Skip to main content

Advertisement

We're creating a new version of this page. See preview

  • Review
  • Open Access

Metabolic syndrome in rheumatic diseases: epidemiology, pathophysiology, and clinical implications

  • 1Email author,
  • 1 and
  • 1
Arthritis Research & Therapy200810:207

https://doi.org/10.1186/ar2397

©  BioMed Central Ltd 2008

  • Published:

Abstract

Subjects with metabolic syndrome–a constellation of cardiovascular risk factors of which central obesity and insulin resistance are the most characteristic–are at increased risk for developing diabetes mellitus and cardiovascular disease. In these subjects, abdominal adipose tissue is a source of inflammatory cytokines such as tumor necrosis factor-alpha, known to promote insulin resistance. The presence of inflammatory cytokines together with the well-documented increased risk for cardiovascular diseases in patients with inflammatory arthritides and systemic lupus erythematosus has prompted studies to examine the prevalence of the metabolic syndrome in an effort to identify subjects at risk in addition to that conferred by traditional cardiovascular risk factors. These studies have documented a high prevalence of metabolic syndrome which correlates with disease activity and markers of atherosclerosis. The correlation of inflammatory disease activity with metabolic syndrome provides additional evidence for a link between inflammation and metabolic disturbances/vascular morbidity.

Keywords

  • Insulin Resistance
  • Systemic Lupus Erythematosus
  • Ankylose Spondylitis
  • Systemic Lupus Erythematosus Patient
  • Abdominal Obesity

Introduction

Cardiovascular diseases (CVDs) cause 38% of all deaths in North America and are the most common cause of death in European men under 65 years of age and the second most common cause in women. Targeting modifiable risk factors for CVD (hypertension, obesity, smoking, and so on) effectively reduces the risk for CVD events. Metabolic syndrome (MetS), also known as syndrome X or the insulin resistance syndrome, is a constellation of metabolic disturbances, all of which are independent risk factors for CVD. The presence of MetS has been associated with increased risk for CVD and type 2 diabetes mellitus (T2DM). MetS in combination with the 10-year risk assessment for CVD events can be used to identify patients who will need lifestyle modification alone from those who will benefit from additional drug therapy.

Epidemiological studies have shown that patients with chronic rheumatic diseases have an increased risk for CVD morbidity and mortality but the pathogenetic factors involved are not yet fully understood. MetS may provide an additional link between accelerated atherosclerosis and inflammation in these diseases.

In this review, we start with a discussion of MetS and its working definitions. Next, we examine recent data about the pathophysiology and epidemiology and their clinical significance in reference to CVD risk assessment. We conclude with a critical analysis of studies addressing the prevalence and significance of MetS in patients with rheumatic diseases.

Metabolic syndrome: overview and proposed criteria

In 1988, Reaven [1] proposed that insulin resistance is central to the etiologies of T2DM, hypertension, and coronary artery disease. In the ensuing years, the concept of insulin resistance and associated metabolic abnormalities leading to increased risk of CVD became known as insulin resistance/MetS. A few years later, Barker and colleagues [2] reported an association between low birth weight and increased risk for MetS.

MetS describes a constellation of cardiovascular risk factors such as atherogenic dyslipidemia (increased free fatty acids, elevated triglycerides, low high-density lipoprotein [HDL] cholesterol levels, and increased small dense low-density lipoprotein [LDL] and apolipoprotein B levels), central obesity, insulin resistance, disturbed glucose metabolism (T2DM, impaired glucose tolerance, and impaired fasting glycemia), and hypertension [3]. Features like a systemic pro-inflammatory state, accelerated hemostasis, and impaired fibrinolysis, though typically associated with the syndrome, are not included in the diagnostic criteria.

Despite abundant research, there has been a lack of consensus regarding the optimal definition and as a result several criteria have been proposed. The primary goal of all of these definitions is to identify individuals at increased risk for CVD and to enable the initiation of lifestyle changes to decrease this risk. The three most widely used definitions are those from the World Health Organization (WHO) [4], the National Cholesterol Education Program (NCEP) [5], and the International Diabetes Federation (IDF) [6] (Table 1). Under the WHO criteria, a disturbance of glucose/insulin metabolism must be present and thus MetS and diabetes are considered to be intersecting diagnostic categories. On the other hand, according to the NCEP criteria, MetS is a precursor to, but does not include, T2DM. The WHO definition is better suited as a research tool, whereas the NCEP definition is simpler and therefore more useful for clinical practice. The most recently proposed criteria released by the IDF include gender- and ethnic group-specific increased waist circumference as a major criterion, underlining the crucial importance of central obesity in MetS.
Table 1

Comparison of definitions of metabolic syndrome

World Health Organization

National Cholesterol Education Program

International Diabetes Federation

Diabetes or impaired fasting glycemia orimpaired glucose tolerance or insulin resistance (hyperinsulinemic, euglycemic clamp-glucose uptake in lowest 25%)

 

Central obesity: waist circumference ≥ 94 cm (male) or ≥ 80 cm (female)a, or ≥ 90 cm (male) or ≥ 80 cm (female)b

Plus two or more of the following

Three or more of the following

Plus two or more of the following

Obesity: body mass index >30 or waist-to-hip ratio >0.9 (male) or >0.85 (female)

Central obesity: waist circumference >102 cm (male) or >88 cm (female)

Fasting plasma glucose ≥ 5.6 mmol/L or medication

Dyslipidemia: triglycerides ≥ 1.7 mmol/L or HDL cholesterol <0.9 mmol/L (male) or <1.0 mmol/L (female)

Hypertriglyceridemia: triglycerides ≥ 1.7 mmol/L

Hypertriglyceridemia: triglycerides ≥ 1.7 mmol/L or medication

Hypertension: blood pressure ≥ 140/90 mm Hg

Low HDL cholesterol: <1.0 mmol/L (male)or <1.3 mmol/L (female)

Low HDL cholesterol: <1.0 mmol/L (male) or <1.3 mmol/L (female) or medication

Microalbuminuria: albumin excretion >20 μg/minute

Hypertension: blood pressure ≥ 130/85 mm Hg

Hypertension: blood pressure ≥ 130/85 mm Hg or medication

 

Fasting plasma glucose ≥ 6.1 mmol/L

 

aEuropeans, Sub-Saharan Africans, and Eastern Mediterranean and Middle East (Arab) populations; bSouth Asians and Ethnic South and Central Americans. HDL, high-density lipoprotein.

Although these criteria are in widespread use, they are currently the subject of intense debate since they do not result from a prospective study nor do they represent the outcome of an evidence-based process. For example, there is much criticism about the reduction of the waist cutoff criterion in men from 102 to 94 cm in the IDF guidelines. As expected, this reduction has considerably increased the number of patients being diagnosed with the syndrome when epidemiologic evidence supports the view that cardiovascular and overall mortality rates are more consistently increased when using a waist cutoff of 102 cm rather than 94 cm [7]. Similarly, reducing the threshold for impaired fasting glucose (IFG) from 6.1 mmol/L (according to NCEP criteria) to 5.6 mmol/L (in the IDF guidelines) did not substantially change the hazard ratio for risk of coronary heart disease, although it did increase the number of individuals identified [8].

Pathophysiology: complementary roles of insulin resistance and abdominal obesity

Insulin signaling

Since insulin resistance is a key feature of this syndrome, a brief overview of insulin signaling is crucial to the understanding of MetS. The insulin receptor has an intrinsic tyrosine kinase activity. Binding of insulin to its receptor induces both autophosphorylation and phosphorylation of tyrosine residues on insulin receptor substrate (IRS)-1 to IRS-4 proteins, thus initiating the intracellular signaling cascade [9]. The two major pathways of insulin signaling are the phosphatidylinositol 3-kinase (PI-3 kinase) and the mitogen-activated protein (MAP) kinase. The PI-3 kinase pathway is initiated by tyrosine phosphorylation by a member of the IRS proteins, which associates with the p85 regulatory subunit of PI-3 kinase, leading to activation of the enzyme. This pathway results in the activation of Akt and other downstream effector molecules that mediate the metabolic response to insulin; this includes, among others, the translocation of the glucose transporter 4 (GLUT4) to the membrane. On the other hand, the MAP kinase pathway begins with phosphorylation of Shc, Grb2/Sos and ras and results in the activation of extracellular signal-regulated kinase (ERK)-1 and ERK-2. Activated ERKs, which are a type of MAP kinase, mediate the mitogenic and pro-inflammatory responses of insulin signaling. In patients with obesity or T2DM who have profound insulin resistance, the pathways leading to the activation of PI-3 kinase are blocked, possibly through serine phosphorylation of the insulin receptor and/or IRS proteins, whereas the MAP kinase pathway remains open and may even be hypersensitive [10].

Inflammatory cytokines and insulin resistance

Inflammatory cytokines like tumor necrosis factor-alpha (TNF-α) can induce insulin resistance and suppression of Glut4 expression by inhibiting insulin receptor autophosphorylation [11] or by inducing serine phosphorylation of IRS-1 [12]. Interleukin-6 also inhibits insulin signal transduction in hepatocytes. This effect seems to be related to SOCS-3 (suppressor of cytokine signalling-3), a protein that associates itself with the insulin receptor, inhibits its autophosphorylation, the tyrosine phosphorylation of IRS-1, the association of the p85 subunit of PI-3 kinase to IRS-1, and the subsequent activation of Akt [13]. Leptin produced by adipose tissue may contribute to insulin resistance through phosphorylation of serine residues of IRS-1 [14]. The involvement of inflammatory cytokines in insulin resistance is very important for two reasons. First, it connects adipose tissue–a major source of inflammatory cytokines in patients with abdominal obesity [15]–with insulin resistance and MetS. Second, it provides a plausible explanation for the interplay between chronic inflammatory diseases (like rheumatoid arthritis [RA]) and MetS/CVD. Insulin resistance may contribute to the pathogenesis of MetS through hyperglycemia, compensatory hyperinsulinemia, and unbalanced insulin action. Among them, hyperinsulinemia seems to be the most important factor (Figure 1).
Figure 1
Figure 1

Pathophysiology of the metabolic syndrome: both insulin resistance and lipid overflow contribute to MetS evolution. IL-6, interleukin-6; MAP, mitogen-activated protein; TNF-α, tumor necrosis factor-alpha.

Abdominal obesity and insulin resistance

Although obesity is a major contributor to MetS pathophysiology, it is not the sole factor nor is it a direct consequence of insulin resistance [16]. Thus, patients with mutations in insulin receptor or autoantibodies to insulin receptor may exhibit huge increases in plasma insulin (up to 100-fold) but typically have no obesity, hypertension, or atherogenic dyslipidemia [17]. On the other hand, abdominal obesity–the most prevalent component of MetS–is associated with atherogenic and diabetogenic abnormalities. There are data supporting that abdominal obesity does not represent a consequence of MetS but rather is a causal factor [18]. In individuals with visceral obesity (due to a surplus of energy), hypertrophic adipocytes are characterized by a hyperlipolytic state that is resistant to the antilipolytic effect of insulin [19]. The non-esterified fatty acids (NEFAs) produced in excess flux to the liver where they may impair liver metabolism (liver insulin resistance); more specifically, they increase hepatic glucose production (contributing to hyperglycemia), decrease apolipoprotein B degradation, and increase triacylglycerolrich lipoproteins [20]. In parallel, the ectopic accumulation of lipids within muscles renders myocytes insulin-resistant, thus contributing to defective glucose metabolism. In addition to NEFA overproduction, visceral fat may contribute to MetS through its action as an endocrine organ that produces – among others – pro-inflammatory cytokines like TNF-α and interleukin-6 (Figure 1). In obesity, the accumulation of macrophages in abdominal fat contributes to pro-inflammatory cytokine production [15]. Moreover, in obese individuals, serum levels of adiponectin – that may facilitate insulin signaling in vitro – are decreased [21]. Overall, these data support a role of the expanded visceral adipose tissue leading to altered NEFA metabolism and pro-inflammatory profile, contributing to both insulin resistance and MetS.

Epidemiology

MetS is widespread throughout the world and its prevalence is expected to increase dramatically in the ensuing years [22, 23]. This increase is associated with the global epidemic of obesity [24]. Irrespective of the definition of MetS employed, its prevalence in the general population is high, increases with age, and varies with gender and ethnicity. Similar to the trend in adults, there is currently an alarming increase in children and young adults [25]. The overall prevalence of MetS in the US is currently estimated at 24% and increases to 44% in adults who are over 60 years. Since several definitions of the syndrome are in use, it is difficult to compare prevalence and impact between countries.

Comparisons of published prevalence for different populations are presented in Table 2.
Table 2

Prevalence of metabolic syndrome in different countries according to the National Cholesterol Education Program criteria

Age group, years

Country

Percentage in males

Percentage in females

>20

US

24

23.7

>18

Greece

24.2

22.8

20–80

Cyprus

26.5

18.3

>20

Italy

22.3

27.2

>20

India

22.9

39.9

>20

Iran

24

42

>25

Poland

16.2

20.9

>25

North Jordan

28.7

40.9

35–74

China

9.8

17.8

55–74

Germany

28

24

50–69

Ireland

21.8

21.5

70

Sweden

26.3

19.2

Clinical significance

In view of the controversy about the clinical criteria and the lack of a unifying pathophysiologic process, the clinical significance of MetS has not been universally accepted [26]. Thus, the US Food and Drug Administration does not consider MetS as a distinct disease entity. Similar statements cautioning against the premature wide adoption of MetS in clinical practice have been made by the American Diabetes Association and the European Association for the Study of Diabetes, which suggest that it requires further study before its designation as a syndrome is truly warranted and at the same time warn physicians against labeling patients with this term. Nevertheless, in the US, a version of MetS has an ICD-9 (International Statistical Classification of Diseases and Related Health Problems, ninth revision) code (277.7), which permits health care reimbursement.

Despite the aforementioned criticisms, numerous published clinical studies have established the association of MetS with an increased risk of both diabetes [27, 28] and CVD [29, 30]. A recent meta-analysis of 21 studies, by Galassi and colleagues [31], demonstrated that individuals with MetS compared with those without had an increased all-cause mortality (relative risk [RR] 1.35) and CVD (RR 1.74) as well as an increased incidence of CVD (RR 1.53), coronary heart disease (RR 1.52), and stroke (RR 1.76). Several studies have also shown that MetS confers an increased risk for the development of T2DM, with a variety of RR estimates ranging from 3.5 in the WOSCOPS (West of Scotland Coronary Prevention Study) [32] up to 6.3 in the San Antonio Heart Study [33] and 17.9 with greater than or equal to 4 MetS traits in the Beaver Dam Study [33, 34]. On the other hand, there are notable exceptions to the large body of evidence documenting the adverse impact of MetS–at least in selected groups of patients. Bruno and colleagues [35] demonstrated that elderly patients with MetS had comparable hazard ratios for all-cause and CVD mortality compared with subjects without the syndrome. Finally, Protopsaltis and colleagues [36], in a recently published study, proposed that MetS per se at baseline or combinations of its components do not predict the development of ischemic stroke in T2DM patients. Accordingly, Bertoni and colleagues [37] found that, although insulin resistance was associated with increased subclinical atherosclerosis, the association was not independent of the risk factors that comprise MetS.

An important clinical question is whether the presence of MetS per se adds to CVD prediction beyond the contribution of the individual risk factors. Sattar and colleagues [32] showed that MetS was not a significant predictor of coronary heart disease when adjusted for its component factors in a multivariate model. Two cross-sectional studies showed that the impact of the syndrome on CVD was greatly attenuated in a multivariate analysis by controlling for certain of its components, thereby suggesting that the whole is not greater than its parts [38, 39]. Moreover, in a prospective study of diabetic and non-diabetic subjects free of CVD and followed for an average of 11 years, the risk of incident coronary heart disease associated with the syndrome was no greater than that explained by the presence of its components [8]. These studies suggest that the syndrome itself conveys no greater information than the sum of its component risk factors.

Metabolic syndrome and other risk assessment algorithms

Although the presence of clinical criteria for MetS is predictive of an increased relative CVD risk, MetS should not replace the need to assess overall cardiovascular risk based on well-established CVD risk factors such as age, gender, smoking, blood pressure, LDL cholesterol, and diabetes [40]. It has also been argued that current risk assessment algorithms such as the Framingham Heart Study calculator [41] and UK Prospective Diabetes Study risk model [42] largely capture the risk associated with MetS.

Several studies have compared the predictive value of MetS with that of the Framingham risk prediction model. Girman and colleagues [43] showed that the increased event rate in subjects with MetS remained significant after adjustment for the Framingham 10-year risk, suggesting that the syndrome carries an additional risk not captured by the Framingham risk scoring. Moreover, a clear gradation in the risk of coronary heart disease outcome is evident with each additional component of MetS; men with three or more components and women with two or more components are at statistically elevated risk [8].

Therapeutic interventions

A 10-year risk assessment is needed in all those individuals who have MetS. If the 10-year risk is high, drug therapy to modify CVD risk factors might be required, whereas if the risk is low, therapeutic lifestyle modification is the first-line therapy [44]. Lifestyle modification, including both weight reduction and increased physical activity, is the cornerstone of treatment for MetS. Although it may not modify any given risk factor as much as a particular drug will, it is beneficial since it produces moderate reduction in all metabolic risk factors [45]. There is general agreement that persons with MetS should adhere to a set of dietary principles: low intake of saturated fats, trans fats, and cholesterol; reduced consumption of simple sugars; and increased intake of fruits, vegetables, and whole grains [44]. Caloric intake should be reduced by 500 to 1,000 calories per day to produce a weight loss of 0.5 to 1.0 kg per week. A reasonable goal for most individuals is moderate exercise such as walking for 30 minutes per day at least 5 days per week [45].

Pharmacotherapy involves the aggressive management of well-established risk factors. For dyslipidemia, a statin or a fibrate might be a reasonable treatment. Recently, a study showed that after 36 weeks of treatment with either simvastatin or atorvastatin, almost 50% of patients with MetS no longer met the classification criteria. Mild elevations of blood pressure can often be controlled with lifestyle changes, but if hypertension persists antihypertensive drugs are usually required [46]. Some investigators believe that angiotensin-converting enzyme inhibitors or angiotensin-receptor blockers are better first-line therapy for MetS patients, especially when T2DM is present, but the issue of the most effective drug has not been entirely resolved. For insulin resistance, metformin or a thiazolidinedione might be considered. Yet at the same time, it is unknown whether treating insulin resistance itself would be of value in preventing CVD in all patients or in a subset of MetS patients. Preliminary reports indicate that metformin or thiazolidinediones also reduce the risk for T2DM in people with IFG or impaired glucose tolerance and improve insulin sensitivity [47, 48].

Because of the strong association between MetS, CVD, and diabetes, there is urgent need for strategies to prevent the emerging global epidemic. Additional research is needed to determine whether treatment of underlying causes of MetS (for example, insulin resistance in the absence of hyperglycemia) results in better outcome beyond the levels achieved by interventions that target conventional cardiovascular risk factors. Until randomized controlled trials have been completed, there is no appropriate pharmacological treatment for MetS, nor should it be assumed that pharmacological therapy to reduce insulin resistance will be beneficial to patients with the syndrome. Thus, treatment should be aimed at well-established risk factors.

Rheumatic diseases: cardiovascular burden and metabolic syndrome

Inflammation is a key feature of obesity and T2DM [49] while patients with chronic inflammatory diseases, like RA or systemic lupus erythematosus (SLE), have an increased risk for CVD [50, 51]. RA patients have almost a four-fold increase in cardiovascular events and most importantly this increased risk ratio is independent of traditional risk factors for CVDs. CVDs are the most common cause of death, with approximately 40% of deaths in RA patients attributed to CVD [52]. It has been proposed that pathogenetic mechanisms attributed to the underlying disease or its treatments are associated with premature atherosclerosis [53]. Although the exact mechanism promoting atherosclerosis in RA remains to be defined, chronic inflammation may alter vascular endothelial biology to a pro-thrombotic/pro-atherogenic state [54].

Similarly to patients with RA, those with SLE have a higher risk for myocardial infarctions, which is even higher in younger patients (up to an eight-fold increase) [55]. Approximately 25% of deaths in SLE are attributed to CVD morbidity, which is the leading cause of death. More importantly, although symptomatic coronary disease is not uncommon (6% to 15%), subclinical atherosclerosis assessed by non-invasive techniques [stress studies using technetium 99 m sestamibi single-photon emission tomography (SPECT)] is much higher and observed in upto 42% of asymptomatic SLE patients [56]. Interestingly, although SLE patients have a high prevalence of traditional risk factors for atherosclerosis [57], the rate of vascular events has been found to be more than seven times that attributed to traditional risk factors [58]. These results suggest the importance of disease-associated factors (like antiphospholipid antibodies) or treatments (like steroids) in the evolution of atherosclerosis.

Several groups have assessed insulin resistance and MetS in patients with rheumatic diseases (Table 3). Homeostatic model assessment of insulin sensitivity (HOMA-S) and the quantitative insulin sensitivity check index (QUICKI) are indices most often applied for insulin sensitivity; homeostatic model assessment of insulin resistance (HOMA-IR) and homeostatic model assessment of beta cell function (HOMA-B) are indices applied for insulin resistance and beta cell function, respectively.
Table 3

High prevalence of metabolic syndrome in patients with rheumatic diseases

    

Metabolic syndrome prevalence, percentage

 

Number

Mean age, years

Women, percentage

NCEP

WHO

NCEP

WHO

 

Rheumatoid arthritis (RA)

Control

Karvounaris, et al. [62]

200

63

74

44

-

41

-

Chung, et al. [63]

       

   Early RA

88

51

64

30

31

22

-

   Established RA

66

59

73

42

42

  

Dessein, et al. [61]

74

56

86

-

19

-

-

 

Systemic lupus erythematosus

Control

Chung, et al. [67]

102

40

91

29

32

20

11

Magadmi, et al. [66]

44

51

100

18

-

-

-

 

Ankylosing spondylitis

Control

Malesci, et al. [68]

24

51

12

46

-

11

-

NCEP, National Cholesterol Education Program; WHO, World Health Organization.

Rheumatoid arthritis: insulin resistance and metabolic syndrome

Dessein and colleagues [59] reported that RA patients have lower insulin sensitivity (assessed by QUICKI) compared with osteoarthritis patients (n = 39 in both groups; P < 0.05), but after controlling for C-reactive protein (CRP) levels, QUICKI was comparable between the two groups. Glucocorticoids were not associated with decreased insulin sensitivity, whereas other factors (waist circumference, CRP, HDL cholesterol, and triglycerides) were associated. Several years later, the same group found that RA patients with high-grade inflammation (high-sensitivity CRP [hsCRP] greater than 1.92 mg/L) had higher insulin resistance compared with those with lower hsCRP [60]. However, in mixed regression models, only abdominal obesity and the patient's assessment of disease activity were predictors of insulin resistance, whereas other disease activity indices (CRP, erythrocyte sedimentation rate, and disease activity index of 28 joint counts [DAS28]) were not. The authors concluded that modifiable factors like obesity and disease activity should be targeted for prevention of CVD in RA patients.

Assessing the correlation of insulin resistance with surrogate markers of atherosclerosis–like carotid artery intima-media thickness (CCA-IMT) or the presence of atherosclerotic plaque–Dessein and colleagues [61] found that QUICKI was associated with both IMT (R = -0.26; P = 0.04) and the presence of plaque (P = 0.03). In this group of RA patients (n = 74, mean age 55.8 years, 86% women), they found that the prevalence rates of MetS were 14% according to WHO criteria and 19% according to NCEP criteria. Only the WHO-defined MetS was associated with CCA-IMT (P = 0.08 to 0.04), but overall both methods performed poorly in identifying RA patients with atherosclerosis.

Our team has studied the prevalence of MetS and its relationship with RA-associated factors in a group of middle-to older-aged (mean age 63 years, 74% women) RA patients (n = 200) and compared them with 400 age- and gender-matched controls in the Mediterranean island of Crete. The prevalence of MetS (according to the NCEP criteria) was high (44%) but comparable to that of the control population (41%). Interestingly, in multivariate logistic regression analysis, the risk of having moderate to high disease activity (DAS28 >3.2) was significantly higher in patients with MetS compared with those without MetS (odds ratio 9.2, 95% confidence interval 1.49 to 57), irrespective of the treatment [62]. This correlation between RA disease activity and MetS is indirect evidence of the role of chronic inflammation in MetS and atherosclerosis development. We are currently investigating the effect of potent anti-TNF-α treatment in insulin resistance in RA patients. After 3 months of treatment, patients with MetS at baseline (n = 31) improved significantly in both insulin resistance (HOMA, from 7.9 ± 7.5 to 2.6 ± 1.6; P = 0.01) and insulin sensitivity (QUCKI, from 0.31 ± 5.1 to 0.35 ± 4.4; P = 0.03) (P.I. Sidiropoulos, S.A. Karvounaris, D.T. Boumpas, unpublished data).

Chung and colleagues [63] studied MetS prevalence according to both WHO and NCEP criteria and its association to coronary atherosclerosis, applying electron beam computed tomography in a group of RA patients (n = 154, mean age 51 years for early RA and 59 years for established disease, 68% women) and compared them with controls. They found that, compared with controls, RA patients had a higher prevalence of WHO-defined (P = 0.001) and NCEP-defined (P = 0.03) MetS; the prevalence rates of MetS (NCEP criteria) were 42% and 30% in patients with longstanding and early disease, respectively, not significantly different compared with 42% and 31% according to WHO criteria. Patients with WHO-defined MetS had an increased risk of having higher coronary artery calcification scores, independent of age and gender (odds ratio = 2; P = 0.04) [63].

Taken together, the studies by Karvounaris and colleagues [62] and Chung and colleagues [63] reported a high prevalence of MetS, albeit comparable to controls. The low prevalence in the report by Dessein and colleagues [61] may be attributed to demographic differences (lower age and higher percentage of women) or to the smaller sample size assessed (Table 3). From these studies, one can conclude that the prevalence of MetS is high in RA patients and correlates with disease activity and markers of atherosclerosis.

Adiponectin is one of the adipokines that has been described to increase insulin sensitivity, while there are data supporting that it has anti-inflammatory properties. As stated previously, low levels of adiponectin have been described in patients with T2DM or obesity [21]. It is believed that pro-inflammatory factors produced by adipose tissue suppress adiponection production and thus increase insulin resistance. Nevertheless, the relationship between adiponectin and inflammation seems to be more complex. In contrast to obesity, in diseases with chronic inflammation like RA and SLE, increased levels of adiponectin have been found, while in vitro data with chondrocytes and synovial fibroblasts suggest that adiponectin may exert pro-inflammatory effects [64, 65]. These apparently controversial data pose more questions about the relationship between adiponectin, inflammation, and insulin signaling which should be addressed.

Systemic lupus erythematosus

El Magadmi and colleagues [66] assessed insulin resistance in a group of women with SLE (n = 44, mean age 50.5 years) and compared them with age-matched controls. They found that SLE patients had significantly lower insulin sensitivity (HOMA-S; P < 0.01), but HOMA-S did not correlate to disease activity or steroid therapy. The prevalence of MetS according to NCEP criteria in this small group was 18%. On the other hand, Chung and colleagues [67] assessed MetS prevalence in an SLE cohort (n = 102, mean age 40 years, 91% women) and compared them to age- and gender-matched controls (n = 101). Insulin resistance was more prevalent in patients (44% versus 25%; P = 0.005) and the prevalence of the WHO-MetS was higher in patients (32.4% versus 10.9%; P < 0.001). Although the NCEP-MetS was more prevalent in patients than controls, this was not statistically significant (29.4% versus 19.8%; P = 0.14), probably because the study was underpowered to detect small differences. In this cohort, the presence of MetS correlated to higher CRP levels, but neither lupus activity nor damage scores were associated with MetS. The authors concluded that MetS is more prevalent in lupus patients, while the correlation of MetS with inflammatory markers underscores a possible common link between chronic inflammation and increased cardiovascular risk in SLE patients.

Ankylosing spondylitis

A small (n = 24) controlled study by Malesci and colleagues [68] found that ankylosing spondylitis (AS) patients had a higher prevalence of NCEP-MetS compared with controls (45.8% versus 10.5%; P = 0.02). In a cohort of AS male patients (n = 63, mean age 40 years) treated with anti-TNF-α agents, we investigated the prevalence of MetS according to NCEP criteria and compared the cohort to age-matched controls. MetS was more prevalent in AS patients (34.9% versus 19%; P < 0.01), whereas AS patients with MetS had higher disease activity (Bath Ankylosing Spondylitis Activity Index; P < 0.05) (P.I. Sidiropoulos, S.A. Karvounaris, D.T. Boumpas, manuscript submitted).

Conclusion

Patients with chronic inflammatory rheumatic diseases have an increased risk for CVD morbidity and mortality. In these patients, a high prevalence of traditional risk factors and MetS has been found. These data, albeit circumstantial, point out chronic inflammation as one of the key contributors to MetS and accelerated atherosclerosis. Aggressive treatment of both underlying disease–to lessen the inflammatory burden–as well as the elimination of traditional risk factors may reduce CVD morbidity and mortality. Assessment of both MetS along with the 10-year risk assessment for CVD events should be applied to identify patients in greater need for lifestyle modification and/or drug therapy.

Abbreviations

AS: 

= ankylosing spondylitis

CCA-IMT: 

= carotid artery intima-media thickness

CRP: 

= C-reactive protein

CVD: 

= cardiovascular disease

DAS28: 

= disease activity index of 28 joint counts

ERK: 

= extracellular signal-regulated kinase

GLUT4: 

= glucose transporter 4

HDL: 

= high-density lipoprotein

HOMA-S: 

= homeostatic model assessment of insulin sensitivity

hsCRP: 

= high-sensitivity C-reactive protein

IDF: 

= International Diabetes Federation

IFG: 

= impaired fasting glucose

IRS: 

= insulin receptor substrate

LDL: 

= low-density lipoprotein

MAP: 

= mitogen-activated protein

MetS: 

= metabolic syndrome

NCEP: 

= National Cholesterol Education Program

NEFA: 

= non-esterified fatty acid

PI-3 kinase: 

= phosphatidylinositol 3-kinase

QUICKI: 

= quantitative insulin sensitivity check index

RA: 

= rheumatoid arthritis

RR: 

= relative risk

SLE: 

= systemic lupus erythematosus

T2DM: 

= type 2 diabetes mellitus

TNF-α: 

= tumor necrosis factor-alpha

WHO: 

= World Health Organization.

Declarations

Acknowledgements

This work was supported by the FP6 European AUTOCURE program.

Authors’ Affiliations

(1)
Department Rheumatology, Clinical Immunology and Allergy, University Hospital, Medical School, University of Crete, 1, Voules Str, Heraklion, 71110, Greece

References

  1. Reaven GM: Banting lecture 1988. Role of insulin resistance in human disease. Diabetes. 1988, 37: 1595-1607. 10.2337/diabetes.37.12.1595.View ArticlePubMedGoogle Scholar
  2. Barker DJ, Hales CN, Fall CH, Osmond C, Phipps K, Clark PM: Type 2 (non-insulin-dependent) diabetes mellitus, hypertension and hyperlipidaemia (syndrome X): relation to reduced fetal growth. Diabetologia. 1993, 36: 62-67. 10.1007/BF00399095.View ArticlePubMedGoogle Scholar
  3. Reilly MP, Rader DJ: The metabolic syndrome: more than the sum of its parts?. Circulation. 2003, 108: 1546-1551. 10.1161/01.CIR.0000088846.10655.E0.View ArticlePubMedGoogle Scholar
  4. Alberti KG, Zimmet PZ: Definition, diagnosis and classification of diabetes mellitus and its complications. Part 1: diagnosis and classification of diabetes mellitus provisional report of a WHO consultation. Diabet Med. 1998, 15: 539-553. 10.1002/(SICI)1096-9136(199807)15:7<539::AID-DIA668>3.0.CO;2-S.View ArticlePubMedGoogle Scholar
  5. 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). JAMA. 2001, 285: 2486-2497. 10.1001/jama.285.19.2486.Google Scholar
  6. Alberti KG, Zimmet P, Shaw J: The metabolic syndrome–a new worldwide definition. Lancet. 2005, 366: 1059-1062. 10.1016/S0140-6736(05)67402-8.View ArticlePubMedGoogle Scholar
  7. Lakka HM, Laaksonen DE, Lakka TA, Niskanen LK, Kumpusalo E, Tuomilehto J, Salonen JT: The metabolic syndrome and total and cardiovascular disease mortality in middle-aged men. JAMA. 2002, 288: 2709-2716. 10.1001/jama.288.21.2709.View ArticlePubMedGoogle Scholar
  8. McNeill AM, Rosamond WD, Girman CJ, Golden SH, Schmidt MI, East HE, Ballantyne CM, Heiss G: The metabolic syndrome and 11-year risk of incident cardiovascular disease in the atherosclerosis risk in communities study. Diabetes Care. 2005, 28: 385-390. 10.2337/diacare.28.2.385.View ArticlePubMedGoogle Scholar
  9. White MF, Kahn CR: The insulin signaling system. J Biol Chem. 1994, 269: 1-4.PubMedGoogle Scholar
  10. Cusi K, Maezono K, Osman A, Pendergrass M, Patti ME, Pratipanawatr T, DeFronzo RA, Kahn CR, Mandarino LJ: Insulin resistance differentially affects the PI 3-kinase- and MAP kinase-mediated signaling in human muscle. J Clin Invest. 2000, 105: 311-320. 10.1172/JCI7535.PubMed CentralView ArticlePubMedGoogle Scholar
  11. Uysal KT, Wiesbrock SM, Marino MW, Hotamisligil GS: Protection from obesity-induced insulin resistance in mice lacking TNF-alpha function. Nature. 1997, 389: 610-614. 10.1038/39335.View ArticlePubMedGoogle Scholar
  12. Gupta D, Varma S, Khandelwal RL: Long-term effects of tumor necrosis factor-alpha treatment on insulin signaling pathway in HepG2 cells and HepG2 cells overexpressing constitutively active Akt/PKB. J Cell Biochem. 2007, 100: 593-607. 10.1002/jcb.21080.View ArticlePubMedGoogle Scholar
  13. Senn JJ, Klover PJ, Nowak IA, Mooney RA: Interleukin-6 induces cellular insulin resistance in hepatocytes. Diabetes. 2002, 51: 3391-3399. 10.2337/diabetes.51.12.3391.View ArticlePubMedGoogle Scholar
  14. Hennige AM, Stefan N, Kapp K, Lehmann R, Weigert C, Beck A, Moeschel K, Mushack J, Schleicher E, Häring HU: Leptin down-regulates insulin action through phosphorylation of serine-318 in insulin receptor substrate 1. FASEB J. 2006, 20: 1206-1208. 10.1096/fj.05-4635fje.View ArticlePubMedGoogle Scholar
  15. Weisberg SP, McCann D, Desai M, Rosenbaum M, Leibel RL, Ferrante AW: Obesity is associated with macrophage accumulation in adipose tissue. J Clin Invest. 2003, 112: 1796-1808.PubMed CentralView ArticlePubMedGoogle Scholar
  16. Miranda PJ, DeFronzo RA, Califf RM, Guyton JR: Metabolic syndrome: definition, pathophysiology, and mechanisms. Am Heart J. 2005, 149: 33-45. 10.1016/j.ahj.2004.07.013.View ArticlePubMedGoogle Scholar
  17. Kahn CR, Flier JS, Bar RS, Archer JA, Gorden P, Martin MM, Roth J: The syndromes of insulin resistance and acanthosis nigricans. Insulin-receptor disorders in man. N Engl J Med. 1976, 294: 739-745.View ArticlePubMedGoogle Scholar
  18. Lebovitz HE, Banerji MA: Point: visceral adiposity is causally related to insulin resistance. Diabetes Care. 2005, 28: 2322-2325. 10.2337/diacare.28.9.2322.View ArticlePubMedGoogle Scholar
  19. Mittelman SD, Van Citters GW, Kirkman EL, Bergman RN: Extreme insulin resistance of the central adipose depot in vivo. Diabetes. 2002, 51: 755-761. 10.2337/diabetes.51.3.755.View ArticlePubMedGoogle Scholar
  20. Despres JP, Lemieux I: Abdominal obesity and metabolic syndrome. Nature. 2006, 444: 881-887. 10.1038/nature05488.View ArticlePubMedGoogle Scholar
  21. Côté M, Mauriège P, Bergeron J, Alméras N, Tremblay A, Lemieux I, Després JP: Adiponectinemia in visceral obesity: impact on glucose tolerance and plasma lipoprotein and lipid levels in men. J Clin Endocrinol Metab. 2005, 90: 1434-1439. 10.1210/jc.2004-1711.View ArticlePubMedGoogle Scholar
  22. Ford ES: Prevalence of the metabolic syndrome defined by the International Diabetes Federation among adults in the U.S. Diabetes Care. 2005, 28: 2745-2749. 10.2337/diacare.28.11.2745.View ArticlePubMedGoogle Scholar
  23. Sarti C, Gallagher J: The metabolic syndrome: prevalence, CHD risk, and treatment. J Diabetes Complications. 2006, 20: 121-132. 10.1016/j.jdiacomp.2005.06.014.View ArticlePubMedGoogle Scholar
  24. Flegal KM, Carroll MD, Ogden CL, Johnson CL: Prevalence and trends in obesity among US adults, 1999–2000. JAMA. 2002, 288: 1723-1727. 10.1001/jama.288.14.1723.View ArticlePubMedGoogle Scholar
  25. Sinha R, Fisch G, Teague B, Tamborlane WV, Banyas B, Allen K, Savoye M, Rieger V, Taksali S, Barbetta G, Sherwin RS, Caprio S: Prevalence of impaired glucose tolerance among children and adolescents with marked obesity. N Engl J Med. 2002, 346: 802-810. 10.1056/NEJMoa012578.View ArticlePubMedGoogle Scholar
  26. Kahn R, Buse J, Ferrannini E, Stern M: The metabolic syndrome: time for a critical appraisal. Joint statement from the American Diabetes Association and the European Association for the Study of Diabetes. Diabetologia. 2005, 48: 1684-1699. 10.1007/s00125-005-1876-2.View ArticlePubMedGoogle Scholar
  27. Wilson PW, D'Agostino RB, Parise H, Sullivan L, Meigs JB: Metabolic syndrome as a precursor of cardiovascular disease and type 2 diabetes mellitus. Circulation. 2005, 112: 3066-3072. 10.1161/CIRCULATIONAHA.105.539528.View ArticlePubMedGoogle Scholar
  28. Kekalainen P, Sarlund H, Pyorala K, Laakso M: Hyperinsulinemia cluster predicts the development of type 2 diabetes independently of family history of diabetes. Diabetes Care. 1999, 22: 86-92. 10.2337/diacare.22.1.86.View ArticlePubMedGoogle Scholar
  29. Isomaa B, Almgren P, Tuomi T, Forsén B, Lahti K, Nissén M, Taskinen MR, Groop L: Cardiovascular morbidity and mortality associated with the metabolic syndrome. Diabetes Care. 2001, 24: 683-689. 10.2337/diacare.24.4.683.View ArticlePubMedGoogle Scholar
  30. Malik S, Wong ND, Franklin SS, Kamath TV, L'Italien GJ, Pio JR, Williams GR: Impact of the metabolic syndrome on mortality from coronary heart disease, cardiovascular disease, and all causes in United States adults. Circulation. 2004, 110: 1245-1250. 10.1161/01.CIR.0000140677.20606.0E.View ArticlePubMedGoogle Scholar
  31. Galassi A, Reynolds K, He J: Metabolic syndrome and risk of cardiovascular disease: a meta-analysis. Am J Med. 2006, 119: 812-819. 10.1016/j.amjmed.2006.02.031.View ArticlePubMedGoogle Scholar
  32. Sattar N, Gaw A, Scherbakova O, Ford I, O'Reilly DS, Haffner SM, Isles C, Macfarlane PW, Packard CJ, Cobbe SM, Shepherd J: Metabolic syndrome with and without C-reactive protein as a predictor of coronary heart disease and diabetes in the West of Scotland Coronary Prevention Study. Circulation. 2003, 108: 414-419. 10.1161/01.CIR.0000080897.52664.94.View ArticlePubMedGoogle Scholar
  33. Lorenzo C, Okoloise M, Williams K, Stern MP, Haffner SM: The metabolic syndrome as predictor of type 2 diabetes: the San Antonio heart study. Diabetes Care. 2003, 26: 3153-3159. 10.2337/diacare.26.11.3153.View ArticlePubMedGoogle Scholar
  34. Klein BE, Klein R, Lee KE: Components of the metabolic syndrome and risk of cardiovascular disease and diabetes in Beaver Dam. Diabetes Care. 2002, 25: 1790-1794. 10.2337/diacare.25.10.1790.View ArticlePubMedGoogle Scholar
  35. Bruno G, Merletti F, Biggeri A, Bargero G, Ferrero S, Runzo C, Prina Cerai S, Pagano G, Cavallo-Perin P, Casale Monferrato Study: Metabolic syndrome as a predictor of all-cause and cardiovascular mortality in type 2 diabetes: the Casale Monferrato Study. Diabetes Care. 2004, 27: 2689-2694. 10.2337/diacare.27.11.2689.View ArticlePubMedGoogle Scholar
  36. Protopsaltis I, Korantzopoulos P, Milionis HJ, Koutsovasilis A, Nikolopoulos GK, Dimou E, Kokkoris S, Brestas P, Elisaf MS, Melidonis A: Metabolic syndrome and its components as predictors of ischemic stroke in type 2 diabetic patients. Stroke. 2008, 39: 1036-1038. 10.1161/STROKEAHA.107.498311.View ArticlePubMedGoogle Scholar
  37. Bertoni AG, Wong ND, Shea S, Ma S, Liu K, Preethi S, Jacobs DR, Wu C, Saad MF, Szklo M: Insulin resistance, metabolic syndrome, and subclinical atherosclerosis: the Multi-Ethnic Study of Atherosclerosis (MESA). Diabetes Care. 2007, 30: 2951-2966. 10.2337/dc07-1042.View ArticlePubMedGoogle Scholar
  38. Alexander CM, Landsman PB, Teutsch SM, Haffner SM: NCEP-defined metabolic syndrome, diabetes, and prevalence of coronary heart disease among NHANES III participants age 50 years and older. Diabetes. 2003, 52: 1210-1214. 10.2337/diabetes.52.5.1210.View ArticlePubMedGoogle Scholar
  39. Yarnell JW, Patterson CC, Bainton D, Sweetnam PM: Is metabolic syndrome a discrete entity in the general population? Evidence from the Caerphilly and Speedwell population studies. Heart. 1998, 79: 248-252.PubMed CentralView ArticlePubMedGoogle Scholar
  40. Kahn R, Buse J, Ferrannini E, Stern M: The metabolic syndrome: time for a critical appraisal: joint statement from the American Diabetes Association and the European Association for the Study of Diabetes. Diabetes Care. 2005, 28: 2289-2304. 10.2337/diacare.28.9.2289.View ArticlePubMedGoogle Scholar
  41. Wilson PW, D'Agostino RB, Levy D, Belanger AM, Silbershatz H, Kannel WB: Prediction of coronary heart disease using risk factor categories. Circulation. 1998, 97: 1837-1847.View ArticlePubMedGoogle Scholar
  42. Stevens RJ, Kothari V, Adler AI, Stratton IM: The UKPDS risk engine: a model for the risk of coronary heart disease in Type II diabetes (UKPDS 56). Clin Sci (Lond). 2001, 101: 671-679.View ArticleGoogle Scholar
  43. Girman CJ, Rhodes T, Mercuri M, Pyörälä K, Kjekshus J, Pedersen TR, Beere PA, Gotto AM, Clearfield M, 4S Group and the AFCAPS/TexCAPS Research Group: The metabolic syndrome and risk of major coronary events in the Scandinavian Simvastatin Survival Study (4S) and the Air Force/Texas Coronary Atherosclerosis Prevention Study (AFCAPS/TexCAPS). Am J Cardiol. 2004, 93: 136-141. 10.1016/j.amjcard.2003.09.028.View ArticlePubMedGoogle Scholar
  44. 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) final report. Circulation. 2002, 106: 3143-3421.Google Scholar
  45. Lakka TA, Laaksonen DE, Lakka HM, Männikkö N, Niskanen LK, Rauramaa R, Salonen JT: Sedentary lifestyle, poor cardiorespiratory fitness, and the metabolic syndrome. Med Sci Sports Exerc. 2003, 35: 1279-1286. 10.1249/01.MSS.0000079076.74931.9A.View ArticlePubMedGoogle Scholar
  46. Chobanian AV, Bakris GL, Black HR, Cushman WC, Green LA, Izzo JL, Jones DW, Materson BJ, Oparil S, Wright JT, Roccella EJ, Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure. National Heart, Lung, and Blood Institute; National High Blood Pressure Education Program Coordinating Committee: Seventh report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure. Hypertension. 2003, 42: 1206-1252. 10.1161/01.HYP.0000107251.49515.c2.View ArticlePubMedGoogle Scholar
  47. Knowler WC, Barrett-Connor E, Fowler SE, Hamman RF, Lachin JM, Walker EA, Nathan DM, Diabetes Prevention Program Research Group: Reduction in the incidence of type 2 diabetes with lifestyle intervention or metformin. N Engl J Med. 2002, 346: 393-403. 10.1056/NEJMoa012512.View ArticlePubMedGoogle Scholar
  48. Gabriel SE, Crowson CS, Kremers HM, Doran MF, Turesson C, O'Fallon WM, Matteson EL: Survival in rheumatoid arthritis: a population-based analysis of trends over 40 years. Arthritis Rheum. 2003, 48: 54-58. 10.1002/art.10705.View ArticlePubMedGoogle Scholar
  49. Hotamisligil GS: Inflammation and metabolic disorders. Nature. 2006, 444: 860-867. 10.1038/nature05485.View ArticlePubMedGoogle Scholar
  50. Boers M, Dijkmans B, Gabriel S, Maradit-Kremers H, O'Dell J, Pincus T: Making an impact on mortality in rheumatoid arthritis: targeting cardiovascular comorbidity. Arthritis Rheum. 2004, 50: 1734-1739. 10.1002/art.20306.View ArticlePubMedGoogle Scholar
  51. Schattner A, Liang MH: The cardiovascular burden of lupus: a complex challenge. Arch Intern Med. 2003, 163: 1507-1510. 10.1001/archinte.163.13.1507.View ArticlePubMedGoogle Scholar
  52. Callahan LF, Pincus T: Mortality in the rheumatic diseases. Arthritis Care Res. 1995, 8: 229-241. 10.1002/art.1790080406.View ArticlePubMedGoogle Scholar
  53. del Rincon ID, Williams K, Stern MP, Freeman GL, Escalante A: High incidence of cardiovascular events in a rheumatoid arthritis cohort not explained by traditional cardiac risk factors. Arthritis Rheum. 2001, 44: 2737-2745. 10.1002/1529-0131(200112)44:12<2737::AID-ART460>3.0.CO;2-#.View ArticlePubMedGoogle Scholar
  54. Bacon PA, Townend JN: Nails in the coffin: increasing evidence for the role of rheumatic disease in the cardiovascular mortality of rheumatoid arthritis. Arthritis Rheum. 2001, 44: 2707-2710. 10.1002/1529-0131(200112)44:12<2707::AID-ART456>3.0.CO;2-M.View ArticlePubMedGoogle Scholar
  55. Ward MM: Premature morbidity from cardiovascular and cerebrovascular diseases in women with systemic lupus erythematosus. Arthritis Rheum. 1999, 42: 338-346. 10.1002/1529-0131(199902)42:2<338::AID-ANR17>3.0.CO;2-U.View ArticlePubMedGoogle Scholar
  56. Sun SS, Shiau YC, Tsai SC, Lin CC, Kao A, Lee CC: The role of technetium-99m sestamibi myocardial perfusion single-photon emission computed tomography (SPECT) in the detection of cardiovascular involvement in systemic lupus erythematosus patients with non-specific chest complaints. Rheumatology (Oxford). 2001, 40: 1106-1111. 10.1093/rheumatology/40.10.1106.View ArticleGoogle Scholar
  57. Manzi S, Selzer F, Sutton-Tyrrell K, Fitzgerald SG, Rairie JE, Tracy RP, Kuller LH: Prevalence and risk factors of carotid plaque in women with systemic lupus erythematosus. Arthritis Rheum. 1999, 42: 51-60. 10.1002/1529-0131(199901)42:1<51::AID-ANR7>3.0.CO;2-D.View ArticlePubMedGoogle Scholar
  58. Esdaile JM, Abrahamowicz M, Grodzicky T, Li Y, Panaritis C, du Berger R, Côte R, Grover SA, Fortin PR, Clarke AE, Senécal JL: Traditional Framingham risk factors fail to fully account for accelerated atherosclerosis in systemic lupus erythematosus. Arthritis Rheum. 2001, 44: 2331-2337. 10.1002/1529-0131(200110)44:10<2331::AID-ART395>3.0.CO;2-I.View ArticlePubMedGoogle Scholar
  59. Dessein PH, Stanwix AE, Joffe BI: Cardiovascular risk in rheumatoid arthritis versus osteoarthritis: acute phase response related decreased insulin sensitivity and high-density lipoprotein cholesterol as well as clustering of metabolic syndrome features in rheumatoid arthritis. Arthritis Res. 2002, 4: R5-10.1186/ar428.PubMed CentralView ArticlePubMedGoogle Scholar
  60. Dessein PH, Stanwix AE, Joffe BI: Insulin resistance and impaired beta cell function in rheumatoid arthritis. Arthritis Rheum. 2006, 54: 2765-2775. 10.1002/art.22053.View ArticlePubMedGoogle Scholar
  61. Dessein PH, Tobias M, Veller MG: Metabolic syndrome and subclinical atherosclerosis in rheumatoid arthritis. J Rheumatol. 2006, 33: 2425-2432.PubMedGoogle Scholar
  62. Karvounaris SA, Sidiropoulos PI, Papadakis JA, Spanakis EK, Bertsias GK, Kritikos HD, Ganotakis ES, Boumpas DT: Metabolic syndrome is common among middle-to-older aged Mediterranean patients with rheumatoid arthritis and correlates with disease activity: a retrospective, cross-sectional, controlled, study. Ann Rheum Dis. 2006, 66: 28-33. 10.1136/ard.2006.053488.PubMed CentralView ArticlePubMedGoogle Scholar
  63. Chung CP, Oeser A, Solus JF, Avalos I, Gebretsadik T, Shintani A, Raggi P, Sokka T, Pincus T, Stein CM: Prevalence of the metabolic syndrome is increased in rheumatoid arthritis and is associated with coronary atherosclerosis. Atherosclerosis. 2008, 196: 756-763. 10.1016/j.atherosclerosis.2007.01.004.View ArticlePubMedGoogle Scholar
  64. Ehling A, Schäffler A, Herfarth H, Tarner IH, Anders S, Distler O, Paul G, Distler J, Gay S, Schölmerich J, Neumann E, Müller-Ladner U: The potential of adiponectin in driving arthritis. J Immunol. 2006, 176: 4468-4478.View ArticlePubMedGoogle Scholar
  65. Sada KE, Yamasaki Y, Maruyama M, Sugiyama H, Yamamura M, Maeshima Y, Makino H: Altered levels of adipocytokines in association with insulin resistance in patients with systemic lupus erythematosus. J Rheumatol. 2006, 33: 1545-1552.PubMedGoogle Scholar
  66. El Magadmi M, Ahmad Y, Turkie W, Yates AP, Sheikh N, Bernstein RM, Durrington PN, Laing I, Bruce IN: Hyperinsulinemia, insulin resistance, and circulating oxidized low density lipoprotein in women with systemic lupus erythematosus. J Rheumatol. 2006, 33: 50-56.PubMedGoogle Scholar
  67. Chung CP, Avalos I, Oeser A, Gebretsadik T, Shintani A, Raggi P, Michael Stein C: High prevalence of the metabolic syndrome in patients with systemic lupus erythematosus: association with disease characteristics and cardiovascular risk factors. Ann Rheum Dis. 2007, 66: 208-214. 10.1136/ard.2006.054973.PubMed CentralView ArticlePubMedGoogle Scholar
  68. Malesci D, Niglio A, Mennillo GA, Buono R, Valentini G, La Montagna G: High prevalence of metabolic syndrome in patients with ankylosing spondylitis. Clin Rheumatol. 2007, 26: 710-714. 10.1007/s10067-006-0380-5.View ArticlePubMedGoogle Scholar

Copyright

© BioMed Central Ltd 2008

Advertisement

Arthritis Research & Therapy

ISSN: 1478-6362

Contact us