Skip to main content
Journal of the Royal Society of Medicine logoLink to Journal of the Royal Society of Medicine
editorial
. 2003 Aug;96(8):371–372. doi: 10.1258/jrsm.96.8.371

Type 2 diabetes is cardiovascular disease

Ketan Dhatariya 1
PMCID: PMC539562  PMID: 12893849

Neurologists are trying to convince generalists to avoid the term cerebrovascular accident, because many of the risk factors for stroke are modifiable: to regard the condition as an act of fate encourages inertia rather than the necessary aggressive approach including rapid brain scanning and thrombolysis in selected cases.1 Just as in myocardial infarction ‘time is muscle’, with an intracerebral event ‘time is brain’. The term ‘brain attack’ serves to remind clinicians that intervention is required long before the 24 hours required for formal definition of a stroke.2

Generalists now have to be persuaded that an equally focused and aggressive approach is required in diabetes mellitus. The day of ‘wait and see’ is past, and the term mild diabetes should be buried forever. Gaining ground is the idea that diabetes mellitus (especially type 2 diabetes) is a ‘state of accelerated cardiovascular disease that just happens to be associated with hyperglycaemia’. People with type 2 diabetes are between two and six times more likely than those without diabetes to have cardiovascular disease and are more than twice as likely to die from it.3,4 Among diabetologists there is a widely held belief that cardiovascular risk reduction should take precedence over reduction of blood glucose.

Whereas in type 1 diabetes the diagnosis is usually made quickly, in type 2 diabetes the patient will probably have had the disorder for 4-7 years before being formally diagnosed.5 Moreover, at the time of diagnosis as many as one fifth will prove to have other risk factors for cardiovascular disease modifiable by lifestyle changes or pharmacological treatment or both.7,8 There is now ample evidence that aspirin,9,10 statins,11,12 and angiotensin converting enzyme (ACE) inhibitors13 reduce the risk of death from cardiovascular disease in diabetes. Gaede and co-workers14 lately reported that, compared with ‘standard care’, an intensive combination of behavioural and pharmaceutical interventions in type 2 diabetes reduced the incidence of cardiovascular disease by 53%, nephropathy by 61%, retinopathy by 58% and autonomic neuropathy by 73% over a mean follow-up of 7.8 years. Today, when a person with diabetes is found to have any cardiovascular risk factor at all, there should be a good reason why they should not be on aspirin, a statin and an ACE inhibitor (‘aspastatapril’). Because hypertension and hypertriglyceridaemia are also widely prevalent in people with type 2 diabetes, beta blockade and fibrates may have to be added.15,16 These results are separate from the benefits of tight blood glucose control seen in both type 1 and type 2 diabetes.17,18 With epidemiological and interventional data showing that the lower the blood pressure or glucose the lower the morbidity and mortality from the complications of diabetes, target values for these indices are being revised downwards.19,20

This aggressive approach is not just for primary prevention. It applies also to people who have already had a cardiovascular event, and the benefits in those with diabetes seem even more impressive than in those without.9 There is, of course, a down-side to this aggressive treatment. Hypoglycaemia is a hazard of intensive regimens to lower blood glucose,17,18 aspirin can cause gastrointestinal haemorrhage, statin therapy (especially in combination with fibrates) can result in myalgias, and ACE inhibitors can impair renal function. All these risks, however, can be limited by individual tailoring of treatment and close follow-up.13,21,22 The emerging epidemic of diabetes23 demands a vigorous clinical counter-attack if its consequences are not to overwhelm our health systems.

References

  • 1.Kwiatkowski TG, Libman RB, Frankel M, et al. Effects of tissue plasminogen activator for acute ischemic stroke at one year. National Institute of Neurological Disorders and Stroke Recombinant Tissue Plasminogen Activator Stroke Study Group. N Engl J Med 1999; 340: 1781-7 [DOI] [PubMed] [Google Scholar]
  • 2.Brown MM. Brain attack: a new approach to stroke. Clin Med 2002;2: 60-5 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Kannel WB, McGee DL. Diabetes and cardiovascular disease. The Framingham Study. JAMA 1979;241: 2035-8 [DOI] [PubMed] [Google Scholar]
  • 4.Saydah SH, Eberhardt MS, Loria CM, Brancati FL. Age and the burden of death attributable to diabetes in the United States. Am J Epidemiol 2002;156: 714-19 [DOI] [PubMed] [Google Scholar]
  • 5.Harris MI, Klein R, Welborn TA, Knuiman MW. Onset of NIDDM occurs at least 4-7 yr before clinical diagnosis. Diabetes Care 1992;15: 815-19 [DOI] [PubMed] [Google Scholar]
  • 6.Turner RC, Millns H, Neil HA, et al. Risk factors for coronary artery disease in non-insulin dependent diabetes mellitus: United Kingdom Prospective Diabetes Study (UKPDS: 23). BMJ 1998;316: 823-8 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Position Statement by the American Diabetes Association. Physical activity/exercise and diabetes mellitus. Diabetes Care 2003;26: S73-7 [DOI] [PubMed] [Google Scholar]
  • 8.Tuomilehto J, Lindstrom J, Eriksson JG, et al. Prevention of type 2 diabetes mellitus by changes in lifestyle among subjects with impaired glucose tolerance. N Engl J Med 2001;344: 1343-50 [DOI] [PubMed] [Google Scholar]
  • 9.Antiplatelet Trialists' Collaboration. Collaborative overview of randomised trials of antiplatelet therapy—I: Prevention of death, myocardial infarction, and stroke by prolonged antiplatelet therapy in various categories of patients. BMJ 1994;308: 81-106 [PMC free article] [PubMed] [Google Scholar]
  • 10.Position Statement by the American Diabetes Association. Aspirin therapy in diabetes. Diabetes Care 2003;26: S87-8 [DOI] [PubMed] [Google Scholar]
  • 11.Heart Protection Study Collaborative Group. MRC/BHF Heart Protection Study of cholesterol lowering with simvastatin in 20536 high-risk individuals: a randomised placebo-controlled trial. Lancet 2002;360: 7-2212114036 [Google Scholar]
  • 12.Position Statement by the American Diabetes Association. Management of dyslipidemia in adults with diabetes. Diabetes Care 2003;26: S83-6 [DOI] [PubMed] [Google Scholar]
  • 13.Effects of ramipril on cardiovascular and microvascular outcomes in people with diabetes mellitus: results of the HOPE study and MICRO-HOPE substudy. Heart Outcomes Prevention Evaluation Study Investigators. Lancet 2000;355: 253-9 [PubMed] [Google Scholar]
  • 14.Gaede P, Vedel P, Larsen N, et al. Multifactorial intervention and cardiovascular disease in patients with type 2 diabetes. N Engl J Med 2003;348: 383-93 [DOI] [PubMed] [Google Scholar]
  • 15.UK Prospective Diabetes Study Group. Tight blood pressure control and risk of macrovascular and microvascular complications in type 2 diabetes: UKPDS 38. BMJ 1998;317: 703-13 [PMC free article] [PubMed] [Google Scholar]
  • 16.Effect of fenofibrate on progression of coronary-artery disease in type 2 diabetes: the Diabetes Atherosclerosis Intervention Study, a randomised study. Lancet 2001;357: 905-10 [PubMed] [Google Scholar]
  • 17.Diabetes Control and Complications Trial Research Group. The effect of intensive treatment of diabetes on the development and progression of long-term complications in insulin-dependent diabetes mellitus. N Engl J Med 1993;329: 977-86 [DOI] [PubMed] [Google Scholar]
  • 18.UK Prospective Diabetes Study Group. Intensive blood-glucose control with sulphonylureas or insulin compared with conventional treatment and risk of complications in patients with type 2 diabetes (UKPDS 33). Lancet 1998;352: 837-53 [PubMed] [Google Scholar]
  • 19.Chobanian AV, Bakris GL, Black HR, et al. The seventh report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure: The JNC 7 report. JAMA 2003;289: 2560-71 [DOI] [PubMed] [Google Scholar]
  • 20.Colagiuri S, Cull CA, Holman RR, the UKPDS Group. Are lower fasting plasma glucose levels at diagnosis of type 2 diabetes associated with improved outcomes?: United Kingdom Prospective Diabetes Study 61. Diabetes Care 2002;25: 1410-17 [DOI] [PubMed] [Google Scholar]
  • 21.Rubins HB, Robins SJ, Collins D, et al. Gemfibrozil for the secondary prevention of coronary heart disease in men with low levels of high-density lipoprotein cholesterol. N Engl J Med 1999;341: 410-18 [DOI] [PubMed] [Google Scholar]
  • 22.Goldberg RB, Mellies MJ, Sacks FM, et al. Cardiovascular events and their reduction with pravastatin in diabetic and glucose-intolerant myocardial infarction survivors with average cholesterol levels: subgroup analyses in the cholesterol and recurrent events (CARE) trial. The Care Investigators. Circulation 1998;98: 2513-19 [DOI] [PubMed] [Google Scholar]
  • 23.Zimmet P, Alberti KG, Shaw J. Global and societal implications of the diabetes epidemic. Nature 2001;414: 782-7 [DOI] [PubMed] [Google Scholar]

Articles from Journal of the Royal Society of Medicine are provided here courtesy of Royal Society of Medicine Press

RESOURCES