Editorials

"Normal" blood glucose and coronary risk

Dose response effect seems consistent throughout the glycaemic continuum

Papers p 15

Although diabetes is a strong risk factor for coronary heart disease, the association between glycaemia within the "normal range" and coronary heart disease has been somewhat controversial.¹ A 1979 collaborative report from 15 countries found the risk ratio in the highest versus the lowest centile of glycaemia to range from 0.34 to 6.07 in men from Finland, Denmark, France, the United Kingdom, and the United States.² In other cohort studies, including Whitehall³ and Framingham,⁴ there appeared to be a threshold effect, with risk observed only at glucose levels approaching or including current diagnostic criteria for diabetes. There are several possible reasons for these contradictory results, including: the failure to exclude people with diabetes from the cohorts, compatible with a threshold effect; the multifactorial aetiology of coronary heart disease, compatible with confounding; or the large intra-individual variation in glucose (especially postchallenge glucose) values, compatible with misclassification bias.

Glycosylated haemoglobin, an integrated estimate of glucose over the preceding 6-12 weeks, provides a more reliable estimate of usual glycaemia, and should, therefore, be a more precise predictor of coronary heart disease risk. An elegant study by Khaw et al in this issue shows that glycosylated haemoglobin levels are positively associated with the risk of future coronary heart disease in a linear stepwise fashion, with no evidence of a threshold effect and independent of other common risk factors for coronary heart disease (p 15).⁵ These are the most convincing data available that the association between glucose and coronary heart disease occurs throughout the normal range of glucose.

Shifting the curve
The finding is important. An association between glycaemia and coronary heart disease in people who do not meet current criteria for a diagnosis of diabetes implies that glucose control for coronary heart disease prevention should begin in those with impaired glucose tolerance, and, as the authors note, points to the desirability of shifting the entire population glycaemia curve to the left. All modifiable risk factors that are continuous variables blur the line between treatment and prevention and lead to the selection of candidates for intervention on feasible and affordable rather than optimal grounds.

Association with microvascular disease
Thus, glycaemia in observational studies and in clinical trials is much more strongly associated with microvascular disease than with coronary heart disease. Is this weaker association because better glucose control is necessary for preventing coronary heart disease than for preventing retinal or renal disease, or because glycaemia is a marker for other risk factors of coronary heart disease more directly in the causal pathway to coronary heart disease? In 1985 Epstein reported an association between glycaemia and coronary heart disease that was independent of cholesterol, blood pressure, and cigarette smoking in five of 13 cohort studies but not in any of the few studies that included women.⁹ The paper by Khaw et al does not describe the association in women in their cohort, apparently because there were too few events for meaningful analysis.

Division of Epidemiology, Department of Family and Preventive Medicine, UCSD School of Medicine, La Jolla, CA 92093-0607, USA (ebarrettconnor{at}ucsd.edu)