Head-to-head comparison of cardiac troponin T and troponin I in patients without acute coronary syndrome: a systematic review

Publikation: Bidrag til tidsskriftReviewForskningfagfællebedømt

Standard

Head-to-head comparison of cardiac troponin T and troponin I in patients without acute coronary syndrome : a systematic review. / Árnadóttir, Ásthildur; Falk Klein, Christine; Iversen, Kasper.

I: Biomarkers, Bind 22, Nr. 8, 2017, s. 701-708.

Publikation: Bidrag til tidsskriftReviewForskningfagfællebedømt

Harvard

Árnadóttir, Á, Falk Klein, C & Iversen, K 2017, 'Head-to-head comparison of cardiac troponin T and troponin I in patients without acute coronary syndrome: a systematic review', Biomarkers, bind 22, nr. 8, s. 701-708. https://doi.org/10.1080/1354750X.2017.1335779

APA

Árnadóttir, Á., Falk Klein, C., & Iversen, K. (2017). Head-to-head comparison of cardiac troponin T and troponin I in patients without acute coronary syndrome: a systematic review. Biomarkers, 22(8), 701-708. https://doi.org/10.1080/1354750X.2017.1335779

Vancouver

Árnadóttir Á, Falk Klein C, Iversen K. Head-to-head comparison of cardiac troponin T and troponin I in patients without acute coronary syndrome: a systematic review. Biomarkers. 2017;22(8):701-708. https://doi.org/10.1080/1354750X.2017.1335779

Author

Árnadóttir, Ásthildur ; Falk Klein, Christine ; Iversen, Kasper. / Head-to-head comparison of cardiac troponin T and troponin I in patients without acute coronary syndrome : a systematic review. I: Biomarkers. 2017 ; Bind 22, Nr. 8. s. 701-708.

Bibtex

@article{8bbb39dfe20d41a399f99f6084891fd3,
title = "Head-to-head comparison of cardiac troponin T and troponin I in patients without acute coronary syndrome: a systematic review",
abstract = "BACKGROUND: Cardiac-specific troponin T (cTnT) and troponin I (cTnI) are considered diagnostically equal in patients with acute coronary syndrome (ACS). The aim of this systematic review was to compare the prevalence and prognostic strength of elevations of cTnT and cTnI in patients with other conditions than ACS.METHODS: A systemic review was conducted in concordance with the PRISMA guidelines. The studies were identified by searching PubMed, EMBASE and Cochrane Central Register, from May to August 2016. Studies measuring both cTnT and cTnI in populations without ACS were eligible.RESULTS: Twenty-nine studies were included (n = 25,859). Seventeen studies reported on prognostic information with follow-up time ranging for 30 d-5 years. Elevation above the 99th percentile (reference value for a healthy population) in non-ACS population was reported to be 0-39% for cTnI and 40-100% for cTnT. Elevation of cTnT tends to be a superior predictor for all-cause mortality and elevation of cTnI tends to be a superior predictor for cardiovascular related mortality.DISCUSSION: In the absence of ACS, elevation of cTnT is more frequent than elevation of cTnI.CONCLUSION: Both cTnT and cTnI elevations have important prognostic information regarding morbidity, cardiac mortality and all-cause mortality.",
author = "{\'A}sthildur {\'A}rnad{\'o}ttir and {Falk Klein}, Christine and Kasper Iversen",
year = "2017",
doi = "10.1080/1354750X.2017.1335779",
language = "English",
volume = "22",
pages = "701--708",
journal = "Biomarkers",
issn = "1354-750X",
publisher = "Taylor & Francis",
number = "8",

}

RIS

TY - JOUR

T1 - Head-to-head comparison of cardiac troponin T and troponin I in patients without acute coronary syndrome

T2 - a systematic review

AU - Árnadóttir, Ásthildur

AU - Falk Klein, Christine

AU - Iversen, Kasper

PY - 2017

Y1 - 2017

N2 - BACKGROUND: Cardiac-specific troponin T (cTnT) and troponin I (cTnI) are considered diagnostically equal in patients with acute coronary syndrome (ACS). The aim of this systematic review was to compare the prevalence and prognostic strength of elevations of cTnT and cTnI in patients with other conditions than ACS.METHODS: A systemic review was conducted in concordance with the PRISMA guidelines. The studies were identified by searching PubMed, EMBASE and Cochrane Central Register, from May to August 2016. Studies measuring both cTnT and cTnI in populations without ACS were eligible.RESULTS: Twenty-nine studies were included (n = 25,859). Seventeen studies reported on prognostic information with follow-up time ranging for 30 d-5 years. Elevation above the 99th percentile (reference value for a healthy population) in non-ACS population was reported to be 0-39% for cTnI and 40-100% for cTnT. Elevation of cTnT tends to be a superior predictor for all-cause mortality and elevation of cTnI tends to be a superior predictor for cardiovascular related mortality.DISCUSSION: In the absence of ACS, elevation of cTnT is more frequent than elevation of cTnI.CONCLUSION: Both cTnT and cTnI elevations have important prognostic information regarding morbidity, cardiac mortality and all-cause mortality.

AB - BACKGROUND: Cardiac-specific troponin T (cTnT) and troponin I (cTnI) are considered diagnostically equal in patients with acute coronary syndrome (ACS). The aim of this systematic review was to compare the prevalence and prognostic strength of elevations of cTnT and cTnI in patients with other conditions than ACS.METHODS: A systemic review was conducted in concordance with the PRISMA guidelines. The studies were identified by searching PubMed, EMBASE and Cochrane Central Register, from May to August 2016. Studies measuring both cTnT and cTnI in populations without ACS were eligible.RESULTS: Twenty-nine studies were included (n = 25,859). Seventeen studies reported on prognostic information with follow-up time ranging for 30 d-5 years. Elevation above the 99th percentile (reference value for a healthy population) in non-ACS population was reported to be 0-39% for cTnI and 40-100% for cTnT. Elevation of cTnT tends to be a superior predictor for all-cause mortality and elevation of cTnI tends to be a superior predictor for cardiovascular related mortality.DISCUSSION: In the absence of ACS, elevation of cTnT is more frequent than elevation of cTnI.CONCLUSION: Both cTnT and cTnI elevations have important prognostic information regarding morbidity, cardiac mortality and all-cause mortality.

U2 - 10.1080/1354750X.2017.1335779

DO - 10.1080/1354750X.2017.1335779

M3 - Review

C2 - 28545334

VL - 22

SP - 701

EP - 708

JO - Biomarkers

JF - Biomarkers

SN - 1354-750X

IS - 8

ER -

ID: 195162989