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Heart 89:589-590 doi:10.1136/heart.89.6.589
  • Editorial

Drug treatment of hypertension: implications of ALLHAT

  1. B Williams
  1. Correspondence to:
    Dr Bryan Williams, Clinical Sciences Building, Leicester Royal Infirmary, PO Box 65, Leicester LE2 7LX, UK;
    bw17{at}le.ac.uk

    The largest ever study of antihypertensive treatment, the ALLHAT trial, has led to some controversial conclusions about the safety and efficacy of the “newer” antihypertensive agents

    The presentation and publication of the primary results of the antihypertensive and lipid lowering treatment to prevent heart attack trial (ALLHAT) has generated much interest and opinion.1 This is because (1) ALLHAT is the largest ever study of antihypertensive therapy; (2) ALLHAT addressed the commercially sensitive issue of appropriate first line therapy for hypertension; and (3) the initial presentation of the results led to some controversial conclusions.

    ALLHAT was designed to compare the effectiveness of initial antihypertensive therapy with three different classes of “newer” antihypertensive drug classes (angiotensin converting enzyme (ACE) inhibitor, calcium channel blocker (CCB) or α adrenergic blocker) with an older established treatment (thiazide diuretic) at reducing a primary end point of fatal coronary heart disease or non-fatal myocardial infarction. ALLHAT was a randomised, double blind controlled clinical trial conducted in 623 centres across North America. ALLHAT initially randomised 42 418 mild to moderate hypertensive patients aged ≥ 55 years (mean age 67 years) with one additional cardiovascular risk factor to one of four antihypertensive treatments; the diuretic, chlorthalidone (12.5–25 mg daily); the ACE inhibitor, lisinopril (10–40 mg daily), the CCB, amlodipine (2.5–10 mg daily), or the α blocker doxazosin (1–8 mg daily). The doxazosin arm was stopped prematurely in 2000 because of a reported excess of cardiovascular events (principally congestive heart failure) when compared to the reference drug chlorthalidone.2 This left 33 357 patients who completed ALLHAT for a mean follow up of 4.9 years.

    NO DIFFERENCE IN PRIMARY END POINT RATE

    At the end of the study, there was no difference in the rate of the primary end point when comparing the reference drug chlorthalidone (11.5%) with amlodipine (11.3%) or with lisinopril (11.4%).1 Moreover, there was no difference in the most important secondary end point—death. Compared with chlorthalidone, all cause mortality with lisinopril was identical and non-significantly 4% lower with amlodipine. Mindful of these outcomes, it was surprising that the investigators, the accompanying editorial in the JAMA, and the subsequent publicity, declared that the thiazide was “the winner”.1,3 If the primary end point and all cause mortality are the same with all three drugs classes, how could this interpretation have arisen? The premise that chlorthalidone was “the winner” comes from analysis of secondary end points and assumptions about cost and thus “cost effectiveness”. However, confidence in the robustness of the effectiveness data is essential before cost effectiveness can be considered.

    There were differences in two secondary outcome measures in ALLHAT: stroke, and heart failure. The incidence of stroke was 15% higher with lisinopril when compared to chlorthalidone, and the rate of heart failure was reported as 19% higher with lisinopril and 38% higher with amlodipine when compared to the diuretic. If this is true, then these findings would represent important differences in drug specific effects. However, there are some troubling inconsistencies in these findings that have more to do with the design of the trial than drug specific effects.

    Blood pressure lowering is a powerful determinant of benefit in clinical trials, even more powerful than often recognised.4 Thus, even small differences in blood pressure between the treatment groups would have a powerful effect on outcome, especially for stroke. The ALLHAT population had a mean age of 67 years and 35% were black. Older people and blacks respond less well to ACE inhibition and much better to diuretics with regard to blood pressure lowering.5,6 Thus, it was unsurprising that systolic blood pressure control was significantly lower in those receiving diuretics when compared to those receiving ACE inhibition throughout the trial.1 This was especially noticeable in blacks. The magnitude of this difference would be sufficient to account for the less effective outcome for lisinopril when compared to chlorthalidone for stroke protection.4

    CONTENTIOUS DATA REGARDING HEART FAILURE

    The data regarding heart failure is more contentious and has been a controversial end point in ALLHAT ever since the premature discontinuation of the doxazosin arm of the study for a reported excess of heart failure when compared to the diuretic.2,7 This again may have much to do with trial design. It is not widely recognised that 90% of patients randomised into ALLHAT were receiving antihypertensive treatment. The details of this baseline treatment have not been reported and it is unclear if they are even available. This is very important because there was no “washout period” or placebo run-in. Patients were simply crossed over to their randomised medications. It is likely that many of this elderly cohort were receiving diuretic treatment at baseline and its cessation and subsequent crossover to an ACE inhibitor or CCB would be expected to unmask occult heart failure. Consistent with this possibility, the rates of heart failure diverge very early and then appear to remain parallel thereafter. Moreover, the expected higher mortality associated with clinical heart failure is inconsistent with the finding that all cause mortality rates are similar with all three drug classes and if anything lower with amlodipine! Heart failure is a difficult end point to validate in such a large clinical trial and in my view the findings of ALLHAT with regard to heart failure should continue to be viewed with caution. The overemphasis given to this end point by the report of the findings of ALLHAT in JAMA and the subsequent publicity distorted the balance of the overall conclusion, away from the primary end point. So much so that even the New York Times felt the need to subsequently publish a correction of its initial front page interpretation of the breaking news from ALLHAT.

    What have we learnt from ALLHAT? We have gained reassurance that the longstanding recommendations of many hypertension societies in Europe are correct and that thiazide diuretics are the most effective initial treatment for lowering blood pressure in older people and should form the platform for drug therapy for hypertension in older people. We have learnt that epidemiologists can at times be more dangerous than the diseases they study and that the misguided publication of scare stories about increased risks of coronary heart disease, cancer, and gastrointestinal bleeding with CCBs has not been confirmed. There is no substitute for a large scale trial when defining treatment modalities to which massive numbers of the population will be exposed. Trials are as much a study of safety as they are of efficacy and the findings of ALLHAT in this regard are reassuring. Finally, we have learnt once again that most people will require more than one drug to control their blood pressure and that the debate about initial therapy is less important than defining the composition of the optimal therapeutic combination for the treatment of hypertension.8,9

    The largest ever study of antihypertensive treatment, the ALLHAT trial, has led to some controversial conclusions about the safety and efficacy of the “newer” antihypertensive agents

    REFERENCE