Introduction
Inflammation-associated anemia represents an important and highly prevalent clinical problem. In 2000, Krause et al. described a peptide that was later called 'hepcidin' based on its hepatic expression and antimicrobial activity [
1,
2]. This β-defensin-like peptide was found to be a principle regulator of systemic iron homeostasis. In concordance with this dual function, its expression is modulated by systemic iron requirements and inflammatory stimuli, as it is induced by cytokines such as IL-6 [
3]. Its role in the development of anemia was first suggested in 2001 [
4]. Since then it has been demonstrated that hepcidin is a central modulator of inflammation-associated anemia, not only by controlling the expression of ferroportin on intestinal cells and macrophages [
5], but also via a direct inhibitory effect of hepcidin on erythropoiesis [
6]. In humans, increased concentrations of hepcidin were detected in patients with chronic infections and severe inflammatory diseases [
7]. The association of increased concentrations of hepcidin with anemia has been determined in patients suffering from chronic inflammation [
8], chronic kidney disease [
9], and cancer [
10]. In addition, acute systemic inflammation evoked by experimental endotoxemia in humans resulted in an increase in hepcidin release, associated with a decrease in serum iron [
11]. Nevertheless, the association between the innate immune response, hepcidin release and consequent decrease in hemoglobin (Hb) has not been established in patients with an acute systemic inflammation.
Human sepsis is a prototypical acute inflammatory syndrome frequently complicated by the development of anemia. As the incidence of sepsis is high [
12], determination of this putative pathway of the development of anemia is of clinical importance. Therefore, we explored the correlation between IL-6 and hepcidin, and the subsequent rate of Hb decrease and number of blood transfusions received in septic patients.
Materials and methods
Subjects and sampling
This is an explorative observational study in which data of the subjects were retrieved from a prospectively aggregated database of patients with sepsis. Following Dutch law, the local Institutional Review Board of Arnhem-Nijmegen indicated that no formal approval was required for this study. Patients were informed, but no written consent was necessary. Ninety-two consecutive septic patients were enrolled after presentation on the emergency ward and subsequent hospital admission. Sepsis was defined by the presence of two or more extended criteria for systemic inflammation (body temperature >38.3 or < 36°C, acutely altered mental status, shivering, heart rate >90 bpm, systolic blood pressure < 90 mmHg or mean arterial pressure < 65 mmHg, respiratory rate >20 breaths/min, hyperglycemia in absence of diabetes) and a proven or suspected source of infection [
13]. The total number of extended systemic inflammatory response syndrome (SIRS) scores were calculated. Patients were given usual care according to the guidelines of the Surviving Sepsis Campaign [
14]. Blood was drawn at day one, two and three of admission for the measurement of IL-6 and hepcidin-25. Hb measurements were not taken as part of a protocol, but Hb levels that were determined as part of standard hospital care during the first 14 days after hospital admission were retrieved and used for further analysis, Hemoblobin levels were checked regularly, but not every day in every patient. Also the accompanying indices of mean corpuscular volume (MCV), mean cell Hb (MCH), and red cell distribution width (RDW) were analyzed. Blood transfusions during hospital stay were recorded. We hypothesized that the effect of sustained elevated levels of hepcidin could be first seen in the Hb level after a period of 7 to 14 days. This was based on the assumption that erythrocytes circulate for approximately 120 days. If erythropoiesis would be abrogated by hypoferremia due to an increased hepcidin level, it would therefore take approximately 12 days to reduce the Hb levels by 10%. A decrease of 10% was considered a clinically relevant and reliably detectable difference. However, due to a possible direct inhibitory effect of hepcidin on erythropoiesis, and a reduced erythrocyte half-life during inflammation, a detectable reduction of Hb from day seven onwards was anticipated.
Laboratory measurements
IL-6 levels were measured on an Immulite 2500 (Siemens, Breda, The Netherlands), based on a solid-phase, enzyme-labelled, chemiluminescent sequential immunometric method. Serum hepcidin-25 measurements were performed by a combination of weak cation exchange chromatography and time-of-flight mass spectrometry (TOF-MS), using a Microflex LT matrix-enhanced laser desorption/ionisation TOF-MS platform (Bruker Daltonics, Bremen, Germany). An internal standard (synthetic hepcidin-24; Peptide International Inc., Louisville, KT, USA) was used for quantification [
15,
16].
Calculations and statistical analysis
Log-transformed IL-6 concentrations were correlated with hepcidin-25 concentrations using Pearson's correlation coefficient. Hepcidin-25 was correlated with the rate of decrease of Hb between day 1 and 14, using Spearman's correlation coefficient. The rate of decrease of Hb was calculated per patient by linear regression using all available Hb measurements. If Hb levels were not measured at days 7 to 14, or if patients received a blood transfusion during their stay, they were excluded from this analysis. Hepcidin levels at admission (prior to any transfusion) of patients who received a blood transfusion during the first 14 days of hospitalization were compared with patients who did not.
To test whether the presence of comorbidity affected the rate of Hb decrease, we divided different forms of comorbidity into eight categories (chronic kidney disease, hematologic, malignancy, pulmonary, rheumatic/autoimmune, cardiologic, urologic, and other) and performed a step-wise multi-variate analysis in which hepcidin levels and the eight categories of comorbidity were added to the model. If a comorbidity was found to significantly attribute to the prediction of Hb decrease, it was left in the model, but otherwise discarded. Data are expressed as mean ± standard error of the mean or median (25th to 75th percentile) depending on their distribution. Correlations were expressed as Spearman's correlation coefficient, except for the correlations between hepcidin and log-transformed IL-6 concentrations that were expressed as Pearson's r.
Paired observations over time were tested with Wilcoxon matched-pairs test and unpaired observations with a Mann-Whitney test.
Discussion
In the present study, three novel findings emerged. This is the first study to show that: hepcidin-25 is increased during human sepsis; in septic patients the degree of inflammation, indicated by IL-6 levels and number of SIRS criteria present, is associated with the elevated concentrations of hepcidin; and persistently increased levels of hepcidin-25 at day two and day three after admission are associated with a decrease in Hb during hospitalization. Naturally, in patients who received a transfusion, the effect of hepcidin on Hb could not be determined and these patients were excluded from this part of the analysis. In a separate analysis, we showed that transfused patients showed a trend towards higher hepcidin levels than those who were not. These findings combined suggest that the observed association between elevated hepcidin and a decrease in Hb is likely to be an underestimation.
This study does not necessarily indicate a causal relation between elevated hepcidin and Hb decrease in septic patients. However, the causal relation of the induction of hepcidin by IL-6 and the development of anemia by sustaining elevated hepcidin levels has been shown by others in separate experiments [
3,
5,
6,
17]. This study is the first to address the combined measurement of hepcidin, IL-6 and Hb levels in patients and shows that hepcidin probably plays a role in sepsis-associated anemia. One may argue that the correlation between inflammation, hepcidin and anemia is an epiphenomenon, because more severely affected patients release higher levels of inflammatory parameters and also receive more fluids during their volume resuscitation, resulting in the more pronounced decrease in Hb. This appears not to be the case, because hepcidin concentrations at admission did not predict the decrease in Hb, in contrast to more prolonged elevations in hepcidin during the first three days. Moreover, the decrease in Hb was determined over 14 days, a period in which the effects of volume resuscitation should have diminished. Nevertheless, it is important that in addition to the physiological role of hepcidin, several other factors that lead to anemia during infection have been described, such as iatrogenic blood loss, inhibition of erythropoietin production [
18], blunted erythropoietic response [
18,
19], and a decreased lifespan of erythrocytes, mediated by increased adherence to the vascular wall and phagocytosis by macrophages [
20]. In addition, in these patients the presence of different comorbidities and the severity of the disease could have influenced the development of anemia. However, we were not able to express these variables in size and number, and therefore could not include these parameters as a continuous variable into a multivariate regression analysis. This may explain the relatively low correlation coefficients we found between hepcidin and Hb decrease.
There are two known ways that hepcidin can result in inflammation-associated anemia. First, hepcidin can abrograte erythroid colony formation in situations where erythropoietin concentrations are reduced, as is the case during sepsis [
6]. Furthermore, inflammation leads to sequestration of iron in cells resulting in a blocked transport of iron to the bone marrow. Considering the fact that the lifespan of erythrocytes of approximately 120 days might be shortened due to inflammation and the fact that hepcidin suppresses erythropoiesis itself, we hypothesized that if hepcidin is upregulated by inflammation and thereby suppresses serum iron levels, a measurable effect on Hb level was expected from seven days onwards after the diagnosis of sepsis. Furthermore, we anticipated a swift decrease in inflammation in treated septic patients. For these reasons we determined IL-6 and hepcidin levels for three days and the rate of Hb decrease within 7 to 14 days.
We were not able to demonstrate a relation of Hb decrease with a change in MCV, MCH, or RDW. This does not invalidate the hypothesis that increased hepcidin attributes to the development of anemia in these patients. It was previously shown that erythrocyte progenitor cells carry iron transporter ferroportin1B on their cell membrane [
21]. During inflammation systemically elevated hepcidin down-regulates ferroportin on these cells, thereby preventing a loss of intracellular iron and the microcytic anemia that is seen in iron-deficiency anemia. Therefore, inflammation-associated anemia is not typically microcytic [
22]. Moreover, the observed effect of hepcidin on the development on anemia may have been mediated by a direct inhibitory effect on erythropoiesis, rather than by blocking iron transport to the bone marrow by sequestration.
Interestingly, hepcidin at day one did not predict the rate of Hb decrease. Probably persistently elevated hepcidin levels are necessary to exert a relevant effect on Hb concentrations. The association we found may be an underestimation, because the patients in this study were already anemic at the time of presentation to the emergency ward and likewise it is possible that before presentation hepcidin levels were even more pronounced. Nevertheless, although statistically significant, the observed association between hepcidin and Hb levels is modest, indicating that other previously mentioned factors that influence Hb are likely to play a role.
Competing interests
The authors declare that they have no competing interests.
Authors' contributions
LTE participated in data collection, performed the statistical analysis and drafted the manuscript. JJCK performed hepcidin measurements and participated in drafting the manuscript. MT collected demographic and SIRS data, built the database and collected the blood samples. JGH revised the manuscript and participated in the design of the study. DWS revised the manuscript and participated in the design of the study and was responsible for hepcidin measurements. PP conceived of the study, participated in its design and coordination and helped to draft the manuscript.