Aim: Few echocardiographic studies have focused on regression of left ventricular hypertrophy (LVH) in patients with renal artery stenosis after revascularization, with inconsistent results. We performed a systematic metaanalysis of these studies in order to offer a comprehensive information on this topic. Methods: The PubMed, OVID-MEDLINE, and Cochrane library databases were analyzed to search English-language articles published from 1 January 1990 up to 31 March 2020. Studies were identified by crossing the following terms: 'renal artery stenosis', 'renovascular hypertension', 'fibromuscular dysplasia', 'renal artery stenting', 'renal artery surgery' with 'cardiac damage', 'hypertensive heart disease' 'left ventricular mass', 'left ventricular hypertrophy', 'echocardiography'. Results: A total of 726 hypertensive patients with renal artery stenosis (mean age 61 years, 64% men, 98% treated, 10% with fibromuscular dysplasia) were included in 13 studies. Baseline and postintervention pooled mean LVM values were 220±15 and 203±19 g, respectively (SMD -0.24±0.06, CI -0.37 to -0.21, P<0.0001); corresponding values for LV mass index were 129.0±6 and 115±7 g/m2, respectively (SMD -0.28±0.04, CI -0.36 to 0.21, P<0.0001). Renal revascularization was associated with a 40% lower risk of LVH. This trend was accompanied by a reduction in the number of antihypertensive drugs (SMD -0.27±0.04, CI -0.37 to 0.17, P<0.0001). Conclusion: The present meta-analysis suggests that renal artery revascularization added to antihypertensive therapy promotes a favourable effect on LV structure, as reflected by a significant decrease in absolute and indexed LV mass index as well by a lower risk of LVH. Limitations include: High prevalence of modest renal artery stenosis (≥50%); small sample of fibromuscular dysplasia; lack of randomized design of most studies.
Cuspidi, C., Tadic, M., Sala, C., Fosca, Q., Gherbesi, E., Mancia, G., et al. (2021). Left ventricular mass reduction and hypertrophy regression following renal artery revascularization: a meta-analysis. JOURNAL OF HYPERTENSION, 39(1), 4-11 [10.1097/HJH.0000000000002586].
Left ventricular mass reduction and hypertrophy regression following renal artery revascularization: a meta-analysis
Cesare Cuspidi
;Fosca Quarti-Trevano;Giuseppe Mancia;Guido Grassi
2021
Abstract
Aim: Few echocardiographic studies have focused on regression of left ventricular hypertrophy (LVH) in patients with renal artery stenosis after revascularization, with inconsistent results. We performed a systematic metaanalysis of these studies in order to offer a comprehensive information on this topic. Methods: The PubMed, OVID-MEDLINE, and Cochrane library databases were analyzed to search English-language articles published from 1 January 1990 up to 31 March 2020. Studies were identified by crossing the following terms: 'renal artery stenosis', 'renovascular hypertension', 'fibromuscular dysplasia', 'renal artery stenting', 'renal artery surgery' with 'cardiac damage', 'hypertensive heart disease' 'left ventricular mass', 'left ventricular hypertrophy', 'echocardiography'. Results: A total of 726 hypertensive patients with renal artery stenosis (mean age 61 years, 64% men, 98% treated, 10% with fibromuscular dysplasia) were included in 13 studies. Baseline and postintervention pooled mean LVM values were 220±15 and 203±19 g, respectively (SMD -0.24±0.06, CI -0.37 to -0.21, P<0.0001); corresponding values for LV mass index were 129.0±6 and 115±7 g/m2, respectively (SMD -0.28±0.04, CI -0.36 to 0.21, P<0.0001). Renal revascularization was associated with a 40% lower risk of LVH. This trend was accompanied by a reduction in the number of antihypertensive drugs (SMD -0.27±0.04, CI -0.37 to 0.17, P<0.0001). Conclusion: The present meta-analysis suggests that renal artery revascularization added to antihypertensive therapy promotes a favourable effect on LV structure, as reflected by a significant decrease in absolute and indexed LV mass index as well by a lower risk of LVH. Limitations include: High prevalence of modest renal artery stenosis (≥50%); small sample of fibromuscular dysplasia; lack of randomized design of most studies.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.