Thorac Cardiovasc Surg 2022; 70(S 02): S67-S103
DOI: 10.1055/s-0042-1743039
Oral and Short Presentations
Tuesday, February 22
DGPK PAH & HTX

Fibrotic Myocardial Remodeling in Children and Adolescents after Cardiac Transplantation—A CMR Native T1 Mapping Study

H. Latus
1   Deutsches Herzzentrum München, München, Deutschland
,
I. Voges
2   Department of Pediatric Cardiology, Kiel, Deutschland
,
A.-E. Blank
3   Pediatric Heart Center, Giessen, Deutschland
,
K. Gummel
3   Pediatric Heart Center, Giessen, Deutschland
,
B. Reich
1   Deutsches Herzzentrum München, München, Deutschland
,
K. Klingel
4   Cardiopathology, Tübingen, Deutschland
,
M. Khalil
3   Pediatric Heart Center, Giessen, Deutschland
,
G. Kerst
5   Department of Pediatric Cardiology, Aachen, Deutschland
,
S. Skrzypek
3   Pediatric Heart Center, Giessen, Deutschland
,
D. Schranz
3   Pediatric Heart Center, Giessen, Deutschland
,
C. Jux
3   Pediatric Heart Center, Giessen, Deutschland
› Author Affiliations
 

    Background: Adverse fibrotic myocardial remodeling has been reported in patients after heart transplantation (HT). The aim of our study was to quantify diffuse myocardial fibrosis using CMR in a cohort of children and adolescents after HT to identify potential underlying factors that are related to increased fibrosis and to assess its hemodynamic relevance.

    Method: A total of 105 HT recipients (age 17.9 ± 7.1 years) without any clinical signs of acute rejection were assessed by CMR 11.8 ± 6.8 years after HT. Left ventricular (LV) volumes and mass were derived from short-axis cine images and LV strain/strain rate was assessed using tissue tracking technique. A T1 mapping sequence (MOLLI) was used to quantify native T1 times within the LV myocardium at a midventricular short axis slice. The collagen volume fraction (CVF) was obtained from histological analysis of endomyocardial biopsy samples.

    Results: Septal native LV T1 times showed a weak but significant association with CVF (r = 0.36, p = 0.01). T1 times were not related to LV size, mass and ejection fraction but correlated inversely with LV mass-to-volume ratio (r = 0.26, p = 0.001) and systolic (r = 0.32, p = 0.001) and diastolic longitudinal (r=0.25, p = 0.01) strain/strain rate. Neither a history of rejection, organ ischemic time, BSA ratio donor-acceptor, and time since HT were significantly related to T1 times.

    Conclusion: Fibrotic myocardial remodeling after HT affects LV systolic and diastolic longitudinal function and is associated with an increased mass-to-volume ratio. Future studies should aim to identify underlying factors and mechanisms that promote the development of fibrotic changes post HT and to assess its prognostic relevance.


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    No conflict of interest has been declared by the author(s).

    Publication History

    Article published online:
    12 February 2022

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