Evidence map›Paper›PMID 37252121›Full record

ArticleFrontiers in cardiovascular medicine2023

Individualized QT interval (QTi) is a powerful diagnostic tool in long QT syndrome: results from a large validation study.

Tomas Robyns, Dieter Nuyens, Bert Vandenberk, Peter Haemers, Jeroen Breckpot, Christophe Garweg, Joris Ector, Rik Willems

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Article in Frontiers in cardiovascular medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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5 · Who and what money

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8 authors.

Tomas RobynsDepartment of Cardiovascular Diseases, University Hospitals Leuven, Leuven, Belgium.
Dieter NuyensDepartment of Cardiology, Ziekenhuis Oost Limburg Genk, Genk, Belgium.
Bert VandenberkDepartment of Cardiovascular Diseases, University Hospitals Leuven, Leuven, Belgium.
Peter HaemersDepartment of Cardiovascular Diseases, University Hospitals Leuven, Leuven, Belgium.
Jeroen BreckpotDepartment of Human Genetics, University Hospitals Leuven, Leuven, Belgium.
Christophe GarwegDepartment of Cardiovascular Diseases, University Hospitals Leuven, Leuven, Belgium.
Joris EctorDepartment of Cardiovascular Diseases, University Hospitals Leuven, Leuven, Belgium.
Rik WillemsDepartment of Cardiovascular Diseases, University Hospitals Leuven, Leuven, Belgium.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aims: Diagnosis of Long QT syndrome (LQTS) is based on prolongation of the QT interval corrected for heart rate (QTc) on surface ECG and genotyping. However, up to 25% of genotype positive patients have a normal QTc interval. We recently showed that individualized QT interval (QTi) derived from 24 h holter data and defined as the QT value at the intersection of an RR interval of 1,000 ms with the linear regression line fitted through QT-RR data points of each individual patient was superior over QTc to predict mutation status in LQTS families. This study aimed to confirm the diagnostic value of QTi, fine-tune its cut-off value and evaluate intra-individual variability in patients with LQTS. Methods: From the Telemetric and Holter ECG Warehouse, 201 recordings from control individuals and 393 recordings from 254 LQTS patients were analysed. Cut-off values were obtained from ROC curves and validated against an in house LQTS and control cohort. Results: ROC curves indicated very good discrimination between controls and LQTS patients with QTi, both in females (AUC 0.96) and males (AUC 0.97). Using a gender dependent cut-off of 445 ms in females and 430 ms in males, a sensitivity of 88% and specificity of 96% were achieved, which was confirmed in the validation cohort. No significant intra-individual variability in QTi was observed in 76 LQTS patients for whom at least two holter recordings were available (483 ± 36 ms vs. 489 ± 42 ms, Conclusions: This study confirms our initial findings and supports the use of QTi in the evaluation of LQTS families. Using the novel gender dependent cut-off values, a high diagnostic accuracy was achieved.

Indexed as

holterindividualized QT correctionlong QT syndromeLQTSQTI

Identifiers

PMID37252121
PMCPMC10213876

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