Background and Objective
Emerging evidence from biological and epidemiological studies has suggested that body iron stores and heme-iron intake may be related to the risk of type 2 diabetes (T2D). We aimed to examine the association of body iron stores and heme-iron intake with T2D risk by conducting a systematic review and meta-analysis of previously published studies.
Research Design and Methods
Systematic review and subsequent meta-analysis were conducted by searching MEDLINE database up to June 22, 2012 to identify studies that analyzed the association of body iron stores or dietary heme-iron intake with T2D risk. The meta-analysis was performed using the effect estimates and 95% confidence intervals (CIs) to calculate the pooled risk estimates, while the heterogeneity among studies was examined using the I2 and Q statistic.
The meta-analysis included 16 high-quality studies: 12 studies analyzed ferritin levels (4,366 T2D patients and 41,091 controls) and 4 measured heme-iron intake (9,246 T2D patients and 179,689 controls). The combined relative risk (RR) comparing the highest and lowest category of ferritin levels was 1.66 (95% CI: 1.15–2.39) for prospective studies, 2.29 (95% CI: 1.48–3.54) for cross-sectional studies with heterogeneity (Q = 14.84, p = 0.01, I2 = 66.3%; Q = 44.16, p<0.001, I2 = 88.7%). The combined RR comparing the highest and lowest category of heme-iron intake was 1.31 (95% CI: 1.21–1.43) with heterogeneity (Q = 1.39, p = 0.71, I2 = 0%). No publication bias was found. Additional 15 studies that were of good quality, had significant results, and analyzed the association between body iron stores and T2D risk were qualitatively included in the systematic review.
Citation: Zhao Z, Li S, Liu G, Yan F, Ma X, Huang Z, et al. (2012) Body Iron Stores and Heme-Iron Intake in Relation to Risk of Type 2 Diabetes: A Systematic Review and Meta-Analysis. PLoS ONE 7(7): e41641. https://doi.org/10.1371/journal.pone.0041641
Editor: Jianping Ye, Pennington Biomedical Research Center, United States of America
Received: March 9, 2012; Accepted: June 24, 2012; Published: July 26, 2012
Copyright: © 2012 Zhao 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.
Funding: These authors have no support or funding to report.
Competing interests: The authors have declared that no competing interests exist.
Iron serves as a potent pro-oxidant in human body and participates in the generation of reactive oxygen species (ROS) such as hydroxyl radical . The susceptibility of β-cells to iron-induced oxidative stress and the iron deposition in β-cells usually leads to apoptosis, and consequently, to insulin deficiency , . Iron deposition also induces insulin resistance by inhibiting glucose uptake in fat and muscle tissues, and reducing the capacity of liver to extract insulin, which results in an abnormal increase in hepatic glucose production –. The causative role of elevated iron store levels in the onset of insulin resistance is well established by prospective data as well as evidence that blood donations improve insulin sensitivity by decreasing iron stores , . Thus, iron deposition and iron-induced oxidative stress contribute to the pathogenesis of type 2 diabetes (T2D) through β-cells apoptosis, hepatic dysfunction, and insulin resistance .
Epidemiological studies have suggested a statistically-significant association between ferritin levels and the risk of T2D , . Heme-iron intake, the major dietary resource of body iron stores, was also positively associated with T2D risk . Recently, a large number of primary studies regarding ferritin levels and T2D have been published, but a meta-analysis has not yet been conducted to evaluate the available data and the consistency of published primary findings. So far, it is also unclear whether some metabolic factors, such as insulin levels and inflammatory score, serve as confounding factors that significantly change the association of ferritin levels and heme-iron intake with T2D risk .
In order to address the need for a cohesive evaluation of existing findings, we performed a systemic review and meta-analysis on the association of body iron stores and heme-iron intake with T2D risk: 1) to summarize the quantitative data respectively from prospective and cross-sectional studies, 2) to qualitatively examine existing studies regarding the association between body iron stores and T2D risk, 3) to examine the association between body iron stores and T2D risk by stratified analysis and meta-regression of parameters, including study design, geographic area, gender, study size, number of patients and controls, metabolic factors, and methods for measuring ferritin levels, and 4) to assess the likelihood of reverse causation and publication bias.
Two investigators (Zhuoxian Zhao, Sheyu Li) independently identified articles and reference lists of selected articles in the MEDLINE database through June 2012 using a manual bibliography search. Search terms for MEDLINE were (“ferritin” or “transferrin” or “iron”) and (“diabetes” or “diabetes mellitus”) without any language or article type restriction. Our search included articles that provided at least an abstract, but unpublished reports were not considered. When several studies from the same group analyzed the same set of patients, the articles that had the largest number of T2D cases were selected. The systemic review and meta-analysis was conducted following the Meta-analysis of Observational Studies in Epidemiology (MOOSE) guidelines .
Inclusion and Exclusion Criteria
Included studies that were used for meta-analysis met the following criteria: 1) study designs were prospective cohort studies or cross-sectional, 2) the exposure of interest was ferritin or iron intake; 3) the outcome of interest was the prevalence or incidence of T2D, and 4) the effect estimates, assessing the association of ferritin or iron intake levels with T2D risk, and the corresponding 95% confidence interval (CI) were reported. Additional studies, where effect estimates were not provided or could not be calculated based on the provided data, were also included for the systematic review, if they analyzed the association between body iron stores and T2D risk. The systematic review also included studies that provided effect estimates and CIs, even if the number of studies was too small to be included in our meta-analysis.
Excluded articles were literature reviews, in vitro or animal studies, and studies concerning children, adolescents, pregnant women, type 1 diabetes (T1D), and/or gestational diabetes. We excluded duplicate studies as well as studies regarding gene polymorphism, hemochromatosis, thalassemia, and hepatitis C.
Data Extraction and the Assessment of Quality
The flow diagram of data extraction is shown in Figure 1. Data were extracted independently by two researchers (Zhuoxian Zhao, Sheyu Li) using a standardized data extraction form. Discrepancies were resolved by consulting a third investigator (Guanjian Liu), who is an expert in evidence-based medicine. Corresponding or first authors of studies, which had potentially collected relevant data, but didn’t provide odds ratio (OR) or relative risk (RR) or hazard risk (HR) values for T2D risk, were contacted through e-mail to inquire about the raw data.
The following data was extracted from the included studies: first author, publication year, country, study design, gender and age of patients, number of T2D patients and controls, criteria for T2D diagnosis, effect estimate and corresponding 95% Cl, duration of follow-up, and adjustments for confounding factors. For the different categories of exposure, such as the tertiles, quartiles or quintiles, we extracted the effect estimates and corresponding 95% CI comparing the highest versus lowest category of ferritin levels or heme-iron intake for T2D risk.
*dotted line represented the combined effect estimate of meta-analysis. Size of square and rhomboids represented weight.
*dotted line represented the combined effect estimate of meta-analysis. Size of square and rhomboids represented weight.
*dotted line represented the combined effect estimate of meta-analysis. Size of square and rhomboids represented weight.
The quality of all included studies was assessed based on the Newcastle-Ottawa scale by determining the selection of participants, adjustments of confounders, description of outcomes, and the duration of follow-up . The approach of the grades of recommendation assessment, development and evaluation (GRADE) approach was used to evaluate the evidence of included studies . The following symbols were chosen to represent the four levels of the quality of evidence: ++++ (high), +++− (moderate), ++−− (low), and +−−− (very low) quality.
STATA v11.0 (Stata-Corp, College Station, TX, USA) was used for all statistical analyses. All tests were two-tailed and p<0.05 was considered statistically significant. All ORs, RRs, and HRs were considered to be estimates of RR used in the meta-analysis. Homogeneity was tested using the Q test and I2 statistic, which represented the variation of effect sizes due to genuine differences across studies rather than chance . A random-effects model described by DerSimonian and Laird was performed to calculate the summarized estimates and corresponding 95% CIs, when significant between-study heterogeneity existed. Alternatively, a fixed effects model was used, when there was no significant heterogeneity across studies. To explore the sources of between-study heterogeneity, subgroup analyses were performed based on study design, geographic area, patient gender, study size, and metabolic factor adjustments. Prospective studies and cross-sectional studies were separately combined in the meta-analysis. Prospective studies, including nested case-control and cohort studies, were separately combined in the subgroup analyses. Sensitivity analyses were also performed to identify the influence of individual studies on the pooled RRs. Both single and multiple models of meta-regression were used to analyze the effect of each covariate on the summarized results and the potential sources of heterogeneity.
Publication bias was assessed using the visual inspection of funnel plots, Begg’s rank correlation, and the Egger weighted regression method (p<0.05 was considered statistically-significant for publication bias). A Galbraith plot was also constructed for visual observation of the outlier studies .
The flow diagram of the literature search strategy is shown in Figure 1. 2,493 articles and abstracts were identified by initial searches, of which 2,347 articles were excluded by manual screening of the titles. An additional 70 papers were excluded after reading the abstract, leaving 76 articles for full publication review. Of these, 15 articles were included after reading the full paper , , , –. Another 16 articles compared ferritin levels or iron intake between T2D patients and controls, but failed to report ferritin levels or iron intake as the exposure to allow the comparison between the highest and lowest category of ferritin levels or iron intake for T2D risk. Therefore, we contacted the authors of these 16 studies and were able to obtain the original data from one author to include in our meta-analysis . Table 1 shows the detailed characteristics of the resulting 16 studies that were included in our meta-analysis.
The systematic review was based on 31 studies, containing additional 15 articles that analyzed the association of ferritin, sTfR (soluble transferrin receptor), transferrin, iron intake, the ratio of transferrin receptors to ferritin or transferrin saturation with T2D risk –. Although the 15 articles that were included for qualitative analysis did not provide the data for effect estimates and corresponding 95% CIs, they analyzed the association between body iron stores and T2D risk, making them eligible to be included in our systematic review. Table S1 showed Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) checklist.
The regression runs through the origin interval (central solid line). Between the two outer parallel lines is the 95% confidence interval.
The results of the quality assessment are shown in Table 2. Every study included in the meta-analysis had a moderate-to-high quality with the appropriated selection of subjects, adequate adjustment for potential confounders, and clearly described exposure or outcome. Among the additional 15 studies that were included only for the qualitative analysis, 9 studies had moderate-to-high quality, 3 showed low quality, and the remaining 3 had very low quality.
For the meta-analysis, 12 studies assessing ferritin levels (4,366 T2D patients and 41,091 controls) and 4 studies assessing heme-iron intake (9,246 T2D patients and 179,689 controls) met the inclusion criteria. These 16 studies consisted of 6 cohort, 1 case-cohort, 3 nested case-control, and 6 cross-sectional studies. Among the 12 studies assessing the association between ferritin levels and T2D risk, 7 studies were conducted in western countries (5 in North America, 2 in Europe) and 5 in Asia. Furthermore, 11 of these 12 studies consisted of men and women, while 1 study consisted entirely of women . In the 12 ferritin studies, all effect estimates and corresponding CIs were adjusted for confounders. In addition, the results of 4 studies were adjusted for metabolic factors including high-density lipoprotein cholesterol (HDL-C), triglyceride, C-reactive protein (CRP), adiponectin, adipokines, liver enzymes, inflammation score, insulin levels and dietary factors. Among the 6 studies assessing the association between iron intake and T2D risk, 5 studies provided the data assessing the association between heme-iron intake and T2D. Of these iron intake studies, 5 analyzed the association between total iron intake (non-heme, heme and supplemental iron intake) and T2D risk, 1 consisted entirely of men , 3 entirely of women –. Furthermore, 4 of these were cohort studies that were quantitatively analyzed in the meta-analysis , –.
The 15 studies that were included for the qualitative analysis of the systematic review consisted of one nested case-control study, one retrospective cohort, 5 case-control, 2 prospective cohort, and 6 cross-sectional studies (Table 3). Of these, 12 studies measured the body iron store indexes without providing the effect estimates, including ferritin (n = 12), sTfR (n = 3), transferrin saturation index (n = 1), and iron intake (n = 1). Also, one study provided OR and CI, comparing the ratio of transferrin receptors to ferritin with T2D risk, and 2 studies provided ORs and CIs comparing transferrin saturation with T2D risk. Of these 15 studies, 8 were conducted in western countries (3 in North America, 5 in Europe), and 7 in Asia. Also, 12 studies consisted of men and women, one consisted entirely of women , and 2 entirely of men , .
Main Analysis and Summary of Results
The ORs, HRs or RRs that were maximally adjusted for confounders, including HDL-C, fasting and 2-h glucose, triglyceride, CRP, adiponectin, adipokines, liver enzymes, insulin level and inflammation score, were used for the meta-analysis. Result of the association of ferritin levels and dietary iron intake with the risk of T2D in the meta-analysis studies is presented in Table 4. The effect estimates, the corresponding CIs, and the pooled RRs are shown in Figure 2, 3 and 4 for prospective, cross-sectional studies of ferritin and cohort studies of heme-iron intake, respectively. The combined RR comparing the highest and lowest category of ferritin levels for T2D risk was 1.66 (95% CI: 1.15–2.39) in prospective studies and 2.29 (95% CI: 1.48–3.54) in cross-sectional studies. The combined RR comparing the highest and lowest category of heme-iron intake for T2D risk was 1.31 (95% CI: 1.21–1.43).
Results of the studies that were included for the qualitative analysis of the systematic review were summarized as follows: 1) ferritin levels were significantly higher in T2D patients than in controls in 8 studies, while they were not significantly different between T2D patients and the controls in 2 studies , , 2) one study suggested significantly higher levels of sTfR in T2D patients compared to control individuals , which was not confirmed by 2 other relevant studies , , 3) transferrin saturation index and iron intake were also not significantly different between patients and control individuals in 2 studies , , 4) one study provided OR value confirming a positive association between the ratio of transferrin receptors to ferritin and T2D risk , and 5) inconsistent results were reported in 2 studies that used ORs and corresponding CIs to analyze the association between transferrin saturation and T2D risk , .
Moderate heterogeneity among prospective cohort studies (Q = 14.84, P = 0.01, I2 = 66.3%), and high heterogeneity among cross-sectional studies (Q = 44.16, P<0.001, I2 = 88.7%) were detected for studies of ferritin levels. Among the studies concerning heme-iron intake levels, on the other hand, no heterogeneity was observed (Q = 1.39, P = 0.71, I2 = 0%). A sensitivity analysis was conducted by omitting 1 study at a time and calculating the pooled RRs for the remaining studies to identify any potential source of heterogeneity. Sensitivity analysis suggested that no single study dramatically influenced the pooled RRs, which ranged from 1.45 (1.15–1.82) to 1.88 (1.51–2.35) comparing the highest versus the lowest category of ferritin levels for T2D risk among prospective studies, 1.98 (1.36–2.88) to 2.65 (1.90–3.70) among cross-sectional studies, and 1.28 (1.16–1.41) to 1.35 (1.19–1.52) for heme-iron intake among prospective cohort studies.
We also performed a stratified analysis to identify potential sources of heterogeneity. For prospective studies, the positive association between ferritin levels and T2D risk was consistently observed when studies were stratified by study design and patient gender, but was not observed when studies were stratified by study size and adjustments of metabolic factors. On the other hand, for cross-sectional studies, the positive association was consistently observed when studies were stratified by study size and metabolic factors, but not observed when stratified by patient gender and ferritin measuring methods (Table 5).
Both single and multiple covariate models of meta-regression were performed using covariates of sample size, number of patients, number of controls and adjustments of metabolic factors for prospective studies, and covariates of country, sample size, number of patients, number of controls, adjustments of metabolic factors, and methods of ferritin measurement for cross-sectional studies. Results of meta-regression models including the number of included studies, β coefficients and corresponding p values are shown in Table 6.
No evidence of publication bias was observed assessing the association between ferritin levels and T2D, as indicated by Begg’s rank correlation and Egger linear regression tests for prospective studies (Figure 5, Begg: P = 0.851; Figure 6, Egger: P = 0.772) and for cross-sectional studies (Figure 7; Begg: P = 0.188; Figure 8, Egger: P = 0.124). Publication bias also did not exist in the association between heme-iron intake and T2D (Figure 9; Begg: P = 0.497; Figure 10, Egger: P = 0.658). Furthermore, Galbraith plot was also used to detect outliers for the studies assessing the association between ferritin and T2D risk. Among the prospective studies (Figure 11), 4 were inside the 95% bounds, 2 were outliers ,  in the Galbraith plot, while among the cross-sectional studies (Figure 12), 3 were within the 95% bounds, and the other 3 were the outliers , , . However, after removing all the outliers, the pooled RRs were just slightly increased from 1.66 (95% CI: 1.15–2.39) to 1.69 (95% CI: 1.31–2.18) for the prospective studies, and 2.29 (95% CI: 1.48–3.54) to 2.03 (95% CI: 1.56–2.63) for the cross-sectional studies, suggesting that the study results were homogenous in nature.
Summary of Findings
Our study provided quantitative pooled estimates of the association of T2D risk with ferritin and dietary heme-iron intake for the first time. Our meta-analysis indicated a significant association between ferritin levels and the risk of T2D, which were performed separately among 6 prospective studies and 6 cross-sectional studies (4,366 T2D cases and 41,091 controls). A significant association between dietary heme-iron intake and the risk of T2D was also observed from 4 prospective cohort studies (9,246 T2D patients and 179,689 controls). The initial results of the meta-analysis were consistent with the results of sensitivity analyses. The qualitative analysis of additional studies suggested a statistically significant association between ferritin and T2D risk in 8 out of 10 studies.
Systematic Review of Current Epidemiological Findings
Cross-sectional and case-control findings.
We found that the cross-sectional studies (1 in U.S., 2 in South Korea, and 3 in China) indicated a statistically significant association between ferritin and T2D risk after adjustments for multiple confounders, with the effect estimates ranging from 1.23 (1.01–1.50) to 4.35 (3.00–6.31) –, , , . Female T2D patients [2.24 (1.23–4.09)] exhibited a higher combined effect estimate than male patients [1.89 (0.97–3.69)], suggesting that hormonal differences may play a role in the association between ferritin levels and T2D risk. When metabolic factors such as hypertension, triglyceride levels, and waist circumference were adjusted, the combined effect estimate was reduced from [2.80 (1.74–4.51)] to [1.80 (1.07–3.04)]. Different methods of ferritin measurement, namely the immunoradiometric assay (RIA) and immunoturbidimetric assay (TIA), also had a significant impact on the association between ferritin levels and T2D risk (RIA: 2.62, 95% CI: 1.66–4.13; TIA: 1.82, 95% CI: 0.82–4.02). The qualitative analysis of six cross-sectional studies from the U.S., China, Japan, Iran, and South Korea found a statistically significant association between ferritin and T2D risk , , –, . The analysis of the five case-control studies indicated that 2 studies showed a positive association between ferritin levels and T2D risk, though an additional study failed to confirm this result. The analysis of the remaining 2 case-control studies indicated a statistically significant association of the elevated transferrin saturation and the ratio of transferrin receptors to ferritin with T2D risk.
Findings of prospective studies.
Six prospective studies (1 case-cohort, 3 nested case-control, 2 cohort), which analyzed the effect of ferritin levels on the incidence of T2D , , , , , , were included in the meta-analysis and had follow-up periods ranging from 2.8 to 10 years. The studies that were smaller than 300 T2D patients or were not adjusted for metabolic factors provided a statistically significant combined RR, while those that were larger than 300 or had adjusted for metabolic factors did not. Jiang et al.  and Forouhi et al.  evaluated large clinical populations (n = 698 and 360, respectively), reporting 2.6- and 3.2-fold increased risk for developing T2D compared to the groups with lowest ferritin levels after adjustment for confounders. Jehn et al. (n = 599)  initially reported a statistically significant association between ferritin levels and T2D risk (1.74, 95% CI: 1.14–2.65) when adjusted for age, study center, patient ethnicity, smoking and alcohol intake status of patients; however, they failed to find a statistically significant association (0.79, 95% CI: 0.48–1.32) after further adjustments for BMI and metabolic syndrome factors. Both Rajpathak et al.  and Salomaa et al.  found no statistically significant association between ferritin and T2D risk (1.61, 95% CI: 0.85–3.02, and 1.44, 95% CI: 0.93–2.24, respectively) after adjusting for multiple confounders, which was consistent with the findings of Le et al.  using female subjects (0.87, 95% CI: 0.37–2.03).
Two studies included in the qualitative analysis measured ferritin and transferrin saturation and found a statistically significant association of T2D risk with ferritin, but not with transferrin saturation, respectively. Thus, although there seems to be a consistent positive association between ferritin levels and T2D risk, we couldn’t completely rule out the possibility that ferritin may only serve as a mediator for metabolic abnormalities that directly contribute to T2D incidence. On the other hand, the meta-analysis of the association between heme-iron intake and T2D risk, which included four prospective cohort studies with larger than 1000 T2D cases with follow-up periods ranging from 8.8 to 20 years , –, found a positive association between heme-iron intake and T2D risk. Considering that these four studies were well designed, the meta-analysis provided convincing combined results for the association of heme-iron intake and T2D incidence.
Genetic iron overload diseases, such as hereditary hemochromatosis, have been well recognized to contribute to diabetes by the excessive accumulation of iron in tissues . Recent studies have mainly focused on the relationship between T2D and moderately elevated iron level that are lower than those in genetic iron overload diseases . Researchers hypothesized that increased iron deposition in tissues initially induces insulin resistance, and the resulting hyperinsulinemia ultimately causes pancreatic islet apoptosis and the progression of T2D . Through transforming poorly-reactive radicals into highly-active ones, catalytic iron damages DNA and the integrity of cell membrane, interferes with the glucose intake of skeletal muscles and adipocytes, and decreases the effect of insulin , , . Indeed, ROS generated by catalytic iron inhibits insulin receptor function, resulting in impaired insulin uptake . Increased iron stores further deteriorate hyperinsulinemia through hepatic dysfunction, decreased capacity for hepatic insulin extraction, and the insulin metabolism . Ultimately, long-term over-secretion of insulin, iron deposition, and the hazardous effect of radicals on β-cells together contribute to β-cells apoptosis and T2D.
Sources of Heterogeneity
Although the random-effect models were used to calculate the combined effect estimates, moderate and high heterogeneity was observed in prospective and cross-sectional studies regarding the association between ferritin levels and T2D risk, respectively. Thus, stratified analysis and meta-regression were introduced to explore the sources of heterogeneity.
Little or no heterogeneity was observed in prospective studies stratified by nested case-control (I2 = 2.6%, p = 0.358) or cohort studies (I2 = 0%, p = 0.559), and in the studies that had less than 300 T2D cases (I2 = 0%, p = 0.842), indicating that study design and size accounted for most of the heterogeneity among these prospective studies. The high heterogeneity of all combined cross-sectional studies was completely eliminated among the studies with less than 300 cases (I2 = 0%, p = 0.344), and partly attenuated among the studies that were adjusted for metabolic factors (I2 = 76.3%, p = 0.015) and the studies that used RIA to measure ferritin levels (I2 = 75.9%, p = 0.006).
Considering the moderate heterogeneity in prospective studies, and high heterogeneity in cross-sectional studies, we further performed a meta-regression analysis to explore the potential sources of heterogeneity , . Heterogeneity was completely eliminated by study design (single covariate: p = 0.026; residual I2 = 0%) in prospective studies, indicating that the three different study types could explain all the sources of heterogeneity. In cross-sectional studies, the country of origin where the studies were conducted had the potential to cause heterogeneity (single covariate: p = 0.125). The OR value of the only western study was 4.35 (95% CI: 3.00–6.31), which was significantly higher than the combined effect estimate of the other five Asian studies (1.98, 95% CI: 1.36–2.88). Other potential sources of heterogeneity could be study size (single covariate: p = 0.195; multiple covariates: p = 0.20) and metabolic factor adjustments (single covariate: p = 0.281). Meta-regression effectively explained the sources of heterogeneity in cross-sectional studies: without using meta-regression, the I2 value of heterogeneity was 88.7%; the residual I2 value was 49.94% when the study size and the adjustments were used as multiple covariates in the meta-regression; I2 value was further reduced to 33.3% when the number of patients and controls, and the study size were used as multiple covariates in the meta-regression.
Measurement errors, including the usage of different measurement methods for ferritin levels and varying times or measurement length may explain part of the variation among the prospective cohort study results. In addition, patients with T1D might have been included in the original studies as well; however, it is unlikely that the inclusion of T1D cases could influence the pooled RRs significantly, considering that the prevalence of T1D is less than 5–10% in adult diabetes patients. Languages might explain part of the heterogeneity, because all the included articles were published in English. However, articles in other languages were also read, if their abstracts were provided in English, which reduced the likelihood of incomplete retrieval of results. Furthermore, publication bias might also influence the pooled RRs, but our Begg and Egger tests did not indicate any potential publication bias.
The results of our meta-analysis were unlikely to be explained by residual confounding due to the strength of the adjusted RRs for ferritin levels and the risk of T2D. The higher combined RR for ferritin levels in cross-sectional studies compared with prospective studies suggests the likelihood of reverse causality. However, the difference in pooled RR between the two study designs was not statistically significant and the strength of RR for prospective studies was high, indicating that reverse causality was unlikely. Since all the included studies were large population-based studies and 4 out of 5 were prospective cohort studies, residual confounding could be ruled out regarding our results for the association of T2D risk with heme-iron intake. Larger prospective studies including both genders, patients from diverse geographic areas, and adjustments for metabolic factors are needed in the future to establish a more definitive conclusion about the association of T2D risk with ferritin levels and heme-iron intake.
Validity of the Meta-analysis
The studies included in the meta-analysis, assessing the association between ferritin levels and T2D risk, were high- (prospective studies) and moderate-quality (cross-sectional studies). The high to moderate quality of all included studies for quantitative analysis ensured the validity of the meta-analysis. High heterogeneity existed among the cross-sectional studies, indicating actual variation rather than pure chance in study results, which was expected, given the diverse ethnic background of patients, inconsistent criteria used for T2D diagnosis, and the varied ferritin measurement methods. Although the results of the stratified analysis and meta-regression indicated that residual confounding among cross-sectional studies might exist, nested case-control and cohort studies were homogeneous. Besides, to exclude the likelihood that ferritin merely served as a surrogate marker for the association with T2D, we included a wide range of metabolic factors, such as HDL-C, triglycerides, CRP, adiponectin, adipokines, liver enzymes, inflammation score, insulin levels, and dietary factors, in our meta-analysis. We calculated the combined RRs of prospective studies before and after the adjustments of metabolic factors. Under both conditions, prospective studies indicated a statistically significant association between ferritin levels and T2D risk, suggesting a causal effect for high ferritin level on T2D independent of known diabetes risk factors.
We thank Dr. Christopher Brooks for improving the English writing of the manuscript.
Conceived and designed the experiments: HMT. Performed the experiments: ZXZ. Analyzed the data: ZXZ SYL. Contributed reagents/materials/analysis tools: GJL. Wrote the paper: ZXZ FFY XLM ZYH.
- 1. Halliwell B, Gutteridge JMC (1990) Role of free radicals and catalytic metal ions in human disease: an overview. Meth Enzymol 186: 1–85.B. HalliwellJMC Gutteridge1990Role of free radicals and catalytic metal ions in human disease: an overview.Meth Enzymol186185
- 2. Cooksey RC, Jouihan HA, Ajioka RS, Hazel MW, Jones DL, et al. (2004) Oxidative stress, beta-cell apoptosis, and decreased insulin secretory capacity in mouse models of hemochromatosis. Endocrinology 145: 5305–5312.RC CookseyHA JouihanRS AjiokaMW HazelDL Jones2004Oxidative stress, beta-cell apoptosis, and decreased insulin secretory capacity in mouse models of hemochromatosis.Endocrinology14553055312
- 3. Tiedge M, Lortz S, Drinkgern J, Lenzen S (1997) Relation between antioxidant enzyme gene expression and antioxidative defense status of insulin-producing cells. Diabetes 46: 1733–1742.M. TiedgeS. LortzJ. DrinkgernS. Lenzen1997Relation between antioxidant enzyme gene expression and antioxidative defense status of insulin-producing cells.Diabetes4617331742
- 4. Ferrannini E (2000) Insulin resistance, iron, and the liver. Lancet 355: 2181–2182.E. Ferrannini2000Insulin resistance, iron, and the liver.Lancet35521812182
- 5. Mendler MH, Turlin B, Moirand R, Jouanolle AM, Sapey T, et al. (1999) Insulin resistance-associated hepatic iron overload. Gastroenterology 117: 1155–1163.MH MendlerB. TurlinR. MoirandAM JouanolleT. Sapey1999Insulin resistance-associated hepatic iron overload.Gastroenterology11711551163
- 6. Green A, Basile R, Rumberger JM (2006) Transferrin and iron induce insulin resistance of glucose transport in adipocytes. Metabolism 55: 1042–1045.A. GreenR. BasileJM Rumberger2006Transferrin and iron induce insulin resistance of glucose transport in adipocytes.Metabolism5510421045
- 7. Fumeron F, Péan F, Driss F, Balkau B, Tichet J, et al. (2006) Ferritin and transferrin are both predictive of the onset of hyperglycemia in men and women over 3 years: the data from an epidemiological study on the Insulin Resistance Syndrome (DESIR) study. Diabetes Care 29(9): 2090–4.F. FumeronF. PéanF. DrissB. BalkauJ. Tichet2006Ferritin and transferrin are both predictive of the onset of hyperglycemia in men and women over 3 years: the data from an epidemiological study on the Insulin Resistance Syndrome (DESIR) study.Diabetes Care29(9)20904
- 8. Ascherio A, Rimm EB, Giovannucci EL, Willett WC, Stampfer MJ (2001) Blood donations and risk of coronary heart disease in men. Circulation 103: 52–57.A. AscherioEB RimmEL GiovannucciWC WillettMJ Stampfer2001Blood donations and risk of coronary heart disease in men.Circulation1035257
- 9. Rajpathak SN, Crandall JP, Rosett JW, Kabat GC, Rohan TE, et al. (2009) The role of iron in type 2 diabetes in humans. Biochimica et Biophysica Acta 1790: 671–681.SN RajpathakJP CrandallJW RosettGC KabatTE Rohan2009The role of iron in type 2 diabetes in humans.Biochimica et Biophysica Acta1790671681
- 10. Jiang R, Manson JE, Meigs JB, Ma J, Rifai N, et al. (2004) Body iron stores in relation to risk of type 2 diabetes in apparently healthy women. JAMA 291(6): 711–7.R. JiangJE MansonJB MeigsJ. MaN. Rifai2004Body iron stores in relation to risk of type 2 diabetes in apparently healthy women.JAMA291(6)7117
- 11. Salomaa V, Havulinna A, Saarela O, Zeller T, Jousilahti P, et al. (2010) Thirty-one novel biomarkers as predictors for clinically incident diabetes. PLos One 5(4): e10100.V. SalomaaA. HavulinnaO. SaarelaT. ZellerP. Jousilahti2010Thirty-one novel biomarkers as predictors for clinically incident diabetes.PLos One5(4)e10100
- 12. Jiang R, Ma J, Ascherio A, Stampfer MJ, Willett WC, et al. (2004) Dietary iron intake and blood donations in relation to risk of type 2 diabetes in men: a prospective cohort study. Am J Clin Nutr 79(1): 70–5.R. JiangJ. MaA. AscherioMJ StampferWC Willett2004Dietary iron intake and blood donations in relation to risk of type 2 diabetes in men: a prospective cohort study.Am J Clin Nutr79(1)705
- 13. Jehn ML, Guallar E, Clark JM, Couper D, Duncan BB, et al. (2007) A prospective study of plasma ferritin level and incident diabetes the Atherosclerosis Risk in Communities (ARIC) Study. Am J Epidemiol 165(9): 1047–54.ML JehnE. GuallarJM ClarkD. CouperBB Duncan2007A prospective study of plasma ferritin level and incident diabetes the Atherosclerosis Risk in Communities (ARIC) Study.Am J Epidemiol165(9)104754
- 14. Stroup DF, Berlin JA, Morton SC, Olkin I, Williamson GD, et al. (2000) Meta-analysis Of Observational Studies in Epidemiology (MOOSE) Group. Meta-analysis of observational studies in epidemiology: a proposal for reporting. JAMA 283(15): 2008–2012.DF StroupJA BerlinSC MortonI. OlkinGD Williamson2000Meta-analysis Of Observational Studies in Epidemiology (MOOSE) Group. Meta-analysis of observational studies in epidemiology: a proposal for reporting.JAMA283(15)20082012
- 15. Wells G, Shea B, O’Connell D, Peterson J, Welch V, et al. The Newcastle-Ottawa Scale (NOS) for assessing the quality of nonrandomised studies in meta-analyses. In. : Ottawa Hospital Research Institute. Wells G, Shea B, O’Connell D, Peterson J, Welch V, et al. The Newcastle-Ottawa Scale (NOS) for assessing the quality of nonrandomised studies in meta-analyses. In.: Ottawa Hospital Research Institute
- 16. Swiglo BA, Murad MH, Schunemann HJ, Kunz R, Vigersky RA, et al. (2008) A case for clarity, consistency, and helpfulness: state-of-the-art clinical practice guidelines in endocrinology using the grading of recommendations, assessment, development, and evaluation system. J Clin Endocrinol Metab 93(3): 666–673.BA SwigloMH MuradHJ SchunemannR. KunzRA Vigersky2008A case for clarity, consistency, and helpfulness: state-of-the-art clinical practice guidelines in endocrinology using the grading of recommendations, assessment, development, and evaluation system.J Clin Endocrinol Metab93(3)666673
- 17. Higgins JP, Thompson SG, Deeks JJ, Altman DG (2003) Measuring inconsistency in meta-analyses. BMJ 327: 557–60.JP HigginsSG ThompsonJJ DeeksDG Altman2003Measuring inconsistency in meta-analyses.BMJ32755760
- 18. Galbraith RF (1988) A note on graphical presentation of estimated odds ratios from several clinical trials. Stat Med 7: 889–894.RF Galbraith1988A note on graphical presentation of estimated odds ratios from several clinical trials.Stat Med7889894
- 19. Shi Z, Hu X, Yuan B, Pan X, Meyer HE, et al. (2006) Association between serum ferritin, hemoglobin, iron intake, and diabetes in adults in Jiangsu, China. Diabetes Care 29(8): 1878–83.Z. ShiX. HuB. YuanX. PanHE Meyer2006Association between serum ferritin, hemoglobin, iron intake, and diabetes in adults in Jiangsu, China.Diabetes Care29(8)187883
- 20. Kim CH, Kim HK, Bae SJ, Park JY, Lee KU (2011) Association of elevated serum ferritin concentration with insulin resistance and impaired glucose metabolism in Korean men and women. Metabolism 60(3): 414–20.CH KimHK KimSJ BaeJY ParkKU Lee2011Association of elevated serum ferritin concentration with insulin resistance and impaired glucose metabolism in Korean men and women.Metabolism60(3)41420
- 21. Lee BK, Kim Y, Kim YI (2011) Association of serum ferritin with metabolic syndrome and diabetes mellitus in the South Korean general population according to the Korean National Health and Nutrition Examination Survey 2008. Metabolism 60(10): 1416–24.BK LeeY. KimYI Kim2011Association of serum ferritin with metabolic syndrome and diabetes mellitus in the South Korean general population according to the Korean National Health and Nutrition Examination Survey 2008.Metabolism60(10)141624
- 22. Rajpathak SN, Wylie-Rosett J, Gunter MJ, Negassa A, Kabat GC, et al. (2009) Biomarkers of body iron stores and risk of developing type 2 diabetes. Diabetes Obes Metab 11(5): 472–9.SN RajpathakJ. Wylie-RosettMJ GunterA. NegassaGC Kabat2009Biomarkers of body iron stores and risk of developing type 2 diabetes.Diabetes Obes Metab11(5)4729
- 23. Luan de C, Li H, Li SJ, Zhao Z, Li X, et al. (2008) Body iron stores and dietary iron intake in relation to diabetes in adults in North China. Diabetes Care 31(2): 285–6.C. Luan deH. LiSJ LiZ. ZhaoX. Li2008Body iron stores and dietary iron intake in relation to diabetes in adults in North China.Diabetes Care31(2)2856
- 24. Ford ES, Cogswell ME (1999) Diabetes and serum ferritin concentration among U.S. adults. Diabetes Care 22(12): 1978–83.ES FordME Cogswell1999Diabetes and serum ferritin concentration among U.S. adults.Diabetes Care22(12)197883
- 25. Le TD, Bae S, Ed Hsu C, Singh KP, Blair SN, et al. (2008) Effects of Cardiorespiratory Fitness on Serum Ferritin Concentration and Incidence of Type 2 Diabetes: Evidence from the Aerobics Center Longitudinal Study (ACLS). Rev Diabet Stud 5(4): 245–52.TD LeS. BaeC. Ed HsuKP SinghSN Blair2008Effects of Cardiorespiratory Fitness on Serum Ferritin Concentration and Incidence of Type 2 Diabetes: Evidence from the Aerobics Center Longitudinal Study (ACLS).Rev Diabet Stud5(4)24552
- 26. Forouhi NG, Harding AH, Allison M, Sandhu MS, Welch A, et al. (2007) Elevated serum ferritin levels predict new-onset type 2 diabetes results from the EPIC-Norfolk prospective study. Diabetologia 50(5): 949–56.NG ForouhiAH HardingM. AllisonMS SandhuA. Welch2007Elevated serum ferritin levels predict new-onset type 2 diabetes results from the EPIC-Norfolk prospective study.Diabetologia50(5)94956
- 27. Sun L, Franco OH, Hu FB, Cai L, Yu Z, et al. (2008) Ferritin concentrations, metabolic syndrome, and type 2 diabetes in middle-aged and elderly Chinese. J Clin Endocrinol Metab 93(12): 4690–6.L. SunOH FrancoFB HuL. CaiZ. Yu2008Ferritin concentrations, metabolic syndrome, and type 2 diabetes in middle-aged and elderly Chinese.J Clin Endocrinol Metab93(12)46906
- 28. Lee DH, Folsom AR, Jacobs DR Jr (2004) Dietary iron intake and Type 2 diabetes incidence in postmenopausal women the Iowa Women’s Health Study. Diabetologia 47(2): 185–94.DH LeeAR FolsomDR Jacobs Jr2004Dietary iron intake and Type 2 diabetes incidence in postmenopausal women the Iowa Women’s Health Study.Diabetologia47(2)18594
- 29. Rajpathak S, Ma J, Manson J, Willett WC, Hu FB (2006) Iron intake and the risk of type 2 diabetes in women a prospective cohort study. Diabetes Care 29(6): 1370–6.S. RajpathakJ. MaJ. MansonWC WillettFB Hu2006Iron intake and the risk of type 2 diabetes in women a prospective cohort study.Diabetes Care29(6)13706
- 30. Song Y, Manson JE, Buring JE, Liu S (2004) A prospective study of red meat consumption and type 2 diabetes in middle-aged and elderly women: the women’s health study. Diabetes Care 27(9): 2108–15.Y. SongJE MansonJE BuringS. Liu2004A prospective study of red meat consumption and type 2 diabetes in middle-aged and elderly women: the women’s health study.Diabetes Care27(9)210815
- 31. Kolberg JA, Jørgensen T, Gerwien RW, Hamren S, McKenna MP, et al. (2009) Development of a type 2 diabetes risk model from a panel of serum biomarkers from the Inter99 cohort. Diabetes Care 32(7): 1207–12.JA KolbergT. JørgensenRW GerwienS. HamrenMP McKenna2009Development of a type 2 diabetes risk model from a panel of serum biomarkers from the Inter99 cohort.Diabetes Care32(7)120712
- 32. Jiang F, Sun ZZ, Tang YT, Xu C, Jiao XY (2011) Hepcidin expression and iron parameters change in Type 2 diabetic patients. Diabetes Res Clin Pract 93(1): 43–8.F. JiangZZ SunYT TangC. XuXY Jiao2011Hepcidin expression and iron parameters change in Type 2 diabetic patients.Diabetes Res Clin Pract93(1)438
- 33. Kim C, Cheng YJ, Beckles GL (2008) Inflammation among women with a history of gestational diabetes mellitus and diagnosed diabetes in the Third National Health and Nutrition Examination Survey. Diabetes Care 31(7): 1386–8.C. KimYJ ChengGL Beckles2008Inflammation among women with a history of gestational diabetes mellitus and diagnosed diabetes in the Third National Health and Nutrition Examination Survey.Diabetes Care31(7)13868
- 34. Wu H, Yu Z, Qi Q, Li H, Sun Q, et al. (2011) Joint analysis of multiple biomarkers for identifying type 2 diabetes in middle-aged and older Chinese a cross-sectional study. BMJ Open 1(1): e000191.H. WuZ. YuQ. QiH. LiQ. Sun2011Joint analysis of multiple biomarkers for identifying type 2 diabetes in middle-aged and older Chinese a cross-sectional study.BMJ Open1(1)e000191
- 35. Freixenet N, Vilardell C, Llauradó G, Giménez-Palop O, Berlanga E, et al. (2011) Men with hyperferritinemia and diabetes in the Mediterranean area do not have a higher iron overload than those without diabetes. Diabetes Res Clin Pract 91(2): e33–6.N. FreixenetC. VilardellG. LlauradóO. Giménez-PalopE. Berlanga2011Men with hyperferritinemia and diabetes in the Mediterranean area do not have a higher iron overload than those without diabetes.Diabetes Res Clin Pract91(2)e336
- 36. Aso Y, Takebayashi K, Wakabayashi S, Momobayashi A, Sugawara N, et al. (2010) Relation between serum high molecular weight adiponectin and serum ferritin or prohepcidin in patients with type 2 diabetes. Diabetes Res Clin Pract 90(3): 250–5.Y. AsoK. TakebayashiS. WakabayashiA. MomobayashiN. Sugawara2010Relation between serum high molecular weight adiponectin and serum ferritin or prohepcidin in patients with type 2 diabetes.Diabetes Res Clin Pract90(3)2505
- 37. Ashourpour M, Djalali M, Djazayery A, Eshraghian MR, Taghdir M, et al. (2010) Relationship between serum ferritin and inflammatory biomarkers with insulin resistance in a Persian population with type 2 diabetes and healthy people. Int J Food Sci Nutr 61(3): 316–23.M. AshourpourM. DjalaliA. DjazayeryMR EshraghianM. Taghdir2010Relationship between serum ferritin and inflammatory biomarkers with insulin resistance in a Persian population with type 2 diabetes and healthy people.Int J Food Sci Nutr61(3)31623
- 38. Kim NH, Oh JH, Choi KM, Kim YH, Baik SH, et al. (2000) Serum ferritin in healthy subjects and type 2 diabetic patients. Yonsei Med J 41(3): 387–92.NH KimJH OhKM ChoiYH KimSH Baik2000Serum ferritin in healthy subjects and type 2 diabetic patients.Yonsei Med J41(3)38792
- 39. Hernández C, Lecube A, Carrera A, Simó R (2005) Soluble transferrin receptors and ferritin in Type 2 diabetic patients. Diabet Med 22(1): 97–101.C. HernándezA. LecubeA. CarreraR. Simó2005Soluble transferrin receptors and ferritin in Type 2 diabetic patients.Diabet Med22(1)97101
- 40. Salonen JT, Tuomainen TP, Nyyssönen K, Lakka HM, Punnonen K (1998) Relation between iron stores and non-insulin dependent diabetes in men case-control study. BMJ 317(7160): 727.JT SalonenTP TuomainenK. NyyssönenHM LakkaK. Punnonen1998Relation between iron stores and non-insulin dependent diabetes in men case-control study.BMJ317(7160)727
- 41. Ren Y, Tian HM, Li XJ, Liang JZ, Zhao GZ (2004) Elevated serum ferritin concentrations in a glucose-impaired population and in normal glucose tolerant first-degree relatives in familial type 2 diabetic pedigrees. Diabetes Care 27(2): 622–3.Y. RenHM TianXJ LiJZ LiangGZ Zhao2004Elevated serum ferritin concentrations in a glucose-impaired population and in normal glucose tolerant first-degree relatives in familial type 2 diabetic pedigrees.Diabetes Care27(2)6223
- 42. Ellervik C, Mandrup-Poulsen T, Andersen HU, Tybjærg-Hansen A, Frandsen M, et al. (2011) Elevated transferrin saturation and risk of diabetes: three population-based studies. Diabetes Care 34(10): 2256–8.C. EllervikT. Mandrup-PoulsenHU AndersenA. Tybjærg-HansenM. Frandsen2011Elevated transferrin saturation and risk of diabetes: three population-based studies.Diabetes Care34(10)22568
- 43. Mainous AG 3rd, King DE, Pearson WS, Garr DR (2002) Is an elevated serum transferrin saturation associated with the development of diabetes. J Fam Pract 51(11): 933–6.Mainous AG 3rd, King DE, Pearson WS, Garr DR2002Is an elevated serum transferrin saturation associated with the development of diabetes.J Fam Pract51(11)9336
- 44. Rowe MW, Bergman RN, Wagenknecht LE, Kolberg JA (2012) Performance of a multi-marker diabetes risk score in the insulin resistance atherosclerosis study (IRAS), a multi-ethnic U.S. cohort. Diabetes Metab Res Rev [Epub 2012 Apr 10]. MW RoweRN BergmanLE WagenknechtJA Kolberg2012Performance of a multi-marker diabetes risk score in the insulin resistance atherosclerosis study (IRAS), a multi-ethnic U.S. cohort.Diabetes Metab Res Rev [Epub 2012 Apr 10]
- 45. Hardikar PS, Joshi SM, Bhat DS, Raut DA, Katre PA, et al. (2012) Spuriously High Prevalence of Prediabetes Diagnosed by HbA(1c) in Young Indians Partly Explained by Hematological Factors and Iron Deficiency Anemia. Diabetes Care 35(4): 797–802.PS HardikarSM JoshiDS BhatDA RautPA Katre2012Spuriously High Prevalence of Prediabetes Diagnosed by HbA(1c) in Young Indians Partly Explained by Hematological Factors and Iron Deficiency Anemia.Diabetes Care35(4)797802
- 46. Adams PC, Reboussin DM, Barton JC, McLaren CE, Eckfeldt JH, et al. (2005) Hemochromatosis and Iron Overload Screening (HEIRS) Study Research Investigators: Hemochromatosis and iron-overload screening in a racially diverse population. N Engl J Med 352: 1769–1778.PC AdamsDM ReboussinJC BartonCE McLarenJH Eckfeldt2005Hemochromatosis and Iron Overload Screening (HEIRS) Study Research Investigators: Hemochromatosis and iron-overload screening in a racially diverse population.N Engl J Med35217691778
- 47. Swaminathan S, Fonseca VA, Alam MG, Shah SV (2007) The Role of Iron in Diabetes and Its Complications. Diabetes Care 30(7): 1926–33.S. SwaminathanVA FonsecaMG AlamSV Shah2007The Role of Iron in Diabetes and Its Complications.Diabetes Care30(7)192633
- 48. Wilson JG, Lindquist JH, Grambow SC, Crook ED, Maher JF (2003) Potential role of increased iron stores in diabetes. Am J Med Sci 325: 332–339.JG WilsonJH LindquistSC GrambowED CrookJF Maher2003Potential role of increased iron stores in diabetes.Am J Med Sci325332339
- 49. Andrews NC (1999) Disorders of iron metabolism. N Engl J Med 341: 1986–1995.NC Andrews1999Disorders of iron metabolism.N Engl J Med34119861995
- 50. Wolff SP (1993) Diabetes mellitus and free radicals: free radicals, transition metals and oxidative stress in the aetiology of diabetes mellitus and complications. Br Med Bull 49: 642–652.SP Wolff1993Diabetes mellitus and free radicals: free radicals, transition metals and oxidative stress in the aetiology of diabetes mellitus and complications.Br Med Bull49642652
- 51. Thompson SG (1994) Systematic review: why sources of heterogeneity in meta-analysis should be investigated. British Medical Journal 309: 1351–1355.SG Thompson1994Systematic review: why sources of heterogeneity in meta-analysis should be investigated.British Medical Journal30913511355
- 52. Higgins JPT, Thompson SG (2002) Quantifying heterogeneity in a meta-analysis. Statistics in Medicine 21: 1539–1558.JPT HigginsSG Thompson2002Quantifying heterogeneity in a meta-analysis.Statistics in Medicine2115391558