|Left ventricular hypertrophy in new hemodialysis patients without symptomatic cardiac disease.|
|PMID: 20378644 Owner: NLM Status: MEDLINE|
|BACKGROUND AND OBJECTIVES: Although left ventricular hypertrophy (LVH) is a characteristic finding in hemodialysis (HD) populations, few risk factors for progressive LVH have been identified.
DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: As part of a multinational, blinded, randomized, controlled trial that demonstrated no effect of hemoglobin targets on LV size, 596 incident HD patients, without symptomatic cardiac disease or cardiac dilation, had baseline echocardiograms within 18 months of starting dialysis and subsequently at 24, 48, and 96 weeks later. A wide array of baseline risk factors were assessed, as were BP and hemoglobin levels during the trial.
RESULTS: The median age and duration of dialysis were 51.5 years and 9 months, respectively. LV mass index (LVMI) rose substantially during follow-up (114.2 g/m(2) at baseline, 121 at week 48, 123.4 at week 48, and 128.3 at week 96), as did fractional shortening, whereas LV volume (68.7, 70.1, 68.7, and 68.1 ml/m(2)) and E/A ratio remained unchanged. At baseline, the only multivariate associations of LVMI were gender and N terminal pro-B type natriuretic peptide. Comparing first and last echocardiograms in those without LVH at baseline, independent predictors of increase in LVMI were higher time-integrated systolic BP and cause of ESRD. An unadjusted association between baseline LVMI and subsequent cardiovascular events or death was eliminated by adjusting for age, diabetes, systolic BP, and N terminal pro-B type natriuretic peptide.
CONCLUSIONS: Progressive concentric LVH and hyperkinesis occur in HD patients, which is partly explained by hypertension but not by a wide array of potential risk factors, including anemia.
|Robert N Foley; Bryan M Curtis; Edward W Randell; Patrick S Parfrey|
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|Type: Journal Article; Multicenter Study; Randomized Controlled Trial Date: 2010-04-08|
|Title: Clinical journal of the American Society of Nephrology : CJASN Volume: 5 ISSN: 1555-905X ISO Abbreviation: Clin J Am Soc Nephrol Publication Date: 2010 May|
|Created Date: 2010-05-10 Completed Date: 2010-08-12 Revised Date: 2013-05-29|
Medline Journal Info:
|Nlm Unique ID: 101271570 Medline TA: Clin J Am Soc Nephrol Country: United States|
|Languages: eng Pagination: 805-13 Citation Subset: IM|
|Chronic Disease Research Group, University of Minnesota, Minneapolis, Minnesota, USA.|
|APA/MLA Format Download EndNote Download BibTex|
Erythropoietin / therapeutic use
Hematinics / therapeutic use
Hemoglobins / metabolism
Hypertension / complications
Hypertrophy, Left Ventricular / blood, etiology*, ultrasonography
Kidney Failure, Chronic / blood, complications, therapy*
Proportional Hazards Models
Renal Dialysis / adverse effects*
|0/Hematinics; 0/Hemoglobins; 0/Recombinant Proteins; 11096-26-7/Erythropoietin|
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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