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European Heart Journal Advance Access originally published online on April 25, 2007
European Heart Journal 2007 28(9):1047-1048; doi:10.1093/eurheartj/ehl573
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© The European Society of Cardiology 2007. All rights reserved. For Permissions, please e-mail: journals.permissions@oxfordjournals.org

Heart failure: are we neglecting the silent majority?

Aengus Murphy and John J.V. McMurray*

Department of Cardiology, Western Infirmary, Dumbarton Road, Glasgow G11 6NT, Scotland, UK

* Corresponding author. Tel: +44 141 330 3479; fax: +44 141 330 6955. E-mail address: j.mcmurray{at}bio.gla.ac.uk

This editorial refers to ‘Prognosis of all-cause heart failure and borderline left ventricular systolic dysfunction: 5 year mortality follow-up of the Echocardiographic Heart of England Screening Study (ECHOES)’{dagger} by F.D.R. Hobbs et al., on page 1128

In the last decade, seminal studies from Europe, the USA, and Australasia have defined the epidemiology of heart failure and left ventricular systolic dysfunction in the population.13 One of those studies, the aptly named Echocardiographic Heart of England Screening study (ECHOES), enrolled over 6000 individuals ≥40 years, living in the West Midlands region of England.4 Hobbs and Colleagues provide further important and incremental insights into the epidemiology of heart failure from their study.

First, they report the number of cases of heart failure with a low left ventricular ejection fraction (LVEF) (LVEF <0.40; n = 219) and ‘preserved’ LVEF (>0.40, n = 230), highlighting, as others have done, that approximately half of patients with the clinical syndrome of heart failure do not have a low LVEF.13,5 Hobbs et al., however, go one step beyond prior studies in better defining the heterogeneous reality of heart failure. They describe the prevalence of heart failure related to valve disease (n = 97) and atrial fibrillation (n = 133), as well as multiple causes (n = 43; all had a low LVEF). We have been lacking these crucial epidemiological data.

Secondly, Hobbs et al. also describe the number of individuals with a low LVEF who did not have symptomatic heart failure (n = 109). This finding that approximately one-third of patients with a low LVEF do not have symptoms confirms prior reports and re-awakens questions about detection and treatment of these individuals, reinforced by knowledge on their prognosis described below.13,6,7

Thirdly, and most importantly, the authors describe long-term prognosis in all these groups of individuals, with some striking findings. Heart failure, irrespective of LVEF, is associated with a greatly reduced survival. Conversely, the risk of premature death is also increased in individuals with a low LVEF, irrespective of whether they have symptomatic heart failure. Specifically, the 5-year mortality rate was 47% in subjects with heart failure and a low LVEF, 38% in those with heart failure and preserved LVEF, and 31% in individuals with a low LVEF without heart failure, but only 7% in the overall population. Crucial new information is shown in Figure 5 of the report from Hobbs et al. Subjects with heart failure and atrial fibrillation, large in number, had a prognosis as poor as individuals with heart failure and a low LVEF. The same was true for individuals with heart failure and valve disease. Patients with heart failure and more than one of these conditions had an even worse prognosis, although the numbers of individuals in these latter two groups were small.

Equally important is the authors' demonstration that individuals with an LVEF in the range 0.40–0.50 (n = 386) also have a considerably reduced survival when compared with those with an LVEF >0.50 (n = 5447), although not as much as individuals with an LVEF < 0.40 (n = 328). This is an important confirmation that ‘left ventricular systolic dysfunction’ is not an ‘all or none’ phenomenon and that there is no magical dividing line between ‘normal’ and ‘abnormal’.6,7 Although the exact numbers are not provided, these data from Hobbs et al. tell us that there are many premature deaths in the population among asymptomatic individuals with either a clearly reduced (<0.40) or borderline (0.40–0.50) LVEF. This silent majority deserves more attention. Who are they? Unfortunately, the authors do not describe their clinical characteristics. What is their natural history? Do these subjects progress to symptomatic heart failure? If so, at what rate and what predicts progression? What are the causes of premature death? Can we better risk stratify these individuals, for example, by measuring blood natriuretic peptides or, perhaps, markers of cardiac electrical instability such as microvolt T-wave alternans? Obviously, the issue underlying these questions is whether progression to the symptomatic state and death can be postponed or avoided.

The broader issue highlighted by this study is how the majority of patients with heart failure or borderline/reduced LVEF have been excluded from clinical trials, which have, until recently, almost exclusively focused on those with symptoms and an LVEF <0.35. At last, we have begun to tackle the problem of heart failure and preserved LVEF.5 Recent studies with renin–angiotensin system blockers in these patients have been encouraging but not definitive; two additional studies are in progress with an angiotensin receptor blocker (I-PRESERVE) and an aldosterone antagonist (TOPCAT).8,9 In contrast, we have done little to investigate the treatment of patients with a low LVEF but without symptomatic heart failure. Other than the prevention arm of the Studies of Left Ventricular Dysfunction, which compared enalapril with placebo, no large-scale trials have been carried out in these patients.10 Might a beta-blocker be of value in these under-studied patients? Are there other treatments that might improve outcome? We should no longer neglect the majority of patients with heart failure, particularly the silent majority.

Conflict of interest: none declared.

Footnotes

The opinions expressed in this article are not necessarily those of the Editors of the European Heart Journal or of the European Society of Cardiology.

{dagger} doi:10.1093/eurheartj/ehm102 Back

References

  1. McMurray JJ, Stewart S. Epidemiology, aetiology, and prognosis of heart failure. Heart (2000) 83:596–602.[Free Full Text]
  2. Petrie M, McMurray J. Changes in notions about heart failure. Lancet (2001) 358:432–434.[CrossRef][Web of Science][Medline]
  3. Abhayaratna WP, Smith WT, Becker NG, Marwick TH, Jeffery IM, McGill DA. Prevalence of heart failure and systolic ventricular dysfunction in older Australians: the Canberra Heart Study. Med J Aust (2006) 184:151–154.[Web of Science][Medline]
  4. Hobbs FDR, Roalfe AK, Davis RC, Davies MK, Hare R, and the Midlands Research Practices Consortium (MidReC). Prognosis of all-cause heart failure and borderline left ventricular systolic dysfunction: 5 year mortality follow-up of the Echocardiographic Heart of England Screening Study (ECHOES). Eur Heart J. doi:10.1093/eurheartj/ehm102.
  5. Hogg K, Swedberg K, McMurray J. Heart failure with preserved left ventricular systolic function; epidemiology, clinical characteristics, and prognosis. J Am Coll Cardiol (2004) 43:317–327.[Abstract/Free Full Text]
  6. McDonagh TA, Cunningham AD, Morrison CE, McMurray JJ, Ford I, Morton JJ, Dargie HJ. Left ventricular dysfunction, natriuretic peptides, and mortality in an urban population. Heart (2001) 86:21–26.[Abstract/Free Full Text]
  7. Gottdiener JS, McClelland RL, Marshall R, Shemanski L, Furberg CD, Kitzman DW, Cushman M, Polak J, Gardin JM, Gersh BJ, Aurigemma GP, Manolio TA. Outcome of congestive heart failure in elderly persons: influence of left ventricular systolic function. The Cardiovascular Health Study. Ann Intern Med (2002) 137:631–639.[Abstract/Free Full Text]
  8. Yusuf S, Pfeffer MA, Swedberg K, Granger CB, Held P, McMurray JJ, Michelson EL, Olofsson B, Ostergren J, CHARM Investigators Committees. Effects of candesartan in patients with chronic heart failure and preserved left-ventricular ejection fraction: the CHARM-Preserved Trial. Lancet (2003) 362:777–781.[CrossRef][Web of Science][Medline]
  9. Cleland JG, Tendera M, Adamus J, Freemantle N, Polonski L, Taylor J, PEP-CHF Investigators. The perindopril in elderly people with chronic heart failure (PEP-CHF) study. Eur Heart J (2006) 27:2338–2345.[Abstract/Free Full Text]
  10. The SOLVD Investigators. Effect of enalapril on mortality and the development of heart failure in asymptomatic patients with reduced left ventricular ejection fractions. N Engl J Med (1992) 327:685–691.[Abstract]

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Related articles in EHJ:

Prognosis of all-cause heart failure and borderline left ventricular systolic dysfunction: 5 year mortality follow-up of the Echocardiographic Heart of England Screening Study (ECHOES)
F.D. Richard Hobbs, Andrea K. Roalfe, Russell C. Davis, Michael K. Davies, Rachel Hare, and and the Midlands Research Practices Consortium (MidReC)
EHJ 2007 28: 1128-1134. [Abstract] [FREE Full Text]  




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