Despite highly successful efforts to improve nutrition in the US Armed Forces(Reference Day, Young and Askew1–Reference Pandolf, Francesconi and Sawka4), mineral deficiencies can still be found among some US military service members (SM) and are also present in some of the civilian populations(5,6) . Prescriptions ordered by military health care providers for several mineral preparations increased from 2005 to 2013 and differed by specific demographic groups(Reference Knapik, Jean and Austin7–Reference Knapik, Jean and Austin9), suggesting that military health care providers determined that mineral supplementation was important to maintain the health of some SM. One mineral of concern in SM is iron, a critical micronutrient incorporated into proteins and enzymes that is important for physical, cognitive and immune functioning(Reference Beard10,Reference Gardner, Edgerton and Senewiratne11) and is deficient in significant numbers of SM(Reference McClung, Marchitelli and Friedl12,Reference McClung, Karl and Cable13) and many civilians especially women of childbearing age(5). In longitudinal studies, iron status deteriorated during deployment among Special Operations soldiers(Reference Farina, Taylor and Means14), as well as during Basic Combat Training, and was associated with a decline in aerobic performance in the latter group(Reference McClung, Karl and Cable13,Reference McClung, Karl and Bass15) . The prevalence of iron deficiency and iron deficiency anaemia was 13 % and 33 % among female Army personnel in Basic Combat Training and Army Advanced Individual Training, respectively, when their iron status was assessed using standard laboratory measures including iron status indicator assays and a microparticle enzyme immunoassay(Reference McClung, Marchitelli and Friedl12).
Low iodine intake causes goitre and hypothyroidism since iodine is an essential component of thyroid hormones(Reference Zimmermann and Boelaert16,Reference Carle, Krejbjerg and Laurberg17) . Thyroid hormones are critical for the regulation of metabolism, and symptoms of thyroid deficiency include fatigue, weight gain, muscle pain and kidney dysfunction(Reference Chaker, Bianco and Jonklaas18). Over 10 000 cases of thyroid disorders were diagnosed in the US military in the period 2008–2017, an incidence rate of 7·4/10,000 person-years (p-y)(Reference Stahlman and Oh19).
In light of the reports cited above, the purpose of this investigation was to examine incidence rates, demographics and secular trends associated with clinically diagnosed iron and iodine disorders in the entire US SM population from 1997 to 2015 as documented in medical records. To date, there has been no large epidemiological investigation that examined the scope of this problem in military or civilian populations to the best of our knowledge. We focused on disorders associated with low dietary intake of iron and iodine since they are of clinical significance and are well documented by International Classification of Diseases, 9th Revision, Clinical Modification (ICD-9) codes.
Methods
Defense Medical Epidemiological Database (DMED) is a comprehensive surveillance system containing inpatient and outpatient medical encounters of all uniformed military personnel and includes demographic data of SM. The number of medically diagnosed cases of any single medical problem can be determined based on ICD-9 codes. The yearly incidence rates of these medical problems can also be obtained since the DMED provides the number of uniformed personnel serving per year. Data can be grouped by a limited number of demographics, including sex, age, race and military service branch.
Participants in this study were the entire population of the US military (Army, Navy, Marine Corps and Air Force) serving between 1997 and 2015. For iron, only ICD-9 codes indicative of iron deficiency anaemia were selected since these are related to low iron intake. Thus, for iron, ICD-9 codes included 280·1, 280·8 and 280·9. An additional code (275·0, disorders of iron metabolism) was not selected because it primarily relates to disorders associated with excessive iron storage (e.g. hemochromatosis, pigmentary cirrhosis of liver). For iodine, ICD-9 codes included 240·0 and 240·9. There were several ICD-9 codes (240–246 series) indicative of disorders of the thyroid gland but only simple and unspecified goitre is related to low dietary intake(Reference Carle, Krejbjerg and Laurberg17). Thyroid gland-related ICD-9 codes that were not included related to conditions of decreased iodine production (241 series), iodine overproduction (242 series) and low production due to acquired or pathological conditions (244-246 series).
The number of first occurrences and primary diagnosis for each individual ICD-9 code were obtained from the DMED for each year from 1997 through 2015 and summed for the selected ICD-9 codes indicating iron and iodine disorders. If a SM had one or more ICD-9 code indicative of one of the mineral disorders, they were included as an incidence case for that particular disorder. Cases involving both hospitalisations and outpatient visits were included. The incidence rate was calculated as the number of new cases of a particular category (grouping) of ICD-9 codes divided by the population for that year and multiplied by 100 000 to obtain cases/100 000 p-y (i.e. (number of new cases/population at risk for the year) × 100 000). Data were plotted by year for the entire male and female cohorts. Linear trend lines were displayed on the graphs along with the equation describing the trend line, variance accounted for (r 2) and standard error of the estimate. In developing the regression equation, years were indicated by sequential numbers (1, 2, 3, etc.) rather than the actual years so that the intercept was at the first year (1997). Percentage changes in the incidence rates of mineral disorders from 1997 to 2015 were calculated as ((incidence rate in 2015 – incidence rate 1997)/incidence rate in 1997) × 100 %.
Cases were also obtained by sex, age (<20, 20–24, 25–29, 30–34, 35–39, ≥40 years), race (white, black, other) and military service (Army, Navy, Air Force, Marine Corps) with the corresponding populations. Incidence rates (cases/100 000 p-y) were calculated for each demographic stratum in both mineral categories. The risk of a mineral disorder was compared across the strata with a referent level of the demographic selected (indicated by an incidence rate ratio = 1·00), and comparisons were made to that level. The Open Source Epidemiologic Calculator was used to determine incident rate ratios with 95 % CI(Reference Dean, Sullivan and Soe20). Power analysis was not conducted since the study involved the entire population of SM.
Results
Table 1 presents descriptive statistics on the demographics of the SM population for the entire 19-year period from 1997 through 2015. The majority of the population was composed of men, whites and those aged 20–29 years. Nonetheless, other demographic groups were also well represented. For example, on average, there were over 200 000 women and over 250 000 blacks in the population per year.
Table 1 Descriptive Statistics on Demographics of Service Member Population, 1997–2015
Table 2 presents the aggregate number of cases and incidence rates for each ICD-9 code and code groupings for both iron and iodine for the entire period. The most commonly diagnosed iron disorder was ‘iron deficiency anemia, unspecified’ (ICD-9 code 280·9) accounting for 85 % of the cases. The most commonly diagnosed iodine deficiency was ‘goiter, unspecified’ (ICD-9 code 240·9), accounting for 82 % of cases. Hospitalisations accounted for only 1·5 % of cases (539/36 897). The overall incidence rate for both mineral disorders combined was 140·5 cases/100 000 p-y.
Table 2 Cases and incidence rates for iron and iodine disorders among US Military Personnel, 1997–2017. Total incidences for each disorder and each individual ICD-9 code
Figure 1 presents the secular trends in iron and iodine disorders by sex. From 1997 to 2015, iron disorder incidence rates (Fig. 1a) for men increased from 23·6 to 49·1 cases/100 000 p-y (108 % increase), at an approximate rate (based on linear regression) of 2·0 cases/100 000 p-y. In this same period, iron disorder incidence rates (Fig. 1b) for women increased from 169·4 to 469·7 cases/100 000 p-y (177 % increase), at an approximate rate of 20 cases/100 000 p-y. From 1997 to 2015, iodine disorder incidence rates in men (Fig. 1c) increased from 8·0 to 15·3 cases/100 000 p-y (91 % increase), at an approximate rate of 0·8 cases/100 000 p-y. Iodine disorder incidence rates in women (Fig. 1 d) increased from 113·3 cases/100 000 p-y in 1997, reached a peak in 2007 (193·0 cases/100 000 p-y) and then declined to 137·3 cases/100 000 p-y by 2015.
Fig. 1 Incidence of iron and iodine disorders in US Military Service Members 1997–2015. (a) Iron disorders (men); (b) iron disorders (women); (c) iodine disorders (men); (d) iodine disorders (women). Straight lines are best fit linear regression lines described by equations on graphs (SEE = standard error of estimate)
Table 3 presents mineral disorders by demographic characteristics. Iron disorder incidence rates were about 12 times higher among women compared with men and were highest in the youngest and oldest age groups compared with other age groups. Higher rates were evident among blacks and those of other races compared with whites; rates were higher in the Army and Air Force than in the Navy and Marine Corps. Iodine disorder incidence rates were about 10 times higher among women compared with men and increased with age in both sexes. Rates were higher among blacks compared with whites and other races and were higher in the Air Force and Army compared with the Navy and Marine Corps.
Table 3 Iron and iodine disorders among US Military Personnel by Demographic characteristics (1997–2015)
Discussion
This study provides the first comprehensive examination of incidence rates of iron and iodine disorders in the entire US military population. Over the 19-year period examined, the incidence of clinically diagnosed iron and iodine deficiencies was low, only 104 and 36 cases/100 000 p-y, respectively. Nonetheless, among both men and women, incidence rates for iron increased dramatically over time. In contrast, while iodine disorder rates increased steadily among men, in women they increased in the early years examined followed by a more recent gradual decline. Overall, women had much higher incidence rates than men for both mineral disorders. Iron disorder rates were highest among the youngest and oldest age groups, but rates for iodine increased with age. For both iron and iodine, black SM had higher incidence rate than white SM and rates were higher among Army and Air Force SM compared with Navy and Marine Corps SM.
A distinction is typically made in the literature between iron deficiency, where iron stores decline and transport is compromised(Reference Dallman21), and iron deficiency anaemia, where iron-containing proteins (especially Hb) decline and fall below a specific cut point(Reference Haas and Brownlie22). Iron deficiency is the most common micronutrient deficiency worldwide(23). In the Global Burden of Diseases, Injuries, and Risk Factors Study involving 328 diseases in 195 countries, iron deficiency anaemia was one of the five most common medical problems contributing to years individuals lived with a disability(24). In the USA, the RDA for iron for 19–50-year-old women is over twice that of comparably aged men, 18 mg/d compared with 8 mg/d, primarily due to menstrual blood loss(25). In general agreement with the present study, a report assessing iron deficiency anaemia in the entire US Armed Forces population from 2002 to 2011 found an increase in the incidence rate over time, as well as higher risk in women, the youngest (<20 year) and oldest (>40 years) age groups, and among black SM(26).
The prevalence of iron deficiencies in the US military has been shown to differ depending on the stage of military training. Among a cohort of Army women followed longitudinally for over 6 months and based on a comprehensive battery of laboratory tests, the prevalence of iron deficiency was 13 % on entry to the Army, increased to 33 % near the end of basic training and decreased to 10 % in a post-basic training assignment; comparable values for iron deficiency anaemia were 6, 21 and 5 %, respectively(Reference McClung, Marchitelli and Friedl12). Iron status also declined among men during basic training(Reference McClung, Karl and Bass15), and similar declines in iron status have been observed in Israeli and New Zealand military recruits during basic training(Reference Martin, Conlon and Smeele27–Reference Epstein, Borohovitz and Merdler29). When laboratory data are collected on SM, rates of deficiency are much higher than the diagnosed rates documented here, suggesting many SM, like the general population and especially women, are not being treated for iron deficiency(30). Cases of iron disorders and the increase over time in both male and female SM documented in the present study are of considerable concern because of the well-known adverse effects of iron deficiency, especially iron deficiency anaemia, on physical(Reference Haas and Brownlie22) and cognitive(Reference Scott and Murry-Kolb31,Reference Scott, Souza and Koehler32) performance and the requirement for high levels of physical and cognitive capability for many military occupational tasks(Reference Sharp, Patton and Vogel33,Reference Kirin and Winkler34) . Once a deficiency is identified, widely accepted standards of care are available for determining the aetiology and providing treatment(Reference Short and Domagalski35,Reference Camaschella36) .
Estimates of the population risk for iodine deficiency are typically based on urinary iodine concentrations (UIC), a reliable biomarker of recent iodine intake(Reference Pearce and Caldwell38). Low iodine intake is a major cause of goitre as demonstrated by many studies that found UIC is related to thyroid gland volume(Reference Carle, Krejbjerg and Laurberg17), but other factors including genetic and environmental influences can be involved(Reference Knudsen and Brix39). In the US military, goitre is a disqualifying medical conditions for entry into the military services(40), but conditions that arise after an individual is in service are treated as any other medical condition. Two previous studies examined incidence rates for goitre in the US Armed Forces from 2002 to 2011(41) and from 2005 to 2017(Reference Stahlman and Oh19). The early study(41) found an increase in incidence rate over time for both men and women, while the later study(Reference Stahlman and Oh19) found increases among men, while rates declined among women. This is in general agreement with the present study which track rates over a longer continuous period: rates steadily increased among men, but increased then decreased among women. Also in agreement with the present study, previous US Armed Forces studies(Reference Stahlman and Oh19,41) found substantially higher incidence rates for goitre among women and Air Force SM and that rates increased with age. The higher incidence rates in women may be related to the action of oestrogens on thyroid tissues(Reference Li42). It has also been suggested(41) that the increased incidence rates of thyroid disease may have been due to increased testing for thyroid function disorders among SM due to psychiatric illnesses(Reference Stahlman and Oetting43) associated with conflicts in Iraq and Afghanistan. Several psychiatric disorders can have symptoms (depression, irritability) similar to thyroid dysfunction. The most recent declines in 2015 may reflect the fact that recently fewer SM are being deployed(Reference Bialik44).
In the US general population, iodine levels appear to be declining over time. Consecutive testing of UIC in NHANES indicated a 52 % decline from NHANES I (1971–1974) to NHANES III (1988–1994), a stabilisation between NHANES III (1988–1994) and NHANES 2007–2008 and then a further 19 % decline between NHANES 2007–2008 and NHANES 2013–2014(Reference Hollowell, Staehling and Hannon45–Reference Herrick, Perrine and Aoki49). A different analytical technique was used in the earliest NHANES, but direct comparison of the two techniques demonstrated that results did not differ between the different assays(Reference Caldwell, Jones and Hollowell46). The early decline in UIC has been attributed to a number of factors including efforts by the dietary industry to improve the quality of their product by reduced use of iodine to sterilise milk, reduced use of erythrosine (a dye containing iodine) in breakfast cereals, commercial bread manufacturers’ replacement of iodine by bromine salts as a dough conditioner and lower intake of iodine-containing table salt(Reference Lee, Bradley and Dwyer50,Reference Pennington and Schoen51) . The reasons for the more recent declines(Reference Corey, Bell and Pleus47) may be more related to lower discretionary intake of table salt and salt used in cooking(Reference Quader, Patel and Gillespie52), but the most recent mean (95 % CI) UIC level of 131(122, 141) ng/ml in the NHANES 2013–2014 data(Reference Corey, Bell and Pleus47) is still considered adequate from a population perspective. The WHO goals are that UIC levels should be >100 ng/ml in 50 % of the population and <50 ng/ml in <20 % of the population(53).
Like iron deficiency, iodine deficiency is a global health problem, but estimates based on WHO data and literature reviews suggest an overall worldwide improvement in iodine status from 2003 to 2011(Reference Andersson, Karumbunathan and Zimmermann54). Nonetheless, there appeared to be a small increase in the prevalence of iodine deficiency over this period in the Americas(Reference Andersson, Karumbunathan and Zimmermann54). Like iron deficiency, low iodine levels are of particular concern in military SM because of detrimental effects on muscle function and exercise capacity(Reference Caraccio, Natali and Sironi55) and adverse effects on work capacity(Reference Nexo, Watt and Pedersen56). Data in the present study suggest that iodine disorder rates are rising in military men but less so in military women. The fact that discretionary intake of salt is declining in the USA(Reference Quader, Patel and Gillespie52) and clinically diagnosed iodine disorders are rising among military men suggests a more focused effort to ensure salt is fortified with iodine may be warranted. Further surveillance efforts will be needed to determine whether the increase in clinically diagnosed iodine disorders requires additional intervention.
Strengths and limitations
This study had the major advantage of examining the entire population of US SM over a period of 19 years using a database that included virtually all clinically diagnosed iron and iodine deficiencies. Deficiencies identified within military facilities were required to be entered into this database and medical personnel who diagnosed conditions outside military facilities were required to enter information into this database for reimbursement, assuring the database was inclusive. Nonetheless, there are limitations in the current analyses. Medical care provided by military unit medics in the field and at deployed locations may not be included in the DMED. However, it is unlikely that the nutritional conditions examined here would be diagnosed by medics who are primarily trained as first responders. Further, only healthy SM can be deployed and if a serious medical condition was detected in pre-deployment physicals, that individual would not deploy until the condition was treated. Another consideration is that this analysis was based on the primary diagnosis of the nutritional condition (first listed condition) in the DMED and thus may not account for comorbidities, pregnancies, dietary supplement use or other conditions that might affect these deficiencies. The DMED provides only the diagnosis (ICD-9 code) of a SM medical condition or the total number of visits for that medical condition (total encounters). If the nutritional condition (ICD-9 code) was listed in position other than the first (primary) because of a comorbid problem, that condition would not be included in this analysis. Thus, this analysis is limited to the nutritional conditions for which the diagnoses were the primary ones. Finally, these data should not be interpreted as reflecting the overall incidence rates of iron or iodine disorders in the military because not all (or a random sample) of SM were tested for the disorders. These data reflect rates at which mineral disorders were clinically diagnosed when a SM saw a medical care provider and that visit resulted in a mineral disorder documented in the medical record.
Conclusions
This study documents a relatively low incidence rate of clinically diagnosed iron and iodine deficiencies in the US Armed Forces. Nonetheless, rates for iron disorders increased substantially over time for both men and women. Iodine disorder rates rose steadily over time among men, while among women there were increases in the early years examined followed by a more recent gradual decline. Women had 10- to 12-fold higher incidence rates than men for both mineral disorders. Iron disorder rates were highest among the youngest (<20 years old) and oldest (≥40 years old) male age groups, but iron deficiency rates increased steadily with age for both sexes. Compared with white SM, black SM had higher incidence rates for both iron and iodine deficiencies. The incidence rates reported here are for those individuals who were clinically diagnosed for these disorders and, as is the case for most diseases, the rates reported here undoubtedly underestimate the underlying incidence of the disorders.
While we are unaware of any other population-based data assessment of medical records to assess incidence of diagnosed dietary deficiencies and disorders, given advancement in digitised medical records and the desire to access and use large data sets, it is likely that such information could be available in the US population in the near future. As such, our results will be useful to those conducting these future analyses. Given the unexpected increases in incidence of the two mineral disorders examined that are associated with significant adverse health outcomes, greater surveillance of the military and civilian populations for these disorders may be appropriate.
Acknowledgements
Acknowledgements: Thanks to Patricia Bremner for assistance in acquiring some of the more difficult to obtain references and to the Defense Health Agency for assistance in obtaining data. Financial support: This work was supported by the Department of Defense Center Alliance for Nutrition and Dietary Supplements Research of the Defense Medical Research and Development Program. Conflict of interest: None. Authorship: J.J.K. contributed to study design, compiled the data, analysed the data, assisted in interpretation and wrote the paper; E.K.F. contributed to study design, assisted in interpretation and critically reviewed drafts of the paper; V.L.F. contributed to study design, assisted in interpretation and critically reviewed drafts of the paper; H.R.L. conceived the study, contributed to study design, assisted in interpretation and critically reviewed drafts of the paper. All authors have read and approved the manuscript. Ethics of human subject participation: The US Army Research Institute of Environmental Medicine Human Research Protection Office approved this retrospective analysis of de-identified data from the Defense Medical Epidemiological Database. Disclaimer: The opinions 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. Citations of commercial organisations and trade names in this report do not constitute an official Department of the Army endorsement or approval of the products or services of these organisations. Approved for public release; distribution is unlimited.
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