Changes in left ventricular mass index in children and adolescents after renal transplantation

Citation
Mm. Mitsnefes et al., Changes in left ventricular mass index in children and adolescents after renal transplantation, PEDIAT TRAN, 5(4), 2001, pp. 279-284
Citations number
23
Categorie Soggetti
Pediatrics
Journal title
PEDIATRIC TRANSPLANTATION
ISSN journal
13973142 → ACNP
Volume
5
Issue
4
Year of publication
2001
Pages
279 - 284
Database
ISI
SICI code
1397-3142(200108)5:4<279:CILVMI>2.0.ZU;2-W
Abstract
Recent reports indicate a high prevalence of left ventricular hypertrophy ( LVH) in children on dialysis and after renal transplantation (Tx), as ident ified by cross-sectional analysis. However. the evolution of LVH in pediatr ic patients with end-stage renal disease after renal Tx is not well establi shed. To assess changes of left ventricular mass (LVM), we prospectively pe rformed echocardiography in 23 children and adolescents between November 19 98 and July 2000. Each patient had an echocardiographic evaluation while on dialysis (for at least 6 weeks) and a follow-up evaluation at least 6 mont hs after successful renal Tx (i.e. with a measured glomerular filtration ra te [GFR] of at least 40 mL/min/1.73 m(2)). The LVM index was estimated by i ndexing LVM to height(2.7). Sixteen patients had a cadaveric transplant and seven had a live donor transplant: the mean duration between the two studi es was 1.9+/-1.6 yr; and the mean GFR was 55.0+/-21.4 mL/min/ 1.73 m(2). Th ere was no significant difference in the mean values of the LVM index while on dialysis and after renal Tx (43.9+/-17.8 g/m(2.7) and 39.3 +/- 12.0 g/m (2.7), respectively, p = 0.19), or in the prevalence of LVH (52% and 56%, r espectively). Interval changes in the LVM index in individual subjects betw een the two studies were significantly associated with interval changes in indexed systolic (r = 0.42, p = 0.04) and diastolic (r = 0.42, p = 0.05) bl ood pressures. Interval changes in hemoglobin, blood urea nitrogen (BUN), c reatinine, and duration after Tx did not correlate with changes in the LVM index. There was no significant difference in LVM index change according to the type of dialysis, donor source, and the cause of renal failure. In mul tivariate analysis, the baseline LVM index and changes in indexed SEP were independent predictors for LVM index change after renal Tx. We conclude tha t LVH persists in children and adolescents after renal Tx. Control of blood pressure might be an important factor in regression or prevention of progr ession of LVH in these patients.