Left atrial structure and function and clinical outcomes in the general population

Left atrial (LA) structural and functional abnormalities may be subclinical phenotypes, which identify individuals at increased risk of adverse outcomes. Maximum LA volume (LAmax) and LA emptying fraction (LAEF) were measured via cardiac magnetic resonance imaging in 1802 participants in the Dallas...

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Published inEuropean heart journal Vol. 34; no. 4; pp. 278 - 285
Main Authors Gupta, Sachin, Matulevicius, Susan A., Ayers, Colby R., Berry, Jarett D., Patel, Parag C., Markham, David W., Levine, Benjamin D., Chin, Kelly M., de Lemos, James A., Peshock, Ronald M., Drazner, Mark H.
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LanguageEnglish
Published England Oxford University Press 01.01.2013
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Abstract Left atrial (LA) structural and functional abnormalities may be subclinical phenotypes, which identify individuals at increased risk of adverse outcomes. Maximum LA volume (LAmax) and LA emptying fraction (LAEF) were measured via cardiac magnetic resonance imaging in 1802 participants in the Dallas Heart Study. The associations of LAEF and LAmax indexed to body surface area (LAmax/BSA) with traditional risk factors, natriuretic peptide levels, and left ventricular (LV) structure [end-diastolic volume (EDV) and concentricity(0.67) (mass/EDV(0.67))] and function (ejection fraction) were assessed using linear regression analysis. The incremental prognostic value of LAmax/BSA and LAEF beyond traditional risk factors, LV ejection fraction, and LV mass was assessed using the Cox proportional-hazards model. Both increasing LAmax/BSA and decreasing LAEF were associated with hypertension and natriuretic peptide levels (P < 0.05 for all). In multivariable analysis, LAmax/BSA was most strongly associated with LV end-diastolic volume/BSA, while LAEF was strongly associated with LV ejection fraction and concentricity(0.67). During a median follow-up period of 8.1 years, there were 81 total deaths. Decreasing LAEF [hazard ratio (HR) per 1 standard deviation (SD) (8.0%): 1.56 (1.32-1.87)] but not increasing LAmax/BSA [HR per 1 SD (8.6 mL/m(2)): 1.14 (0.97-1.34)] was independently associated with mortality. Furthermore, the addition of LAEF to a model adjusting Framingham risk score, diabetes, race, LV mass, and ejection fraction improved the c-statistic (c-statistics: 0.78 vs. 0.77; P < 0.05, respectively), whereas the addition of LAmax/BSA did not (c-statistics: 0.76, P = 0.20). In the general population, both LAmax/BSA and LAEF are important subclinical phenotypes but LAEF is superior and incremental to LAmax/BSA.
AbstractList Left atrial (LA) structural and functional abnormalities may be subclinical phenotypes, which identify individuals at increased risk of adverse outcomes.AIMSLeft atrial (LA) structural and functional abnormalities may be subclinical phenotypes, which identify individuals at increased risk of adverse outcomes.Maximum LA volume (LAmax) and LA emptying fraction (LAEF) were measured via cardiac magnetic resonance imaging in 1802 participants in the Dallas Heart Study. The associations of LAEF and LAmax indexed to body surface area (LAmax/BSA) with traditional risk factors, natriuretic peptide levels, and left ventricular (LV) structure [end-diastolic volume (EDV) and concentricity(0.67) (mass/EDV(0.67))] and function (ejection fraction) were assessed using linear regression analysis. The incremental prognostic value of LAmax/BSA and LAEF beyond traditional risk factors, LV ejection fraction, and LV mass was assessed using the Cox proportional-hazards model. Both increasing LAmax/BSA and decreasing LAEF were associated with hypertension and natriuretic peptide levels (P < 0.05 for all). In multivariable analysis, LAmax/BSA was most strongly associated with LV end-diastolic volume/BSA, while LAEF was strongly associated with LV ejection fraction and concentricity(0.67). During a median follow-up period of 8.1 years, there were 81 total deaths. Decreasing LAEF [hazard ratio (HR) per 1 standard deviation (SD) (8.0%): 1.56 (1.32-1.87)] but not increasing LAmax/BSA [HR per 1 SD (8.6 mL/m(2)): 1.14 (0.97-1.34)] was independently associated with mortality. Furthermore, the addition of LAEF to a model adjusting Framingham risk score, diabetes, race, LV mass, and ejection fraction improved the c-statistic (c-statistics: 0.78 vs. 0.77; P < 0.05, respectively), whereas the addition of LAmax/BSA did not (c-statistics: 0.76, P = 0.20).METHODS AND RESULTSMaximum LA volume (LAmax) and LA emptying fraction (LAEF) were measured via cardiac magnetic resonance imaging in 1802 participants in the Dallas Heart Study. The associations of LAEF and LAmax indexed to body surface area (LAmax/BSA) with traditional risk factors, natriuretic peptide levels, and left ventricular (LV) structure [end-diastolic volume (EDV) and concentricity(0.67) (mass/EDV(0.67))] and function (ejection fraction) were assessed using linear regression analysis. The incremental prognostic value of LAmax/BSA and LAEF beyond traditional risk factors, LV ejection fraction, and LV mass was assessed using the Cox proportional-hazards model. Both increasing LAmax/BSA and decreasing LAEF were associated with hypertension and natriuretic peptide levels (P < 0.05 for all). In multivariable analysis, LAmax/BSA was most strongly associated with LV end-diastolic volume/BSA, while LAEF was strongly associated with LV ejection fraction and concentricity(0.67). During a median follow-up period of 8.1 years, there were 81 total deaths. Decreasing LAEF [hazard ratio (HR) per 1 standard deviation (SD) (8.0%): 1.56 (1.32-1.87)] but not increasing LAmax/BSA [HR per 1 SD (8.6 mL/m(2)): 1.14 (0.97-1.34)] was independently associated with mortality. Furthermore, the addition of LAEF to a model adjusting Framingham risk score, diabetes, race, LV mass, and ejection fraction improved the c-statistic (c-statistics: 0.78 vs. 0.77; P < 0.05, respectively), whereas the addition of LAmax/BSA did not (c-statistics: 0.76, P = 0.20).In the general population, both LAmax/BSA and LAEF are important subclinical phenotypes but LAEF is superior and incremental to LAmax/BSA.CONCLUSIONIn the general population, both LAmax/BSA and LAEF are important subclinical phenotypes but LAEF is superior and incremental to LAmax/BSA.
Left atrial (LA) structural and functional abnormalities may be subclinical phenotypes, which identify individuals at increased risk of adverse outcomes. Maximum LA volume (LAmax) and LA emptying fraction (LAEF) were measured via cardiac magnetic resonance imaging in 1802 participants in the Dallas Heart Study. The associations of LAEF and LAmax indexed to body surface area (LAmax/BSA) with traditional risk factors, natriuretic peptide levels, and left ventricular (LV) structure [end-diastolic volume (EDV) and concentricity(0.67) (mass/EDV(0.67))] and function (ejection fraction) were assessed using linear regression analysis. The incremental prognostic value of LAmax/BSA and LAEF beyond traditional risk factors, LV ejection fraction, and LV mass was assessed using the Cox proportional-hazards model. Both increasing LAmax/BSA and decreasing LAEF were associated with hypertension and natriuretic peptide levels (P < 0.05 for all). In multivariable analysis, LAmax/BSA was most strongly associated with LV end-diastolic volume/BSA, while LAEF was strongly associated with LV ejection fraction and concentricity(0.67). During a median follow-up period of 8.1 years, there were 81 total deaths. Decreasing LAEF [hazard ratio (HR) per 1 standard deviation (SD) (8.0%): 1.56 (1.32-1.87)] but not increasing LAmax/BSA [HR per 1 SD (8.6 mL/m(2)): 1.14 (0.97-1.34)] was independently associated with mortality. Furthermore, the addition of LAEF to a model adjusting Framingham risk score, diabetes, race, LV mass, and ejection fraction improved the c-statistic (c-statistics: 0.78 vs. 0.77; P < 0.05, respectively), whereas the addition of LAmax/BSA did not (c-statistics: 0.76, P = 0.20). In the general population, both LAmax/BSA and LAEF are important subclinical phenotypes but LAEF is superior and incremental to LAmax/BSA.
Author Peshock, Ronald M.
Matulevicius, Susan A.
Patel, Parag C.
Levine, Benjamin D.
Markham, David W.
de Lemos, James A.
Gupta, Sachin
Chin, Kelly M.
Berry, Jarett D.
Drazner, Mark H.
Ayers, Colby R.
AuthorAffiliation 1 Division of Cardiology, Department of Internal Medicine , University of Texas Southwestern Medical Center , 5323 Harry Hines Blvd, Dallas, TX 75390-9047 , USA
3 Division of Pulmonary and Critical Care, Department of Internal Medicine , University of Texas Southwestern Medical Center , 5323 Harry Hines Blvd, Dallas, TX 75390-9047 , USA
2 Donald W. Reynolds Cardiovascular Clinical Research Center , University of Texas Southwestern Medical Center , 5323 Harry Hines Blvd, Dallas, TX 75390-9047 , USA
AuthorAffiliation_xml – name: 1 Division of Cardiology, Department of Internal Medicine , University of Texas Southwestern Medical Center , 5323 Harry Hines Blvd, Dallas, TX 75390-9047 , USA
– name: 2 Donald W. Reynolds Cardiovascular Clinical Research Center , University of Texas Southwestern Medical Center , 5323 Harry Hines Blvd, Dallas, TX 75390-9047 , USA
– name: 3 Division of Pulmonary and Critical Care, Department of Internal Medicine , University of Texas Southwestern Medical Center , 5323 Harry Hines Blvd, Dallas, TX 75390-9047 , USA
Author_xml – sequence: 1
  givenname: Sachin
  surname: Gupta
  fullname: Gupta, Sachin
– sequence: 2
  givenname: Susan A.
  surname: Matulevicius
  fullname: Matulevicius, Susan A.
– sequence: 3
  givenname: Colby R.
  surname: Ayers
  fullname: Ayers, Colby R.
– sequence: 4
  givenname: Jarett D.
  surname: Berry
  fullname: Berry, Jarett D.
– sequence: 5
  givenname: Parag C.
  surname: Patel
  fullname: Patel, Parag C.
– sequence: 6
  givenname: David W.
  surname: Markham
  fullname: Markham, David W.
– sequence: 7
  givenname: Benjamin D.
  surname: Levine
  fullname: Levine, Benjamin D.
– sequence: 8
  givenname: Kelly M.
  surname: Chin
  fullname: Chin, Kelly M.
– sequence: 9
  givenname: James A.
  surname: de Lemos
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– sequence: 10
  givenname: Ronald M.
  surname: Peshock
  fullname: Peshock, Ronald M.
– sequence: 11
  givenname: Mark H.
  surname: Drazner
  fullname: Drazner, Mark H.
BackLink https://www.ncbi.nlm.nih.gov/pubmed/22782941$$D View this record in MEDLINE/PubMed
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Copyright Published on behalf of the European Society of Cardiology. All rights reserved. © The Author 2012. For permissions please email: journals.permissions@oup.com 2012
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7641364 - Circulation. 1995 Aug 15;92(4):835-41
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Snippet Left atrial (LA) structural and functional abnormalities may be subclinical phenotypes, which identify individuals at increased risk of adverse outcomes....
Left atrial (LA) structural and functional abnormalities may be subclinical phenotypes, which identify individuals at increased risk of adverse...
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SubjectTerms Atrial Function, Left - physiology
Biomarkers - blood
Cardiac Volume - physiology
Cause of Death
Clinical Research
Female
Heart Atria - anatomy & histology
Hemodynamics - physiology
Humans
Magnetic Resonance Angiography
Male
Middle Aged
Natriuretic Peptide, Brain - blood
Peptide Fragments - blood
Prognosis
Sex Factors
Texas - epidemiology
Troponin T - blood
Title Left atrial structure and function and clinical outcomes in the general population
URI https://www.ncbi.nlm.nih.gov/pubmed/22782941
https://www.proquest.com/docview/1273785183
https://pubmed.ncbi.nlm.nih.gov/PMC3549524
Volume 34
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