Effects of a 7-day military training exercise on inflammatory biomarkers, serum hepcidin, and iron status
© McClung et al.; licensee BioMed Central Ltd. 2013
Received: 5 August 2013
Accepted: 26 October 2013
Published: 4 November 2013
Hepcidin, a peptide that is released into the blood in response to inflammation, prevents cellular iron export and results in declines in iron status. Elevated serum and urinary levels of hepcidin have been observed in athletes following exercise, and declines in iron status have been reported following prolonged periods of training. The objective of this observational study was to characterize the effects of an occupational task, military training, on iron status, inflammation, and serum hepcidin.
Volunteers (n = 21 males) included Norwegian Soldiers participating in a 7-day winter training exercise that culminated in a 3-day, 54 km ski march. Fasted blood samples were collected at baseline, on day 4 (PRE, prior to the ski march), and again on day 7 (POST, following the ski march). Samples were analyzed for hemoglobin, serum ferritin, soluble transferrin receptor (sTfR), interleukin-6 (IL-6), and serum hepcidin. Military training affected inflammation and serum hepcidin levels, as IL-6 and hepcidin concentrations increased (P < 0.05) from the baseline to POST (mean ± SD, 9.1 ± 4.9 vs. 14.5 ± 8.4 pg/mL and 6.5 ± 3.5 vs. 10.2 ± 6.9 ng/mL, respectively). Iron status was not affected by the training exercise, as sTfR levels did not change over the course of the 7-day study.
Military training resulted in significant elevations in IL-6 and serum hepcidin. Future studies should strive to identify the role of hepcidin in the adaptive response to exercise, as well as countermeasures for the prevention of chronic or repeated elevations in serum hepcidin due to exercise or sustained occupational tasks which may result in longer term decrements in iron status.
KeywordsPhysical activity Operational stress Military Ferritin Inflammation Iron absorption Soluble transferrin receptor
The relationships between iron status and physical and neuropsychological performance in humans are well established and relate to the biological action of iron dependent proteins and enzymes [1, 2]. Examples include hemoglobin and myoglobin, which support oxygen storage and transport, and aconitase and cytochrome c, which function in energy metabolic pathways. Maintaining optimal iron status is paramount for athletes and individuals with physically demanding occupations, such as military service, as poor iron status has been linked to diminished performance in such individuals [3, 4], and iron status may decline in response to sustained physical activity [4–6].
Several mechanisms have been proposed to explain declines in iron status associated with physical activity, to include gastrointestinal bleeding  and iron losses in sweat  and urine . The biological activity of hepcidin, a 25-amino acid protein that arises in response to proinflammatory cytokines, including interleukin-6 (IL-6), may represent another mechanism by which iron status declines in response to physical activity . Hepcidin affects iron export from the enterocyte, macrophage, and hepatocyte through binding of ferroportin 1 (FPN1), the primary cellular iron export protein . The binding of hepcidin to FPN1 results in the degradation of the hepcidin-FPN1 complex, effectively sequestering iron, thereby limiting availability for incorporation into iron-dependent proteins and enzymes.
Recent studies have investigated the effects of endurance-type exercises, such as running and cycling, on serum hepcidin and inflammatory biomarkers in athletes. For example, Newlin et al.  observed significant elevations in serum hepcidin following treadmill running in female athletes, and Sim et al.  observed elevated IL-6 and serum hepcidin in male triathletes following both running and cycling activities. However, the effects of more complex occupational tasks, such as short-term military training, on hepcidin levels and iron status have not been investigated. The objective of this observational study was to characterize the effects of a 7-day winter military training exercise on iron status, biomarkers of inflammation, and serum hepcidin.
20 ± 1
182 ± 7
82 ± 9
25 ± 2
7-Day winter training exercise
3842 ± 153
161 ± 13
425 ± 20
160 ± 10
5177 ± 325
213 ± 13
572 ± 19
218 ± 41
3115 ± 437
128 ± 22
360 ± 57
122 ± 19
3415 ± 977
139 ± 42
384 ± 125
138 ± 38
Blood samples were collected after an overnight fast (Vacutainer, Becton Dickson, Franklin Lakes, NJ). Serum was frozen and shipped to the Pennington Biomedical Research Center (Baton Rouge, LA) for analysis of ferritin (Siemens Medical Solutions USA Inc, Malbern, PA), soluble transferrin receptor (sTfR, Quantikine IVD; R&D Systems Inc, Minneapolis, MN), hepcidin (DRG International, Inc, Springfield, NJ) and IL-6 (Milliplex MAP; Millipore, Billerica, MA). Hemoglobin was assayed in whole blood at the Kirkenes Hospital (NO) using an automated hematology analyzer (Sysmex® XN-Series, Sysmex Norge, Oslo, NO). Multiple indicators of iron status and inflammation were incorporated into the biochemical panel utilized in this study, as alterations in hydrations status are known to affect the interpretation of hematology data.
Baseline volunteer characteristics were described using common descriptive statistics. Shapiro-Wilk tests confirmed data were normally distributed. Repeated measures ANOVAs were used to evaluate changes over time for circulating indices of iron status, hepcidin, and IL-6. Post hoc analyses were completed using Bonferroni corrections. Correlations were assessed using Pearson’s product–moment correlations. Significance was set at P < 0.05. Data were analyzed using SPSS (version 19.0; SPSS Inc., Chicago, IL) and expressed as means ± SD.
Changes in iron status during a 7-day winter military training exercise
14.7 ± 0.8a
14.5 ± 0.9a
14.1 ± 0.9b
109.2 ± 44.1a
137.0 ± 54.5b
133.0 ± 55.2b
18.9 ± 4.2a
18.7 ± 3.8a
18.7 ± 3.2a
6.5 ± 3.5a
6.8 ± 4.1a
10.2 ± 6.9b
9.1 ± 4.9a
7.9 ± 3.9a
14.5 ± 8.4b
Serum hepcidin remained constant (P > 0.05) from baseline to PRE, yet concentrations increased (P < 0.05) nearly 57% in response to the 3-day ski march (POST, Table 3). Similarly, IL-6 concentrations were steady (P > 0.05) from baseline to PRE but were approximately 60% higher (P < 0.05) POST (Table 3). Significant (P < 0.05) associations were identified between POST serum hepcidin, IL-6 (r = 0.6) and ferritin (r = 0.5).
The major finding of this longitudinal, repeated measures study was that a 7-day winter military training activity resulted in significant elevations in IL-6 and serum hepcidin. This is the first report of elevated IL-6 and serum hepcidin in response to an applied occupational task, and may raise the possibility that repeated exposures to strenuous occupational tasks could degrade iron status, which could eventually affect physical and neuropsychological performance over time.
Findings from the present study are consistent with previous studies in athletes. For example, Roecker et al.  reported elevated urinary hepcidin in female athletes following a marathon. Subsequently, Newlin et al.  reported elevated IL-6, serum ferritin, and hepcidin in response to treadmill running (60 and 120 mins at 65% of maximal oxygen consumption) in female volunteers. Similarly, Sim et al.  reported elevated levels of IL-6 and serum hepcidin following low intensity steady-state running (40 mins at 65% of peak running velocity), low intensity steady-state cycling (40 mins at 65% of peak cycling power output), high-intensity interval running (8 × 3 min intervals at 85% of peak running velocity) and high-intensity interval cycling (8 × 3 min intervals at 85% of peak cycling power output) in male triathletes. Similar to Newlin et al.  and Sim et al. , both serum ferritin and hepcidin were elevated in response to physical activity. However, in the present study, the increase in serum ferritin (PRE) preceded the increase in hepcidin (POST), suggesting that ferritin could be more sensitive to immediate changes in inflammation (or occur more rapidly) than hepcidin, although further study would be required to directly address this hypothesis.
In the present study, hepcidin was detected using a commercially available kit (DRG International). Others have used different techniques for hepcidin analysis, including a combination of weak cation exchange chromatography and time-of-flight mass spectrometry . The use of multiple techniques across laboratories makes comparison of absolute levels of hepcidin difficult, although the repeated measures design of the current study provides confidence in the relative change in hepcidin concentrations over time.
Although the military training exercise had a significant effect on inflammation and serum hepcidin, iron status was unchanged. sTfR, the gold-standard iron status indicator, was unaffected by the exercise, and hemoglobin declined minimally (4%). Serum ferritin was elevated in response to the training exercise, probably reflecting the effects of acute inflammation, and not improved iron status . The lack of change in iron status may reflect the duration of data collection, as decrements may have become apparent if subsequent samples were collected. Since the male Soldiers that participated in this training exercise had robust iron stores at baseline, it is unlikely that decrements in iron status would have an immediate effect on performance. However, individuals that begin similar training exercises with moderate or poor iron status, such as female Soldiers (4, 6, 17), may experience declines in iron status that affect performance, especially if training exercises were extended over longer periods, or followed by other physically demanding, occupational tasks (e.g., operational deployment).
Future studies should focus on identifying the role of hepcidin in the adaptive response to exercise, as well as the efficacy of hepcidin antagonism for the preservation of iron status in individuals that experience repeated bouts of physical activity that may result in an inflammatory response. Work from our laboratory indicates that providing supplemental iron may prevent declines in iron status in women that begin training with poor iron status [4, 6, 17], although the effects of supplemental iron on serum hepcidin remain understudied. Two studies have assessed the effects of carbohydrate ingestion on IL-6 and serum hepcidin during endurance running, although the inflammatory response to exercise was not affected by carbohydrate ingestion [18, 19]. To the best of our knowledge, the effects of anti-inflammatory nutrients or pharmacologic agents on serum hepcidin in response to physical activity have not been determined.
Occupational tasks, such as sustained, physically demanding military training, may result in the release of IL-6, and subsequent elevations in serum hepcidin. Chronic or repeated elevations in serum hepcidin may result in diminished iron status, which could affect human performance. Future studies should strive to identify the role of hepcidin in the adaptive response to exercise, as well as appropriate countermeasures for the prevention of decrements in iron status that may occur in response to physical activity-induced elevations in serum hepcidin.
Soluble transferrin receptor
The authors thank the volunteers that participated in this research experiment. The authors acknowledge Holly McClung and Susan McGraw for their significant contributions to ration analysis. This work was supported by the U.S. Army Medical Research and Material Command and the Norwegian Defense Research Establishment, under agreement NO. W81XWH-12-0279. The investigators adhered to the policies for protection of human subjects as prescribed in Army Regulation 70–25, and the research was conducted in adherence with the provisions of 32 CFR part 219. The opinions or assertions contained herein are the private views of the authors and are not to be construed as official or as reflecting the views of the Army or the Department of Defense. Any citations of commercial organizations and trade names in this report do not constitute an official Department of the Army endorsement of approval of the products or services of these organizations.
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