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Cardiac Magnetic Resonance Reveals Incipient Cardiomyopathy Traits in Adult Patients With Phenylketonuria
BACKGROUND: Phenylketonuria is the most common inborn error of amino acid metabolism, where oxidative stress and collateral metabolic abnormalities are likely to cause cardiac structural and functional modifications. We aim herein to characterize the cardiac phenotype of adult subjects with phenylke...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8649272/ https://www.ncbi.nlm.nih.gov/pubmed/34423658 http://dx.doi.org/10.1161/JAHA.120.020351 |
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author | Tanacli, Radu Hassel, Jan‐Hendrik Gebker, Rolf Berger, Alexander Gräfe, Michael Schneeweis, Christopher Doeblin, Patrick Fleck, Eckart Stehning, Christian Tacke, Frank Pieske, Burkert Spranger, Joachim Plöckinger, Ursula Ziagaki, Athanasia Kelle, Sebastian |
author_facet | Tanacli, Radu Hassel, Jan‐Hendrik Gebker, Rolf Berger, Alexander Gräfe, Michael Schneeweis, Christopher Doeblin, Patrick Fleck, Eckart Stehning, Christian Tacke, Frank Pieske, Burkert Spranger, Joachim Plöckinger, Ursula Ziagaki, Athanasia Kelle, Sebastian |
author_sort | Tanacli, Radu |
collection | PubMed |
description | BACKGROUND: Phenylketonuria is the most common inborn error of amino acid metabolism, where oxidative stress and collateral metabolic abnormalities are likely to cause cardiac structural and functional modifications. We aim herein to characterize the cardiac phenotype of adult subjects with phenylketonuria using advanced cardiac imaging. METHODS AND RESULTS: Thirty‐nine adult patients with phenylketonuria (age, 30.5±8.7 years; 10‐year mean phenylalanine concentration, 924±330 µmol/L) and 39 age‐ and sex‐matched healthy controls were investigated. Participants underwent a comprehensive cardiac magnetic resonance and echocardiography examination. Ten‐year mean plasma levels of phenylalanine and tyrosine were used to quantify disease activity and adherence to treatment. Patients with phenylketonuria had thinner left ventricular walls (septal end‐diastolic thickness, 7.0±17 versus 8.8±1.7 mm [P<0.001]; lateral thickness, 6.1±1.4 versus 6.8±1.2 mm [P=0.004]), more dilated left ventricular cavity (end‐diastolic volume, 87±14 versus 80±14 mL/m(2) [P=0.0178]; end‐systolic volume, 36±9 versus 29±8 mL/m(2) [P<0.001]), lower ejection fraction (59±6% versus 64±6% [P<0.001]), reduced systolic deformation (global circumferential strain, −29.9±4.2 % versus −32.2±5.0 % [P=0.027]), and lower left ventricular mass (38.2±7.9 versus 47.8±11.0 g/m(2) [P<0.001]). T1 native values were decreased (936±53 versus 996±26 ms [P<0.001]), with particular low values in patients with phenylalanine >1200 µmol/L (909±48 ms). Both mean phenylalanine (P=0.013) and tyrosine (P=0.035) levels were independently correlated with T1; and in a multiple regression model, higher phenylalanine levels and higher left ventricular mass associate with lower T1. CONCLUSIONS: Cardiac phenotype of adult patients with phenylketonuria reveals some traits of an early‐stage cardiomyopathy. Regular cardiology follow‐up, tighter therapeutic control, and prophylaxis of cardiovascular risk factors, in particular dyslipidemia, are recommended. |
format | Online Article Text |
id | pubmed-8649272 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-86492722022-01-14 Cardiac Magnetic Resonance Reveals Incipient Cardiomyopathy Traits in Adult Patients With Phenylketonuria Tanacli, Radu Hassel, Jan‐Hendrik Gebker, Rolf Berger, Alexander Gräfe, Michael Schneeweis, Christopher Doeblin, Patrick Fleck, Eckart Stehning, Christian Tacke, Frank Pieske, Burkert Spranger, Joachim Plöckinger, Ursula Ziagaki, Athanasia Kelle, Sebastian J Am Heart Assoc Original Research BACKGROUND: Phenylketonuria is the most common inborn error of amino acid metabolism, where oxidative stress and collateral metabolic abnormalities are likely to cause cardiac structural and functional modifications. We aim herein to characterize the cardiac phenotype of adult subjects with phenylketonuria using advanced cardiac imaging. METHODS AND RESULTS: Thirty‐nine adult patients with phenylketonuria (age, 30.5±8.7 years; 10‐year mean phenylalanine concentration, 924±330 µmol/L) and 39 age‐ and sex‐matched healthy controls were investigated. Participants underwent a comprehensive cardiac magnetic resonance and echocardiography examination. Ten‐year mean plasma levels of phenylalanine and tyrosine were used to quantify disease activity and adherence to treatment. Patients with phenylketonuria had thinner left ventricular walls (septal end‐diastolic thickness, 7.0±17 versus 8.8±1.7 mm [P<0.001]; lateral thickness, 6.1±1.4 versus 6.8±1.2 mm [P=0.004]), more dilated left ventricular cavity (end‐diastolic volume, 87±14 versus 80±14 mL/m(2) [P=0.0178]; end‐systolic volume, 36±9 versus 29±8 mL/m(2) [P<0.001]), lower ejection fraction (59±6% versus 64±6% [P<0.001]), reduced systolic deformation (global circumferential strain, −29.9±4.2 % versus −32.2±5.0 % [P=0.027]), and lower left ventricular mass (38.2±7.9 versus 47.8±11.0 g/m(2) [P<0.001]). T1 native values were decreased (936±53 versus 996±26 ms [P<0.001]), with particular low values in patients with phenylalanine >1200 µmol/L (909±48 ms). Both mean phenylalanine (P=0.013) and tyrosine (P=0.035) levels were independently correlated with T1; and in a multiple regression model, higher phenylalanine levels and higher left ventricular mass associate with lower T1. CONCLUSIONS: Cardiac phenotype of adult patients with phenylketonuria reveals some traits of an early‐stage cardiomyopathy. Regular cardiology follow‐up, tighter therapeutic control, and prophylaxis of cardiovascular risk factors, in particular dyslipidemia, are recommended. John Wiley and Sons Inc. 2021-08-21 /pmc/articles/PMC8649272/ /pubmed/34423658 http://dx.doi.org/10.1161/JAHA.120.020351 Text en © 2021 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Research Tanacli, Radu Hassel, Jan‐Hendrik Gebker, Rolf Berger, Alexander Gräfe, Michael Schneeweis, Christopher Doeblin, Patrick Fleck, Eckart Stehning, Christian Tacke, Frank Pieske, Burkert Spranger, Joachim Plöckinger, Ursula Ziagaki, Athanasia Kelle, Sebastian Cardiac Magnetic Resonance Reveals Incipient Cardiomyopathy Traits in Adult Patients With Phenylketonuria |
title | Cardiac Magnetic Resonance Reveals Incipient Cardiomyopathy Traits in Adult Patients With Phenylketonuria |
title_full | Cardiac Magnetic Resonance Reveals Incipient Cardiomyopathy Traits in Adult Patients With Phenylketonuria |
title_fullStr | Cardiac Magnetic Resonance Reveals Incipient Cardiomyopathy Traits in Adult Patients With Phenylketonuria |
title_full_unstemmed | Cardiac Magnetic Resonance Reveals Incipient Cardiomyopathy Traits in Adult Patients With Phenylketonuria |
title_short | Cardiac Magnetic Resonance Reveals Incipient Cardiomyopathy Traits in Adult Patients With Phenylketonuria |
title_sort | cardiac magnetic resonance reveals incipient cardiomyopathy traits in adult patients with phenylketonuria |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8649272/ https://www.ncbi.nlm.nih.gov/pubmed/34423658 http://dx.doi.org/10.1161/JAHA.120.020351 |
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