School-based routine screenings of electrocardiograms for the diagnosis of long QT syndrome

Author:

Fukuyama Megumi1ORCID,Horie Minoru1ORCID,Aoki Hisaaki2,Ozawa Junichi3,Kato Koichi1ORCID,Sawayama Yuichi1ORCID,Tanaka-Mizuno Sachiko4,Makiyama Takeru5,Yoshinaga Masao6,Nakagawa Yoshihisa1,Ohno Seiko7ORCID

Affiliation:

1. Department of Cardiovascular Medicine, Shiga University of Medical Science, Otsu, Japan

2. Department of Pediatric Cardiology, Osaka Women’s and Children’s Hospital, Osaka, Japan

3. Department of Pediatrics, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan

4. Department of Medical Statistics, Shiga University of Medical Science, Otsu, Japan

5. Department of Cardiovascular Medicine, Kyoto University Graduate School of Medicine, Kyoto, Japan

6. Department of Pediatrics, National Hospital Organization Kagoshima Medical Center, Kagoshima, Japan

7. Department of Bioscience and Genetics, National Cerebral and Cardiovascular Center, 5-7-1 Fujishirodai, Suita, Osaka 565-8565, Japan

Abstract

Abstract Aims School-based routine screenings of electrocardiograms (ECGs) have been performed upon admission to primary school (PS), junior high school (JHS), and high school (HS) in Japan. Though ECGs with prolonged QT intervals are occasionally found, the role of regular ECG screening tests in identifying long QT syndrome (LQTS) remains to be determined. We investigated the usefulness of the ECG screenings by comparing the results of genetic tests between students who showed QT-prolongation in the screenings and patients with LQTS. Methods and results We genetically screened 341 students (106 PS, 173 JHS, and 62 HS). Of these, 230 subjects showed QT-prolongation during regular screenings (S-S group), and the other 111 patients were clinically consulted with suspected LQTS by paediatricians (C-C group). Genotype–phenotype relationships were compared between the two groups. The positive rates in the genetic tests were comparable among the two groups; however, symptomatic subjects were significantly fewer in the S-S group than the C-C group (3% vs. 70%). Compared to the genotype-negative subjects, the positive subjects showed significantly longer QTc (P < 0.0001) and more frequently presented LQTS risk scores with ≥3.5 points (P < 0.0001). Lethal arrhythmic events (LAE) occurred only in the C-C group; 18 subjects experienced LAE and 83% of them were found to carry variant(s) in the LQTS-related genes. Conclusion The school-based ECG screenings are effective in identifying young patients with LQTS who require genetic analysis. If individuals are screened at a younger age, we can identify patients at risk earlier and provide preventative treatments.

Funder

MEXT KAKENHI

Ministry of Education, Culture, Sports, Science, and Technology of Japan

Ministry of Health, Labor and Welfare of Japan for Clinical Research on Intractable Disease

Publisher

Oxford University Press (OUP)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

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