Post hoc analyses of SYMPLICITY HTN-3 shed light on potential source of unexpected trial outcome
Several potential confounding factors are revealed that may explain the unexpected blood pressure responses in the sham control and renal denervation arm. These insight can guide future trial designs.
Predictors of blood pressure response in the SYMPLICITY HTN-3 trialLiterature - Kandzari DE et al., Eur Heart J. 2014
KandzariDE, Bhatt DL, Brar S, et al.
Eur Heart J. 2014 Nov 16. pii: ehu441
Background
Several strategies have been explored to interrupt the sympathetic contribution to hypertension, especially in patients with resistant hypertension. Surgical sympathectomy yielded reduction of blood pressure for some patients, but also had serious side effects [1,2].A catheter-based approach to renal denervation (RDN) has shown sensory and sympathetic efferent denervation with decreased renal norepinephrine spill over, halving of renin activity and increased renal plasma flow [3]. Clinically significant, sustained reductions in office systolic blood pressure (SBP) have also been observed after RDN, in unblinded studies [4,5]. In a less-selected real-world patient population BP reductions were seen across a broader range of baseline BPs and the safety of radiofrequency RDN was confirmed [6].
The SYMPLICITY HTN-3 trial also confirmed safety of RDN, but did not show a significant difference in BP decline at 6 months, between the real and a sham procedure, in 535 patients with treatment resistant hypertension [7].
This study explored key factors that may have contributed to the puzzling results in SYMPLICITY HTN-3, namely the less than expected RDN treatment effect and a more pronounced response to a sham procedure. Information on changes in antihypertensive medications, outcomes in selected subgroups and detailed assessment of procedural data were studied, in order to identify potential confounding factors that may have impacted the delivery of effective RDN.
Main results
- In the overall group, multivariable analysis identified baseline office SBP>180 mmHg and prescription of an aldosterone antagonist at baseline as positive predictions for increasing 6-months change from baseline in office SBP.
Prescription of a vasodilator at baseline was a negative predictor of office BP reduction. - After randomisation, 39% of patients had a change in dose or drug class between baseline and 6-months.
- Vasodilators were the only baseline medications that were differentially prescribed between treatment groups. Among African-Americans, more sham patients (56%) than RDN patients (46.7%) received them, and among non-African-Americans 40.5% (sham) vs. 33.7% (RDN) respectively received vasodilators.
African-Americans undergoing a sham procedure and receiving a vasodilator showed a particularly large decline in SBP (-21.9+29.1 mmHg), which was not seen in the other subgroups. In non-African-Americans, patients not prescribed a vasodilator showed a greater change in office SBP (-17.6 mmHg in RDN and -10.4 mmHg in sham group, difference: -7.1, 95%CI: -13.7 to -0.6, P=0.03). - When control and RDN patients were propensity matched according to baseline characteristics, statistically significant increasing trends were seen for the difference in office SBP, and heart rate, with increasing numbers of ablations delivered to the RDN group.
No increase in safety events occurred with increasing number of renal artery ablations.
Conclusion
These post hoc analyses of the SYMPLICITY HTN-3 trial critically examined the results in the context of existing RDN data and clinical trial design. The unexpectedly large SBP decline in African-American control patients may indicate a change in medical adherence or type of therapy in this group. African-Americans indeed received vasodilators more often. While the exact reasons for the observed difference remain unclear, it underscores the importance of standardised and consistent BP care in future trials. A better understanding of how RDN translates to sympathetic activity is needed, and may require revisiting the basic science of RDN.Find this article on Pubmed
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