Association of Serum Gamma-Glutamyl Transferase and Ferritin with the Metabolic Syndrome

Wei, Dong; Chen, Tao; Li, Jie; Gao, Yun; Ren, Yan; Zhang, Xiangxun; Yu, Hongling; Tian, Haoming

doi:https://doi.org/10.1155/2015/741731

Journal of Diabetes Research

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Abstract Introduction Materials and Methods Results Discussion and Conclusions Acknowledgments References Copyright Related Articles

Research Article | Open Access

Volume 2015 | Article ID 741731 | https://doi.org/10.1155/2015/741731

Association of Serum Gamma-Glutamyl Transferase and Ferritin with the Metabolic Syndrome

Dong Wei,^1,2Tao Chen,¹Jie Li,³Yun Gao,¹Yan Ren,¹Xiangxun Zhang,⁴Hongling Yu,⁴and Haoming Tian^1,4

Academic Editor: Toshiyasu Sasaoka

Received11 Feb 2015

Revised24 May 2015

Accepted26 May 2015

Published21 Jun 2015

Abstract

Aim. To investigate the relationship among GGT, ferritin, and the risk of metabolic syndrome. Methods. A total of 1024 eligible individuals of the Chinese Yi ethnic group were enrolled in this cross-sectional study. The presence of metabolic syndrome was determined using the revised NCEP-ATP III and CDS criteria. Odds ratios for the metabolic syndrome and its components for different groups based on the levels of GGT and ferritin were calculated using multiple logistic regressions. Results. Serum GGT and ferritin concentrations were significantly higher in subjects with metabolic syndrome compared to those without metabolic syndrome in both genders (p < 0.05). Serum GGT was positively correlated with ferritin (p < 0.05). The risk of the metabolic syndrome was significantly higher in female subjects who had elevated GGT and ferritin levels (p < 0.05). Furthermore, the increased risk of having each of the metabolic syndrome components (overweight or obesity, hypertriglyceridemia, hypertension, hyperglycemia, and insulin resistance) was also observed in those subjects after adjustment for possible confounders (p < 0.05). Conclusions. These data indicate that GGT and ferritin synergistically correlate with the risk of the metabolic syndrome, suggesting that they could potentially be used as predictive biomarkers for the metabolic syndrome.

1. Introduction

The metabolic syndrome is a cluster of interrelated metabolic abnormalities that directly promote the development of atherosclerotic cardiovascular disease. Its main components are obesity, dyslipidemia, hypertension, insulin resistance, and abnormal glucose tolerance. Currently, there is not a standard definition of the metabolic syndrome that spans different populations, although some criteria have been proposed by various organizations to address this issue [1–5]. Insulin resistance is generally considered to be the central component that is involved in the common pathogenesis of the metabolic syndrome.

Gamma-glutamyl transferase (GGT) and ferritin participate in common pathophysiological processes, including oxidative stress and lipid peroxidation, which are important to the pathogenesis and development of insulin resistance and the metabolic syndrome [6–8]. A number of studies have shown that the serum level of GGT directly correlates with increased risk of death, hypertension, diabetes, and metabolic syndrome, even after adjustment for alcohol consumption and established risk factors [6–11]. In addition, several studies have shown that a high level of serum ferritin, a sensitive indicator of body iron stores, is associated independently with an increased risk of type 2 diabetes and the metabolic syndrome [12–14]. However, conflicts exist among these studies with regard to these associations among different ethnicities/races, gender, and alcohol consumption status. Furthermore, most of these studies focused specifically on either GGT or ferritin rather than addressing the synergistic association of GGT and ferritin with the metabolic syndrome.

Previously, our group conducted a novel investigation in a Chinese ethnic minority cohort of the synergistic association between GGT and ferritin and the risk of developing type 2 diabetes, an individual component of the metabolic syndrome [15]. We confirmed the synergistic association of GGT and ferritin with type 2 diabetes in women and suggested oxidative stress and lipid peroxidation as potential mechanisms. In this study, we investigated the relationship between these two metabolic markers and the metabolic syndrome in both genders.

2. Materials and Methods

2.1. Design

The study was part of the China National Diabetes and Metabolic Disorders Study, a population-based cross-sectional study designed to investigate the prevalence of type 2 diabetes and metabolic syndrome in the Chinese population [16]. A total of 1288 individuals of the Yi ethnic group from Xichang of Liangshan Yi Nationality Autonomous District, Sichuan Province of China, participated in this survey. This study was approved by China-Japan Friendship Hospital’s Drugs/Medical Apparatus & Instruments Ethics Committee and was registered on the website of the Chinese Clinical Trial Registry (ChiCTR-OCS-09000361). Written informed consent was obtained from each participant before data collection. This study was carried out in compliance with the Helsinki Declaration II.

2.2. Measurements and Populations

A standard questionnaire collecting demographic characteristics, medical history, and lifestyle factors was provided to the subjects. The medical history included the diagnosis and treatment of diabetes, hypertension, dyslipidemia, cardiovascular events, liver diseases, and malignant diseases. Those with a known history of liver disease (e.g., acute and chronic active hepatitis, liver cirrhosis), biliary tract diseases, malignant diseases, acute infectious or inflammatory disorders, history of transfusion, and iron therapy were all excluded. Lifestyle factors assessed by the questionnaire included alcohol consumption, smoking habits, and recreational physical activity. Heavy smoking and heavy drinking were defined as exposure to more than 25 cigarettes per day and consumption of more than 60 mL of alcohol per day, respectively [15]. Regular recreational physical activity was defined as participation in moderate or vigorous activity for at least 30 minutes or longer per day at least 3 days a week [17].

Blood pressure (BP) was measured by standard methods. Body weight, height, and waist circumference were obtained. Body mass index (BMI) was calculated as weight in kilograms divided by the square of height in meters (kg/m²). Blood samples were taken at the time of enrollment. The participants were asked to fast for at least 8 hours before their examinations. A standard 75 g glucose solution or a steamed bun that contained approximately 80 g of complex carbohydrates was provided as oral glucose tolerance test (OGTT). Plasma glucose was measured by a hexokinase enzymatic method. Serum ferritin was measured with a radioimmunoassay kit (Beijing North Institute of Biological Technology). Alanine aminotransferase (ALT), aspartate aminotransferase (AST), and GGT were determined using enzymatic methods. Serum lipids, uric acid (UA), hepatitis B surface antigen (HBsAg), and anti-hepatitis C virus (anti-HCV) as well as urinary albumin-to-creatinine ratio (UACR) were determined according to standard laboratory procedures. All measurements were conducted within 2 hours of sample collection. Insulin resistance was examined by the homeostatic model of assessment for insulin resistance (HOMA-IR). The HOMA-IR index was calculated using the following formula: fasting serum insulin (mU/mL) × fasting plasma glucose (mmol/L)/22.5. A HOMA-IR index score above the upper quartile of normal glucose tolerance (NGT) populations was used to determine the presence of insulin resistance according to World Health Organization (WHO) criteria [1].

The presence of metabolic syndrome was determined using two definitions: one proposed by the revised National Cholesterol Education Program Expert Panel on Detection, Evaluation and Treatment of High Blood Cholesterol in Adults Adult Treatment Panel III (NCEP-ATP III) and one proposed by the China Diabetes Society (CDS) [3, 5]. According to the revised NCEP ATP-III criteria, a participant has the metabolic syndrome if he or she meets three or more of the following criteria: (1) abdominal obesity (waist circumference ≥ 90 cm in men, ≥80 cm in women); (2) hypertriglyceridemia (triglycerides (TG) ≥ 1.70 mmol/L or on drug treatment for elevated TG); (3) low high density lipoprotein-cholesterol (HDL-C) (HDL-C < 1.03 mmol/L in men, <1.3 mmol/L in women, or on drug treatment for reduced HDL-C); (4) hypertension (systolic blood pressure (SP) ≥ 130 mmHg, diastolic pressure (DP) ≥ 85 mmHg, or on antihypertensive medication); (5) high fasting glucose (fasting plasma glucose (FPG) ≥ 5.6 mmol/L or under treatment for diabetes). The CDS definition of the metabolic syndrome requires three or more abnormalities of the following criteria: (1) overweight or obesity (BMI ≥ 25.0 kg/m²); (2) dyslipidemia (TG ≥ 1.70 mmol/L and/or low HDL-cholesterol [<0.9 mmol/L in men, <1.0 mmol/L in women]); (3) hypertension (SP ≥ 140 mmHg, DP ≥ 90 mmHg, or on antihypertensive medication); (4) hyperglycemia (FPG ≥ 6.1 mmol/L and/or 2-hour postprandial plasma glucose (PG) ≥ 7.8 mmol/L, or under treatment for diabetes).

2.3. Statistical Analysis

Data were presented as mean (standard deviation) or medians (interquartile range) for continuous data and as numbers (in percentage) for categorical measures. Data that were not normally distributed were logarithmically transformed for analysis. Student’s -test, Mann-Whitney test, or Chi-square test was used to compare the difference of clinical and laboratory characteristics between the subjects with and without the metabolic syndrome. Spearman’s rank-order correlation coefficient and multiple linear regression analyses were applied to determine the relationship between GGT and ferritin. Participants were divided into three groups based on the levels of GGT and ferritin: Group 1 including subjects with both GGT and ferritin lower than median values, Group 2 with only GGT or ferritin higher than median values, and Group 3 with both GGT and ferritin higher than median values. Differences of clinical and laboratory data among groups were calculated using one-way analysis of variance or Kruskal-Wallis rank-sum test. Odds ratios (ORs) for the metabolic syndrome and its components in Group 2 and Group 3 compared with Group 1 were analyzed by multiple logistic regressions. Statistical analysis was performed using SPSS (version 15.1; SPSS, Inc., Chicago, IL). value of less than 0.05 was considered to be statistically significant.

3. Results

3.1. Clinical and Laboratory Characteristics of Subjects

A total of 1288 individuals, aged 20–74 years, participated in this survey. 1024 individuals (84.0%), including 436 men and 588 women, were eligible subjects whose data proceeded to final analysis. Clinical and laboratory characteristics of the study participants are presented in Table 1. In total, 197 (19.2%) subjects were identified as having metabolic syndrome and 827 (80.8%) as not having metabolic syndrome according to the revised NCEP-ATP III criteria; 135 (13.2%) subjects were identified as having metabolic syndrome and 889 (86.8%) as not having metabolic syndrome according to the CDS criteria. In female participants, we identified 161 (27.4%) using the revised NCEP-ATP III definition and 79 (13.4%) using the CDS definition as having metabolic syndrome. The numbers and percentages of the metabolic syndrome in male subjects were 36 (8.3%) according to the revised NCEP-ATP III definition and 56 (12.8%) according to the CDS definition, respectively (Table 1). Serum GGT and ferritin levels were significantly higher in subjects with metabolic syndrome compared to those without metabolic syndrome in both genders. (Serum GGT: according to the revised NCEP-ATP III and CDS definitions in females; according the revised NCEP-ATP III definition and according the CDS definition in males. Serum ferritin: according to the revised NCEP-ATP III and CDS definitions in females; according the revised NCEP-ATP III definition and according the CDS definition in males.) In both genders, BMI, waist circumference, SP, DP, TG, 2h PG, and HOMA-IR were significantly higher in subjects with metabolic syndrome compared to those without (). FPG was significantly higher in the metabolic syndrome in female subjects () but not in males. There was no significant difference in HDL-C level in subjects with or without metabolic syndrome in females () (Table 1).

3.2. Association between GGT and Ferritin

Spearman correlation analysis showed that GGT was significantly correlated with ferritin (, ), and both of them were significantly correlated with gender (, for ferritin; , for GGT). Spearman correlation analysis confirmed that GGT was significantly correlated with ferritin in both genders (, for females; , for males). The multiple linear regression model was performed using ferritin/GGT as well as residence, age, TC, LDL-C, UA, UACR, education, income, regular recreational physical activity, heavy drinking, heavy smoking, HBsAg, anti-HCV, AST, and ALT as the independent variables and serum GGT/ferritin as the dependent variable. Stepwise linear regression analysis further confirmed that GGT was independently correlated with ferritin in both genders and showed different independent correlations in different genders (). In females, when GGT was used as dependent variable, the standard β was calculated as 0.156 (, ); when ferritin was used as dependent variable, the standard β was calculated as 0.150 (, ). In males, when GGT was used as dependent variable, the standard β was calculated as 0.205 (, ); when ferritin was used as dependent variable, the standard β was calculated as 0.170 (, ).

3.3. Clinical and Laboratory Characteristics of Subjects by GGT and Ferritin Levels

As described earlier, subjects in each gender were divided into three groups according to their serum levels of GGT and ferritin. The detailed clinical and laboratory findings by group and gender are presented in Table 2. Female subjects in Groups 2 and 3 exhibited higher BMI, waist circumference, SP, DP, 2h PG, TG, and HOMA-IR compared to Group 1, with the highest values in Group 3 (), and higher FPG in Group 3 compared with Group 1 (). Male subjects exhibited higher BMI, waist circumference, DP, and TG from Group 1 to Group 3 () and higher SP, FPG, 2h PG, HDL-C, and HOMA-IR in Group 3 compared with Group 1 ().

3.4. Risk of Metabolic Syndrome by GGT and Ferritin Levels

Multiple logistic regression tests showed that the risk of metabolic syndrome increased 3.7-fold (95% CI, 2.3–5.7; ) for Group 3 and 2.8-fold (95% CI, 1.8–4.4; ) for Group 2 compared to Group 1 according to the revised NCEP-ATP III criteria, and 9.6-fold (95% CI, 5.4–17.4; ) for Group 3 and 3.1-fold (95% CI, 1.6–5.7; ) for Group 2 compared to Group 1 according to the CDS criteria. After adjustment for gender, the risk of metabolic syndrome increased 6.1-fold (95% CI, 3.7–9.9; ) for Group 3 and 3.2-fold (95% CI, 2.0–5.1; ) for Group 2 compared to Group 1 according to the revised NCEP-ATP III criteria, and 10.7-fold (95% CI, 5.9–19.5; ) for Group 3 and 3.1-fold (95% CI, 1.7–5.8; ) for Group 2 compared to Group 1 according to the CDS criteria.

Multiple logistic regression analyses were conducted in both genders separately. The risk of metabolic syndrome increased 7.9-fold (95% CI, 4.6–13.5) according to the revised NCEP-ATP III criteria and 10.3-fold (95% CI, 5.0–21.5) according to the CDS criteria for Group 3 compared to Group 1 in female subjects (). This was independent of subjects’ residence, age, TC, LDL-C, UA, UACR, recreational physical activity, income, education, heavy drinking, heavy smoking, HBsAg, anti-HCV, ALT, or AST (OR [95% CI] 3.1 1.7–5.9, according to the NCEP-ATP III criteria; OR [95% CI] 3.5 1.6–8.2, according to the CDS criteria). However, the risk of metabolic syndrome did not significantly increase for Group 3 compared to Group 1 in male subjects () (Table 3).

3.5. Components of the Metabolic Syndrome Risks between Groups in Women

Given the strong association of GGT and ferritin levels with risk of metabolic syndrome in women indicated by our data, we went on to evaluate the likelihood of possessing each of the diagnostic components of the metabolic syndrome (as defined by NCEP-ATP III and CDS) for these groups in female subjects. Specifically, we assessed the association of GGT and ferritin with overweight or obesity, abdominal obesity, hypertriglyceridemia, hypertension, hyperglycemia, and insulin resistance. These results are presented in Table 4. The risk of possessing metabolic syndrome components was significantly higher overall in Group 3 compared with Group 1 (), although the risk of low HDL-C did not significantly increase in Group 3 () (Table 4). The statistical significance of these findings persisted even after adjustment for subjects’ residence, age, TC, LDL-C, UA, UACR, education, income, recreational physical activity, heavy drinking, heavy smoking, HBsAg, anti-HCV, AST, and ALT conditions () (Table 4).

4. Discussion and Conclusions

The Yi people are the seventh largest of the 55 ethnic minority groups officially recognized by the People’s Republic of China. They live primarily in rural areas of Southwest China, usually in mountainous regions. From the standpoint of conducting population-based studies, these particular demographic characteristics provided this study with the advantage of performing a detailed study within a relatively homogeneous group of people. This study showed, for the first time, the prevalence of the metabolic syndrome in a relatively large population of Liangshan Yi ethnic minority, out of a total population of 2.31 million.

Our study produced several important findings. First, in our study population, the prevalence of the metabolic syndrome was 197 (19.2%) in the overall population, 161 (27.4%) in female and 36 (8.3%) in male, based on the revised NCEP-ATP III criteria, while it was 135 (13.2%) in the overall population, 79 (13.4%) in female and 56 (12.8%) in male by the CDS definition. Second, serum GGT and ferritin concentrations were significantly higher in subjects with metabolic syndrome compared to those without metabolic syndrome in both genders. Third, serum GGT and ferritin were independently significantly correlated with each other in both genders. Finally, the risks of having metabolic syndrome and each of its diagnostic components (overweight or obesity, abdominal obesity, hypertriglyceridemia, hypertension, hyperglycemia, and insulin resistance) were significantly increased in those female subjects who had elevated GGT and ferritin levels. All these observations remained statistically significant after adjustment for possible confounders.

In clinical practice, an elevated serum GGT level is conventionally interpreted as a marker of alcohol abuse and liver dysfunction. It is still controversial whether elevated GGT or elevated ferritin is a cause or a consequence of the metabolic syndrome. A growing body of evidence suggests that GGT may serve as a predictor of type 2 diabetes and the metabolic syndrome [9–11]. Prospective studies have also found that increased serum ferritin is associated with the development of the metabolic syndrome [13, 14]. In our present study, serum GGT and ferritin were found to be significantly correlated with each other. Multiple regression analysis revealed that the risks of the metabolic syndrome and its components increased significantly in subjects with elevated levels of GGT and ferritin after adjustment for possible confounders, which further confirmed their synergistic associations with the metabolic syndrome and its constituent abnormalities.

From a mechanistic standpoint, GGT and ferritin are both recognized to be involved in oxidative stress, lipid peroxidation, and mitochondrial dysfunction. GGT is the principal enzyme that influences the extracellular hydrolysis of glutathione (GSH). Interestingly, ferritin plays an important role in the catalytic activities of GGT. The reactive products originating from GGT-mediated cleavage of GSH may cause the reduction of ferric iron to ferrous iron. Elevated levels of GGT and ferritin then result in increased production of reactive oxygen species (ROS), aggravating oxidative stress and leading to peroxidation of lipids by highly reactive free radicals. The adverse effects of ferritin overload and increased GGT mutually reinforce each other, ultimately leading to tissue injury [6–8, 18]. Our results are compatible with these findings, and the mechanisms need to be verified and further investigated.

Prior studies have identified regional and sexual variation in the demographics of metabolic syndrome [17, 19–21]. The causes of this observed sexual dimorphism in metabolic syndrome are not well understood. In our study, the significant association between GGT and ferritin and the metabolic syndrome was found in females but not in males. This difference might be attributed to the larger amount of alcohol consumption by males versus females (), which could affect GGT levels and distort the ability of GGT levels to reflect oxidative stress. The effect of alcohol consumption on insulin resistance and the metabolic syndrome is considered to be relative to the amount of alcohol intake and patterns and multiple other factors. Whether alcohol consumption is protective or is a risk factor for the metabolic syndrome and/or its components remains controversial in recent studies [22–25]. Furthermore, in this study, the percentage of individuals with the metabolic syndrome was higher in females than in male subjects (according to the revised NCEP ATP-III criteria; ), though the male population consumed larger amounts of alcohol overall. Further studies should be carried out to understand whether the sexual dimorphism disappears after controlling for the effect of alcohol consumption.

Interestingly, there were a higher proportion of female subjects with larger waist circumference than males in this cohort. This might explain why the prevalence of the metabolic syndrome (according to the revised NCEP-ATP III criteria) is much higher in females than in males. Also, the number of subjects with larger waist circumference was higher than those with larger BMI, especially in females, and this might be one of the reasons why the prevalence of the metabolic syndrome according to the revised NCEP ATP-III criteria was higher than the prevalence according to CDS criteria. Thus, it is important to note that the prevalence of the metabolic syndrome may vary in part due to different metabolic syndrome definitions being applied.

Since the incidence of the metabolic syndrome is increasing rapidly worldwide and carries with it high morbidity and mortality, finding predictive biomarkers may help to improve prevention, treatment, and prognosis for patients. The findings from our study suggest that utilization of the common laboratory values serum GGT and ferritin might be useful in clinical practice. In conclusion, this study showed that GGT and ferritin were significantly correlated with each other and increased in subjects with metabolic syndrome in both genders, while elevated levels of both GGT and ferritin were associated with increased risk of the metabolic syndrome only in females. Further mechanistic and clinical studies are needed to determine the potential use of GGT and ferritin as predictive biomarkers of the metabolic syndrome and its related diseases.

Disclaimer

The funders had no direct role in study design; in the collection, analysis, and interpretation of data; in the writing of the report; and in the decision to submit the paper for publication. The researchers are independent of researchers from funders.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

Acknowledgments

The authors acknowledge the residents and nurses of Department of Endocrinology of the First People’s Hospital of Liangshan Yi Autonomy Prefecture for their diligent work on collecting demographic data and blood samples. This study was supported by Chinese National Natural Science Foundation for the Youth (Grant 81100572), Health Department of Sichuan Province (Grant 100011), and Chengdu Health Bureau (Grant 0905).

References

K. G. M. M. Alberti and P. Z. Zimmet, “Definition, diagnosis and classification of diabetes mellitus and its complications. Part 1: diagnosis and classification of diabetes mellitus. Provisional report of a WHO consultation,” Diabetic Medicine, vol. 15, no. 7, pp. 539–553, 1998.
View at: Publisher Site | Google Scholar
J. I. Cleeman, “Executive summary of the third report of the National Cholesterol Education Program (NCEP) expert panel on detection, evaluation, and treatment of high blood cholesterol in adults (adult treatment panel III),” Journal of the American Medical Association, vol. 285, no. 19, pp. 2486–2497, 2001.
View at: Google Scholar
S. M. Grundy, J. I. Cleeman, S. R. Daniels et al., “Diagnosis and management of the metabolic syndrome: an American Heart Association/National Heart, Lung, and Blood Institute scientific statement,” Circulation, vol. 112, no. 17, pp. 2735–2752, 2005.
View at: Google Scholar
K. G. M. M. Alberti, P. Zimmet, and J. Shaw, “Metabolic syndrome—a new world-wide definition. A consensus statement from the International Diabetes Federation,” Diabetic Medicine, vol. 23, no. 5, pp. 469–480, 2006.
View at: Publisher Site | Google Scholar
Metabolic Syndrome Study Group of the Chinese Diabetes Society, “Metabolic syndrome: Chinese Diabetes Society consultation,” Chinese Journal of Diabetes, vol. 12, pp. 156–561, 2004 (Chinese).
View at: Google Scholar
O. Turgut and I. Tandogan, “Gamma-glutamyltransferase to determine cardiovascular risk: shifting the paradigm forward,” Journal of Atherosclerosis and Thrombosis, vol. 18, no. 3, pp. 177–181, 2011.
View at: Publisher Site | Google Scholar
M. Iciek, G. Chwatko, H. Rokita, E. Bald, and L. Włodek, “The effects of modulation of γ-glutamyl transpeptidase activity in HepG2 cells on thiol homeostasis and caspase-3-activity,” Biochimica et Biophysica Acta: Molecular Cell Research, vol. 1773, no. 2, pp. 201–208, 2007.
View at: Publisher Site | Google Scholar
R. Bataller-Sifré, V. Guiral-Olivan, and L. Bataller-Alberola, “New clinical and toxicological scenario of gammaglutamyltranspeptidase,” Revista Espanola de Enfermedades Digestivas, vol. 103, no. 11, pp. 586–590, 2011.
View at: Publisher Site | Google Scholar
P. André, B. Balkau, S. Vol, M. A. Charles, and E. Eschwège, “γ-glutamyltransferase activity and development of the metabolic syndrome (International Diabetes Federation Definition) in middle-aged men and women: data from the Epidemiological Study on the Insulin Resistance Syndrome (DESIR) cohort,” Diabetes Care, vol. 30, no. 9, pp. 2355–2361, 2007.
View at: Publisher Site | Google Scholar
S. K. Kunutsor, T. A. Apekey, and D. Seddoh, “Gamma glutamyltransferase and metabolic syndrome risk: a systematic review and dose-response meta-analysis,” International Journal of Clinical Practice, vol. 69, no. 1, pp. 136–144, 2015.
View at: Publisher Site | Google Scholar
G. Targher, “Elevated serum γ-glutamyltransferase activity is associated with increased risk of mortality, incident type 2 diabetes, cardiovascular events, chronic kidney disease and cancer—a narrative review,” Clinical Chemistry and Laboratory Medicine, vol. 48, no. 2, pp. 147–157, 2010.
View at: Publisher Site | Google Scholar
Y. Ren, H. Tian, X. Li, J. Liang, and G. Zhao, “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, vol. 27, no. 2, pp. 622–623, 2004.
View at: Publisher Site | Google Scholar
I. S. Vari, B. Balkau, A. Kettaneh et al., “Ferritin and transferrin are associated with metabolic syndrome abnormalities and their change over time in ageneral population: data from an Epidemiological Study on the Insulin Resistance Syndrome (DESIR),” Diabetes Care, vol. 30, no. 7, pp. 1795–1801, 2007.
View at: Publisher Site | Google Scholar
P. Hämäläinen, J. Saltevo, H. Kautiainen, P. Mäntyselkä, and M. Vanhala, “Serum ferritin levels and the development of metabolic syndrome and its components: a 6.5-year follow-up study,” Diabetology & Metabolic Syndrome, vol. 6, no. 1, article 114, 2014.
View at: Publisher Site | Google Scholar
T. Chen, Y. Ren, Y. Liu et al., “Serum gamma-glutamyl transferase, ferritin and the risk of type 2 diabetes in women from a Chinese minority,” Diabetes Research and Clinical Practice, vol. 90, no. 3, pp. 352–357, 2010.
View at: Publisher Site | Google Scholar
W. Yang, J. Lu, J. Weng et al., “Prevalence of diabetes among men and women in China,” The New England Journal of Medicine, vol. 362, no. 12, pp. 1090–1101, 2010.
View at: Publisher Site | Google Scholar
L. L. Han, Y. X. Wang, J. Li et al., “Gender differences in associations of serum ferritin and diabetes, metabolic syndrome, and obesity in the China Health and Nutrition Survey,” Molecular Nutrition & Food Research, vol. 58, no. 11, pp. 2189–2195, 2014.
View at: Publisher Site | Google Scholar
D.-H. Lee, R. Blomhoff, and D. R. Jacobs, “Is serum gamma glutamyltransferase a marker of oxidative stress?” Free Radical Research, vol. 38, no. 6, pp. 535–539, 2004.
View at: Publisher Site | Google Scholar
W. H. H. Sheu, Y. T. Chen, W. J. Lee, C. W. Wang, and L. Y. Lin, “A relationship between serum ferritin and the insulin resistance syndrome is present in non-diabetic women but not in non-diabetic men,” Clinical Endocrinology, vol. 58, no. 3, pp. 380–385, 2003.
View at: Publisher Site | Google Scholar
N. M. Pham, A. Nanri, S. Yi et al., “Serum ferritin is associated with markers of insulin resistance in Japanese men but not in women,” Metabolism, vol. 62, no. 4, pp. 561–567, 2013.
View at: Publisher Site | Google Scholar
S. Ryu, Y. Chang, H. Y. Woo et al., “Longitudinal increase in γ-glutamyltransferase within the reference interval predicts metabolic syndrome in middle-aged Korean men,” Metabolism, vol. 59, no. 5, pp. 683–689, 2010.
View at: Publisher Site | Google Scholar
M. Stoutenberg, D.-C. Lee, X. Sui et al., “Prospective study of alcohol consumption and the incidence of the metabolic syndrome in US men,” British Journal of Nutrition, vol. 110, no. 5, pp. 901–910, 2013.
View at: Publisher Site | Google Scholar
J. R. Churilla, T. M. Johnson, R. Curls et al., “Association between alcohol consumption patterns and metabolic syndrome,” Diabetes & Metabolic Syndrome, vol. 8, no. 2, pp. 119–123, 2014.
View at: Publisher Site | Google Scholar
H. Im, S. Park, J. Choi, and E. Choi, “Binge drinking and its relation to metabolic syndrome in korean adult men,” Korean Journal of Family Medicine, vol. 35, no. 4, pp. 173–181, 2014.
View at: Publisher Site | Google Scholar
I. Wakabayashi, “Frequency of heavy alcohol drinking and risk of metabolic syndrome in middle-aged men,” Alcoholism: Clinical and Experimental Research, vol. 38, no. 6, pp. 1689–1696, 2014.
View at: Publisher Site | Google Scholar

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Copyright © 2015 Dong Wei et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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