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dc.contributor.authorForså, Marianne Inngjerdingen
dc.contributor.authorSmedsrud, Marit Kristine
dc.contributor.authorHaugaa, Kristina Ingrid Helena Hermann
dc.contributor.authorBjerring, Anders W.
dc.contributor.authorFruh, Andreas
dc.contributor.authorSarvari, Sebastian I.
dc.contributor.authorLandgraff, Hege Elisabeth Wilson
dc.contributor.authorHallén, Jostein
dc.contributor.authorEdvardsen, Thor
dc.date.accessioned2024-03-18T13:34:08Z
dc.date.available2024-03-18T13:34:08Z
dc.date.created2024-02-15T08:27:35Z
dc.date.issued2023
dc.identifier.citationEuropean Journal of Preventive Cardiology. 2023, Artikkel zwad361.en_US
dc.identifier.issn2047-4873
dc.identifier.urihttps://hdl.handle.net/11250/3122923
dc.descriptionThis is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited.en_US
dc.description.abstractAims: Echocardiographic characteristics to distinguish physiological left ventricular (LV) hypertrophy from pathology are warranted in early adolescent athletes. This study aimed to explore the phenotype, progression, and potential grey zone of LV hypertrophy during adolescence in athletes and hypertrophic cardiomyopathy (HCM) genotype–positive patients. Methods and results: In this longitudinal observation study, we compared seventy-six 12-year-old athletes with 55 age-matched and sex-matched HCM genotype–positive patients. Echocardiographic parameters were evaluated by using paediatric reference values (Z-scores). Hypertrophic cardiomyopathy genotype–positive patients were included if they had no or mild LV hypertrophy [maximum wall thickness <13 mm, Z-score <6 for interventricular septum diameter (ZIVSd), or posterior wall thickness]. We collected clinical data, including data on cardiac events. The mean follow-up-time was 3.2 ± 0.8 years. At baseline, LV hypertrophy was found in 28% of athletes and 21% of HCM genotype–positive patients (P = 0.42). Septum thickness values were similar (ZIVSd 1.4 ± 0.9 vs. 1.0 ± 1.3, P = 0.08) and increased only in HCM genotype–positive patients {ZIVSd progression rate −0.17 [standard error (SE) 0.05], P = 0.002 vs. 0.30 [SE 0.10], P = 0.001}. Left ventricular volume Z-scores (ZLVEDV) were greater in athletes [ZLVEDV 1.0 ± 0.6 vs. −0.1 ± 0.8, P < 0.001; ZLVEDV progression rate −0.05 (SE 0.04), P = 0.21 vs. −0.06 (SE 0.04), P = 0.12]. Cardiac arrest occurred in two HCM genotype–positive patients (ages 13 and 14), with ZIVSd 8.2–11.5. Conclusion: Left ventricular hypertrophy was found in a similar proportion in early adolescence but progressed only in HCM genotype–positive patients. A potential grey zone of LV hypertrophy ranged from a septum thickness Z-score of 2.0 to 3.3. Left ventricular volumes remained larger in athletes. Evaluating the progression of wall thickness and volume may help clinicians distinguish physiological LV hypertrophy from early HCM.en_US
dc.language.isoengen_US
dc.subjectadolescenten_US
dc.subjectathleteen_US
dc.subjectcardiac remodellingen_US
dc.subjectechocardiographyen_US
dc.titleDistinguishing left ventricular hypertrophy from hypertrophic cardiomyopathy in adolescents: A longitudinal observation studyen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.rights.holder© The Author(s) 2023en_US
dc.source.pagenumber8en_US
dc.source.journalEuropean Journal of Preventive Cardiologyen_US
dc.identifier.doi10.1093/eurjpc/zwad361
dc.identifier.cristin2246206
dc.description.localcodeInstitutt for fysisk prestasjonsevne / Department of Physical Performanceen_US
dc.source.articlenumberzwad361en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2


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