Factors associated with serum fetuin-A concentrations after long-term use of different phosphate binders in hemodialysis patients

The original clinical trial was a multi-center, prospective, randomized, open-label, parallel comparison of 48-week treatment of sevelamer (sevelamer HCl, Renagel) versus a calcium-based phosphate binder (calcium carbonate) in maintenance HD patients with hyperphosphatemia. The primary objective was to compare the proportion of patients achieving the National Kidney Foundation’s Kidney Disease Outcomes Quality Initiative (NKF-K/DOQI) recommend treatment goal for maintenance HD patients. It was approved by China medical university and hospital research ethics committees and was registered on ClinicalTrials.gov (NCT01755078). The study design and methods also have been reported in detail elsewhere [22]. We conducted a post-hoc analysis to compare the long-term effects of sevelamer versus calcium carbonate on the changes of serum fetuin-A levels. The ethics committees approved consent procedure and the written informed consent was obtained from all patients. This is a per-protocol analysis including only the population who have completed the 48-week treatment.

Adult (age ≥ 45 years) ESRD patients with anuria attending routine HD sessions 3 times per week for at least 3 months with adequate dialysis dose (KT/V >1.2) were evaluated. The different calcium concentrations in dialysate of studied patients included low calcium bath (LCB, calcium concentration 2.5 meq/L) and non- low calcium bath (non-LCB, calcium concentration 3.0 meq/L or 3.5 meq/L). Patients were excluded from the study if they had the following conditions: hypercalcemia (corrected serum total calcium > 10.5 mg/dL) during the 2 weeks of washout period; ALT or AST > 3 times upper normal limit or iPTH > 1000 pg/mL before screening; clinical inflammatory or infectious diseases, gastrointestinal bleeding or any other cause of hospital admission within 3 months before enrollment; thyroid disease, parathyroidectomy, swallowing disorders, gastrectomy or intestinal resection; osteoporosis and concurrently receiving related medications (including bisphosphonates, calcitonin or hormone replacement therapy) and known hypersensitivity to any components of the formulation of the study medications. Commonly used and studied calcium-based phosphate binders include calcium carbonate and calcium acetate. Calcium acetate was not chosen in this study because of the large tablet size manufactured in Taiwan and poor taste, it is unpleasant for seniors to swallow.

At the screening visit, patients who fulfilled the entrance criteria and who gave their written informed consent entered a washout period. They discontinued phosphate binders for two weeks. Patients who had hyperphosphatemia (serum phosphorus > 5.5 mg/dL and ≤ 8.5 mg/dL) during the 2-week washout period were randomized to receive either sevelamer or calcium carbonate for 48 weeks. The randomization schedule was generated using a validated system that automates the random assignment of treatment groups to randomized numbers. All randomized patients attended bi-weekly clinic visits for the first month (week 2 and 4), monthly clinic visits for the subsequent 2 months (week 8 and 12) and tri-monthly clinic visits for the last 9 months (week 24, 36 and 48). The starting dose of the medications was based on the baseline serum phosphate (P) level. All patients in different treatment groups took sevelamer (800mg per tablet) or calcium carbonate (500mg per tablet) three times per day with 1 tablet (5.5 < P < 6.5 mg/dL), 2 tablets (6.5 ≦ P < 7.5 mg/dL), or 3 tablets (P ≧ 7.5 mg/dL). The medications were given with meals and doses were titrated according to a fixed algorithm: increase 1 tablet per meal (if P > 5.5 mg/dL), no change (3.5 ≦ P ≦ 5.5 mg/dL), or decrease 1 tablet per meal (if P < 3.5 mg/dL). If the serum total calcium level rose above 10.5 mg/dL, the investigator reduced the calcium carbonate dosage by 1 tablet per meal to bring the serum calcium below 10.5 mg/dL. The largest daily dose was 12 tablets of sevelamer or calcium carbonate. The total duration of this trial was 50 weeks (i.e, 2 weeks washout plus 48 weeks of treatment). The patients were instructed to take trial medication per day and returned the trial medication bottle in next visit. A record of the number of tablets dispensed, taken and returned for each patient was documented on the case report form (CRF). Compliance was assessed from information recorded in the CRF, including trial medication count and starting and ending date of therapy. All patients in the analysis maintained their regular dialysis schedule, dietary habits and prescribed medication for diabetes mellitus (insulin or oral anti-diabetic drugs, except for metformin and glitazones), dyslipidemia (statin), hypertension (anti-hypertension drugs) and secondary hyperparathyroidism (active vitamin D, either alfacalcidol or calcitriol, dosage adjusted by KDOQI guideline) throughout the study period by the physicians in the three centers. Magnesium-containing drugs, other vitamin D analogs and calcimimetics were not prescribed to the patients.

After enrollment, the serum phosphate, total calcium and albumin levels were measured at week 0, 2, 4, 6, 8,12, 24, 36 and 48. The serum ALK-P, LDL-C, hsCRP and iPTH levels were measured at week 0, 12, 24, 36 and 48. The serum fetuin-A levels were measured at week 0 and 48. The serum phosphate, total calcium, lipid profiles, triglyceride, albumin, ALK-P and hsCRP were measured using standard laboratory techniques with an automatic analyzer in the central laboratory. Intact PTH was measured by immunoradiometric assay (Beckman Coulter PTH IRMA).

For the analysis of fetuin-A, the serum was centrifuged and harvested according to standard procedures at 4 °C and frozen immediately afterwards at −80 °C. Serum analysis for fetuin-A was performed in duplicate by a highly sensitive two-site enzyme linked immunoassay (ELISA) (Immunology Consultants Laboratory, Inc. OR, USA.) The interassay and intraassay coefficients of variations were <8 %. Fetuin-A was batch analyzed after completion of the study.

The sample size and power was estimated by G*Power software. We estimated that a sample size of 70 (35 in each one group) with an anticipated dropout rate of 30 % would provide more than 80 % power to detect a significant difference between two independent or dependent means with a two-sided α = 0.05. Shapiro-Wilk test was used to verify the distribution normality of investigated parameters. Normally distributed data were given as mean ± standard deviation, whereas non-normally distributed data were expressed as median (inter-quartile range). Continuous and ordinal data were analyzed using the Student t test. Changes in parameters from the baseline data were compared with a paired samples t test. The Mann-Whitney U test and the Wilcoxon signed-rank test were used for testing nonparametric measurements. Categorical data were analyzed using Fisher’s exact test or the chi-square test. Bivariate relationships were calculated using Pearson or Spearman’s rank correlation coefficient.

In this post-hoc analysis, 75 randomized patients from three large HD centers were included. In the sevelamer group, 13 patients withdrew early (8 patients withdrew in eight weeks because of GI problems, 1 died with sepsis at week 12, 1 received a kidney transplant at week 24, 1 loss to follow-up at week 24, 1 withdrew consent at week 36, and 1 died with gastric cancer at week 36). In the calcium group, 12 patients withdrew early (1 died with pneumonia at week two, 7 patients withdrew in 12 weeks because of GI problems, 2 withdrew their consent at week 24 and week 36, and 1 received a kidney transplant at week 36). Finally, 50 patients completed the 48-week treatment, including 23 patients treated with sevelamer and 27 patients with calcium carbonate. The flow chart was shown in Fig. 1.

Baseline demographic data of 50 completed treatment patients are shown in Table 1. Variables of HD duration and serum levels of iPTH, hsCRP, TG and fetuin-A were not normally distributed. There were no differences between the two groups with respect to age, sex, hemodialysis duration, patients with DM, use of active vitamin D, low calcium dialysate, statin and anti-hypertension drugs. The sevelamer group had lower basal serum phosphate levels (6.54 ± 0.91 vs 7.22 ± 0.98 mg/dL in calcium group, P = 0.015) before treatment. No other significant differences of basal serum Ca, iPTH, ALK-P, hsCRP, Hct, Albumin, LDL-C, TG and fetuin-A levels were noted between two groups (Table 1). The baseline serum fetuin-A levels had a significant correlation with HD duration (ρ = -0.324, P = 0.022) and basal serum albumin levels (ρ = 341, P = 0.015) (Table 2). For the 25 (33.3 %) patients who withdrew early, the clinical characteristics of them were not different from the 50 analyzed patients in age, sex, hemodialysis duration, number of patients with DM, use of vitamin D, use of low calcium dialysate, use of statin and anti-hypertension drugs, basal serum Ca, P, iPTH, ALK-P, hsCRP, Hct, serum albumin, LDL-C and TG levels (data not shown).

The average daily dose of study medication was 7.81 ± 3.22 tablets (6248 ± 2576 mg) in sevelamer group and 6.52 ± 2.61 tablets (3260 ± 1305 mg) in calcium carbonate group. The incidence of combined adverse events was similar between sevelamer and calcium carbonate group. The most commonly reported adverse event in sevelamer group was upper abdominal pain (8.0 %, vs. 0 %, P < 0.001). Constipation was more common in the calcium carbonate group (7.3 %, vs. 4.5 %, P = 0.022). There were no cardiovascular events in either study group during the follow-up period.

In the sevelamer group, there were significant changes after the 48-week treatment with increased serum calcium, decreased serum phosphate, increased ALK-P, decreased hsCRP, decreased LDL-C and decreased fetuin-A levels (from 210.61 (104.73) to 153.85 (38.64) ug/dl, P = 0.003) (Table 3). In the calcium group, there were significant changes after the 48-week treatment with increased serum calcium, decreased phosphate, decreased iPTH and decreased fetuin-A levels (from 203.95 (107.87) to 170.90 (58.02) ug/mL, P =0.002) (Table 3).

After the 48-week treatment, the sevelamer group had less serum calcium increment (0.26 ± 0.55 vs. 0.80 ± 0.93 mmol/L, P = 0.015), less iPTH decrement (12.10 (216.60) vs. -137.10 (255.70) pg/mL, P = 0.026), more ALK-P increment (30.26 ± 45.78 vs. -2.26 ± 22.69 IU/L, P = 0.004), more hsCRP decrement (−0.9 (2.7) vs. 0.1(3.8) mg/L, P = 0.025) and more LDL-C decrement (1.16 ± 0.73 vs. 0.20 ± 0.71 mmol/L, P < 0.0001). There was no significant difference in the serum fetuin-A decrement between two treatment groups (sevelamer group −49.44 (113.78) vs. calcium carbonate group −38.21 (78.51) ug/mL, P = 0.345) (Table 4).

We further analyzed the correlations of fetuin-A decrement with related parameters in 50 studied patients. Bivariate correlation analysis (Table 5) showed the decrement in serum fetuin-A (Δfetuin-A) levels was associated with the changes in serum calcium (ΔCa) (ρ = −0.230, P = 0.040), iPTH (ΔiPTH) (ρ = 0.306, P = 0.031) and albumin (Δalbumin) levels (ρ = 0.408, P = 0.003), not associated with sevelamer use, changes in serum phosphate (ΔP) and hsCRP (ΔhsCRP) levels.