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Long Troponin T to Separate Troponin Elevations Among Patients With Atrial Fibrillation Versus Myocardial Infarction




TekijätAiraksinen, K. E. Juhani; Teppo, Konsta; Vasankari, Tuija; Paana, Tuomas; Junes, Helea; Salonen, Selma; Tuominen, Tuulia; Simonen, Sara; Strandberg, Marjatta; Hellman, Tapio; Linko‐Parvinen, Anna; Pallari, Hanna‐Mari; Jaakkola, Samuli; Wittfooth, Saara

KustantajaOvid Technologies (Wolters Kluwer Health)

Julkaisuvuosi2026

Lehti: Journal of the American Heart Association

Artikkelin numeroe044092

Vuosikerta15

Numero6

eISSN2047-9980

DOIhttps://doi.org/10.1161/JAHA.125.044092

Julkaisun avoimuus kirjaamishetkelläAvoimesti saatavilla

Julkaisukanavan avoimuus Kokonaan avoin julkaisukanava

Verkko-osoitehttps://doi.org/10.1161/jaha.125.044092

Rinnakkaistallenteen osoitehttps://research.utu.fi/converis/portal/detail/Publication/515754724

Rinnakkaistallenteen lisenssiCC BY NC ND

Rinnakkaistallennetun julkaisun versioKustantajan versio


Tiivistelmä
Background

Elevated troponin levels are a frequent finding in patients presenting with atrial fibrillation or atrial flutter (AF) to the emergency department but are seldom caused by myocardial infarction (MI). The current high‐sensitivity cTnT (cardiac troponin T) assay measures both the intact and highly fragmented cTnT forms (total cTnT) and detects cTnT elevations in conditions causing myocardial injury or MI without distinction between the 2.

Methods

The SuperTROPO (Better Diagnostics of Myocardial Infarction With a Test for Special Forms of Troponin) study included 521 consecutive patients with AF only and 188 patients with MI only (139 Type 1 MI), all with a total cTnT value ≥14 ng/L at emergency department admission. Intact and long forms of cTnT (long cTnT) were analyzed from the first plasma samples using a novel immunoassay. The diagnostic performance of long cTnT and total cTnT assays was compared in these cases with elevated total cTnT.

Results

Long cTnT was superior to total cTnT in discriminating troponin elevations in patients with MI from those in patients with AF (area under the curve for type 1 MI: 0.879 versus 0.783; for any MI: 0.864 versus 0.779; both P<0.001) when measured from the first blood sample without a significant effect of sex, age, estimated glomerular filtration rate, or total cTnT <200 ng/L. The difference in long cTnT levels was most notable in patients presenting within 12 hours of symptom onset.

Conclusions

The long cTnT immunoassay shows that the troponin release in AF is composed mainly of smaller troponin fragments. This novel test holds promise that measuring long cTnT forms could help to separate troponin elevations caused by AF from those of acute Type 1 MI from a single sample with better accuracy than the commercial high‐sensitivity cTnT test.


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Julkaisussa olevat rahoitustiedot
Research funding from Business Finland, Research grants from the Finnish Foundation for Cardiovascular Research. The funders had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, or approval of the article; and decision to submit the article for publication.


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