Antihypertensive effects of angiotensin converting enzyme inhibition by lisinopril in post-transplant patients
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Published on: October 26, 2020
Lionel H Opie1, Matthias Haus, Patrick J Commerford
1Hypertension Clinic, Department of Medicine, Groote Schuur Hospital and Cape Heart Centre, University of Cape Town, Observatory, South Africa. opie@capeheart.uct.ac.za
Insights
Strictly controlling blood pressure (BP) with lisinopril in transplant patients reduced BP and left ventricular mass. This improved outcomes without negatively impacting cardiac function.
Area of Science:
- Nephrology
- Cardiology
- Pharmacology
Background:
- Post-transplant hypertension management remains unclear regarding strict blood pressure (BP) control benefits.
- Assessing the efficacy of adding lisinopril to standard therapy for ambulatory BP (ABP) in transplant recipients is crucial.
Purpose of the Study:
- To evaluate the antihypertensive effects of lisinopril on post-transplant patients' ambulatory BP (ABP).
- To monitor echocardiographic and hemodynamic changes as secondary endpoints.
Main Methods:
- A double-blind, randomized, prospective study involving post-transplant patients with abnormal 24-h ABP.
- Patients received either lisinopril plus standard therapy or placebo, with evaluations at 6, 12, 18, and 24 months post-transplantation.
Main Results:
- Lisinopril significantly reduced clinic BP and ABP compared to placebo.
- Fewer patients on lisinopril required additional antihypertensive medication (amlodipine).
- Lisinopril use led to a significant decrease in left ventricular (LV) mass and index, while the placebo group showed no change. LV end-diastolic diameter increased only in the placebo group.
Conclusions:
- Adding lisinopril to existing therapy effectively controlled BP in post-transplant patients.
- This stricter BP control modestly reduced LV mass without adverse effects on cardiac hemodynamic function.
Background:
It is not known whether strict control of blood pressure (BP) in mild post-transplant hypertension gives any benefit. Our primary objective was to test the antihypertensive effects of lisinopril added to standard therapy on ambulatory BP (ABP) of post-transplant patients. The secondary objective was to monitor echocardiographic and hemodynamic end points.
Methods:
Post-transplant patients with an abnormality of the 24-h ABP recording were recruited to this double-blind randomized prospective study that started 2 to 3 months after transplantation. Patients were then evaluated at 6, 12, 18, and 24 months after transplantation.
Results:
Lisinopril decreased the clinic BP and ABP, the latter from 134/85 to 126/82 mm Hg at 6 months (P =.01 v placebo) and 121/79 mm Hg after 2 years (P =.03 v placebo). Fewer patients in the lisinopril group required added amlodipine to control the BP (P =.01). Data on left ventricular (LV) mass are difficult to interpret because by coincidence in this small study, the lisinopril group had lower initial values than placebo. However, in the lisinopril group mean LV mass decreased by 10% (P =.02) and mass index by 13% (P =.01), whereas placebo LV mass and index did not change. The LV end-diastolic diameter increased only in the placebo group (P =.008). There were no significant changes in any of the other secondary outcomes, including the cardiac index and systemic vascular resistance.
Conclusions:
Thus, in these post-transplant patients, stricter BP control to normal levels by the addition of lisinopril to existing therapy, reduced BP and modestly decreased LV mass without altering cardiac hemodynamic function.
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