Literature DB >> 23124781

Change in cardiac geometry and function in CKD children during strict BP control: a randomized study.

Maria Chiara Matteucci1, Marcello Chinali, Gabriele Rinelli, Elke Wühl, Aleksandra Zurowska, Marina Charbit, Giacomo Pongiglione, Franz Schaefer.   

Abstract

BACKGROUND AND OBJECTIVES: Left ventricular hypertrophy (LVH) and abnormal systolic function are present in a high proportion of children with CKD. This study evaluated changes in left ventricular (LV) geometry and systolic function in children with mild to moderate CKD as an ancillary project of the Effect of Strict Blood Pressure Control and ACE Inhibition on Progression of Chronic Renal Failure in Pediatric Patients trial. DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: Echocardiograms and ambulatory BP monitoring were performed at baseline and at 1- or 2-year follow-up in 84 patients with CKD and 24-hour mean BP above the 50th percentile and/or receiving fixed high-dose angiotensin converting enzyme inhibition and randomized to conventional or intensified BP control.
RESULTS: LVH prevalence decreased from 38% to 25% (P<0.05). Changes in LV mass index (LVMI) were restricted to patients with LVH at baseline (-7.9 g/m(2.7); P<0.02). Changes in LVMI were independent of randomization, reduction in BP, hemoglobin, and estimated GFR. A significant increase in midwall fractional shortening was observed in the total cohort (P<0.05), and was greater in the intensified group compared with the conventional BP control group (12%±1.9% versus 8%±1.5%; P=0.05). In multivariate analysis, improvement in myocardial function was associated with reduction in BP (r=-0.4; P<0.05), independently of LVMI reduction.
CONCLUSIONS: In children with CKD, angiotensin converting enzyme inhibition with improved BP control, LVH regression, and improved systolic function was observed within 12 months. Lowering BP to the low-normal range led to a slightly more marked improvement in myocardial function but not in LVMI.

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Year:  2012        PMID: 23124781      PMCID: PMC3562867          DOI: 10.2215/CJN.08420811

Source DB:  PubMed          Journal:  Clin J Am Soc Nephrol        ISSN: 1555-9041            Impact factor:   8.237


  42 in total

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2.  Prognostic significance of serial changes in left ventricular mass in essential hypertension.

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Journal:  J Hypertens       Date:  1995-11       Impact factor: 4.844

4.  Ambulatory blood pressure is superior to clinic blood pressure in predicting treatment-induced regression of left ventricular hypertrophy. SAMPLE Study Group. Study on Ambulatory Monitoring of Blood Pressure and Lisinopril Evaluation.

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5.  Management of essential hypertension in patients with different degrees of left ventricular hypertrophy. Multicenter trial.

Authors:  A P Yurenev; H G Dyakonova; I D Novikov; A Vitols; L Pahl; G Haynemann; D Wallrabe; R Tsifkova; L Romanovska; P Niderle
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Authors:  G de Simone; S R Daniels; R B Devereux; R A Meyer; M J Roman; O de Divitiis; M H Alderman
Journal:  J Am Coll Cardiol       Date:  1992-11-01       Impact factor: 24.094

8.  Association of change in left ventricular mass with prognosis during long-term antihypertensive treatment.

Authors:  M L Muiesan; M Salvetti; D Rizzoni; M Castellano; F Donato; E Agabiti-Rosei
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9.  Comparison of five antihypertensive monotherapies and placebo for change in left ventricular mass in patients receiving nutritional-hygienic therapy in the Treatment of Mild Hypertension Study (TOMHS).

Authors:  P R Liebson; G A Grandits; S Dianzumba; R J Prineas; R H Grimm; J D Neaton; J Stamler
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10.  The relative effects of left ventricular hypertrophy, coronary artery disease, and ventricular dysfunction on survival among black adults.

Authors:  Y Liao; R S Cooper; D L McGee; G A Mensah; J K Ghali
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2.  Relationship of FGF23 to indexed left ventricular mass in children with non-dialysis stages of chronic kidney disease.

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4.  Longitudinal assessment of myocardial function in childhood chronic kidney disease, during dialysis, and following kidney transplantation.

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8.  Left ventricular diastolic dysfunction by tissue Doppler echocardiography in pediatric chronic kidney disease.

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Review 9.  Evidence-based guidelines for the management of hypertension in children with chronic kidney disease.

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Review 10.  The role of bone in CKD-mediated mineral and vascular disease.

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