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Metabolic syndrome: definitions and controversies

  • Eva Kassi1,
  • Panagiota Pervanidou2,
  • Gregory Kaltsas3 and
  • George Chrousos2Email author
BMC Medicine20119:48

https://doi.org/10.1186/1741-7015-9-48

©  Kassi et al; licensee BioMed Central Ltd. 2011

Received: 6 January 2011

Accepted: 5 May 2011

Published: 5 May 2011

Open Peer Review reports

Abstract

Metabolic syndrome (MetS) is a complex disorder defined by a cluster of interconnected factors that increase the risk of cardiovascular atherosclerotic diseases and diabetes mellitus type 2. Currently, several different definitions of MetS exist, causing substantial confusion as to whether they identify the same individuals or represent a surrogate of risk factors. Recently, a number of other factors besides those traditionally used to define MetS that are also linked to the syndrome have been identified. In this review, we critically consider existing definitions and evolving information, and conclude that there is still a need to develop uniform criteria to define MetS, so as to enable comparisons between different studies and to better identify patients at risk. As the application of the MetS model has not been fully validated in children and adolescents as yet, and because of its alarmingly increasing prevalence in this population, we suggest that diagnosis, prevention and treatment in this age group should better focus on established risk factors rather than the diagnosis of MetS.

Keywords

Waist CircumferenceImpaired Fasting GlucoseInternational Diabetes FederationCholesterol Education Program Adult TreatmentEducation Program Adult Treatment Panel

Introduction

Metabolic syndrome (MetS) is a complex disorder with high socioeconomic cost that is considered a worldwide epidemic. MetS is defined by a cluster of interconnected factors that directly increase the risk of coronary heart disease (CHD), other forms of cardiovascular atherosclerotic diseases (CVD), and diabetes mellitus type 2 (DMT2). Its main components are dyslipidemia (elevated triglycerides and apolipoprotein B (apoB)-containing lipoproteins, and low high-density lipoproteins (HDL)), elevation of arterial blood pressure (BP) and dysregulated glucose homeostasis, while abdominal obesity and/or insulin resistance (IR) have gained increasing attention as the core manifestations of the syndrome. Recently, other abnormalities such as chronic proinflammatory and prothrombotic states, non-alcoholic fatty liver disease and sleep apnea have been added to the entity of to the syndrome, making its definition even more complex. Besides the many components and clinical implications of MetS, there is still no universally accepted pathogenic mechanism or clearly defined diagnostic criteria. Furthermore, there is still debate as to whether this entity represents a specific syndrome or is a surrogate of combined risk factors that put the individual at particular risk. A main evolving aspect of MetS is its increasing prevalence in both childhood and young adulthood and the future implications to the global health burden this may confer. In the present work we discuss the importance of establishing clear criteria to define MetS, highlighting the latest research, which we use to provide a critical review of currently existing controversies in this field and expand on the childhood and adulthood aspect of the syndrome.

Currently used criteria to define MetS

Historically, Reaven was the first to put forward the concept of 'syndrome X', (which he later renamed MetS), hypothesizing that it was a central feature in the development of CHD and DMT2, mainly through target tissue resistance to insulin action [1]. Since then, many international organizations and expert groups, such as the World Health Organization (WHO), the European Group for the study of Insulin Resistance (EGIR), the National Cholesterol Education Program Adult Treatment Panel III (NCEP:ATPIII), the American Association of Clinical Endocrinology (AACE), the International Diabetes Federation (IDF), and the American Heart Association/National Heart, Lung, and Blood Institute (AHA/NHLBI), have attempted to incorporate all the different parameters used to define MetS (Appendix 1).

The first attempt was made in 1998 by the WHO, which proposed that MetS may be defined by the presence of IR or its surrogates, impaired glucose tolerance (IGT) or DMT2, as essential components of the syndrome, along with at least two of the following parameters: raised BP, hypertriglyceridemia and/or low HDL-cholesterol, obesity (as measured by waist/hip ratio or body mass index (BMI)), and microalbuminuria [2]. Shortly thereafter, the EGIR excluded microalbuminuria as an integral component of the syndrome, while it required hyperinsulinemia to be present [3]. In addition, waist circumference and not BMI was regarded as the main indicator to assess obesity, while introducing different cut-offs from those previously used for the other components of the syndrome. In 2001, the NCEP:ATPIII published a new set of criteria that included waist circumference, blood lipids, BP, and fasting glucose [4]. The NCEP:ATPIII definition differed from both the WHO and EGIR definitions in that IR was not considered as a necessary diagnostic component. In 2005, the International Diabetes Federation (IDF) published newer criteria in an attempt to define the syndrome more precisely so that it could be used by different clinical and research groups. The aim of this new definition was to enable comparisons between study results, in the hope that it would be a better predictor of risk particularly for CHD, stroke and DMT2 [5]. The IDF introduced abdominal obesity as a prerequisite of the diagnosis of MetS, with particular emphasis on waist measurement as a simple screening tool that was also adopted by AHA/NHLBI [6].

The remaining four components of MetS were identical in the AHA/NHLBI definition to those of the IDF, although abdominal obesity was defined differently. The IDF recommended that the threshold for waist circumference in Europeans should be 94 cm for men and 80 cm for women, while the AHA/NHLBI recommended cut-off points of 102 and 88 cm, respectively.

Currently, the two most widely used definitions are those of the NCEP:ATP III and IDF focusing specifically on waist circumference, which is a surrogate measure of central obesity. In contrast, the AACE, WHO and the EGIR definitions are all largely focused on insulin resistance.

However, a major problem with the WHO and NCEP:ATPIII definitions has been their applicability to different ethnic groups, especially when trying to define obesity cut-offs. This is particularly evident for the risk of DMT2, which is apparent at much lower levels of obesity in Asians compared to Europeans. The IDF, having recognized the difficulties in identifying unified criteria for MetS that were applicable across all ethnicities, has proposed a new set of criteria with ethnic/racial specific cut-offs [7]. However, even in Westerners, a difference of 14 cm in current abdominal obesity criteria across genders may be debatable, leading to dilution of MetS in women or a failure of encompassing men with MetS at increased cardiometabolic risk.

In view of these difficulties and until more evidence that can elucidate the cause of MetS accumulate, the Joint Interim Statement (consensus definition in Appendix 1) highlighting that there should be no obligatory component for MetS but rather all individual components should be considered important on risk prediction, is currently mostly accepted.

Although prevalence estimates for the syndrome have been mostly similar in any given population regardless of the definition used, different individuals are identified [8]. This is attributed to the different focus of each definition, from the glucocentric WHO definition to an obesity-centric IDF one, and to a collection of statistically related CVD risk factors by the NCEP:ATPIII definition. Taking into account the burgeoning epidemic of DMT2 and CVD worldwide, the need for one practical definition that would identify accurately individuals with MetS is becoming imperative.

Epidemiology of MetS according to the various definitions used

Clearly, the prevalence of MetS varies and depends on the criteria used in different definitions, as well as the composition (sex, age, race and ethnicity) of the population studied [9]. No matter which criteria are used, the prevalence of MetS is high and rising in all western societies, probably as a result of the obesity epidemic [10–12]. According to National Health and Examination Survey (NHANES) 2003-2006 [13], approximately 34% of people studied met the NCEP:ATPIII revised criteria for MetS. Differences in the age-adjusted prevalence estimates using the various definitions of MetS within three NHANES cohorts (1988-1994, 1999-2002 and 2003-2006) are shown in Table 1. Using the revised NCEP:ATPIII criteria, the estimated prevalence of MetS increased up to 5% during the last 15 years. The WHO criteria, although more restrictive, estimated nearly the same prevalence of MetS, whereas the IDF definition which adopted a lower cut-off point for waist circumference, estimated a higher prevalence [14]. Despite the differing prevalence estimates when employing the various definitions, they all add up to a shocking figure of a vast proportion of the population being at high risk of developing CHD and DMT2.
Table 1

Age-adjusted prevalence according to MetS definition within NHANES cohorts.

 

N

ATPIII 2001

ATPIII revised

WHO

IDF

NHANES 1988-1994 [143]

8,814

23.7%

   

NHANES 1988-1994 [144]

8,608

23.9%

 

25.1%

 

NHANES 1988-1994 [145]

6,436

24.1%

29.2%

  

NHANES 1999-2002 [145]

1,677

27.0%

32.3%

  

NHANES 1999-2002 [10]

3,601

 

34.6%

 

39.1%

NHANES 2003-2006 [13]

3,423

 

34%

  

ATPIII = National Cholesterol Education Program Adult Treatment Panel III; IDF = International Diabetes Federation; MetS = metabolic syndrome; NHANES = National Health and Examination Survey; WHO = World Health Organization.

Both the unadjusted prevalence and age-adjusted prevalence of MetS increased from NHANES-III (1988-1994) to NHANES 1999-2006, from 27.9% to 34.1% and 29% to 34.2%, respectively, but remained the same over the last NHANES cohorts (1999-2002, and 2003-2006 cohort). In countries from areas other than Europe and Africa, the IDF guidelines also identify a greater prevalence of MetS than the NCEP:ATPIII [15–19]. A similar prevalence of MetS in the Iranian population was recently reported, applying both the IDF and ATPIII criteria (32.1% and 33.2% respectively) [20].

In the NHANES 2003-2006 cohort, the prevalence of MetS was found to increase with age: approximately 20% of males and 16% of females under 40 years of age, 41% of males and 37% of females between 40-59 years, and 52% of males and 54% of females 60 years and over [13]. The trend for a higher prevalence of MetS with advancing age was similar to that observed in other populations [8, 21–25]. This increase with age continues up to the sixth decade; however, different studies have estimated a variable prevalence after the sixth or seventh decades, probably as individuals most susceptible to obesity-related mortality have already died [22, 24, 26].

The prevalence of MetS increases even more dramatically as BMI increases. In the NHANES 2003-2006 cohort, overweight males and females were found, respectively, to be more than 6 and 5.5 times as likely to meet the criteria for MetS compared to underweight and normal weight individuals. In obese males and females compared to underweight and normal weight individuals these figures spiked to 32 and 17 times, respectively [13]. Similarly to western societies, the prevalence of MetS is rapidly increasing in developing countries, ranging from 9.8% in male urban North Indians to 42% in female urban Iranians [27]. This increase is observed regardless of the criteria used and reflects the transition from a traditional to a Western-like lifestyle. The emergence of obesity and MetS in developing countries is related to a number of factors. Demographic transition (shift to low fertility, low mortality, and higher life expectancy), and epidemiological transition (from widely prevalent infectious diseases to a pattern of a high prevalence of lifestyle related diseases) evolved in developing countries as they become economically more resourceful, leading to significant shifts in dietary and physical activity patterns. These changes cause significant effects on body composition and metabolism, often resulting in an increase in BMI, generalized and abdominal obesity, and an increase in dyslipidemia and DMT2 [27].

It should be noted however, that even lean individuals may develop features of MetS adding further to the complexity of its pathogenesis [28].

Thus, the importance of identifying markers for MetS to supplement age-related and obesity-related measures cannot be overstated. Understanding how to use definition criteria in clinical settings will aid physicians in treating the right cohort of at-risk patients.

Morbidities related to MetS

The need to precisely define MetS stems from the need to detect accurately individuals at high risk for CVD and DMT2. All the components of the various MetS definitions are involved in conferring risk for CVD and DMT2. In particular, the three components of atherogenic dyslipidemia (increased low-density lipoprotein (LDL), decreased HDL and high blood triglyceride concentrations) are individually associated with a cardiovascular risk [29], while IR significantly increases the risk of developing DMT2, although approximately 25% of insulin resistant patients have normal glucose tolerance [30]. Central obesity has been shown in several studies to be associated with an increased risk of CVD and DMT2 [31].

Several epidemiological studies have confirmed the increased risk of CVD in individuals with MetS, independently of the diagnostic criteria used [32–39]. Overall a range of 1.5-3 times greater risk of CVD and CHD mortality has been found in several prospective studies (REFS), whereas a recent meta-analysis showed that MetS was associated with a twofold increase in cardiovascular outcomes and a 1.5-fold increase in all-cause mortality [40]. It should be noted however, that several studies amongst which the Casale Monferrato Study and PROSPER conducted in older people, failed to reveal an association between MetS and an increased risk of CVD [41, 42]. Due to these inconsistencies several recent studies have aimed to investigate which of the proposed definitions of MetS is particularly related to excessive CVD risk, and thus which one should be implemented in clinical practice. A recent meta-analysis suggested that the WHO definition was associated with a slightly greater risk than the NCEP:ATPIII definition [43]. It is of interest that the INTERHEART study, the first large-scale multiethnic international investigation, has demonstrated that using either the WHO or IDF definition, the presence of MetS is associated with a > 2.5-fold increase in the risk of acute myocardial infarction (MI) [44], while Cabre et al. recently reported similar findings for CVD using these definitions [45].

The assessment of whether the risk of MetS on MI is greater than the risk conferred by the sum of individual component risk factors has also been studied. A recent report suggested that the MetS-related CVD risk was more than that of the sum of its parts in subjects with MetS, with or without DMT2 [46]. In the recent INTERHEART study, MI risk increased as more component factors of MetS were present, and this is consistent with previous observations showing that the presence of more risk factors was associated with an incremental increase in subclinical atherosclerosis and incident CHD [38, 47–49]. One major point of note was that the risk of CHD when three components of MetS were present did not appear to be greater than the risk of individual components such as DMT2 and hypertension, and this was in agreement with other reports [50, 51]. In this regard, in a recent appraisal of MetS, the American Diabetes Association (ADA) in conjunction with the European Association for the Study of Diabetes, issued a joint statement raising concerns over the value of using MetS as a CVD risk marker and recommended that clinicians should evaluate and treat all CVD risk factors without considering whether a patient meets the criteria for diagnosis of MetS [52].

The observation of the presence of MetS predicting the risk for DMT2 has also been examined by numerous studies; according to these reports, it is well accepted that the presence of MetS not only increases this risk, but is also highly predictive of new-onset DMT2 [6, 42, 53–55]. Indeed, MetS is associated with an approximately five times higher risk for incident DMT2 [56].

The presence of MetS predicting the incidence of DMT2 also varies depending on how MetS is defined. It has previously been demonstrated that definitions like that of the WHO, which imposes as a prerequisite the presence of impaired fasting glucose (IFG) and/or IGT, confer a higher risk than the NCEP:ATPIII and IDF definitions, which consider elevated fasting plasma glucose as an essential, but not required component [57]. IFG and IGT can predict the development of DMT2, independently of other components of MetS [56]. However, recent studies have shown that the IDF and NCEP:ATPIII definitions of MetS predicted DMT2 at least as well as the WHO definition [58, 59].

Although the presence of MetS can predict the CVD and DMT2 risk, it cannot estimate the exact risk, as a significant part may be related to other factors such as age, smoking or gender. In particular, women have higher concentrations of inflammatory markers, such as high sensitivity C reactive protein (hs-CRP), compared to men, attributed possibly to their increased accumulation of subcutaneous and/or visceral fat [60, 61]. Additionally, factors others than those included in the existing definitions of MetS, such as endothelial dysfunction, small dense oxidized LDL, insulin resistance, prothrombotic tendency and a proinflammatory state that are essential components and determinant of future cardiometabolic risk have been left out. Indeed, a substantial amount of knowledge on cardiometabolic risk is provided by markers that define a proinflammatory state, such as hs-CRP, γ-glutamyltransferase (γ-GT), uric acid, apoB, apoE, fibrinogen, along with the associated dysfunction of apolipoprotein A-I (ApoA-I) and HDL [62–67]. In particular, HDL dysfunctionality is closely linked to obesity and low-grade inflammation yet seems to act partly independently of them. Although it is not as yet clear what is the exact contribution of these risk factors to the development of CVD and DMT2, it is probable that along with the mechanisms delineated further below, may account for the residual risk not attributed to the traditional risk factors of these disorders.

Conditions contributing to the pathogenesis of MetS (Figure 1)

Figure 1
Figure 1

A schematic image of the conditions implicated in the pathophysiology of the metabolic syndrome and their potential interactions. IR: Insulin Resistance; HTN: Hypertension; HPA axis : Hypothalamic-Pituitary-Adrenal Axis; DMT2: Diabetes Mellitus type 2; CVD: Cardiovascular disease; CRH: Corticotropin Releasing Hormone; AVP: Arginine Vasopressin.

Despite advances in pathophysiology and delineation of risk factors that predispose to MetS, there are many key aspects that remain unclear. The great variation in susceptibility and age of onset in individuals with a very similar risk profile, suggests a major interaction between genetic and environmental factors [68]. Although obesity and IR remain at the core of the pathophysiology of MetS, a number of other factors such as chronic stress and dysregulation of the hypothalamic-pituitary-adrenal (HPA) axis and autonomic nervous system (ANS), increases in cellular oxidative stress, renin-angiotensin-aldosterone system activity, and intrinsic tissue glucocorticoid actions, as well as currently discovered molecules such as micro RNAs can also be involved in its pathogenesis (Figure 1).

Conditions epidemiologically confirmed

Obesity/insulin resistance and MetS

Although not all overweight or obese individuals are metabolically disturbed, the majority are IR [69–71]. Central obesity is thought to be an early step, as visceral adipose tissue secretes a variety of bioactive substances termed adipocytokines, such as leptin, resistin, tumor necrosis factor α (TNFα), interleukin-6 (IL-6), and angiotensin II which induce IR, along with plasminogen activator inhibitor 1 (PAI-1), which is related to thrombogenic vascular diseases [72]. Notably, adiponectin, an important adipocytokine that protects against the development of DMT2, hypertension, inflammation, and atherosclerotic vascular diseases, is decreased in individuals with visceral fat accumulation, and this may be causally related to MetS [73, 74]. Moreover, newly recognized adipocytokines such as visfatin, as well as enzymes expressed in adipose tissue, such as neprilysin, and growth factors, like fibroblast growth factor 21, an important regulator of glucose and lipid metabolism, are currently under investigation regarding their role in the pathogenesis of MetS [75–77]. In particular, visfatin has been suggested to exert insulin-mimicking/sensitizing effects but can also contribute to the inflammatory processes by triggering cytokine production and nuclear factor κB (NF-κB) activation, while vice versa visfatin secretion is upregulated in response to proinflammatory cytokines [78].

Other compounds produced by adipose tissue possibly implicated in the pathogenesis of MetS, are the non-esterified free fatty acids (FFAs). In the presence of IR the process of FFAs mobilization from stored adipose tissue triglycerides is accelerated. In the liver, FFAs result (due to hepatic insulin resistance) in increased production of glucose and triglycerides and secretion of very low-density lipoprotein (VLDL), maintaining a vicious cycle. FFAs also reduce insulin sensitivity in muscle by inhibiting insulin-mediated glucose uptake and increase fibrinogen and PAI-1 production [9, 79].

Conditions related to MetS without epidemiological confirmation

Chronic stress: dysregulation of HPA axis/ANS and MetS

Chronic hypersecretion of stress mediators, such as cortisol, in individuals with a genetic predisposition exposed to a permissive environment, may lead to visceral fat accumulation as a result of chronic hypercortisolism, low growth hormone secretion and hypogonadism [80, 81]. Moreover, hypercortisolism directly causes IR of peripheral target tissues in proportion to glucocorticoid (GC) levels and a particular target tissue's sensitivity to them as shown by studying polymorphisms of the glucocorticoid receptor gene [82]. These hormonal alterations may lead to reactive insulin hypersecretion, and increasing visceral obesity and sarcopenia, resulting to dyslipidemia, hypertension and DMT2 [83]. Stress-related IL-6 hypersecretion plus adipose-tissue-generated inflammatory hypercytokinemia, as well as hypercortisolism, contribute to increased production of acute phase reactants and blood hypercoagulation, which have been recently recognized as components of MetS [84, 85].

Moreover, since intracellular GC levels are regulated by 11β-hydroxysteroid dehydrogenase type 1 (11β-HSD1), which converts inactive cortisone to cortisol, a large number of studies have focused on evaluating tissue specific alterations in 11β-HSD1 expression and activity in obesity and IR. In obesity global 11β-HSD1 activity, as measured by urinary corticosteroid metabolite analysis, is impaired [86, 87], while selective 11β-HSD1 inhibitors, are in development with promising results showing improvements in metabolic profile in rodents [88].

A possible association between visceral fat/insulin resistance, inflammatory cytokines, stress hormones, and sleep apnea has recently been suggested [89–91]. Visceral obesity/insulin resistance, determined by both genetic/constitutional and environmental factors, may be the principal culprit leading to sleep apnea, which, in turn, may accelerate these metabolic abnormalities, possibly through progressive elevation of stress hormones and cytokines such as noradrenaline, cortisol, IL-6, and TNFα [92].

Apart from the stress HPA axis and its end effectors glucocorticoids, another system, the circadian CLOCK system may also be implicated in the pathogenesis of MetS. Interestingly, most of the metabolic phenotypes associated with dysregulation of the CLOCK system and the HPA axis overlap [93].

Cellular oxidative stress/renin-angiotensin-aldosterone system and MetS

Emerging evidence suggests that nitric oxide (NO), inflammatory and oxidative stress also play important roles in the pathophysiology of MetS hypertension and DMT2 [94, 95]. Increased production of reactive oxygen species (ROS) in numerous tissues, including skeletal muscle and cardiovascular tissues, has been linked (amongst others) to activation of the renin-angiotensin-aldosterone system [96, 97], which is also implicated in the development of IR [98]. Elevation of angiotensin II can induce IR via reactive oxygen species (ROS) production in various tissues, including vascular smooth muscle and skeletal muscle in patients with MetS [96, 98]. Furthermore, either use of angiotensin II type 1 receptor antagonists or genetic knockout of angiotensin II type 1 receptor are known to effectively attenuate lipid accumulation in the liver [99–105].

Micro RNAs and MetS

Micro RNAs (miRNAs) play important regulatory roles in a variety of biological processes including adipocyte differentiation, metabolic integration, IR and appetite regulation [106]. Although the exact mechanism of action remains to be elucidated, miRNAs may regulate cellular gene expression at the transcriptional or post-transcriptional level, by suppressing translation of protein-coding genes, or cleaving target messenger RNAs (mRNAs) to induce their degradation, through imperfect pairing with target mRNAs [107, 108]. Antagomirs (cholesterol conjugated antisense oligonucleotides) which target and silence miRNAs, as evidenced by hepatic miR-122 blockade in vivo [109], have already been successfully tested in a phase I clinical trial. Further studies are needed to explore the full potential of miRNAs as novel biomarkers and therapeutic agents against MetS.

Fetal/developmental basis of MetS

The concept of fetal/developmental origin of MetS, since the first study linking intrauterine undernutrition with later obesity, continues to raise interest [110]. Evidence from both human [111, 112] and animal studies [113, 114] suggests that the nutritional, hormonal, and metabolic environment of the mother, as well as the early postnatal environment, may permanently reprogram the structure and physiology of the offspring toward the development of metabolic disease, in later life [80, 84, 115, 116].

Since in vitro fertilization (IVF) has been widely used, the possible effect of IVF (as a result of either intrauterine growth restriction or periconceptual manipulation of the blastocysts per se) in the incidence of MetS manifestations has been studied, producing conflicting results [117–119]. More prospective studies on the metabolic profile of children conceived by IVF, with longer follow-up are necessary to draw safe conclusions.

Although the role of the all these components as integral parts of MetS has not been evaluated in epidemiological and interventional studies, they may represent the missing link that provides full susceptibility to CVD besides the traditionally accepted components of MetS. This is particularly relevant for the fetal programming as it may suggest intervention at an earlier stage with lifestyle therapies, since the incidence of MetS in children and adolescents is increasing alarmingly.

Is the pediatric metabolic syndrome real or a myth? A developmental perspective

The increasing worldwide prevalence of childhood obesity and, in parallel, of DMT2 in the young [120, 121], has highlighted the importance of MetS diagnosis in children and adolescents, as a state of high risk for progression to later disease. Since the first publication of MetS in children, in 1999, [122], a growing interest emerged investigating MetS prevalence and the potential utility of this diagnosis, as well as therapeutic interventions in adolescents fulfilling it. Later, findings from the Third National Health and Nutrition Examination Survey (NHANES), 1988-1994 [123] revealed that 4.2% of adolescents in general, and almost 30% of overweight and obese adolescents, in the US met diagnostic criteria for MetS. A variety of subsequent studies [120, 123–131], using three or four criteria and variable definitions, revealed diversity in MetS prevalence in childhood. The NHANES 1999-2000, using the ATPIII definition modified for age, identified a further increase in the prevalence of MetS among US adolescents, from 4.2% in NHANES III (1988-1994) to 6.4% in NHANES (1999-2000) [127]. The prevalence of MetS was almost exclusively found to be high among obese adolescents.

Definitions

Similarly to adults, no general consensus exists regarding the definition of MetS in children and adolescents [132]. Furthermore, studies published so far have used their own set of variables, number of criteria (three or four) and different cut-off points to define risk factors associated with MetS. Obesity has been defined as the 85th to 97th percentile of BMI or waist circumference, while accordingly, a variety of cut-off percentiles have been used for blood pressure, triglycerides, HDL, insulin and glucose [133]. In 2007, a consensus report was published by the IDF group [134], including three age groups: 6 to < 10, 10 to < 16 and 16 + years (adult criteria). Based on this report, obesity is defined as waist circumference ≥ 90th percentile, or adult cut-off if lower, while all other parameters are defined based on absolute numbers, rather than percentiles. These numbers are: ≥ 150 mg/dl for triglycerides (or specific treatment for triglycerides), < 40 mg/dl for HDL and < 50 mg/dl in females older than 10 (or specific treatment for HDL), ≥ 130 mmHg for systolic and ≥ 85 mmHg for diastolic blood pressure (or treatment of previously diagnosed hypertension) and fasting plasma glucose ≥ 100 mg/dl or known type 2 diabetes. The rationale of using absolute numbers as cut-offs is based on the heterogeneity of clinical, biochemical and hormonal values during childhood and adolescence, as well as, on the large diversity of proposed percentile cut-offs of different definitions. The IDF definition is presented in detail in Table 2.
Table 2

International Diabetes Federation (IDF) definition for pediatric metabolic syndrome (MetS) [134]

Age group (years)

Obesity (WC)

Triglycerides

HDL-C

Blood pressure

Glucose

6 to < 10a

≥ 90th percentile

    

10 to < 16

≥ 90th percentile or adult cut-off if lower

≥ 1.7 mmol/l (≥ 150 mg/dl)

< 1.03 mmol/l (< 40 mg/dl)

Systolic BP ≥ 130 or diastolic BP ≥ 85 mm Hg

FPG ≥ 5.6 mmol/l (100 mg/dl)b or known T2DM

16+ (adult criteria)

WC ≥ 94 cm for Europid males and ≥ 80 cm for Europid females, with ethnic-specific values for other groupsc

≥ 1.7 mmol/l (≥ 150 mg/dl) or specific treatment for high triglycerides

< 1.03 mmol/l (< 40 mg/dl) in males and < 1.29 mmol/l (< 50mg/dl) in females, or specific treatment for low HDL

Systolic BP ≥ 130 or diastolic BP ≥ 85 mm Hg or treatment of previously diagnosed hypertension

FPG ≥ 5.6 mmol/l (100 mg/dl)b or known T2DM

Diagnosing metabolic syndrome requires the presence of central obesity plus any two of the other four factors.

aMetabolic syndrome cannot be diagnosed, but further measurements should be made if there is a family history of metabolic syndrome, T2DM, dyslipidemia, cardiovascular disease, hypertension and/or obesity.

bFor clinical purposes, but not for diagnosing MetS, if FPG: 5.6-6.9 mmol/l (100-125 mg/dl) and not known to have diabetes, an oral glucose tolerance test should be performed.

cFor those of South and South-East Asian, Japanese, and ethnic South and Central American origin, the cut-offs should be ≥ 90 cm for men, and ≥ 80 cm for women. The IDF Consensus group recognizes that there are ethnic, gender and age differences, but research is still needed on outcomes to establish risk.

BP = blood pressure; FPG = fasting plasma glucose; HDL-C = high-density lipoprotein cholesterol; IDF = International Diabetes Federation; T2DM = type 2 diabetes mellitus; WC = waist circumference.

The pediatric perspective: challenges in conceptual models

The main concern for pediatric clinicians is that all childhood MetS definitions originate from adult definitions and use criteria extrapolated from an adult diagnosis to a younger age group, while, in fact, the utility and predictive value of this diagnosis in young age groups has not been fully established. Indeed, large longitudinal studies linking pediatric MetS with adult cardiovascular disease are limited, and although it is hypothesized that MetS in childhood is related to MetS in adulthood, this hypothesis has not yet been tested. A second important issue is the lack of a developmental perspective in MetS definition: MetS as an entity is developing progressively, according to age and pubertal changes, so that the full MetS cannot in general be easily diagnosed in childhood [124]. Developmentally-appropriate risk or protective factors, such as gestational age, birth weight and breastfeeding, as well as parental obesity and family history, are not typically taken into account [133]. More importantly, none of the MetS definitions consider the influences of growth and puberty, for instance the 'normal' insulin resistance in puberty [135, 136], the changes in fat and fat-free mass and the changes in growth and sex steroid secretion. Further to these changes, it has been shown that in obese children, insulin resistance (as measured by the homeostasis model assessment-insulin resistance (HOMA-IR) index) increases progressively across Tanner stages and is higher in all pubertal stages than in normal weight children [137].

MetS consistency in adolescence

Recently published studies examined MetS stability in large epidemiological samples of adolescents, using factor analysis. It was found that, though metabolic risk factor clustering was consistent, the categorical diagnosis of MetS was not stable during adolescence [138], including both gain and loss of diagnosis. A second, more recent study from the same group, examined the stability of three alternative models of MetS factor structure across three developmental changes [139]. The researchers suggested that the concepts used to support the utility of MetS in the young do not fit to pediatric populations and may vary by maturation. In addition to these large epidemiological studies, from US, clinical data also support this idea. Our research group examined the prevalence and stability of MetS diagnosis in children and adolescents aged 8-16. Data from our cohort showed that in a clinical population of obese children followed at our obesity outpatient clinic, almost 10% had the full MetS, and another 30% had partial MetS (two positive parameters of MetS). When examining the effects of puberty, we found that pubertal children had a higher prevalence of full and partial MetS than the prepubertal population. However, this diagnosis presented a within-person variability when examined at different time points during adolescence [140]. This new information is further supported by recently published data from the Bogalusa Heart Study and the Cardiovascular Risk in Young Finns [141]. This study has shown that although children and adolescents with MetS are indeed at an increased risk of adult MetS, subclinical atherosclerosis and diabetes type 2, the BMI alone is an equally accurate measure as MetS in identifying youth at risk for adult MetS and subsequent atherosclerotic disease.

Clinical implications for pediatric MetS

MetS as a concept was originally developed to identify adults at a greatest risk for CVD and DMT2, however, the application of this model has not yet been fully validated in children and adolescents. Furthermore, the effects of growth and puberty on reference values is a critical issue, because diverse age-dependent cut-off points are needed to define a pathological state, such as MetS. Longitudinally, the high level of diagnostic inconsistency through adolescence suggests that MetS classification may not be a valuable method for risk identification in the pediatric age group.

These limitations, as well as new data from longitudinal studies in pediatric MetS, suggest that prevention and treatment in childhood and adolescence should better focus on established risk factors rather than the diagnosis of MetS. Pediatric clinicians may put more emphasis on healthy lifestyle promotion and obesity prevention and treatment rather than targeting specific metabolic alterations. Indeed, advocating weight maintenance rather than weight loss during the years of physical growth, may lead to BMI reduction and cardiovascular risk minimization and may be a more cost-effective approach than pursuing fluctuating biochemical abnormalities.

Conclusions

Due to its impact upon health and financial implications, the mechanisms that contribute to the pathogenesis of MetS remain under intense investigation since their understanding may help design novel therapeutic strategies. A number of potential mechanisms contributing to the pathogenesis of MetS include fetal programming, dyshomeostasis of the stress system, and the development of a proinflammatory and prothrombotic state as a result of cytokine production and/or dysregulation from the excessive adipose tissue. Delineation of the role of these factors along with the established ones and others that are currently being studied may help clarify the exact pathogenesis of the syndrome and may expand the clinical criteria of MetS. This is particularly important as there is still a need to develop uniform criteria that can be used by different clinical and research groups, enabling comparisons between study results, in the hope to better predictor the risk, for CVD and DMT2. In this direction, further studies exploring the relation of waist circumference thresholds to metabolic risk and cardiovascular outcomes in different populations are encouraged. However, until this aim is achieved, the consensus definition incorporating IDF and AHA/NHLBI is, in our opinion, the most suitable for practical use in clinical medicine. Adoption of these criteria seem to incorporate the most important aspects of the syndrome, recognizing that the risk associated with a particular waist measurement will differ in different populations, albeit with the limitations that it has when applied to mixed ethnicities. Finally, the application of the MetS model has not been fully validated in children and adolescents as yet, suggesting that prevention and treatment in childhood and adolescence should better focus on established risk factors rather than the diagnosis of MetS.

Appendix 1

Criteria for metabolic syndrome (MetS) definitions in adults

World Health Organization criteria (1998) [2]

Insulin resistance is defined as type 2 diabetes mellitus (DM) or impaired fasting glucose (IFG) (> 100 mg/dl) or impaired glucose tolerance (IGT), plus two of the following:

  • Abdominal obesity (waist-to-hip ratio > 0.9 in men or > 0.85 in women, or body mass index (BMI) > 30 kg/m2.

  • Triglycerides 150 mg/dl or greater, and/or high-density lipoprotein (HDL)-cholesterol < 40 mg/dl in men and < 50 mg/dl in women.

  • Blood pressure (BP) 140/90 mmHg or greater.

  • Microalbuminuria (urinary albumin secretion rate 20 μg/min or greater, or albumin-to-creatinine ratio 30 mg/g or greater).

European Group for the Study of Insulin Resistance criteria (1999) [3]

Insulin resistance defined as insulin levels > 75th percentile of non-diabetic patients, plus two of the following:

  • Waist circumference 94 cm or greater in men, 80 cm or greater in women.

  • Triglycerides 150 mg/dl or greater and/or HDL-cholesterol < 39 mg/dl in men or women.

  • BP 140/90 mmHg or greater or taking antihypertensive drugs.

  • Fasting glucose 110 mg/dl or greater.

National Cholesterol Education Program Adult Treatment Panel III (NCEP:ATPIII) criteria (2001) [4]

Any three or more of the following:

  • Waist circumference > 102 cm in men, > 88 cm in women.

  • Triglycerides 150 mg/dl or greater.

  • HDL-cholesterol < 40 mg/dl in men and < 50 mg/dl in women.

  • BP 130/85 mmHg or greater.

  • Fasting glucose 110 mg/dl* or greater.

* In 2003, the American Diabetes Association (ADA) changed the criteria for IFG tolerance from 110 mg/dl to 100 mg/dl.

American Association of Clinical Endocrinology criteria (2003) [142]

IGT plus two or more of the following:

  • BMI 25 kg/m2 or greater.

  • Triglycerides 150 mg/dl or greater and/or HDL-cholesterol < 40 mg/dl in men and < 50 mg/dl in women.

  • BP 130/85 mmHg or greater.

International Diabetes Federation (IDF) criteria (2005) [5]

Central obesity (defined as waist circumference but can be assumed if BMI > 30 kg/m2) with ethnicity-specific values,* plus two of the following:

  • Triglycerides 150 mg/dl or greater.

  • HDL-cholesterol < 40 mg/dl in men and < 50 mg/dl in women.

  • BP 130/85 mmHg or greater.

  • Fasting glucose 100 mg/dl or greater.

*To meet the criteria, waist circumference must be: for Europeans, > 94 cm in men and > 80 cm in women; and for South Asians, Chinese, and Japanese, > 90 cm in men and > 80 cm in women. For ethnic South and Central Americans, South Asian data are used, and for sub-Saharan Africans and Eastern Mediterranean and Middle East (Arab) populations, European data are used.

American Heart Association/National Heart, Lung, and Blood Institute (AHA/NHLBI) criteria (2004) [6]

Any three of the following:

  • Waist circumference 102 cm or greater in men, 88 cm or greater in women.

  • Triglycerides 150 mg/dl or greater.

  • HDL-cholesterol < 40 mg/dl in men and < 50 mg/dl in women.

  • BP 130/85 mmHg or greater.

  • Fasting glucose 100 mg/dl or greater.

Consensus definition (incorporating IDF and AHA/NHLBI definitions) [7]

Any three of the following:

  • Elevated waist circumference (according to population and country-specific definitions).

  • Triglycerides 150 mg/dl or greater.

  • HDL-cholesterol < 40 mg/dl in men and < 50 mg/dl in women.

  • BP 130/85 mmHg or greater.

  • Fasting glucose 100 mg/dl or greater.

Declarations

Authors’ Affiliations

(1)
Department of Biochemistry, National and Kapodistrian University of Athens, Athens, Greece
(2)
First Department of Paediatrics, National and Kapodistrian University of Athens, Athens, Greece
(3)
Department of Pathophysiology, National and Kapodistrian University of Athens, Athens, Greece

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