Age- and sex-dependent upper reference limits for the high-sensitivity cardiac troponin T assay

The study sought to determine the 99th percentile upper reference limit for the high-sensitivity cardiac troponin T assay (hs-cTnT) in 3 large independent cohorts. The presently recommended 14 ng/l cut point for the diagnosis of myocardial infarction using the hs-cTnT assay was derived from small st...

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Vydáno v:Journal of the American College of Cardiology Ročník 63; číslo 14; s. 1441
Hlavní autoři: Gore, M Odette, Seliger, Stephen L, Defilippi, Christopher R, Nambi, Vijay, Christenson, Robert H, Hashim, Ibrahim A, Hoogeveen, Ron C, Ayers, Colby R, Sun, Wensheng, McGuire, Darren K, Ballantyne, Christie M, de Lemos, James A
Médium: Journal Article
Jazyk:angličtina
Vydáno: United States 15.04.2014
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ISSN:1558-3597, 1558-3597
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Abstract The study sought to determine the 99th percentile upper reference limit for the high-sensitivity cardiac troponin T assay (hs-cTnT) in 3 large independent cohorts. The presently recommended 14 ng/l cut point for the diagnosis of myocardial infarction using the hs-cTnT assay was derived from small studies of presumably healthy individuals, with relatively little phenotypic characterization. Data were included from 3 well-characterized population-based studies: the Dallas Heart Study (DHS), the Atherosclerosis Risk in Communities (ARIC) Study, and the Cardiovascular Health Study (CHS). Within each cohort, reference subcohorts were defined excluding individuals with recent hospitalization, overt cardiovascular disease, and kidney disease (subcohort 1), and further excluding those with subclinical structural heart disease (subcohort 2). Data were analyzed stratified by age, sex, and race. The 99th percentile values for the hs-cTnT assay in DHS, ARIC, and CHS were 18, 22, and 36 ng/l (subcohort 1) and 14, 21, and 28 ng/l (subcohort 2), respectively. These differences in 99th percentile values paralleled age differences across cohorts. Analyses within sex/age strata yielded similar results between cohorts. Within each cohort, 99th percentile values increased with age and were higher in men. More than 10% of men 65 to 74 years of age with no cardiovascular disease in our study had cardiac troponin T values above the current myocardial infarction threshold. Use of a uniform 14 ng/l cutoff for the hs-cTnT assay may lead to over-diagnosis of myocardial infarction, particularly in men and the elderly. Clinical validation is needed of new age- and sex-specific cutoff values for this assay.
AbstractList The study sought to determine the 99th percentile upper reference limit for the high-sensitivity cardiac troponin T assay (hs-cTnT) in 3 large independent cohorts. The presently recommended 14 ng/l cut point for the diagnosis of myocardial infarction using the hs-cTnT assay was derived from small studies of presumably healthy individuals, with relatively little phenotypic characterization. Data were included from 3 well-characterized population-based studies: the Dallas Heart Study (DHS), the Atherosclerosis Risk in Communities (ARIC) Study, and the Cardiovascular Health Study (CHS). Within each cohort, reference subcohorts were defined excluding individuals with recent hospitalization, overt cardiovascular disease, and kidney disease (subcohort 1), and further excluding those with subclinical structural heart disease (subcohort 2). Data were analyzed stratified by age, sex, and race. The 99th percentile values for the hs-cTnT assay in DHS, ARIC, and CHS were 18, 22, and 36 ng/l (subcohort 1) and 14, 21, and 28 ng/l (subcohort 2), respectively. These differences in 99th percentile values paralleled age differences across cohorts. Analyses within sex/age strata yielded similar results between cohorts. Within each cohort, 99th percentile values increased with age and were higher in men. More than 10% of men 65 to 74 years of age with no cardiovascular disease in our study had cardiac troponin T values above the current myocardial infarction threshold. Use of a uniform 14 ng/l cutoff for the hs-cTnT assay may lead to over-diagnosis of myocardial infarction, particularly in men and the elderly. Clinical validation is needed of new age- and sex-specific cutoff values for this assay.
The study sought to determine the 99th percentile upper reference limit for the high-sensitivity cardiac troponin T assay (hs-cTnT) in 3 large independent cohorts.OBJECTIVESThe study sought to determine the 99th percentile upper reference limit for the high-sensitivity cardiac troponin T assay (hs-cTnT) in 3 large independent cohorts.The presently recommended 14 ng/l cut point for the diagnosis of myocardial infarction using the hs-cTnT assay was derived from small studies of presumably healthy individuals, with relatively little phenotypic characterization.BACKGROUNDThe presently recommended 14 ng/l cut point for the diagnosis of myocardial infarction using the hs-cTnT assay was derived from small studies of presumably healthy individuals, with relatively little phenotypic characterization.Data were included from 3 well-characterized population-based studies: the Dallas Heart Study (DHS), the Atherosclerosis Risk in Communities (ARIC) Study, and the Cardiovascular Health Study (CHS). Within each cohort, reference subcohorts were defined excluding individuals with recent hospitalization, overt cardiovascular disease, and kidney disease (subcohort 1), and further excluding those with subclinical structural heart disease (subcohort 2). Data were analyzed stratified by age, sex, and race.METHODSData were included from 3 well-characterized population-based studies: the Dallas Heart Study (DHS), the Atherosclerosis Risk in Communities (ARIC) Study, and the Cardiovascular Health Study (CHS). Within each cohort, reference subcohorts were defined excluding individuals with recent hospitalization, overt cardiovascular disease, and kidney disease (subcohort 1), and further excluding those with subclinical structural heart disease (subcohort 2). Data were analyzed stratified by age, sex, and race.The 99th percentile values for the hs-cTnT assay in DHS, ARIC, and CHS were 18, 22, and 36 ng/l (subcohort 1) and 14, 21, and 28 ng/l (subcohort 2), respectively. These differences in 99th percentile values paralleled age differences across cohorts. Analyses within sex/age strata yielded similar results between cohorts. Within each cohort, 99th percentile values increased with age and were higher in men. More than 10% of men 65 to 74 years of age with no cardiovascular disease in our study had cardiac troponin T values above the current myocardial infarction threshold.RESULTSThe 99th percentile values for the hs-cTnT assay in DHS, ARIC, and CHS were 18, 22, and 36 ng/l (subcohort 1) and 14, 21, and 28 ng/l (subcohort 2), respectively. These differences in 99th percentile values paralleled age differences across cohorts. Analyses within sex/age strata yielded similar results between cohorts. Within each cohort, 99th percentile values increased with age and were higher in men. More than 10% of men 65 to 74 years of age with no cardiovascular disease in our study had cardiac troponin T values above the current myocardial infarction threshold.Use of a uniform 14 ng/l cutoff for the hs-cTnT assay may lead to over-diagnosis of myocardial infarction, particularly in men and the elderly. Clinical validation is needed of new age- and sex-specific cutoff values for this assay.CONCLUSIONSUse of a uniform 14 ng/l cutoff for the hs-cTnT assay may lead to over-diagnosis of myocardial infarction, particularly in men and the elderly. Clinical validation is needed of new age- and sex-specific cutoff values for this assay.
Author Gore, M Odette
Defilippi, Christopher R
Ballantyne, Christie M
Christenson, Robert H
Hoogeveen, Ron C
Ayers, Colby R
McGuire, Darren K
Sun, Wensheng
Seliger, Stephen L
de Lemos, James A
Hashim, Ibrahim A
Nambi, Vijay
Author_xml – sequence: 1
  givenname: M Odette
  surname: Gore
  fullname: Gore, M Odette
  organization: Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, Texas
– sequence: 2
  givenname: Stephen L
  surname: Seliger
  fullname: Seliger, Stephen L
  organization: Department of Medicine, University of Maryland School of Medicine, Baltimore, Maryland
– sequence: 3
  givenname: Christopher R
  surname: Defilippi
  fullname: Defilippi, Christopher R
  organization: Department of Medicine, University of Maryland School of Medicine, Baltimore, Maryland
– sequence: 4
  givenname: Vijay
  surname: Nambi
  fullname: Nambi, Vijay
  organization: Department of Medicine, Baylor College of Medicine, Center for Cardiovascular Disease Prevention, Methodist DeBakey Heart and Vascular Center, Houston, Texas; Michael E. DeBakey Veterans Affairs Hospital, Houston, Texas
– sequence: 5
  givenname: Robert H
  surname: Christenson
  fullname: Christenson, Robert H
  organization: Department of Pathology, University of Maryland School of Medicine, Baltimore, Maryland
– sequence: 6
  givenname: Ibrahim A
  surname: Hashim
  fullname: Hashim, Ibrahim A
  organization: Department of Pathology, University of Texas Southwestern Medical Center, Dallas, Texas
– sequence: 7
  givenname: Ron C
  surname: Hoogeveen
  fullname: Hoogeveen, Ron C
  organization: Department of Medicine, Baylor College of Medicine, Center for Cardiovascular Disease Prevention, Methodist DeBakey Heart and Vascular Center, Houston, Texas
– sequence: 8
  givenname: Colby R
  surname: Ayers
  fullname: Ayers, Colby R
  organization: Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, Texas; Department of Clinical Sciences, University of Texas Southwestern Medical Center, Dallas, Texas
– sequence: 9
  givenname: Wensheng
  surname: Sun
  fullname: Sun, Wensheng
  organization: Department of Medicine, Baylor College of Medicine, Center for Cardiovascular Disease Prevention, Methodist DeBakey Heart and Vascular Center, Houston, Texas
– sequence: 10
  givenname: Darren K
  surname: McGuire
  fullname: McGuire, Darren K
  organization: Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, Texas; Donald W. Reynolds Cardiovascular Clinical Research Center, University of Texas Southwestern Medical Center, Dallas, Texas
– sequence: 11
  givenname: Christie M
  surname: Ballantyne
  fullname: Ballantyne, Christie M
  organization: Department of Medicine, Baylor College of Medicine, Center for Cardiovascular Disease Prevention, Methodist DeBakey Heart and Vascular Center, Houston, Texas
– sequence: 12
  givenname: James A
  surname: de Lemos
  fullname: de Lemos, James A
  email: James.deLemos@UTSouthwestern.edu
  organization: Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, Texas; Donald W. Reynolds Cardiovascular Clinical Research Center, University of Texas Southwestern Medical Center, Dallas, Texas. Electronic address: James.deLemos@UTSouthwestern.edu
BackLink https://www.ncbi.nlm.nih.gov/pubmed/24530665$$D View this record in MEDLINE/PubMed
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Keywords diagnosis
troponin
myocardial infarction
population
Language English
License Copyright © 2014 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.
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PublicationTitle Journal of the American College of Cardiology
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References 24530670 - J Am Coll Cardiol. 2014 Apr 15;63(14):1449-50. doi: 10.1016/j.jacc.2013.12.031.
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Snippet The study sought to determine the 99th percentile upper reference limit for the high-sensitivity cardiac troponin T assay (hs-cTnT) in 3 large independent...
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SubjectTerms Adult
Age Factors
Aged
Biological Assay - methods
Biomarkers - analysis
Biomarkers - blood
Blood Chemical Analysis
Cohort Studies
Cross-Sectional Studies
Female
Humans
Male
Middle Aged
Myocardial Infarction - blood
Myocardial Infarction - diagnosis
Reference Values
Risk Assessment
Sensitivity and Specificity
Severity of Illness Index
Sex Factors
Troponin T - analysis
Troponin T - blood
Title Age- and sex-dependent upper reference limits for the high-sensitivity cardiac troponin T assay
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