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The role of omega-3 fatty acids and aspirin in primary prevention

Hypertension, raised blood lipids and diabetes are among the risk factors for coronary heart disease (CHD). For primary prevention, omega-3 fatty acid supplementation and aspirin are preferred. But is that still up to date?

Almost every heart attack is due to coronary heart disease. That makes prevention all the more important, especially in at-risk patients. Alongside giving up nicotine, a healthy lifestyle with enough exercise, a balanced diet and little stress certainly plays a major part in primary prevention. In addition, all guidelines recommend a fish-rich diet and 1 g of fish oil capsules, as Prof. Dr. med. Franz Eberli of Zurich explained. This was based on study results from the 1980s [1–6], in which omega-3 fatty acid supplementation was associated with a reduction in cardiovascular mortality.

However, this hypothesis could not be confirmed in follow-up studies. Only in open-label studies was a trend towards an effect apparent. In 2018 a Cochrane review [7] analysed the results of 79 randomised clinical trials. It found little or no effect of omega-3 fatty acids on all-cause mortality, cardiovascular mortality, cardiovascular events, stroke and arrhythmias. A recently published study [8] of 25,871 patients without cardiovascular disease confirmed the new findings. There was no difference in cardiovascular events between 1 g of fish oil and placebo.

Aspirin brings no benefit

Several studies in different patient groups that examined the benefit of aspirin in primary prevention reached similar results. A multicentre study [9] randomised 12,546 patients 1:1 to take 100 mg/day of ASA or placebo. The primary endpoint was a combination of cardiovascular death, heart attack, unstable angina or stroke/transient ischaemic attack. One of these events occurred in 269 patients (4.29%) in the verum group and 281 patients (4.48%) in the placebo group. So there was no clear advantage.

A second study [10] examined the protection ASA offers against cardiovascular events in 15,480 people with diabetes (average age 63). Here too, one group was given 100 mg/day of ASA or placebo. The primary efficacy endpoint was a serious vascular event. Over a follow-up period of 7.4 years, the risk of a vascular event was indeed moderately reduced, by 12%. However, a high number of severe haemorrhagic complications (up 29%) cancelled out this benefit. 'Good treatment of hypertension and lowering cholesterol therefore remain the most important primary preventive measures in high-risk patients,' Prof. Eberli concluded.

Source: 85th Medical Congress Davos, 7–9 February 2019

References:

  1. NEJM 1985; 312: 1205–1209.
  2. NEJM 1985; 313: 820–824.
  3. Circulation 202; 106: 2747.
  4. Lancet 189; 334:757–761.
  5. Lancet 1999; 354: 474–455.
  6. Circulation 2017; 135: 867–884.
  7. Cochrane Database Syst Rev 2018; 7: CD03177.
  8. NEJM 2019; 380: 23–32.
  9. Lancet 10152; 392: 1036–1046.
  10. Am Heart J 2018; 198: 135–144.

Leoni Burggraf

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