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Stroke. 2007;38:1713-1714
Published online before print April 12, 2007, doi: 10.1161/STROKEAHA.107.487223
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(Stroke. 2007;38:1713.)
© 2007 American Heart Association, Inc.


Editorials

Should Stroke Be Considered Both a Brain Attack and a Heart Attack?

Seemant Chaturvedi, MD, FAHA, FAAN

From the Department of Neurology and Stroke Program, Wayne State University, Detroit, Mich.

Correspondence to Seemant Chaturvedi, MD, Department of Neurology & Stroke Program, Wayne State University, 8C-UHC, 4201 St. Antoine, Detroit, MI 48201. E-mail SChaturv{at}med.wayne.edu


Key Words: cardiac disease • statins

See related article, pages 1752–1758.

The concept of coronary risk equivalents has gained increased acceptance in recent years. In the 2001 National Cholesterol Education Program (NCEP) Adult Treatment Panel III guidelines, diabetes mellitus, peripheral arterial disease, abdominal aortic aneurysm, and "symptomatic carotid artery disease" were cited as coronary risk equivalents.1 These conditions carry a 10-year risk of coronary heart disease events of >20%.

In 2004, the tent containing coronary risk equivalent conditions was expanded by the NCEP committee to symptomatic carotid disease or ">50% obstruction of a carotid artery."2 In addition, whereas in 2001, the low-density lipoprotein target for coronary risk equivalents was <100 mg/dL, in 2004, an optional target of <70 mg/dL was established for high-risk patients.

In this issue of Stroke, Dhamoon et al, using data from the Northern Manhattan Study, provide further ammunition to support the enlargement of the coronary risk equivalent umbrella.3 These authors followed 655 patients (aged 40 years or older) with a first ischemic stroke for a 5-year period. In their overall population, the 5-year risk of myocardial infarction (MI) or vascular death (VD) was 17.4%. There was an increased "up front" risk of 8.2% at one year. Their study also identified age >70 years, history of coronary artery disease, and atrial fibrillation as independent predictors of MI or VD. Embolic stroke subtype was particularly ominous, whereas lacunar stroke subtype was less risky. The 5-year risk of MI or VD was 11.5% in patients aged 70 years and over with lacunar infarcts, whereas the corresponding risk was 6.0% in lacunar stroke patients <70 years.

This comprehensive study poses several challenges and questions for clinicians and policy makers. First, because MI and VD are common in the first 5 years after stroke, should there be more widespread screening for occult heart disease? The data from Northern Manhattan resonate well with a previous American Stroke Association recommendation that patients with large-vessel atherosclerotic stroke should be considered for cardiac screening whereas lacunar stroke patients may not require screening.4 Second, the risk of both recurrent stroke events and cardiac events calls for a strategy of "intensive medical therapy" after the first stroke, especially considering that previous studies have shown unsatisfactory results with use of vascular medications or risk factor modification in various stroke-prone populations.5–7 Third, the increased first-year stroke of MI or VD should prompt consideration of cardioprotective therapies at an early stage. For example, use of β blockers or statins have shown value in vascular surgery patients and may be of use in decreasing major vascular events in the days and months after a stroke.8,9 For policy makers, designating ischemic stroke as a coronary risk equivalent should be strongly considered, with the possible exception of younger lacunar stroke patients.

As with all studies, the current report has limitations. The Northern Manhattan cohort is not entirely representative of the broader North American population. In this report, 51.3% of patients were Hispanic and 45.1% had diabetes. These figures do not reflect the larger stroke population. The high frequency of diabetes could overestimate the risk of coronary events. In addition, the authors do not provide information on medication use after the first stroke, so we do not know whether these risk estimates occurred while receiving "state of the art" or "usual" preventative treatment, although it was likely the latter.

Despite these limitations, this report is extremely thought-provoking for clinicians. It should prod those who are standing on the sidelines to jump on the bandwagon of intensive medical therapy, in recognition of the stroke survivor’s multifaceted vascular risks.

Acknowledgments

Disclosures

None.

Footnotes

The opinions in this editorial are not necessarily those of the editors or of the American Heart Association.

References

  1. Expert Panel on Detection Evaluation, and Treatment of High Blood Cholesterol in Adults. 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.[Free Full Text]
  2. Grundy SM, Cleeman JI, Merz CNB, Brewer HB Jr, Clark LT, Hunninghake DB, Pasternak RC, Smith SC Jr, Stone NJ; for the Coordinating Committee of the National Cholesterol Education Program, Endorsed by the National Heart L, and Blood Institute, American College of Cardiology Foundation, and American Heart Association. Implications of recent clinical trials for the national cholesterol education program adult treatment panel III guidelines. Circulation. 2004; 110: 227–239.[Abstract/Free Full Text]
  3. Dhamoon M, Tai W, Boden-Albala B, Runek T, Paik MC, Sacco RL, Elkind MSV. Risk of myocardial infarction or vascular death after first ischemic stroke: The Northern Manhattan study. Stroke. 2007; 38: 1752–1758.
  4. Adams RJ, Chimowitz MI, Alpert JS, Awad IA, Cerqueria MD, Fayad P, Taubert KA; American Heart Association/American Stroke Association. Coronary risk evaluation in patients with transient ischemic attack and ischemic stroke: a scientific statement for healthcare professionals from the Stroke Council and the Council on Clinical Cardiology of the American Heart Association/American Stroke Association. Stroke. 2003; 34: 2310–2322.[Free Full Text]
  5. Joseph LN, Babikian VL, Allen NC, Winter MR. Risk factor modification in stroke prevention: the experience of a stroke clinic. Stroke. 1999; 30: 16–20.[Abstract/Free Full Text]
  6. Ovbiagele B, Saver JL, Bang H, Chambless LE, Nassief A, Minuk J, Toole JF, Crouse JR; for the VISP Study Investigators. Statin treatment and adherence to national cholesterol guidelines after ischemic stroke. Neurology. 2006; 66: 1164–1170.[Abstract/Free Full Text]
  7. Betancourt M, Van Stavern RB, Share D, Gardella P, Martus M, Chaturvedi S. Are patients receiving maximal medical therapy following carotid endarterectomy? Neurology. 2004; 63: 2011–2015.[Abstract/Free Full Text]
  8. Mangano DT, Layug EL, Wallace A, Tateo I; The Multicenter Study of Perioperative Ischemia Research Group. Effect of atenolol on mortality and cardiovascular morbidity after noncardiac surgery. N Engl J Med. 1996; 335: 1713–1721.[Abstract/Free Full Text]
  9. Kennedy J, Quan H, Buchan AM, Ghali WA, Feasby TE. Statins are associated with better outcomes after carotid endarterectomy in symptomatic patients. Stroke. 2005; 36: 2072–2076.[Abstract/Free Full Text]

Related Article:

Risk of Myocardial Infarction or Vascular Death After First Ischemic Stroke: The Northern Manhattan Study
Mandip S. Dhamoon, Wanling Tai, Bernadette Boden-Albala, Tanja Rundek, Myunghee C. Paik, Ralph L. Sacco, and Mitchell S.V. Elkind
Stroke 2007 38: 1752-1758. [Abstract] [Full Text] [PDF]




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