2,998
Views
8
CrossRef citations to date
0
Altmetric
Editorial

The INTERSTROKE Study: hypertension is by far the most important modifiable risk factor for stroke

, , &
Pages 131-132 | Received 04 Feb 2017, Accepted 05 Feb 2017, Published online: 15 Feb 2017

The Global Burden of Disease Study 2015 [Citation1] reported that the five largest contributors to global disability-adjusted life-years (DALYs) among diseases, injuries and risk factors were high systolic blood pressure (212 million), smoking (149 million), high fasting plasma glucose (143 million), high body mass index (120 million million) and childhood undernutrition (113 million). We [Citation2] believe that the Global Burden of Disease Study is both the most useful global effort to inform governments, health care providers and the population at large of the real issues of risk factors, diseases and injuries in the world and the most important global study to reveal that hypertension has remained the leading risk factor for disease and death worldwide for the past quarter century.

Similarly, the INTERSTROKE investigators recently quantified the importance of modifiable risk factors for acute stroke in different regions of the world, in key populations, and in major stroke subtypes [Citation3]. From early 2007 and through mid-2015, as many as 10,388 patients with ischemic stroke and 3059 patients with intracerebral haemorrhage were compared with 13,472 control persons in 32 countries. Ten potentially modifiable risk factors were collectively associated with approximately 90% of the population attributable risks of stroke in each major region of the world. These associations were consistent in different ethnic groups, both genders and all age groups. Estimations of population attributable risks of stroke were based on logistic models; using this method [Citation4] addition of population attributable risks for individual risk factors usually exceeds 100% although the overall attributable risk for the composite of these risk factors is less than 100%. Previous history of hypertension or blood pressure of 140/90 mm Hg or higher (Odds ratio 2.98, 99% CI 2.72–3.28, attributable risk 47.9%, 99% CI 45.1–50.6) was by far the most important of the modifiable risk factors. Other population attributable modifiable risk factors, in descending order of importance, included physical activity (35.8%), apolipoprotein B/A1 ratio (26.8%), diet (23.2%), waist-to-hip ratio (18.6%), psychosocial factors (17.4%), current smoking (12.4%), cardiac causes (9.1%), alcohol consumption (5.8%), and diabetes mellitus (3.9%). The INTERSTROKE investigators found evidence of regional and ethnic variations in magnitude of importance of individual risk factors, though the collective contribution of these ten risk factors to stroke risk was consistent in all populations, suggesting that general approaches to prevention of stroke can be similar worldwide.

Since 70–80% of strokes can be prevented by reducing blood pressure with antihypertensive drug treatment, e.g. 30/15 mm Hg [Citation5], as an example reduction from average baseline blood pressure of 174/98 to achieved average 144/81 mmHg in the Losartan Intervention For Endpoint (LIFE) reduction in hypertension study [Citation6], the INTERSTROKE investigators have reminded us once again about the need for careful assessment and treatment of hypertension. We are not sure of the optimal blood pressure treatment target, but we are sure that treatment of hypertension is effective in preventing stroke, and there seems to be no J-curve at low target levels, as in the Valsartan Antihypertensive Long-term Use Evaluation (VALUE) trial [Citation7,Citation8]. It is our opinion then that a target blood pressure of 130/80 mm Hg or lower is beneficial, particularly in people at high risk of stroke.

Sverre E. Kjeldsen

Department of Cardiology, University of Oslo, Ullevaal Hospital, Oslo, Norway

[email protected]

Krzysztof Narkiewicz

Department of Hypertension and Diabetology, Medical University of Gdansk, Poland

Michel Burnier

Service of Nephrology and Hypertension, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland

Suzanne Oparil

Vascular Biology and Hypertension Program, Department of Medicine, University of Alabama at Birmingham, AL, USA

Disclosure statement

SEK, KN, MB and SO are editors of Blood Pressure and report no relevant conflicts of interest to disclose related to this commentary.

References

  • GBD 2015 Risk Factors Collaborators. Global, regional, and national comparative risk assessment of 79 behavioural, environmental and occupational, and metabolic risks or clusters of risk, 1990–2015: a systematic analysis for the Global Burden of Disease Study 2015. Lancet. 2016;388:1659–1724.
  • Kjeldsen SE, Narkiewicz K, Burnier M, Oparil S. The Global Burden of Disease Study 2015 and Blood Pressure. Blood Press. 2017;26:1.
  • O’Donnell MJ, Chin SL, Rangarajan S, et al. On behalf of the INTERSTROKE investigators. Global and regional effects of potentially modifiable risk factors associated with acute stroke in 32 countries (INTERSTROKE): a case-control study. Lancet. 2016;388:761–775.
  • Benichou J, Gail MH. Variance calculations and confidence intervals for estimates of the attributable risk based on logistic models. Biometrics. 1990;46:991–1003.
  • Law MR, Morris JK, Wald NJ. Use of blood pressure lowering drugs in in the prevention of cardiovascular disease: meta-analysis of 147 randomised trials in the context of expectations from prospective epidemiological studies. BMJ. 2009;338:b1665.
  • Dahlöf B, Devereux RB, Kjeldsen SE, et al. Cardiovascular morbidity and mortality in the Losartan Intervention For Endpoint reduction in hypertension study (LIFE): a randomised trial against atenolol. Lancet. 2002;359:995–1003.
  • Kjeldsen SE, Berge E, Bangalore S, et al. No evidence for a J-shaped curve in treated hypertensive patients with increased cardiovascular risk: the VALUE trial. Blood Press. 2016;25:83–92.
  • Mancia G, Kjeldsen SE, Zappe DH, et al. Cardiovascular outcomes at different on-treatment blood pressures in the hypertensive patients of the VALUE trial. Eur Heart J. 2016;37:955–964.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.