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Effects of exercise training on Fetuin-a in obese, type 2 diabetes and cardiovascular disease in adults and elderly: a systematic review and Meta-analysis



Elevated levels of fetuin-A are associated with increased risks of metabolic syndrome, type 2 diabetes and nonalcoholic fatty liver disease. This meta-analysis investigated whether exercise interventions can reduce fetuin-A in adults.


We searched clinical trials that objectively assessed fetuin-A and included study arms with exercise intervention. The pre-intervention and post-intervention data were used for meta-analysis. The effect sizes were calculated as standardized mean differences or changes in fetuin-A and expressed as Hedges’ g using random-effects models.


The overall Hedges’ g for fetuin-A in all included interventions was − 0.640 (95%CI − 1.129 to − 0.151; n = 9), but this effect was not observed in obese (g = − 0.096; 95%CI, − 0.328 to 0.135) and type 2 diabetes/dysglycemia (g = − 0.56; 95%CI, − 1.348 to 0.236) individuals. Additionally, the random-effects meta-regression analysis showed that there was not a greater decrease in fetuin-A in individuals who achieved greater body mass index reductions (regression coefficient = 0.065; 95%CI, − 0.185 to 0.315).


Supervised exercise is associated with reductions in fetuin-A levels in adults and elderly. However, the results of the present meta-analysis should be interpreted with caution because of the variety of type of exercises and individual obesity related-disorders involve. Therefore, additional high-quality randomized controlled trials describing the effect of supervised exercise interventions on fetuin-A in adults are still needed. 


Human fetuin-A (formerly named α2-Heremans-Schmid glycoprotein) is a 64-kDa glycoprotein that is found in relatively high concentrations in serum (300–1000 μg/ml) [1]. Fetuin-A is mainly expressed and secreted from the liver and adipose tissue [2]. Recent studies suggest that the liver may control whole-body energy homeostasis through the regulation of glucose and lipid metabolism by the secretion of fetuin-A [3, 4]. For example, in an animal model of diet-induced obesity that is commonly associated with hepatic steatosis, an increase in fetuin-A mRNA expression was observed in the liver [4]. Cross-sectional [5, 6] and large cohort studies [7, 8] have demonstrated consistently that elevated fetuin-A levels are associated with increased risks of subclinical and clinical cardiovascular disease (CVD).

Circulating levels of fetuin-A are increased in obesity and related disorders such as the metabolic syndrome, type 2 diabetes, and myocardial infarction/stroke [9,10,11,12]. Fetuin A stimulates the production of pro-inflammatory cytokines from adipocytes and macrophages [13] and acts as an endogenous ligand for Toll-like receptor 4, which enables free fatty acids to activate Toll-like receptor 4 signaling to induce insulin resistance [14]. Moreover, fetuin-A levels is also associated with type 2 diabetes risk [9] due to been shown to inhibit skeletal muscle insulin receptor tyrosine phosphorylation and reduce Akt activity, which in turn, contributes to decreased peripheral glucose uptake [15]. Interestingly, this liver-derived protein is also associated with fatty liver and correlates with non-alcoholic fatty liver disease (NAFLD) in humans [16].

Recent research studies have investigated the mechanisms that underlie the relationship between fetuin-A and subclinical-clinical CVD-related complications [17, 18]. Trepanowski et al. reported fetuin-A is involved in the mechanism regulating the insulin downstream signaling pathway and acts as an inhibitor of insulin resistance in muscle, liver and fat [11]. Fetuin-knockout mice exhibit improved glucose and insulin tolerance and are resistant to high-fat diet-induced weight gain [19]. Although the regulation of fetuin-A synthesis is not completely understood, its strong association within metabolic diseases has made it an attractive target for the development of novel research approaches related to metabolic health, such as insulin sensitivity, glucose tolerance or circulating lipid level treatments.

In particular, fetuin-A is the contributor which plays a critical role in the impairment of two metabolic sensors, Sirtuin 1 and AMP-activated protein kinase, in inflamed adipocytes of high fat diet mice [20]. Several studies was proposed that increased circulating fetuin-A in humans after a chronic exercise program may promote increased weight loss and improved metabolic control through elevation of adiponectin expression [20] and decrease of inflammatory cytokines in the liver and muscle [21] via fetuin-A inhibition through the AMP-activated protein kinase-nuclear factor kappa-light-chain-enhancer of activated B cells pathway [4]. Furthermore, fetuin-A directly correlated with two cardiometabolic risk markers, Apo B and C-reactive protein that, together with insulin resistance, are important components of the metabolic syndrome. This hypothesis seemed plausible, as studies demonstrated fetuin-A lowered expression of stimulated oxygen consumption and had an inverse association with blood postprandial insulin, c-peptide, and lipid peroxidation levels [21] and a positive association with adiponectin concentrations [22].

The exact role of exercise in regulating circulating fetuin-A concentration remains to be fully established. As a possible biological link between physical exercise and fetuin-A levels, cardiorespiratory fitness and muscular strength are inversely associated with liver fat and abdominal obesity [23, 24], and fetuin-A is associated with liver fat accumulation in humans [25]. A few studies have assessed the effects of lifestyle interventions such as hypocaloric diets [26] physical exercise [27, 28] or combined interventions [29] on fetuin-A, showing contradictory results. Some biological alterations promoting the protective effects of exercise on insulin sensitivity may be explained by changes in circulating fetuin-A and free fatty acids, supporting less toll-like receptor 4 signaling in adipose tissue perhaps by modulating adipose tissue macrophages [30]. In general, results on the effects of exercise on circulating fetuin-A have been rather ambiguous; diverse exercise amount and intensity within interventions may explain the highly discrepant results thus far.

In 2015, Trepanowski et al. [31] published the first comprehensive review to exclusively focus on the relationship between fetuin-A and obesity. To the best of the investigative team’s knowledge, no systematic review, with or without meta-analysis, has analyzed the effects of exercise on fetuin-A levels in humans. Hence, the present work was undertaken [31]. Due to heterogeneity between studies in terms of results, we used a meta-analytic approach to determine the effectiveness of supervised exercise interventions on fetuin-A in adults.


Protocol and registration

The study was undertaken in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) statement [32]. The review was registered with PROSPERO (CRD42017073872) at the University of York, UK. However, no study protocol was published before the initiation of the meta-analysis. All analyses were based on aggregate data from previously published studies, and thus, no ethical approval was required.

Eligibility criteria

The a priori inclusion criteria for this study were as follows: (1) adults aged 18 years old; (2) interventions of physical exercise without hypocaloric diet intervention; and (3) assessment of serum fetuin-A.

Information sources

A search of the literature was performed using the electronic databases Cochrane Central Register of Controlled Trials (CENTRAL), EMBASE, and MEDLINE (all: from 1998 until 15 November 2017). The terms used were as follows: [‘Fetuin-A and ‘alpha2hsglycoprotein’ OR], [‘Exercise’ and ‘training’ and ‘physical activity’ and ‘sport’ OR].


Two researchers (AG-H and RR-V) independently carried out the search. As an example, the search strategy in MEDLINE database was as follows: “Fetuin-A and alpha2hsglycoprotein” AND “metabolic risk” OR “cardiometabolic risk” OR “type 2 diabetes” “metabolic syndrome” OR “obesity”) AND (“exercise” OR “physical activity” OR “exercise intervention” OR “training”) AND (“intervention” OR “program” OR “trial” OR “treatment” OR “pre-post study”). Additionally, the reference lists of retrieved studies were examined to identify other articles. Studies reported in languages other than English were not explored.

Study selection

Two authors (AG-H and RR-V) independently screened the titles and abstracts of potentially eligible studies identified by the search strategy. If necessary, a third researcher (MI) was consulted. The bibliographic management software EndNote version X7.0 for Windows was used for all searches. Any differences between the two authors were discussed and, if necessary, the third author was referred to for arbitration. Reasons for exclusion of identified articles were recorded in all cases.

Data collection process and data items

Two researchers (AG-H and RR-V) independently abstracted all data. For each study, data were extracted regarding the first author’s last name, year of publication, characteristics of the subjects, exercise programs (type, frequency, duration, intensity, etc.), assessment of fetuin-A, sample size, and mean values with corresponding standard deviations of fetuin-A and BMI (pre- and post-test). The reviewers created a study-specific database in Excel (Microsoft Corp., USA) for data collection. Any differences between the two authors were discussed and, if necessary, the third author was referred to for arbitration.

Risk of bias of individual studies

The methodological quality of non-RCT studies and studies without a control group was assessed using the Quality Assessment Tool for Quantitative Studies of the Effective Public Health Practice Project (EPHPP) [33]. This tool is used to evaluate a variety of intervention study designs, such as non-RCT or pre-post studies [33]. EPHPP assesses study quality in six domains: selection bias, study design, confounders, blinding, data collection method, and withdrawals/dropouts. Each study was assessed for quality by 2 reviewers (AG-H and RR-V), and any discrepancy in the final grade was resolved through group discussion or discussion among the primary authors.

Summary measures

All analyses were carried out using Comprehensive Meta-analysis Software (second version, Biostat, Englewood, NJ, USA) to calculate the standardized mean difference and expressed as Hedges’ g to correct for possible small-sample bias [34]. For studies that were randomized and non-randomized controlled trials, the Hedges’ g was calculated taking the change outcome difference between the exercise and control groups and then dividing that difference by the pooled standard deviation of the change outcome difference. For single group studies, the Hedges’ g value of the fetuin-A was calculated by the mean pre- to post-intervention in each study (i.e., in all cases the pre-intervention and the post-intervention data were used to meta-analyze), dividing the result by the pooled standard deviation, and correcting for small sample bias. We used the continuous random-effect analysis with the DerSimonian-Laird method to pool results. For studies where means and standard deviations were not reported and could not be obtained from the authors, we transformed dichotomous data into the standardized mean difference using the formulas implemented in Comprehensive Meta-analysis [35] or used other statistics, such as t-values or exact p-values to calculate the standardized mean difference. In the cumulative meta-analysis, outcome data for fetuin-A from all available studies were included sequentially according to the year in which they first became available.

Synthesis of results

Heterogeneity between trial results was tested with Cochran’s Q test [34] and the I2 statistic. I2 values of < 25%, 25–50, and > 50% are considered to represent small, medium, and large amounts of inconsistency [36]. Each study was deleted from the model once to analyze its influence on the overall results.

Risk of bias across studies

Small-study effects was assessed in two ways: 1) visual inspection of the asymmetry of the funnel plot and Egger’s test of the intercept to test the symmetry of the funnel plot [37].

Additional analysis

Subgroup analyses were conducted to determine whether fetuin-A differed according to population characteristics by stratifying the meta-analyses by each of these factors (i.e., healthy, type 2 diabetes/dysglycemia and obese) using the random-effect model. Additionally, random-effects meta-regression analyses were used to evaluate whether the results differed with BMI changes (as Hedges’ g) [38]. The effect of individual studies on the pooled Hedges’ g was assessed with influence analysis, in which the analysis was repeated omitting one study at a time, to establish the contribution of each study to the effect size.

Patient involvement

Due to the nature of the study, no participants were involved in the systematic review and meta-analysis. Furthermore, no patients were involved in the development of the research question or outcome measures, nor were they involved in the design, implementation, recruitment, or conduct of the study. Finally, no patients were asked to advise on the interpretation or writing up of the results. There are no plans to disseminate the results of the research to the study participants.


Study selection

A total of 189 studies were identified through the database search. The titles and abstracts of the returned articles were examined for suitability, leading to the retrieval of 23 full texts. Of those 13, 4 were rejected—3 because of the type of intervention criterion (interventions with hypocaloric diet), and one because of the population issues (adolescents). Nine trials met the inclusion criteria and were included in the meta-analysis [5, 21, 27,28,29,30, 39,40,41]. A flow diagram summarizing the study selection process of the systematic review and meta-analysis is shown in Fig. 1. Exclusion criteria and the list of excluded articles are in online Additional file 1.

Fig. 1

Flow chart for the identification of the meta-analyses included in the study

The characteristics of the nine studies included in the systematic review sorted by study design are available in Table 1. All studies were single-group pre-post design except two randomized controlled trials [40, 41] and one a randomized trial without a control group [21]. A total of 163 individuals were included in the meta-analysis. Two studies included only women [29, 39], one included only men [30], and five included mixed samples of men and women [5, 21, 27, 28, 40, 41] who were relative healthy [30], were obese [21, 27,28,29, 39], suffered from nonalcoholic fatty liver disease [21, 28], or had type 2 diabetes/dysglycemia or were undergoing hemodialysis [5, 30, 41].

Table 1 Characteristics of the included trials

Relative to exercise programs, all studies used aerobic exercise except two that used a combined aerobic plus resistance exercise protocol (concurrent exercise) [29, 30]. Overall, the programs mainly used treadmill walking/running, cycle ergometer cycling and whole-body resistance training. The study durations ranged from one to 16 weeks, and the training frequency ranged from three to seven times weekly with 40–70 min session duration. All exercise interventions were supervised.

Measurement of fetuin-a

All studies measured fetuin-A using enzyme-linked immunosorbent assays (ELISA) according to the manufacturer’s protocols.

Risk of bias within studies

Only three trials had random allocation between groups [21, 40, 41]. All studies provided points and estimates of variability. Blinding of the participants and therapists was not possible because of the nature of the interventions. The studies’ “bias” score ranged from two to four with a mean total score of 2.62.

Synthesis of results

Overall, supervised exercise training was associated with a significant reduction in the random-effects models (g = − 0.640; 95% CI, − 1.129 to − 0.151; p = 0.010) with high heterogeneity (I2 = 87.60%) (Fig. 2).

Fig. 2

Forest plot for changes in fetuin-A. The black horizontal lines represent the 95% confidence intervals while the squares represent the Hedge’s g estimate. The first red diamond represents the overall point estimate and 95% confidence intervals from all individual studies included in each meta-analysis. All analyses are based on the random-effects model. RCT, randomized controlled trial

Risk of bias across studies

Small-study effects by means of visual inspection of funnel plots was evaluated and the Egger’s regression asymmetry test. As shown in Fig. 3, the funnel plot was symmetrical and Egger’s linear regression tests provided no evidence for existence of small-study effects (Egger regression intercept, − 4.42 [95% CI, − 8.44 to 0.11, p = 0.052]).

Fig. 3

Funnel plot of precision by difference in means (Hedge’s g). Circles represent the Hedge’s g for each study and the diamond represents pooled Hedge’s g

Additional analysis

Regarding subgroup analysis, in obese individuals, physical exercise favored a reduction in fetuin-A the overall same effect was not observed in individuals with obesity (g = − 0.096; 95%CI, − 0.328 to 0.135; p = 0.415; I2 = 29.04%) and type 2 diabetes/dysglycemia (g = − 1.698; 95% CI, − 3.570 to 0.174; p = 0.075; I2 = 94.24%). The independent effects of potential moderating variables were examined using meta-regression and are presented in Fig. 4. The meta-regression analysis shows that there was not a greater decrease in fetuin-A in individuals who achieved greater BMI changes. The slope regression coefficient was 0.065 [95% CI, − 0.185 to 0.315] and was not significant (p = 0.609).

Fig. 4

Meta-regression analysis of changes in body mass index (BMI) (X axis) against the Hedges’s g fetuin-A levels (Y axis)

Finally, the influence analysis showed that no particular trial affected the pooled effect size (Fig. 5).

Fig. 5

Influence analysis. RCT, randomized controlled trial


To our knowledge, this is the first systematic review and meta-analytic approach assessing the effects of supervised exercise training on fetuin-A in adults. The main findings of our study are as follows: (i) supervised exercise interventions is associated with reductions in fetuin-A in adults and older participants; (ii) both aerobic and resistance exercise at vigorous or moderate intensity, with a volume of 60 min/session and a minimum frequency of 4 to 7 sessions/week, significantly reduced fetuin-A levels in dysglycemic and overweight/obese individuals; and (iii) greater BMI reductions after the supervised exercise intervention are not associated with greater reductions in fetuin-A. These findings could help to provide more specific exercise recommendations for cardiometabolic risk factor management in the adult population. However, due to population heterogeneity and the high risk of bias, our findings should be interpreted with caution.

Our results show that supervised exercise training alone is associated with reductions in fetuin-A levels in adults. This finding is consistent with recently published systematic reviews and meta-analyses showing that exercise significantly modulates adipokine levels, inflammatory cytokine and glycemic control in youths [42] and patients with type 2 diabetes [30]. Jenkins et al. [43] have suggested an inverse correlation between cardiorespiratory fitness and fetuin-A, which would suggest that physical fitness level may regulate to some degree fetuin-A concentrations. However, in contrast with this conclusion, Malin et al., [27] showed that exercise-induced changes in fetuin-A were not associated with cardiorespiratory fitness in healthy adults. Two other narrative reviews [31, 44] also suggested that exercise alone might improve adipokine levels, such as fetuin-A. Our results show that supervised exercise training on fetuin-A was statistically significant when comparing post vs. pre-intervention values with large heterogeneity (I2 = 87.60%), even though some of the studies showed no changes after the exercise intervention. However, these results should be treated with caution given the limited number of studies included in our analysis. The differences between the results observed in the analyses examining the effect of exercise could be due to the large heterogeneity and lack of comparison with control groups. Also, these discrepancies can likely be explained by the wide range of characteristics of the participants (> 50 years old, diseases, etc.), study duration, intervention exercise program (i.e., cycling, treadmill and/or elliptical, weight machines), and extent of change in body composition across these studies.

Fetuin-A may attenuate lipogenesis and accelerate lipolysis in adipocytes, thereby promoting obesity and insulin resistance [31]. Regarding both diseases and according to subgroup analysis (individuals with type 2 diabetes/dysglycemia or obese individuals), we found no evidence to support that supervised exercise was associated with a reduction in serum fetuin-A levels. Stefan and associates conducted a study involving a complex lifestyle intervention program including dietary counseling and increased physical activity and found different results. They reported body weight decreased by ~ 3.2 kg, liver fat by 34%, and energy and, in particular, saturated fat intake by 7 and 11%, respectively, and fetuin-A levels decreased over an ~ 9-month period in subjects with a high risk for type 2 diabetes [45]. Recently, another randomized trial in obese adults confirm our findings and did not detect significant reductions in fetuin-A after applied two different exercise programs at moderate and high intensity [21]. Therefore, it is unclear whether these divergent findings are attributable to differences in the duration and intensity of the intervention, in health status, in the timing of fetuin-A measurement (e.g., within 24 h versus 36–48 h after the last exercise session), or in the sex of the participants; however, there is some evidence that relationships between fetuin-A levels and “outcomes” vs. “status” exist [45]. Reduced fetuin-A in response to intervention is often associated with improvement in insulin-related parameters [46], which was confirmed in all of the studies showing decreases in this hepatokine. For example, the study published by Lee et al. [30] demonstrated that changes in circulating fetuin-A might predict some of the benefits seen on insulin sensitivity after long-term exercise. Another study in older obese subjects also reveals that lower fetuin-A after exercise correlated with lower hepatic insulin resistance [27]. These authors suggest that fetuin-A down regulates glucose transporter-4 translocation and contributes to the improvement in skeletal muscle glucose disposal after exercise.

The meta-regression analyses showed that there was not a greater decrease in fetuin-A in individuals who achieved greater BMI changes. These findings are partly in accordance with those reported in adults with different health statuses. For example, six weeks of supervised aerobic exercise showed modest changes in body composition without affecting serum fetuin-A levels in obese older women [39]; however, 12 weeks of aerobic-exercise with significant weight loss did reduce plasma fetuin-A levels in a study of obese older men and women [28]. Additionally, a recent review suggests that weight loss seems to be effective for reducing fetuin-A level, which is not consistent with our findings [31]. Some previous studies suggest that dietary changes and weight loss [47] as well as pharmacological treatment with thiazolidinediones [5] or metformin [48] might be more potent factors than aerobic exercise alone in the regulation of hepatic fetuin-A release. Hennige et al. [49] also suggested that fetuin-A induces low-grade inflammation and represses adiponectin production in animals and in humans. Collectively, it appears likely that hepatic fat content and thus serum fetuin-A levels respond to changes in energy balance rather than to changes in body composition [39]. These data suggest an important role of fatty liver in the pathophysiology of insulin resistance and atherosclerosis. In this context, the decrease in fetuin-A observed in the present study, along with changes in BMI, could be interpreted as overall beneficial to reduce CVD risk through supervised exercise training in humans. Nonetheless, the disparate findings suggest more research and comprehensive studies of changes in fetuin-A levels as a function of exercise interventions and body composition change appears necessary.

The current meta-analytic approach was not designed to establish the exact mechanism responsible for exercise reducing fetuin-A in humans, but our data indicate that exercise is associated with lower fetuin-A, as suggested previously by others [45]. The plausible mechanisms by which supervised exercise lowers fetuin-A include the following: (i) reducing intrahepatic fat content by down-regulating sterol regulatory element-binding protein-1c and up-regulating peroxisome proliferator-activated receptor γ expression levels [50]; (ii) decreasing hepatic glucolipotoxicity through modulating the reactive oxygen species, along with inhibition of proinflammatory mediators [51]; and (iii) activating protein kinase B (also known as Akt) and Akt substrate of 160 kDa (AS160) phosphorylation, which itself has been shown to improve glucose tolerance and decrease insulin resistance [52].

The current study has several limitations. First, we included both randomized controlled trials and clinical trials, which introduced some risk of bias [53]. Second, there is a high degree of heterogeneity among the analyzed studies, in part due to the differences in inclusion criteria, health status, and the type, intensity, and duration of the supervised-exercise interventions within individual studies. Third, meta-analysis and meta-regression analyses included a reduced number of studies, some of them with small sample sizes and control groups (no intervention). A high risk of bias (i.e., quality of the studies) could be considered another limitation. Fourth, since this was an aggregate data meta-analysis, the potential for ecological fallacy exists. Fifth, since studies are not randomly assigned to covariates in meta- analysis, they are considered to be observational in nature.

Consequently, the results of subgroup and meta-regression analyses conducted in our meta-analysis do not support causal inferences and should hence be viewed as association. Large, well- designed randomized controlled trials are needed to address this issue adequately. Given the former, future randomized controlled trials may want to address some of the differences and associations observed in our current meta-analysis. In the same line, future RCT studies would need to account for baseline levels, change in other cardiometabolic traits in addition to change in BMI, and effect of medication status, alcohol and smoking patterns, and diet patterns throughout the study period. Finally, since we ran a number of analyses, some of our findings could have been nothing more than chance occurrence. Therefore, the results should be taken with caution, and more research on the effect of exercise interventions is needed to reinforce the current recommendation on exercise in the regulation of hepatic fetuin-A in humans.


This meta-analysis shows that supervised exercise alone is associated with reductions in fetuin-A levels in adults and older participants. However, high quality randomized controlled trials describing the effects of supervised exercise interventions on fetuin-A in adults are few. Here in we have identify important components for future research that should be addressed as well as the limitations found in reviewing the studies for our analysis. By doing so, we hope to advance this area of research and aid in the answering of questions on exercise, hepatokines, and health, an area that is growing in interest and importance.



Beats per minute


Cardiovascular disease


Effective Public Health Practice Project


Maximum heart rate


Preferred Reporting Items for Systematic Reviews and Meta-Analyses


Randomized controlled trial


  1. 1.

    Pedersen KO. Fetuin, a new globulin isolated from serum. Nature. 1944;154(3914):575.

    CAS  Article  Google Scholar 

  2. 2.

    Mori K, Emoto M, Inaba M. Fetuin-A: a multifunctional protein. Recent Pat Endocr Metab Immune Drug Discov. 2011;5(2):124–46.

    CAS  Article  Google Scholar 

  3. 3.

    Iroz A, Couty J-P, Postic C. Hepatokines: unlocking the multi-organ network in metabolic diseases. Diabetologia. 2015;58(8):1699–703.

    CAS  Article  Google Scholar 

  4. 4.

    Jung TW, Youn B-S, Choi HY, Lee SY, Hong HC, Yang SJ, et al. Salsalate and adiponectin ameliorate hepatic steatosis by inhibition of the hepatokine fetuin-a. Biochem Pharmacol. 2013;86(7):960–9.

    CAS  Article  Google Scholar 

  5. 5.

    Mori K, Emoto M, Araki T, Yokoyama H, Lee E, Teramura M, et al. Effects of pioglitazone on serum fetuin-a levels in patients with type 2 diabetes mellitus. Metabolism. 2008;57(9):1248–52.

    CAS  Article  Google Scholar 

  6. 6.

    Sun Q, Cornelis MC, Manson JE, Hu FB. Plasma levels of fetuin-a and hepatic enzymes and risk of type 2 diabetes in women in the US. Diabetes. 2013;62(1):49–55.

    CAS  Article  Google Scholar 

  7. 7.

    Laugsand LE, Ix JH, Bartz TM, Djousse L, Kizer JR, Tracy RP, et al. Fetuin-a and risk of coronary heart disease: a Mendelian randomization analysis and a pooled analysis of AHSG genetic variants in 7 prospective studies. Atherosclerosis. 2015;243(1):44–52.

    CAS  Article  Google Scholar 

  8. 8.

    Aroner SA, St-Jules DE, Mukamal KJ, Katz R, Shlipak MG, Criqui MH, et al. Fetuin-a, glycemic status, and risk of cardiovascular disease: the multi-ethnic study of atherosclerosis. Atherosclerosis. 2016;248:224–9.

    CAS  Article  Google Scholar 

  9. 9.

    Laughlin GA, Barrett-Connor E, Cummins KM, Daniels LB, Wassel CL, Ix JH. The Sex-specific association of fetuin-a with type 2 diabetes in older community-dwelling adults: the rancho Bernardo study. Diabetes Care. 2013;36(7):1994–2000.

  10. 10.

    Ix JH, Shlipak MG, Brandenburg VM, Ali S, Ketteler M, Whooley MA. Association between human fetuin-a and the metabolic syndrome: data from the heart and soul study. Circulation. 2006;113(14):1760–7.

    CAS  Article  Google Scholar 

  11. 11.

    Temesszentandrási G, Vörös K, Böröcz Z, Kaszás E, Prohászka Z, Falus A, et al. Association of human fetuin-a rs4917 polymorphism with obesity in 2 cohorts. J Investig Med. 2015;63(3):548–53.

    Article  Google Scholar 

  12. 12.

    Weikert C, Stefan N, Schulze MB, Pischon T, Berger K, Joost H-G, et al. Plasma fetuin-a levels and the risk of myocardial infarction and ischemic stroke. Circulation. 2008;118(24):2555–62.

    CAS  Article  Google Scholar 

  13. 13.

    Mukhopadhyay S, Bhattacharya S. Plasma fetuin-a triggers inflammatory changes in macrophages and adipocytes by acting as an adaptor protein between NEFA and TLR-4. Diabetologia. 2016;59(4):859–60.

    Article  Google Scholar 

  14. 14.

    Pal D, Dasgupta S, Kundu R, Maitra S, Das G, Mukhopadhyay S, et al. Fetuin-a acts as an endogenous ligand of TLR4 to promote lipid-induced insulin resistance. Nature Med. 2012;18(8):1279–85.

  15. 15.

    Mathews ST, Rakhade S, Zhou X, Parker GC, Coscina DV, Grunberger G. Fetuin-null mice are protected against obesity and insulin resistance associated with aging. Biochem Biophys Res Commun. 2006;350(2):437–43.

    CAS  Article  Google Scholar 

  16. 16.

    Ou H-Y, Yang Y-C, Wu H-T, Wu J-S, Lu F-H, Chang C-J. Increased fetuin-a concentrations in impaired glucose tolerance with or without nonalcoholic fatty liver disease, but not impaired fasting glucose. J Clin Endocrinol Metab. 2012;97(12):4717–23.

    CAS  Article  Google Scholar 

  17. 17.

    Jung TW, Yoo HJ, Choi KM. Implication of hepatokines in metabolic disorders and cardiovascular diseases. BBA Clin. 2016;5:108–13.

    Article  Google Scholar 

  18. 18.

    Mori K, Emoto M, Inaba M. Fetuin-A and The cardiovascular system. Adv Clin Chem. 2012;56:175–95.

  19. 19.

    Oh K-J, Lee D, Kim W, Han B, Lee S, Bae K-H. Metabolic adaptation in obesity and type II diabetes: myokines, adipokines and hepatokines. Int J Mol Sci. 2016;18(1).

  20. 20.

    Chattopadhyay M, Mukherjee S, Chatterjee SK, Chattopadhyay D, Das S, Majumdar SS, et al. Impairment of energy sensors, SIRT1 and AMPK, in lipid induced inflamed adipocyte is regulated by Fetuin a. Cell Signal. 2018;42:67–76.

    CAS  Article  Google Scholar 

  21. 21.

    Winn NC, Liu Y, Rector RS, Parks EJ, Ibdah JA, Kanaley JA. Energy-matched moderate and high intensity exercise training improves nonalcoholic fatty liver disease risk independent of changes in body mass or abdominal adiposity—a randomized trial. Metabolism. 2017;78:128–40.

    Article  Google Scholar 

  22. 22.

    Blumenthal JB, Gitterman A, Ryan AS, Prior SJ. Effects of exercise training and weight loss on plasma Fetuin-a levels and insulin sensitivity in overweight older men. J Diabetes Res. 2017;2017:1492581.

  23. 23.

    Church TS, Kuk JL, Ross R, Priest EL, Biltoff E, Blair SN. Association of cardiorespiratory fitness, body mass index, and waist circumference to nonalcoholic fatty liver disease. Gastroenterology. 2006;130(7):2023–30.

    CAS  Article  Google Scholar 

  24. 24.

    Pietiläinen KH, Kaprio J, Borg P, Plasqui G, Yki-Järvinen H, Kujala UM, et al. Physical inactivity and obesity: a vicious circle. Obesity. 2008;16(2):409–14.

    Article  Google Scholar 

  25. 25.

    Stefan N, Kantartzis K, Häring H-U. Causes and metabolic consequences of fatty liver. Endocr Rev. 2008;29(7):939–60.

    CAS  Article  Google Scholar 

  26. 26.

    König D, Zdzieblik D, Deibert P, Berg A, Gollhofer A, Büchert M. Internal fat and cardiometabolic risk factors following a meal-replacement regimen vs. comprehensive lifestyle changes in obese subjects. Nutrients. 2015;7(12):9825–33.

    Article  Google Scholar 

  27. 27.

    Malin SK, Del Rincon JP, Huang H, Kirwan JP. Exercise-induced lowering of fetuin-a may increase hepatic insulin sensitivity. Med Sci Sports Exerc. 2014;46(11):2085–90.

  28. 28.

    Malin SK, Mulya A, Fealy CE, Haus JM, Pagadala MR, Scelsi AR, et al. Fetuin-a is linked to improved glucose tolerance after short-term exercise training in nonalcoholic fatty liver disease. J Appl Physiol. 2013;115(7):988–94.

    CAS  Article  Google Scholar 

  29. 29.

    Yang SJ, Hong HC, Choi HY, Yoo HJ, Cho GJ, Hwang TG, et al. Effects of a three-month combined exercise programme on fibroblast growth factor 21 and fetuin-a levels and arterial stiffness in obese women. Clin Endocrinol. 2011;75(4):464–9.

    CAS  Article  Google Scholar 

  30. 30.

    Lee S, Norheim F, Gulseth HL, Langleite TM, Kolnes KJ, Tangen DS, et al. Interaction between plasma fetuin-a and free fatty acids predicts changes in insulin sensitivity in response to long-term exercise. Physiol Rep. 2017;5(5).

  31. 31.

    Trepanowski J, Mey J, Varady K. Fetuin-a: a novel link between obesity and related complications. Int J Obes. 2015;39(5):734–41.

  32. 32.

    Liberati A, Altman DG, Tetzlaff J, Mulrow C, Gøtzsche PC, Ioannidis JP, et al. The PRISMA statement for reporting systematic reviews and meta-analyses of studies that evaluate health care interventions: explanation and elaboration. PLoS Med. 2009;6(7):e1000100.

    Article  Google Scholar 

  33. 33.

    Armijo-Olivo S, Stiles CR, Hagen NA, Biondo PD, Cummings GG. Assessment of study quality for systematic reviews: a comparison of the Cochrane collaboration risk of Bias tool and the effective public health practice project quality assessment tool: methodological research. J Eval Clin Pract. 2012;18(1):12–8.

    Article  Google Scholar 

  34. 34.

    Higgins JP, Thompson SG, Deeks JJ, Altman DG. Measuring inconsistency in meta-analyses. BMJ. 2003;327(7414):557.

    Article  Google Scholar 

  35. 35.

    Borenstein M, Hedges LV, Higgins JP, Rothstein HR. A basic introduction to fixed-effect and random-effects models for meta-analysis. Res Synth Methods. 2010;1(2):97–111.  

  36. 36.

    Higgins JP, Thompson SG. Quantifying heterogeneity in a meta-analysis. Stat Med. 2002;21(11):1539–58.

    Article  Google Scholar 

  37. 37.

    Egger M, Smith GD, Schneider M, Minder C. Bias in meta-analysis detected by a simple, graphical test. BMJ. 1997;315(7109):629–34.

    CAS  Article  Google Scholar 

  38. 38.

    Thompson SG, Sharp SJ. Explaining heterogeneity in meta-analysis: a comparison of methods. Stat Med. 1999;18(20):2693–708.

    CAS  Article  Google Scholar 

  39. 39.

    Schultes B, Frick J, Ernst B, Stefan N, Fritsche A. The effect of 6-weeks of aerobic exercise training on serum fetuin-a levels in non-diabetic obese women. Exp Clin Endocrinol Diabetes. 2010;118(10):754–6.

  40. 40.

    Wilund KR, Tomayko EJ, Wu P-T, Ryong Chung H, Vallurupalli S, Lakshminarayanan B, et al. Intradialytic exercise training reduces oxidative stress and epicardial fat: a pilot study. Nephrol Dial Transplant. 2010;25(8):2695–701.

    CAS  Article  Google Scholar 

  41. 41.

    Zhang L-Y, Liu T, Teng Y-Q, Yao X-Y, Zhao T-T, Lin L-Y, et al. Effect of a 12-week aerobic exercise training on serum fetuin-a and adipocytokine levels in type 2 diabetes. Exp Clin Endocrinol Diabetes. 2017;126(08):487–92.

    PubMed  Google Scholar 

  42. 42.

    García-Hermoso A, Ceballos-Ceballos R, Poblete-Aro C, Hackney A, Mota J, Ramírez-Vélez R. Exercise, adipokines and pediatric obesity: a meta-analysis of randomized controlled trials. Int J Obes. 2017;41(4):475-82.

  43. 43.

    Jenkins NT, McKenzie JA, Hagberg JM, Witkowski S. Plasma fetuin-a concentrations in young and older high-and low-active men. Metabolism. 2011;60(2):265–71.

    CAS  Article  Google Scholar 

  44. 44.

    Pedersen BK. Anti-inflammatory effects of exercise: role in diabetes and cardiovascular disease. Eur J Clin Investig. 2017;47(8):600–11.

    CAS  Article  Google Scholar 

  45. 45.

    Stefan N, Hennige AM, Staiger H, Machann J, Schick F, Kröber SM, et al. α2-Heremans-Schmid glycoprotein/fetuin-a is associated with insulin resistance and fat accumulation in the liver in humans. Diabetes Care. 2006;29(4):853–7.

    CAS  Article  Google Scholar 

  46. 46.

    Srinivas P, Wagner AS, Reddy LV, Deutsch D, Leon MA, Goustin AS, et al. Serum alpha 2-HS-glycoprotein is an inhibitor of the human insulin receptor at the tyrosine kinase level. Mol Endocrinol. 1993;7(11):1445–55.

    CAS  PubMed  Google Scholar 

  47. 47.

    Brix JM, Stingl H, Höllerl F, Schernthaner GH, Kopp H-P, Schernthaner G. Elevated Fetuin-a concentrations in morbid obesity decrease after dramatic weight loss. J Clin Endocrinol Metab. 2010;95(11):4877–81.

    CAS  Article  Google Scholar 

  48. 48.

    Haukeland JW, Dahl TB, Yndestad A, Gladhaug IP, Løberg EM, Haaland T, et al. Fetuin a in nonalcoholic fatty liver disease: in vivo and in vitro studies. Eur J Endocrinol. 2012;166(3):503–10.

    CAS  Article  Google Scholar 

  49. 49.

    Hennige AM, Staiger H, Wicke C, Machicao F, Fritsche A, Häring H-U, et al. Fetuin-a induces cytokine expression and suppresses adiponectin production. PLoS One. 2008;3(3):e1765.

    Article  Google Scholar 

  50. 50.

    González-Ruiz K, Ramirez-Velez R, Correa-Bautista JE, Peterson MD, Garcia-Hermoso A. The effects of exercise on abdominal fat and liver enzymes in pediatric obesity: a systematic review and meta-analysis. Child Obes. 2017;13(4):272–82.

    Article  Google Scholar 

  51. 51.

    Guo R, Liong EC, So KF, Fung M-L, Tipoe GL. Beneficial mechanisms of aerobic exercise on hepatic lipid metabolism in non-alcoholic fatty liver disease. Hepatobiliary Pancreat Dis Int. 2015;14(2):139–44.

  52. 52.

    Xu XJ, Valentine RJ, Ruderman NB. AMP-activated protein kinase (AMPK): does this master regulator of cellular energy state distinguish insulin sensitive from insulin resistant obesity? Curr Obes Rep. 2014;3(2):248–55.

    Article  Google Scholar 

  53. 53.

    Sacks H, Chalmers TC, Smith H Jr. Randomized versus historical controls for clinical trials. Am J Med. 1982;72(2):233–40.

    CAS  Article  Google Scholar 

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The contribution of each author for this paper was as follows, RR-V, AG-H and MI designed the experimental study. RR-V and MI provide technical assistance regarding research and data interpretation. AC-H helped for drafting the manuscript. It is evident that all authors read and approved the final manuscript.

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Correspondence to Robinson Ramírez-Vélez.

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Ramírez-Vélez, R., García-Hermoso, A., Hackney, A.C. et al. Effects of exercise training on Fetuin-a in obese, type 2 diabetes and cardiovascular disease in adults and elderly: a systematic review and Meta-analysis. Lipids Health Dis 18, 23 (2019).

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  • Fetuin-a
  • Obesity
  • Type 2 diabetes
  • Metabolic syndrome
  • Cardiovascular disease
  • Exercise training
  • Meta-analysis
  • Systematic review