Objective To examine the clinical and epidemiological utility of the concepts of metabolic syndrome and insulin resistance syndrome in two prospective cohort studies of white men.
Methods Men aged 45–63 years were screened for evidence of ischaemic heart disease (IHD) between 1979 and 1982 and followed up at regular intervals thereafter. Non-fatal coronary events were validated from hospital records and fatal coronary events from death certificates.
Results Analysis of serum insulin concentrations in non-diabetic individuals measured at entry to the study showed no independent contribution to the prediction of subsequent IHD at 10 year follow up. Blood glucose concentrations, however, showed a small independent contribution in the combined cohort in the upper fifth of the distribution. Three different models of metabolic syndrome among non-diabetic individuals were defined based on tertiles, medians, and clusters. The predictive value of each model was assessed using logistic regression before and after adjustment for conventional and metabolic risk factors. After adjustment the odds were non-significant and close to unity.
Conclusions This study did not detect any complex relation among the five variables defining metabolic syndrome; the excess risk seems to be no greater than can be explained by individual effects of the defining variables in a multiple logistic model.
- metabolic syndrome
- insulin resistance
- ischaemic heart disease
Statistics from Altmetric.com
Hyperinsulinaemia, insulin resistance, and cardiovascular risk factors, such as dyslipidaemia, hypertension, and obesity,1 2 are closely linked with non-insulin dependent diabetes mellitus.3-8 Reaven9 has suggested that insulin resistance labelled as metabolic syndrome may occur in up to 25% of the normal population. We examined evidence for the existence of this syndrome in two general population based cohorts of British men. Previous studies of insulin10 (Caerphilly cohort) and glucose11 (Caerphilly and Speedwell cohorts) were based on five year follow up of these populations. These analyses have been combined and extended in a 10 year follow up.
Men were selected from a defined area in Caerphilly. They were aged between 45 and 59 years when first examined. A total of 2512 (89%) of 2818 men eligible for study were seen. In Speedwell men were selected from the age sex registers of 16 general practitioners working from two neighbouring health centres. The men were between 45 and 59 years of age when chosen, immediately before the study started. They were aged between 45 and 63 years when first examined. A total of 2348 (92%) of 2552 men eligible for study were seen. The total number of men for the combined cohort was 4860.
SURVEY METHODS AND FOLLOW UP
The two studies had a common core protocol and procedures, which have been described elsewhere.10-12 Briefly, at recruitment, the men attended an afternoon or evening clinic at which they completed a standard medical and smoking history, and the London School of Hygiene and Tropical Medicine chest pain questionnaire. Height, weight, and blood pressure were also measured and a 12 lead electrocardiogram (ECG) recorded. The men were asked whether they had ever been diagnosed as having diabetes. They returned, after an overnight fast, to an early morning clinic where a blood sample was taken with minimal venous stasis. Fasting samples were obtained from 4641 men. The results reported refer to the second follow up in Caerphilly. This was at a nearly constant interval of mean (SD) 120 (6) months. The results in Speedwell relate to the third follow up and the mean (SD) interval was 112 (3) months. The chest pain questionnaire was administered at follow up and a second ECG recorded. The questionnaire was extended to include questions about hospitalisation for severe chest pain. These, together with hospital activity analysis notifications of admissions coded as 410–414—ischaemic heart disease (IHD) in the International classification of diseases, (9th revision) (ICD-9)—were used as the basis for a search of hospital notes for events that satisfied the World Health Organisation (WHO) criteria for definite acute myocardial infarction. A copy of the death certificate of men who died before the end of follow up was automatically received from the National Health Service Central Register. This information enabled three categories of incident IHD events to be defined: IHD death (cause of death coded as 410–414 in the ICD-9); clinical non-fatal myocardial infarction (an event satisfying WHO criteria); and electrocardiographic myocardial infarction (major or moderate Q/QS waves, Minnesota codes 1-1-1 to 1-2-5 or 1-2-7 on any follow up ECG when there were no Q/QS waves, Minnesota codes 1-1-any, 1-2-any, or 1-3-any on the recruitment ECG). ECGs were read by experienced observers. The same observers read, independently, baseline and follow up ECGs for both studies. A major IHD event was defined as one or more of the three possible outcomes described.
Blood samples were taken with minimum haemostasis after an overnight fast. Methods for the determination of fasting insulin, glucose, and lipid variables have been reported elsewhere.10 11 Insulin was measured only in samples from the Caerphilly cohort.10
Assessment of the nature of the interrelations among the variables used to define metabolic syndrome was performed using log linear models for multidimensional contingency tables.13 In these models the results on each of the variables for any man were simply considered as being above or below a cut off. An analysis involving n variables therefore gives rise to a contingency table with 2n cells. The number of men assessed as having the syndrome—that is, values of each variable above the cut off, is given by the entry in one cell of the contingency table and may be compared to the number predicted by models specifying various patterns of association among the variables. A χ2 statistic provides a test of the goodness of fit of a model to the actual pattern of association observed among the variables across the whole contingency table. Cluster analysis was performed using a non-hierarchical K means algorithm. This method clusters men into a prespecified number, K, of groups the composition of which is not initially known. After specifying a suitable centre for each cluster, each man is assigned to the cluster in which the centre is closest. When all men have been assigned, the cluster centres are recalculated. The assignment then takes place again, typically resulting in some men being reassigned to a different cluster. This process is repeated until there is convergence. Here, the number of groups was preset at two (K = 2), and closeness to a cluster centre was defined using Euclidean distance calculated with the variables standardised to zero mean and unit variance. Insulin and total triglyceride concentrations were log transformed before standardising. In anticipation of two clusters of unequal size, the initial cluster centres were placed at values of 0.00 and 1.645 for each of the standardised variables, corresponding roughly to the 50th and the 95th centiles of the distributions. Analysis of events during follow up was performed using multiple logistic regression with the occurrence, or not, of a major IHD event as the principal outcome variable. Men with evidence of IHD when first examined were not excluded from the analyses but their increased risk was allowed for by including pre-existing IHD as a factor in the regression model. In this instance a broad epidemiological definition of pre-existing IHD was used: men with severe chest pain and/or angina on the chest pain questionnaire and/or probable or possible ECG ischaemia according to Whitehall criteria.14 Death from any cause was also analysed as a separate outcome variable. Any difference in incidence between the two study areas—for example, arising from their slightly different lengths of follow up, was allowed for by including area as a two level factor in the logistic model. The assumption that IHD risks associated with independent variables in the two areas were parallel on the logit scale was tested by including interactions with area in the model. None was statistically significant. No time to event was available for incidence cases of IHD defined by significant changes in the Minnesota ECG codes. Time to event analyses were not performed for this reason and because the average length of follow up was nearly constant within each area.
Ninety four men said that diabetes was diagnosed by their general practitioner or a consultant physician before our baseline examination. An additional 53 individuals had fasting glucose concentrations of 7.8 mmol/l, which is the threshold value presently used by the WHO15 to define diabetes. Diabetic men as defined earlier were excluded from further analyses.
Analyses are based on 4197 of 4462 non-diabetic men in the combined cohort who had a complete set of data relevant to risk of IHD, with the possible exception of insulin. A total of 527 of 4197 men died and there were 492 incident IHD events. In the Caerphilly cohort there were 1896 non-diabetic men with insulin results among whom there were 223 deaths and 221 incident IHD events. Metabolic syndrome has been defined using different variables but we constructed two versions to simplify subsequent analyses: one included five variables—namely, insulin, glucose, triglyceride, body mass index, and diastolic blood pressure; and the other excluded insulin, which was not measured in the Speedwell cohort. Table 1 shows association among the variables in the non-diabetic population. The correlation coefficients given separately for the two cohorts are very similar.
Three empirical definitions of metabolic syndrome were made. Tertiles: men had to be in the top third of the distribution of each of the variables. There were 154 men (3.7%) (n = 4197) with four metabolic variables and 50 (2.6%) (n = 1896) with five. Medians: men had to be in the top half of the distribution of each variable. There were 463 (11.0%) men (n = 4197) with four metabolic variables and 167 (8.8%) (n = 1896) with five. Clusters: the clustering algorithm with four variables gave a metabolic syndrome cluster of 1876 (45%) of 4197 men, while with five variables there was a cluster of 860 (45%) of 1896 men. Both clusters were characterised by high values for each variable. The composition of the clusters changed only slightly when different initial cluster centres were specified. Log linear model analysis to investigate the pattern of association among variables defining the syndrome was applied using both the tertile and the median cut off points obtained in the first two definitions of the syndrome. When four metabolic variables were used to define the syndrome a contingency table with 24 = 16 cells was obtained. A model specifying independence of the four variables was first fitted. Not surprisingly, in light of the associations shown in table 1, there was very poor fitting of the data with this model, giving highly significant lack of fit tests and grossly under-predicting the number of men with the syndrome.
A more relevant model specifying no more complicated interrelations among variables than association between each pair was fitted (first two columns of table 2). The data fitted well with this model and enabled prediction of the number of men with the syndrome, which accorded closely with the observed number. When five variables were used to define the syndrome a contingency table with 25 = 32 cells was obtained and findings from the analysis were similar (final two columns of table 2).
To assess the relative predictive value and independence of glucose, insulin, and other risk factors multiple logistic regression analyses were performed separately for each cohort and for the combined cohort. Glucose was measured in both cohorts but insulin was measured only in the Caerphilly cohort. The following variables were included as potential confounders: age, smoking habit (never, ex or current), pre-existing IHD, diastolic blood pressure, body mass index, total cholesterol, high density lipoprotein cholesterol, and log triglyceride. Table 3 shows the relative odds of incident IHD by 10 year follow up by increasing fifths of the insulin distribution in the Caerphilly cohort. A significant trend is shown in univariate analysis but adjustment for potential confounder variables shows that fasting serum insulin concentrations no longer make a statistically significant independent contribution to the risk of an IHD event. The exclusion of glucose from the model increased the size of the relative odds marginally but no trend was detectable.
Table 4 shows data for glucose for the combined cohort. Although there is a significant relation between glucose and incident IHD, this effect is confined to the top 20% of the glucose distribution. Table 5subdivides the upper three fifths of the glucose distribution by arbitrary units (from 4.8 mmol/l). An association between glucose and incident IHD is detectable at 5.8 mmol/l, but the association is stronger and significant in both univariate and multivariate analysis at 6.8 mmol/l. In this population of non-diabetic individuals approximately 7% of men have glucose concentrations of 5.8 mmol/l or more and 1% have levels of 6.8 mmol/l or greater. Table 6 shows the ability of these three definitions of metabolic syndrome to predict an IHD event during follow up for the combined cohort. The relative odds of incident IHD associated with presence of the syndrome is statistically significant but is reduced to non-significance when all components of the syndrome and standard IHD risk factors are added to the models. These data suggest that, although the syndrome may be helpful in defining a group with an increased risk of IHD, this increase is no greater than would be expected on the basis of the increases in risk associated with individual variables defining the syndrome. Table 7 shows that similar findings were obtained using the Caerphilly data with insulin included in the definition.
The purpose of the present study was to examine the clinical and epidemiological utility of the concept of metabolic syndrome or insulin resistance syndrome among non-diabetic individuals. In our study populations undiagnosed diabetic individuals with fasting blood glucose values of 7.8 mmol/l were also excluded. Several variables included in previous definitions of metabolic syndrome were considered (table 1) and showed moderately strong intercorrelation. Log linear modelling of the two arbitrary definitions of metabolic syndrome (all individuals with a complete set of variables in the upper third or half of the distributions respectively) (table 2) suggested that simple pair wise association of these variables was sufficient to explain these associations; there was no evidence of any complex interrelation among variables.
Cluster analyses were carried out to define metabolic syndrome in a less arbitrary and possibly more physiologically relevant manner. For four and five variable analyses 45% of men were assigned to a cluster that was characterised by higher mean values for each of the defining variables, these men were regarded as having metabolic syndrome. As in previous analyses, adjustment for individual risk factors removed the excess risk associated with metabolic syndrome defined in this way. These data support the findings of the five year follow up that indicate that a raised serum insulin concentration, a marker for insulin resistance,16 is not an independent risk factor for IHD in non-diabetic individuals. A threshold effect for non-fasting insulin concentrations was reported for a specific insulin assay in the British regional heart study.17 We also reviewed other studies that investigated insulin as a risk factor for IHD, some of which had a positive relation,18-23 while others had no independent relation with subsequent IHD.24-30
Blood glucose concentrations, however, show an overall significant association with subsequent IHD but the effect is confined to the top 7% of the non-diabetic population. The Whitehall study also reported a threshold effect for glucose and subsequent IHD.31 The American Diabetes Association and the WHO have recently been considering a redefinition of non-insulin dependent diabetes mellitus.32 Our data tend to support the suggestion33 that the definition based on fasting blood glucose should be reduced from 7.8 mmol/l or greater to 7.0 mmol/l or more, as individuals with fasting glucose concentrations of more than 6.8 mmol/l are at increased risk of subsequent IHD at 511or 10 year follow up.
Various models of insulin resistance have been proposed,34 35 and we have shown that a simple model based on the product of fasting insulin and glucose does not carry an increased risk of subsequent IHD in the Caerphilly cohort.36
This study has attempted to examine a cluster of variables frequently cited as components of metabolic syndrome.37 Our definitions are arbitrary but cover a range of possibilities; using these definitions there is no suggestion of a complex relation among these variables that would justify definition of a separate disease entity. Our definition of metabolic syndrome did not include high density lipoprotein cholesterol but including this factor made no difference to the outcome. There remains, however, the possibility that different components of the syndrome may be more relevant than others to a biological/pathological definition of a syndrome. In other clinically defined syndromes—for example, Paterson-Kelly syndrome (post-cricoid web and dysphagia associated with iron deficiency anaemia) population data have led to redefinition of components of the syndrome.38
Further analyses using different components of a possible syndrome may provide alternative evidence for the existence of such a syndrome in non-diabetic individuals but are beyond the scope of the present study. For example, we did not measure waist:hip ratio, which may provide a measure of abdominal obesity.39 This may be more closely associated with metabolic syndrome than an overall measure of body mass index such as that used in this study. Further studies will be required to test these hypotheses.
We thank Dr Tom Trinick for his helpful suggestions and Professor Vincent Marks for the insulin assays.
If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.