Assessing liver disease in cyanotic CHD using multiparametric MRI: a call to prevent future burden

article
Autores

Póvoa-Corrêa, Mariana

Innocenzi, Adriana M.

Fernandes, Fernanda P.

Costermani, Igor

Secco, José Carlos P.

Terzi, Flávia V.O.

Pittella, Ana Maria

Rangel, Isabela

Barbosa, Rosa Célia P.

Medei, Emiliano

Silvestre-Sousa, Andrea

Rodrigues, Rosana S.

Luiz, Ronir R.

Perez, Renata M.

Camargo, Gabriel C.

Parente, Daniella

Moll-Bernardes, Renata

Data de Publicação

1 de dezembro de 2025

Resumo

Abstract Background & aims: Patients with cyanotic CHD and those with metabolic dysfunction–associated steatotic liver disease are at risk of liver fibrosis. We compared hepatic extracellular volumes and native T1 values to better understand the burden of liver disease in these populations. Methods: The sample comprised 136 patients in 5 groups: control ( n = 23), metabolic dysfunction–associated steatotic liver disease [mild (F0–F1) and significant (F2–F4) fibrosis; n = 45], repaired tetralogy of Fallot ( n = 30), and Fontan circulation ( n = 38). Differences were assessed using linear regression models, with adjustment for the body mass index and sex. Results: The hepatic extracellular volume was significantly larger in the Fontan group (43.96% ± 4.22%) than in the other groups, even with adjustment. Patients with Fallot had significantly larger extracellular volumes (36.77% ± 5.63%) than did controls and mild liver disease ( p < 0.001 and p = 0.011, respectively), although smaller extracellular volumes than patients with significant liver disease ( p = 0.042). These trends were corroborated by native T1 values, which were highest in patients with Fontan (1013.7 ± 86.1 ms), although not significantly different from patients with F2–F4 steatotic liver disease. Conclusions: The potential burden of CHD-related hepatic injury and steatotic liver disease highlights the importance of early identification. Given the possible additional risk of liver fibrosis in patients with coexisting metabolic dysfunction and CHD, comprehensive clinical management should prioritise regular metabolic risk assessment and the promotion of a healthy lifestyle to reduce the likelihood of liver disease development in this vulnerable population.

Citação

BibTeX
@online{mariana2025,
  author = {Mariana , Póvoa-Corrêa and Adriana M. , Innocenzi and
    Fernanda P. , Fernandes and Igor , Costermani and José Carlos P. ,
    Secco and Flávia V.O. , Terzi and Ana Maria , Pittella and Isabela ,
    Rangel and Rosa Célia P. , Barbosa and Emiliano , Medei and Andrea ,
    Silvestre-Sousa and Rosana S. , Rodrigues and Ronir R. , Luiz and
    Renata M. , Perez and Gabriel C. , Camargo and Daniella , Parente
    and Renata , Moll-Bernardes},
  title = {Assessing liver disease in cyanotic CHD using multiparametric
    MRI: a call to prevent future burden},
  volume = {35},
  number = {12},
  date = {2025-12-01},
  doi = {10.1017/S1047951125110792},
  langid = {pt-BR},
  abstract = {Abstract Background \& aims: Patients with cyanotic CHD
    and those with metabolic dysfunction–associated steatotic liver
    disease are at risk of liver fibrosis. We compared hepatic
    extracellular volumes and native T1 values to better understand the
    burden of liver disease in these populations. Methods: The sample
    comprised 136 patients in 5 groups: control ( n = 23), metabolic
    dysfunction–associated steatotic liver disease {[}mild (F0–F1) and
    significant (F2–F4) fibrosis; n = 45{]}, repaired tetralogy of
    Fallot ( n = 30), and Fontan circulation ( n = 38). Differences were
    assessed using linear regression models, with adjustment for the
    body mass index and sex. Results: The hepatic extracellular volume
    was significantly larger in the Fontan group (43.96\% ± 4.22\%) than
    in the other groups, even with adjustment. Patients with Fallot had
    significantly larger extracellular volumes (36.77\% ± 5.63\%) than
    did controls and mild liver disease ( p \textless{} 0.001 and p =
    0.011, respectively), although smaller extracellular volumes than
    patients with significant liver disease ( p = 0.042). These trends
    were corroborated by native T1 values, which were highest in
    patients with Fontan (1013.7 ± 86.1 ms), although not significantly
    different from patients with F2–F4 steatotic liver disease.
    Conclusions: The potential burden of CHD-related hepatic injury and
    steatotic liver disease highlights the importance of early
    identification. Given the possible additional risk of liver fibrosis
    in patients with coexisting metabolic dysfunction and CHD,
    comprehensive clinical management should prioritise regular
    metabolic risk assessment and the promotion of a healthy lifestyle
    to reduce the likelihood of liver disease development in this
    vulnerable population.}
}
Por favor, cite este trabalho como:
Mariana, Póvoa-Corrêa, Innocenzi Adriana M., Fernandes Fernanda P., Costermani Igor, Secco José Carlos P., Terzi Flávia V.O., Pittella Ana Maria, et al. 2025. “Assessing liver disease in cyanotic CHD using multiparametric MRI: a call to prevent future burden.” Cardiology in the Young. December 1, 2025. https://doi.org/10.1017/S1047951125110792.