Document Detail


Left ventricular hypertrophy in new hemodialysis patients without symptomatic cardiac disease.
MedLine Citation:
PMID:  20378644     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
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.
Authors:
Robert N Foley; Bryan M Curtis; Edward W Randell; Patrick S Parfrey
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Publication Detail:
Type:  Journal Article; Multicenter Study; Randomized Controlled Trial     Date:  2010-04-08
Journal Detail:
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 
Date Detail:
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    
Other Details:
Languages:  eng     Pagination:  805-13     Citation Subset:  IM    
Affiliation:
Chronic Disease Research Group, University of Minnesota, Minneapolis, Minnesota, USA.
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MeSH Terms
Descriptor/Qualifier:
Anemia / blood,  complications,  drug therapy
Canada
Disease Progression
England
Erythropoietin / therapeutic use
Female
Hematinics / therapeutic use
Hemoglobins / metabolism
Humans
Hypertension / complications
Hypertrophy, Left Ventricular / blood,  etiology*,  ultrasonography
Kidney Failure, Chronic / blood,  complications,  therapy*
Linear Models
Logistic Models
Male
Middle Aged
Odds Ratio
Proportional Hazards Models
Prospective Studies
Recombinant Proteins
Renal Dialysis / adverse effects*
Risk Factors
Time Factors
Chemical
Reg. No./Substance:
0/Hematinics; 0/Hemoglobins; 0/Recombinant Proteins; 11096-26-7/Erythropoietin
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