Effects of body size and hypertension treatments on cardiovascular event rates: subanalysis of the ACCOMPLISH randomised controlled trial
- PMID: 23219284
- DOI: 10.1016/S0140-6736(12)61343-9
Effects of body size and hypertension treatments on cardiovascular event rates: subanalysis of the ACCOMPLISH randomised controlled trial
Abstract
Background: In previous clinical trials in high-risk hypertensive patients, paradoxically higher cardiovascular event rates have been reported in patients of normal weight compared with obese individuals. As a prespecified analysis of the Avoiding Cardiovascular Events through Combination Therapy in Patients Living with Systolic Hypertension (ACCOMPLISH) trial, we aimed to investigate whether the type of hypertension treatment affects patients' cardiovascular outcomes according to their body size.
Methods: On the basis of body-mass index (BMI), we divided the full ACCOMPLISH cohort into obese (BMI ≥30, n=5709), overweight (≥25 to <30, n=4157), or normal weight (<25, n=1616) categories. The ACCOMPLISH cohort had already been randomised to treatment with single-pill combinations of either benazepril and hydrochlorothiazide or benazepril and amlodipine. We compared event rates (adjusted for age, sex, diabetes, previous cardiovascular events, stroke, or chronic kidney disease) for the primary endpoint of cardiovascular death or non-fatal myocardial infarction or stroke. The analysis was by intention to treat. This trial is registered with ClinicalTrials.gov, number NCT00170950.
Findings: In patients allocated benazepril and hydrochlorothiazide, the primary endpoint (per 1000 patient-years) was 30·7 in normal weight, 21·9 in overweight, and 18·2 in obese patients (overall p=0·0034). However, in those allocated benazepril and amlodipine, the primary endpoint did not differ between the three BMI groups (18·2, 16·9, and 16·5, respectively; overall p=0·9721). In obese individuals, primary event rates were similar with both benazepril and hydrochlorothiazide and benazepril and amlodipine, but rates were significantly lower with benazepril and amlodipine in overweight patients (hazard ratio 0·76, 95% CI 0·59-0·94; p=0·0369) and those of normal weight (0·57, 0·39-0·84; p=0·0037).
Interpretation: Hypertension in normal weight and obese patients might be mediated by different mechanisms. Thiazide-based treatment gives less cardiovascular protection in normal weight than obese patients, but amlodipine-based therapy is equally effective across BMI subgroups and thus offers superior cardiovascular protection in non-obese hypertension.
Funding: Novartis Pharmaceuticals.
Copyright © 2013 Elsevier Ltd. All rights reserved.
Comment in
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Diuretic-based regimens for obese patients?Lancet. 2013 Feb 16;381(9866):512-3. doi: 10.1016/S0140-6736(12)61819-4. Epub 2012 Dec 6. Lancet. 2013. PMID: 23219285 No abstract available.
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Hypertension: Should thiazides be used for hypertension in obese patients?Nat Rev Nephrol. 2013 Feb;9(2):66. doi: 10.1038/nrneph.2012.278. Epub 2013 Jan 8. Nat Rev Nephrol. 2013. PMID: 23296295 No abstract available.
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[BMI influences the success of antihypertensive therapy].Dtsch Med Wochenschr. 2013 Feb;138(7):298. doi: 10.1055/s-0032-1331862. Dtsch Med Wochenschr. 2013. PMID: 23520618 German. No abstract available.
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Obesity, blood pressure, and cardiovascular outcomes.Lancet. 2013 Jun 8;381(9882):1981-2. doi: 10.1016/S0140-6736(13)61194-0. Lancet. 2013. PMID: 23746889 No abstract available.
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Obesity, blood pressure, and cardiovascular outcomes.Lancet. 2013 Jun 8;381(9882):1981. doi: 10.1016/S0140-6736(13)61192-7. Lancet. 2013. PMID: 23746890 No abstract available.
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Obesity, blood pressure, and cardiovascular outcomes.Lancet. 2013 Jun 8;381(9882):1981. doi: 10.1016/S0140-6736(13)61193-9. Lancet. 2013. PMID: 23746891 No abstract available.
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Obesity, blood pressure, and cardiovascular outcomes - Authors' reply.Lancet. 2013 Jun 8;381(9882):1982-3. doi: 10.1016/S0140-6736(13)61196-4. Lancet. 2013. PMID: 23746892 No abstract available.
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Obesity, blood pressure, and cardiovascular outcomes.Lancet. 2013 Jun 8;381(9882):1982. doi: 10.1016/S0140-6736(13)61195-2. Lancet. 2013. PMID: 23746893 No abstract available.
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