythropoietin

ESA:

Erythropoiesis-stimulating agents

FGF23:

Fibroblast growth factor-23

Hb:

Hemoglobin

MBD:

Mineral and  bone disorder

PTH:

Parathyroid hormone

References

  1. Babitt JL, Lin HY. Mechanisms of anemia in CKD. J Am Soc Nephrol. 2012;23:1631–4.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  2. Dhingra R, Gaziano JM, Djoussé L. Chronic kidney disease and the risk of heart failure in men. Circ Heart Fail. 2011;4:138–44.

    Article  PubMed  PubMed Central  Google Scholar 

  3. Go AS, Yang J, Ackerson LM, Lepper K, Robbins S, Massie BM, et al. Hemoglobin level, chronic kidney disease, and the risks of death and hospitalization in adults with chronic heart failure: the Anemia in Chronic Heart Failure: Outcomes and Resource Utilization (Anchor) Study. Circulation. 2006;113:2713–23.

    Article  CAS  PubMed  Google Scholar 

  4. Gouva C, Nikolopoulos P, Ioannidis JP, Siamopoulos KC. Treating anemia early in renal failure patients slows the decline of renal function: a randomized controlled trial. Kidney Int. 2004;66:753–60.

    Article  PubMed  Google Scholar 

  5. Hayashi T, Suzuki A, Shoji T, Togawa M, Okada N, Tsubakihara Y, et al. Cardiovascular effect of normalizing the hematocrit level during erythropoietin therapy in predialysis patients with chronic renal failure. Am J Kidney Dis. 2000;35:250–6.

    Article  CAS  PubMed  Google Scholar 

  6. Kazmi WH, Kausz AT, Khan S, Abichandani R, Ruthazer R, Obrador GT, et al. Anemia: an early complication of chronic renal insufficiency. Am J Kidney Dis. 2001;38:803–12.

    Article  CAS  PubMed  Google Scholar 

  7. Kalantar-Zadeh K, Lee GH, Miller JE, Streja E, Jing J, Robertson JA, et al. Predictors of hyporesponsiveness to erythropoiesis-stimulating agents in hemodialysis patients. Am J Kidney Dis. 2009;53:823–34.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  8. Jablonski KL, Chonchol M, Pierce GL, Walker AE, Seals DR. 25-Hydroxyvitamin D deficiency is associated with inflammation-linked vascular endothelial dysfunction in middle-aged and older adults. Hypertension. 2011;57:63–9.

    Article  CAS  PubMed  Google Scholar 

  9. Komaba H, Fukagawa M. The role of FGF23 in CKD–with or without klotho. Nat Rev Nephrol. 2012;8:484–90.

    Article  CAS  PubMed  Google Scholar 

  10. Nam KH, Kim H, An SY, Lee M, Cha MU, Park JT, et al. Circulating fibroblast growth Factor-23 levels are associated with an increased risk of anemia development in patients with nondialysis chronic kidney disease. Sci Rep. 2018;8:7294.

    Article  PubMed  PubMed Central  Google Scholar 

  11. Akizawa T, Makino H, Matsuo S, Watanabe T, Imai E, Nitta K, et al. Management of anemia in chronic kidney disease patients: baseline findings from Chronic Kidney Disease Japan Cohort Study. Clin Exp Nephrol. 2011;15:248–57.

    Article  CAS  PubMed  Google Scholar 

  12. Tsai MH, Leu JG, Fang YW, Liou HH. High fibroblast growth factor 23 levels associated with low hemoglobin levels in patients with chronic kidney disease Stages 3 and 4. Medicine (Baltimore). 2016;95:e3049.

    Article  CAS  PubMed  Google Scholar 

  13. Mehta R, Cai X, Hodakowski A, Lee J, Leonard M, Ricardo A, et al. Fibroblast growth factor 23 and anemia in the chronic renal insufficiency cohort study. Clin J Am Soc Nephrol. 2017;12:1795–803.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  14. Usui T, Zhao J, Fuller DS, Hanafusa N, Hasegawa T, Fujino H, et al. Association of erythropoietin resistance and fibroblast growth factor 23 in dialysis patients: results from the Japanese Dialysis Outcomes and Practice Patterns Study. Nephrology (Carlton). 2021;26:46–53.

    Article  CAS  PubMed  Google Scholar 

  15. National Kidney Foundation. K/DOQI clinical practice guidelines for chronic kidney disease: evaluation, classification, and stratification. Am J Kidney Dis. 2002;39:S1-266.

    Google Scholar 

  16. Matsuo S, Imai E, Horio M, Yasuda Y, Tomita K, Nitta K, et al. Revised equations for estimated GFR from serum creatinine in Japan. Am J Kidney Dis. 2009;53:982–92.

    Article  CAS  PubMed  Google Scholar 

  17. Watanabe Y, Yamagata K, Nishi S, Hirakata H, Hanafusa N, Saito C, et al. Japanese society for dialysis therapy clinical guideline for “hemodialysis initiation for maintenance hemodialysis.” Ther Apher Dial. 2015;19:93–107.

    Article  PubMed  Google Scholar 

  18. Shimada T, Hasegawa H, Yamazaki Y, Muto T, Hino R, Takeuchi Y, et al. FGF-23 is a potent regulator of vitamin D metabolism and phosphate homeostasis. J Bone Miner Res. 2004;19:429–35.

    Article  CAS  PubMed  Google Scholar 

  19. Shimada T, Kakitani M, Yamazaki Y, Hasegawa H, Takeuchi Y, Fujita T, et al. Targeted ablation of FGF23 demonstrates an essential physiological role of FGF23 in phosphate and vitamin D metabolism. J Clin Invest. 2004;113:561–8.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  20. Isakova T, Wahl P, Vargas GS, Gutiérrez OM, Scialla J, Xie H, et al. Fibroblast growth factor 23 is elevated before parathyroid hormone and phosphate in chronic kidney disease. Kidney Int. 2011;79:1370–8.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  21. Rebholz CM, Grams ME, Coresh J, Selvin E, Inker LA, Levey AS, et al. Serum fibroblast growth factor-23 is associated with incident kidney disease. J Am Soc Nephrol. 2015;26:192–200.

    Article  CAS  PubMed  Google Scholar 

  22. Khan AM, Chirinos JA, Litt H, Yang W, Rosas SE. FGF-23 and the progression of coronary arterial calcification in patients new to dialysis. Clin J Am Soc Nephrol. 2012;7:2017–22.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  23. Gutiérrez OM, Januzzi JL, Isakova T, Laliberte K, Smith K, Collerone G, et al. Fibroblast growth factor 23 and left ventricular hypertrophy in chronic kidney disease. Circulation. 2009;119:2545–52.

    Article  PubMed  PubMed Central  Google Scholar 

  24. Scialla JJ, Xie H, Rahman M, Anderson AH, Isakova T, Ojo A, et al. Fibroblast growth factor-23 and cardiovascular events in CKD. J Am Soc Nephrol. 2014;25:349–60.

    Article  CAS  PubMed  Google Scholar 

  25. Isakova T, Xie H, Yang W, Xie D, Anderson AH, Scialla J, et al. Fibroblast growth factor 23 and risks of mortality and end-stage renal disease in patients with chronic kidney disease. JAMA. 2011;305:2432–9.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  26. Gutiérrez OM, Mannstadt M, Isakova T, Rauh-Hain JA, Tamez H, Shah A, et al. Fibroblast growth factor 23 and mortality among patients undergoing hemodialysis. N Engl J Med. 2008;359:584–92.

    Article  PubMed  PubMed Central  Google Scholar 

  27. Czaya B, Faul C. The role of fibroblast growth factor 23 in inflammation and anemia. Int J Mol Sci. 2019;20:4195.

    Article  PubMed  PubMed Central  Google Scholar 

  28. Coe LM, Madathil SV, Casu C, Lanske B, Rivella S, Sitara D. FGF-23 is a negative regulator of prenatal and postnatal erythropoiesis. J Biol Chem. 2014;289:9795–810.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  29. David V, Francis C, Babitt JL. Ironing out the cross talk between FGF23 and inflammation. Am J Physiol Renal Physiol. 2017;312:F1-8.

    Article  CAS  PubMed  Google Scholar 

  30. Eisenga MF, Emans ME, van der Putten K, Cramer MJ, Diepenbroek A, Velthuis BK, et al. Epoetin beta and C-terminal fibroblast growth factor 23 in patients with chronic heart failure and chronic kidney disease. J Am Heart Assoc. 2019;8:e011130.

    Article  PubMed  PubMed Central  Google Scholar 

  31. Iwasaki T, Fujimori A, Nakanishi T, Okada S, Hanawa N, Hasuike Y, et al. Saccharated ferric oxide attenuates haematopoietic response induced by epoetin beta pegol in patients undergoing haemodialysis. BMC Nephrol. 2021;22:124.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  32. Yokoyama K, Hirakata H, Akiba T, Fukagawa M, Nakayama M, Sawada K, et al. Ferric citrate hydrate for the treatment of hyperphosphatemia in nondialysis-dependent CKD. Clin J Am Soc Nephrol. 2014;9:543–52.

    Article  PubMed  PubMed Central  Google Scholar 

  33. Silverberg DS, Wexler D, Iaina A. The importance of anemia and its correction in the management of severe congestive heart failure. Eur J Heart Fail. 2002;4:681–6.

    Article  PubMed  Google Scholar 

  34. Duque EJ, Elias RM, Moysés RMA. Parathyroid hormone: a uremic toxin. Toxins (Basel). 2020;12:189.

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgements

Not applicable.

Funding

Not applicable.

Author information

Authors and Affiliations

  1. Division of Nephrology and Hypertension, Department of Internal Medicine, The Jikei University School of Medicine, 3-25-8 Nishi-Shimbashi Minato-Ku, Tokyo, 105-8461, Japan

    Kazuhiko Kato, Akio Nakashima, Ichiro Ohkido & Takashi Yokoo

  2. Department of Internal Medicine, Fuji City General Hospital, Takashima-Cho 50, Fuji-Shi, Shizuoka, Japan

    Kazuhiko Kato & Kenji Kasai

Authors
  1. Kazuhiko Kato
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Akio Nakashima
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Ichiro Ohkido
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Kenji Kasai
    View author publications

    You can also search for this author in PubMed Google Scholar

  5. Takashi Yokoo
    View author publications

    You can also search for this author in PubMed Google Scholar

Contributions

Research idea and study design: KK, AN; data acquisition: KK; data analysis/interpretation: KK, AN; statistical analysis: KK, AN; supervision or mentorship: IO, K. Kasai, TY. Each author contributed important intellectual content during manuscript drafting or revision and accepts accountability for the overall work by ensuring that questions pertaining to the accuracy or integrity of any portion of the work are appropriately investigated and resolved.

Corresponding author

Correspondence to Kazuhiko Kato.

Ethics declarations

Ethics approval and consent to participate

All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee at which the studies were conducted (Institutional Review Board of the Fuji City General Hospital, Shizuoka, Japan; Approval No.: 244) and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. As this was a retrospective cross-sectional study, and we provided patients with information regarding the study design and gave them the opportunity to opt out, the requirement for informed consent was waived.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Kato, K., Nakashima, A., Ohkido, I. et al. Association between serum phosphate levels and anemia in non-dialysis patients with chronic kidney disease: a retrospective cross-sectional study from the Fuji City CKD Network. BMC Nephrol 24, 244 (2023). https://doi.org/10.1186/s12882-023-03298-9

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12882-023-03298-9

Keywords

BMC Nephrology

ISSN: 1471-2369

Contact us