Figures
Abstract
Hepcidin is the key regulator of iron homeostasis but data are limited regarding its temporal response to iron therapy, and response to intravenous versus oral iron. In the 56-week, open-label, multicenter, prospective, randomized FIND-CKD study, 626 anemic patients with non-dialysis dependent chronic kidney disease (ND-CKD) and iron deficiency not receiving an erythropoiesis stimulating agent were randomized (1:1:2) to intravenous ferric carboxymaltose (FCM), targeting higher (400–600μg/L) or lower (100–200μg/L) ferritin, or to oral iron. Serum hepcidin levels were measured centrally in a subset of 61 patients. Mean (SD) baseline hepcidin level was 4.0(3.5), 7.3(6.4) and 6.5(5.6) ng/mL in the high ferritin FCM (n = 17), low ferritin FCM (n = 16) and oral iron group (n = 28). The mean (SD) endpoint value (i.e. the last post-baseline value) was 26.0(9.1),15.7(7.7) and 16.3(11.0) ng/mL, respectively. The increase in hepcidin from baseline was significantly smaller with low ferritin FCM or oral iron vs high ferritin FCM at all time points up to week 52. Significant correlations were found between absolute hepcidin and ferritin values (r = 0.65, p<0.001) and between final post-baseline increases in both parameters (r = 0.70, p<0.001). The increase in hepcidin levels over the 12-month study generally mirrored the cumulative iron dose in each group. Hepcidin and transferrin saturation (TSAT) absolute values showed no correlation, although there was an association between final post-baseline increases (r = 0.42, p<0.001). Absolute values (r = 0.36, p = 0.004) and final post-baseline increases of hepcidin and hemoglobin (p = 0.30, p = 0.030) correlated weakly. Baseline hepcidin levels were not predictive of a hematopoietic response to iron therapy. In conclusion, hepcidin levels rose in response to either intravenous or oral iron therapy, but the speed and extent of the rise was greatest with intravenous iron targeting a higher ferritin level. However neither the baseline level nor the change in hepcidin was able to predict response to therapy in this cohort.
Citation: Gaillard CA, Bock AH, Carrera F, Eckardt K-U, Van Wyck DB, Bansal SS, et al. (2016) Hepcidin Response to Iron Therapy in Patients with Non-Dialysis Dependent CKD: An Analysis of the FIND-CKD Trial. PLoS ONE 11(6): e0157063. https://doi.org/10.1371/journal.pone.0157063
Editor: Kathrin Eller, Medical University of Graz, AUSTRIA
Received: March 15, 2016; Accepted: May 23, 2016; Published: June 8, 2016
Copyright: © 2016 Gaillard et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All relevant data are with the paper and its supporting information files.
Funding: The FIND-CKD study was funded by Vifor Pharma, Glattbrugg, Switzerland. Medical writing supported was provided by a freelance medical writer funded by Vifor Pharma (C Dunstall). MC, YM, and SL are employed by Vifor Pharma Ltd. Vifor Pharma Ltd provided support in the form of salaries for MC, YM, and SL, and contributed to the study design and data analysis, and these authors reviewed the manucript prior to publication. The specific roles of these authors are articulated in the ‘author contributions’ section. DBVW is employed by Davita Healthcare Partners. Davita Healthcare Partners provided support in the form of salary for author DBVW, but did not have any additional role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript. The specific role of this author is articulated in the ‘author contributions’ section.
Competing interests: Carlo Gaillard has received speakers’ fees, honoraria, and consultancy fees from several manufacturers of erythropoietin-stimulating agents and intravenous iron products, including Amgen, Pharmacosmos, Hoffmann-La Roche, Takeda, and Vifor Pharma. Andreas H. Bock has received speaker's honoraria and consultancy fees from Amgen, Hoffmann-La Roche, and Vifor Pharma. Fernando Carrera has no conflicts of interest to declare. Kai-Uwe Eckardt has received speaker’s fees and consultancy fees from several manufacturers of ESAs and IV iron, including Affymax, Amgen, Bayer, Johnson & Johnson, Hoffmann-La Roche, and Vifor Pharma. David B. Van Wyck is employed by Davita Healthcare Partners. Davita Healthcare Partners provided support in the form of salary for author DBVW, but did not have any additional role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript. The specific role of this author is articulated in the ‘author contributions’ section. Sukhvinder S. Bansal has no conflicts of interest to declare. Maureen Cronin, Yvonne Meier, and Sylvain Larroque are employed by Vifor Pharma Ltd. Vifor Pharma Ltd provided support in the form of salaries for MC, YM, and SL, and contributed to the study design and data analysis, and these authors reviewed the manucript prior to publication. The specific roles of these authors are articulated in the ‘author contributions’ section. Simon D. Roger has received speakers’ fees, honoraria, and consultancy fees from several manufacturers of ESAs and IV iron, including Amgen, Hoffmann-La Roche, Janssen-Cilag, Novartis, Sandoz, Takeda, and Vifor Pharma. Iain C Macdougall has received speakers’ fees, honoraria, and consultancy fees from several manufacturers of ESAs and IV iron, including Affymax, AMAG, Amgen, Ortho Biotech, Pharmacosmos, Hoffmann-La Roche, Takeda, and Vifor Pharma. The FIND-CKD study was funded by Vifor Pharma, Glattbrugg, Switzerland. The study was undertaken in collaboration with Luitpold Pharmaceuticals Inc, Shirley, NY, USA. The involvement of Luitpold was limited to a local protocol amendment for US sites and to proposing US sites for inclusion. The clinical research organisation ICON (Dublin, Ireland) coordinated the study with funding from Vifor Pharm. Medical writing supported was provided by a freelance medical writer funded by Vifor Pharma (C Dunstall). There are no patents, products in development, or marketed products to declare. This does not alter the authors' adherence to PLOS ONE policies on sharing data and materials.
Introduction
Since its discovery in 2001 [1, 2], the peptide hormone hepcidin has been identified as the principal regulator of iron availability in the body. It maintains iron homeostasis by controlling intestinal absorption of dietary iron and release of iron from the liver and spleen [3]. Hepcidin acts by binding to, and inducing internalization of, the transmembrane iron transporter protein ferroportin, thus blocking export of iron from enterocytes, macrophages and parenchymal hepatocytes into the circulation. When iron availability is inadequate, low hepcidin levels promote enhanced intestinal iron uptake and release of stored iron. Hepcidin levels rise in response to iron repletion such that iron absorption and release are reduced. Stimulation of erythropoiesis, conversely, lowers hepcidin levels through increased production of erythroferrone by erythroblasts [4]. Furthermore, hepcidin levels are increased in the presence of chronic inflammation, such as in patients with chronic kidney disease (CKD) [5–8], contributing to the functional iron deficiency which is frequently observed in this patient population.
The key regulatory role of hepcidin has prompted interest in the possibility that it may represent a more reliable indicator of iron status than current biomarkers such as ferritin [3, 9, 10] and indeed may represent a useful therapeutic target [11]. As with ferritin, however, the predictive value of hepcidin is complicated by the influence of inflammation on hepcidin levels [3, 12], and by high intra-individual variation [13]. Data are conflicting regarding an association between hepcidin and the erythropoietic response to erythropoiesis stimulating agent (ESA) therapy [13–17], or iron therapy [13, 16, 18–22]. The longitudinal response of hepcidin levels to iron therapy has not been examined, nor are there any data comparing the short- or long-term hepcidin response to intravenous (IV) versus oral iron therapy. Additionally, the associations between hepcidin and other markers of iron status, or anemia, are poorly defined.
The Ferinject® assessment in patients with Iron deficiency anemia and Non-Dialysis dependent Chronic Kidney Disease (FIND-CKD) study was a randomized, international, trial of IV ferric carboxymaltose (FCM) versus oral iron in patients with non-dialysis dependent CKD, anemia, and iron deficiency not receiving ESA therapy [23]. As part of the study protocol, hepcidin levels were measured in a subset of patients throughout the 12-month study. The current exploratory analysis was undertaken post hoc with the objective of determining the response of hepcidin levels to IV or oral iron treatment over time.
Methods
Study design
FIND-CKD was a 56-week, open-label, multicenter, prospective, randomized, three-arm study undertaken at 193 nephrology centers in 20 countries (ClinicalTrials.gov NCT00994318). The first patient visit took place in December 2009, with the final patient visit in January 2012. The study design has been described in full elsewhere [24] and is summarized here. The study protocol was approved at all participating sites (see S1 Appendix for a list of Ethics Committees). The study was conducted according to the principles of the Declaration of Helsinki and the ICH Guidelines for Good Clinical Practice. All patients provided written informed consent.
The primary endpoint of the study was time to initiation of other anemia management, specified as ESAs, blood transfusion, use of an alternative iron therapy, or occurrence of a Hb trigger (two consecutive Hb values <10 g/dL on or after week 8). Pre-planned analyses included the correlations between hepcidin and iron parameters (ferritin and transferrin saturation [TSAT]) at baseline and by visit, both for absolute values and for change from baseline. Other analyses reported here were performed post hoc.
Study population
Full eligibility criteria have been published previously [24]. In brief, adult (≥18 years) patients with non-dialysis dependent CKD were enrolled if (a) at least one Hb level was 9–11 g/dL within four weeks of randomization, (b) any ferritin level was <100 μg/L, or <200 μg/L with TSAT <20%, within four weeks of randomization, (c) estimated glomerular filtration rate (eGFR) was ≤60 mL/min/1.73m2 (d) no ESA had been administered within four months of randomization, (e) no documented history of gastrointestinal intolerability to oral iron (e) no known active infection and baseline C-reactive protein (CRP) ≤ 20 mg/L.
Study treatment
Patients were randomized in 1:1:2 ratio to high ferritin FCM: low ferritin FCM: oral iron. FCM dose (Ferinject®, Vifor International, St Gallen, Switzerland) in the high ferritin and low ferritin FCM groups was adjusted to target a ferritin level of 400–600 μg/L and 100–200 μg/L, respectively. An initial single dose was administered on day 0: 1000 mg iron as FCM in the high ferritin FCM group (500 mg iron on days 0 and 7 in patients weighing ≤66 kg) and 200 mg iron as FCM in the low ferritin FCM group if ferritin was <100 μg/L. During weeks 4 to 48, FCM was administered every four weeks in the high ferritin FCM group at a dose of 500 mg iron if ferritin was in the range 200 to <400 μg/L, and at a dose of 1000 mg iron if ferritin was <200 μg/L, and in the low ferritin FCM group at a dose of 200 mg iron if ferritin was <100 μg/L. In both groups, dosing was withheld if TSAT was ≥40%. Oral iron therapy consisted of commercially-available ferrous sulfate at a dose of 304 mg (100 mg of iron) twice daily.
Until week 8 post-randomization, patients were not to receive ESAs, blood transfusion or any anemia therapy other than study drug unless there was an absolute requirement.
Hepcidin
All UK patients had hepcidin levels in serum samples measured at baseline (week 0) and at weeks 4, 8, 12, 24, 36 and 52 post-randomization. Hepcidin was measured at King’s College London in serum using ultra-high pressure liquid chromatography (UPLC) and a triple-quadruple mass spectrometer based on published methodology [25]. Due to a change of mass spectrometer, the assay has undergone a further validation [26]. The lower limit of quantitation was 0.1 ng/mL with less than 20% precision and accuracy.
Statistical analysis
All patients who received at least one dose of randomized treatment (or according to the protocol were not treated due to ferritin level) and who attended at least one post-baseline visit were included in the intention-to-treat (ITT) population. Hepcidin data were analyzed for all ITT patients with a baseline hepcidin value and at least one post-baseline value (i.e. the 'hepcidin subpopulation'). The statistical analysis plan specified that hepcidin values were included only up to the point at which the primary endpoint was met (i.e. another anemia therapy was initiated) or the end of the study (for patients who did not meet primary endpoint).
All analyses were based on the natural scale (i.e. untransformed data). Summary statistics are provided for baseline and post-baseline hepcidin levels by treatment group. The change in hepcidin level from baseline to each post-baseline time point was compared within each treatment group using the Student paired t-test. The pairwise comparisons of treatment groups in the change in hepcidin values from baseline to all post-baseline visits were assessed by a mixed model with repeated measures procedure, using treatment group, baseline hepcidin value, visit, age at baseline and interaction between visit and treatment as covariates. The correlation between observed hepcidin levels versus ferritin, TSAT, Hb and estimated GFR (GFR) levels, and between changes in levels from baseline, was assessed by Pearson coefficients across patients in all treatment groups, using endpoint values (i.e. the last non-missing post-baseline value recorded). Correlations were analyzed similarly within each treatment group at weeks 8 and 24. Patient numbers were considered too low after week 24 for within-group analyses, although positive correlations in either FCM treatment arm prompted an additional assessment at week 52 or endpoint, and/or in pooled FCM groups. All assessments of correlations between hepcidin and ferritin, TSAT, Hb and eGFR included only values recorded on the same sample date. Ferritin and Hb values measurements were based on central analysis; TSAT values were obtained locally. eGFR based on locally-measured serum creatinine values was calculated based on the Modification of Diet in Renal Disease-4 (MDRD-4) equation.
As an exploratory analysis, the hazard ratios and associated 95% confidence intervals for the primary endpoint of the study (time to initiation of other anemia management or occurrence of hepcidin trigger [24]) were calculated using Cox proportional hazards modeling adjusting for (a) hepcidin at baseline (b) change in hepcidin to week 8 and (c) change in hepcidin to week 24.
All statistical analyses were performed using SAS Version 9.3 (SAS Institute Inc. SAS/STAT, Cary, NC, USA).
Results
Study population
In total, 613 patients formed the ITT population, of whom 71 patients were recruited in the UK and were candidates for the hepcidin substudy. Of these, 61 provided both a baseline and ≥1 post-baseline value and formed the hepcidin subpopulation (17 high ferritin FCM, 16 low ferritin FCM, 28 oral iron). During the 12-month study, a total of 10 patients received an alternative anemia therapy at some point (2 high ferritin FCM, 2 low ferritin FCM, 6 oral iron), and in these patients subsequent hepcidin values were excluded from analysis since this could have affected hepcidin concentrations. Overall, hepcidin data were available from 59, 56, 57, 48, 41 and 28 patients at weeks 4, 8, 12, 24, 36 and 52, respectively (Fig 1) (S1 Table).
Disposition according to treatment group is shown in S1 Table.
The characteristics of the patients included in the hepcidin subpopulation (Table 1) showed no relevant differences to the rest of the study population [21].
Hepcidin levels over time
Mean (SD) hepcidin level at baseline was 4.0 (3.5), 7.3 (6.4) and 6.5 (5.6) ng/mL in the high ferritin FCM, low ferritin FCM and oral iron groups, respectively. These values were broadly similar to the normal range for healthy individuals of this age group based on the assay used in this analysis [25].
Post-baseline, the highest hepcidin values were observed in the high ferritin FCM group at all time points (Fig 2a). The change from baseline was statistically significant at all post-baseline visits in the high ferritin FCM group and the low ferritin group while for the oral iron group the change was significant except for week 8 (p = 0.063) (Fig 2a). The mean (SD) endpoint value (i.e. the last non-missing value recorded after baseline) was 26.0 (9.1), 15.7 (7.7) and 16.3 (11.0) ng/mL in the high ferritin FCM, low ferritin FCM and oral iron groups, respectively.
(a) Observed mean (SD) hepcidin level at each visit by treatment group. The p values indicate change from baseline (student paired t test). (b) Least square [LS] mean change in hepcidin level from baseline to each visit by treatment group by a mixed model with repeated measures procedure, with treatment group and baseline hepcidin as covariates. The p values refer to the comparison of change from baseline in the low ferritin FCM group or oral group versus the high ferritin FCM group. All differences between the low ferritin FCM and oral iron groups for the mean change in hepcidin level from baseline were non-significant (p>0.05). In both graphs, only values obtained prior to the start of alternative anemia therapy are included.
The increase in hepcidin was significantly smaller in the low ferritin FCM group and the oral iron group compared to the high ferritin FCM group at all post-baseline time points other than week 52 (Fig 2b). Other predictive factors for the increase in hepcidin were baseline hepcidin (p = 0.038) and time from start of treatment (i.e. study visit) (p<0.001). The post-baseline hepcidin increase was similar in the low ferritin FCM group and the oral iron group at all times (Fig 2b).
Hepcidin level and iron dose
The change in hepcidin level over the 12-month study generally mirrored the cumulative iron dose administered in each of the three treatment groups (Fig 3). However, most FCM in the high ferritin group was administered at the early study visits (S1 Fig), as was a high proportion of FCM in the low ferritin group, whereas daily oral dosing was continued throughout the study (Fig 3). The mean hepcidin level increased rapidly and remained elevated after the first high ferritin FCM dose (Fig 3a), with a similar but less profound pattern of change in the low FCM group (Fig 3b). Hepcidin levels increased more slowly and progressively over the 52-week study in response to oral iron therapy (Fig 3c).
Bars indicate iron dose per visit and cumulative iron dose, lines indicate mean hepcidin level. Only values obtained prior to the start of alternative anemia therapy are included BL, baseline; FCM, ferric carboxymaltose.
Association between hepcidin level and markers for iron status
Serum ferritin.
In the total hepcidin substudy population, there was a significant correlation between hepcidin and ferritin levels at baseline (r = 0.43, p<0.001) and at the study endpoint (i.e. the last available post-baseline visit values) (r = 0.65, p<0.001) (Fig 4a). At higher ferritin levels the association between hepcidin and ferritin seems to plateau although the patient numbers at these high levels are too low to draw firm conclusions. There was also a close correlation between change in hepcidin and change in ferritin from baseline to the endpoint value (r = 0.70, p<0.001) (Table 2). Fig 5 shows the correlation between hepcidin and ferritin levels in the high ferritin FCM group at baseline, week 8 and week 24, illustrating that the correlation was similar at low or high ferritin levels (i.e. before or after the start of high ferritin FCM administration).
Only values with the same sample date, and obtained prior to the start of alternative anemia therapy, are included. Solid lines indicate the quadratic regression line. Shaded areas indicate 95% CI of the regression line.
Only values with the same sample date, and obtained prior to the start of alternative anemia therapy, are included Correlation between hepcidin levels and (a) ferritin level (b) TSAT level (c) Hb level at study endpoint for the hepcidin substudy population. Only values with the same sample date, and obtained prior to the start of alternative anemia therapy, are included. Solid lines indicate the quadratic regression line. Shaded areas indicate 95% CI of the regression line. Correlation between hepcidin levels and (a) ferritin level (b) TSAT level (c) Hb level at study endpoint for the hepcidin substudy population. Only values with the same sample date, and obtained prior to the start of alternative anemia therapy, are included. Solid lines indicate the quadratic regression line. Shaded areas indicate 95% CI of the regression line.
Significant p values are shown in bold.
TSAT.
Hepcidin did not correlate with TSAT at baseline in the overall hepcidin study population (r = -0.01, p = 0.91). Neither was any significant correlation observed for absolute hepcidin and TSAT based on endpoint values (r = 0.12, p = 0.34) (Fig 4b). The change in hepcidin versus the change in TSAT from baseline to the endpoint value, however, was significant (r = 0.42, p<0.001) but the correlation was less strong than for serum ferritin (Table 2). The correlations between hepcidin and TSAT remained significant based on endpoint values for the pooled FCM cohort, both for absolute values (r = 0.59, p<0.001; n = 33) and change from baseline (r = 0.69, p<0.001; n = 33).
Association between hepcidin level and Hb.
At baseline, there was no association between absolute values for hepcidin and Hb values across all patients (r = 0.02, p = 0.88). There was a relatively weak, albeit significant, positive correlation for endpoint values (r = 0.36, p = 0.004) (Fig 4c) and between the change in hepcidin and change in Hb from baseline to the endpoint value (r = 0.30, p = 0.030) (Table 2).
Hepcidin as a predictor of response to iron therapy.
Baseline hepcidin values and the mean hepcidin increase from baseline to week 8 and week 24 were calculated within each treatment group for the subsets of patients with or without an increase in Hb of >1g/dL, >0.5g/dL or 0 g/dL at the same time point. No association was observed between baseline hepcidin or hepcidin increase and the Hb increase in either FCM treatment group using any of the cut-off points. In the oral iron group, mean baseline hepcidin was lower in patients who achieved an increase in Hb of >1 g/dL versus patients who did not at week 8 (mean 0.1 ng/mL [n = 1] versus 7.4 ng/mL [n = 20]) and at week 24 (mean 4.9 ng/mL [n = 6] versus 7.4 ng/mL [n = 11]), but patient numbers were low.
Multivariate exploratory analysis showed no association between the primary endpoint of the study (time to initiation of other anemia management or occurrence of Hb trigger) with hepcidin level at baseline (HR 0.92; 95% CI 0.73, 1.16; p = 0.49), the change in hepcidin from baseline to week 8 (HR 0.96; 95% CI 0.83, 1.11; p = 0.56) or the change to week 24 (HR 1.22; 95% CI 0.88, 1.68; p = 0.24) as covariates.
Discussion
These are the first results from a prospective, randomized trial using defined iron therapy regimens to examine the three-way relationship between iron therapy, ferritin and hepcidin in patients with non-dialysis dependent CKD. Data over a one-year period show that hepcidin levels rise in response to iron therapy regardless of when the iron is administered periodically via IV administration or continuously via daily oral dosing. However, the speed and extent of the rise was greatest with IV iron targeting a higher ferritin level than with oral iron or when IV iron was used to target a lower ferritin level, reflecting differences in the rate of delivery of iron with each type of treatment.
Baseline hepcidin levels were within, or close to, the upper threshold for healthy controls in this population of non-dialysis dependent patients with CKD. This reflects the fact that this was an iron-deficient, relatively healthy cohort in which low levels of CRP indicated minimal chronic inflammation. At all time points there was a clear and significant correlation between serum hepcidin level and ferritin level. This is consistent with published data in hemodialysis patients [5, 6, 15, 18, 19, 27] and, as in our population, non-dialysis dependent patients with CKD [5, 20]. The utility of hepcidin as a marker for iron stores is limited, however, due to the high intra-individual variation in hepcidin levels [13]. An important regulator of hepcidin is inflammation, which stimulates production of hepcidin [3, 12], and chronic inflammation becomes most prominent as renal function declines [28]. Hepcidin levels correlate with the inflammatory marker C-reactive protein in patients on dialysis [13, 29, 30] or in non-dialysis dependent CKD [7, 20], and the wide intra-patient variability in hepcidin levels may reflect short-term fluctuations in the inflammatory state [13]. Thus, hepcidin levels may not be a reliable guide to whether iron therapy is required for patients with chronic inflammation, a situation which is already known to apply when ferritin is used as a biomarker for iron status.
In the complete cohort the correlation between hepcidin and TSAT levels was not significant, although the change from baseline to endpoint in both values did attain significance. However the window between iron administration and sampling may have influenced this result [21] since in the oral iron group, iron was administered daily whereas in the IV iron group iron was administered at least 4 weeks prior to blood sampling. Other authors have observed a significant positive association between hepcidin and TSAT in peritoneal dialysis [27] and non-dialysis dependent patients with CKD [20], but Ford et al, in their assessment of 28 hemodialysis patients, also found no significant correlation [13].
Neither baseline hepcidin levels nor change in hepcidin levels predicted the response to iron therapy whereas a very weak association between endpoint hepcidin levels and hemoglobin levels was found. Theoretically low baseline levels of hepcidin are associated with reduced systemic iron levels and increased capacity to absorb oral iron, and thus identify successful candidates for oral iron therapy. The effect of a marked increase in hepcidin on treatment response is harder to anticipate. If hepcidin is a marker of iron load and concurs with increased iron stores, increased levels are associated with successful therapy. However, if increased levels of hepcidin designate reduced absorption and reduced iron release from the iron stores a marked increase in hepcidin would be associated with resistance to therapy. In this study we observed no evidence that the latter contention is true. Overexpression of ferroportin in response to high iron levels may permit export of iron from macrophages into the circulation even when hepcidin levels are elevated [31]. In our analysis, there was no significant association between change in hepcidin levels and achievement of Hb thresholds or the primary endpoint of the study. Reports in the literature regarding a role for hepcidin in predicting response to therapy are relatively limited [10, 13, 16–20]. A single-arm study in 51 patients on hemodialysis with iron deficiency examined the association between hepcidin levels and response to oral iron therapy [18]. All patients had been receiving an ESA but no iron therapy for the three month prior to study entry, at which point oral ferrous fumarate 50 mg/ day was given for eight weeks. In the 16 patients who were Hb responders (i.e. Hb increase of 2 g/dL or higher), mean hepcidin was significantly lower than in non-responders (10.8 versus 32.8 ng/mL, p<0.05) [18]. Chand et al studied 129 patients with non-dialysis CKD given IV iron therapy, and on multivariable analysis observed hepcidin to be significantly predictive of Hb increase by week 8 after the start of iron infusion (p = 0.002) [20]. In contrast, Tessitore et al found baseline hepcidin levels to show no significant association with the response to IV iron [19]. In their series of 56 hemodialysis patients, multivariate analysis indicated that serum hepcidin level was not a significant predictor for an increase in Hb following IV iron therapy in addition to maintenance ESA therapy [19].
Research into the role of serum hepcidin as a biomarker has been hampered by accurate, consistent concentration measurements [32]. Different assay methods and a lack of standardization have made between-study comparisons difficult [33]. Absolute values for hepcidin in urine or plasma samples can vary by up to 10-fold between assay types and centers [34, 35]. Here, we used a validated liquid chromatography tandem mass spectrometry assay. This is more robust than immunoassays for detecting hepcidin (such as ELISA) which have been used in other investigative studies of hepcidin as a biomarker, and which cross-react with other hepcidin isoforms such as hepcidin-22 and hepcidin-20. The study also benefitted from its prospective, randomized design, and the extended 12-month longitudinal recording of hepcidin values. The population size was limited by the fact that only patients recruited in the UK took part in the substudy, but this ensured consistent measurement of hepcidin at a single center using a single assay. It should be noted that hepcidin values were excluded if patients reached the primary endpoint—which included initiation of ESA therapy—so these findings do not necessarily apply to CKD patients receiving ESAs. Similarly, baseline hepcidin values were low, indicating that the patient population did not have chronic inflammation (the study protocol excluded patients with active infection or baseline CRP ≥ 20 mg/L), limiting extrapolation to more inflamed patient groups. Lastly, we recognise that over the course of this one-year study hepcidin data were available in a declining number of patients, with fewer than half the hepcidin population providing values at one year. This effect was exacerbated by exclusion of patients in whom alternative anemia management was started. This avoided contamination of data regarding the relative effect of the randomized therapies, and effectively provided a 'per protocol analysis', but it also substantially reduced the data set over time.
This is the first analysis to prospectively assess the response of hepcidin levels to different iron treatments. Results from these pre-specified and post hoc analyses showed that baseline hepcidin levels were in the normal range, consistent with the presence of iron deficiency, anemia and low inflammatory state. With either IV or oral iron therapy, the increase in hepcidin correlated with the administered dose of iron. Changes in hepcidin levels showed a close correlation with the level of stored iron, as measured by ferritin, but not either TSAT or Hb levels. Hepcidin levels were not predictive for hematopoietic response to iron therapy in this population, although the size of this population and the increasing proportion of non-evaluable patients as the study progressed precludes firm conclusions. Further prospective studies, specifically in patients with chronic inflammation, are awaited.
Supporting Information
S1 Appendix. FIND-CKD trial: Ethics Committee approvals.
https://doi.org/10.1371/journal.pone.0157063.s001
(DOCX)
S1 Fig. Proportion of patients receiving high dose FCM over time (FCM group, n = 154).
https://doi.org/10.1371/journal.pone.0157063.s002
(EPS)
Author Contributions
Conceived and designed the experiments: CAG AHB FC KUE DBVW SDR ICM. Performed the experiments: CAG AHB FC KUE DBVW SDR ICM. Analyzed the data: CAG AHB FC KUE DBVW MC YM SDR ICM. Wrote the paper: CAG. Provided biostatistical support: SL. Performed the hepcidin assays: SSB.
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