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The extent of postpartum cardiac reverse remodeling is reflected in urine proteome

  • Ana F. Ferreira
  • , Fábio Trindade
  • , Maria J. Azevedo
  • , Juliana Morais
  • , Thibaut Douché
  • , Sílvia O. Diaz
  • , Francisca A. Saraiva
  • , Carla Sousa
  • , Ana P. Machado
  • , Mariette Matondo
  • , Adelino Leite-Moreira
  • , Carla Ramalho
  • , Rui Vitorino
  • , Inês Falcão-Pires
  • , António S. Barros

Research output: Contribution to JournalArticleAcademicpeer-review

Abstract

The association of postpartum cardiac reverse remodeling (RR) with urinary proteome, particularly in pregnant women with cardiovascular (CV) risk factors who show long-term increased risk of cardiovascular disease and mortality is unknown. We aim to profile the urinary proteome in pregnant women with/without CV risk factors to identify proteins associated with postpartum RR. Our study included a prospective cohort of 32 healthy and 27 obese and/or hypertensive and/or diabetic pregnant women who underwent transthoracic echocardiography, pulse-wave-velocity, and urine collection at the 3rd trimester and 6 months postpartum. Shotgun HPLC-MS/MS profiled proteins. Generalized linear mixed-effects models were used to identify associations between urinary proteins and left ventricle mass (LVM), a surrogate of RR. An increase in arterial stiffness was documented from 3rd trimester to 6 months after delivery, being significantly elevated in women with CV risk factors. In addition, the presence of at least one CV risk factor was associated with worse LVM RR. We identified 6 and 11 proteins associated with high and low LVM regression, respectively. These proteins were functionally linked with insulin-like growth factor (IGF) transport and uptake regulation by IGF binding-proteins, platelet activation, signaling and aggregation and the immune system's activity. The concentration of IGF-1 in urine samples was associated with low LVM regression after delivery. Urinary proteome showed a predicting potential for identifying pregnant women with incomplete postpartum RR.

Original languageEnglish
Article number14815
Pages (from-to)1-12
Number of pages12
JournalScientific Reports
Volume14
Early online date27 Jun 2024
DOIs
Publication statusPublished - 2024

Bibliographical note

Publisher Copyright:
© 2024. The Author(s).

Funding

This work has been supported by EPIC-XS, project number 318, funded by the Horizon 2020 program of the European Union; Bolsa de Estudo Jo\u00E3o Porto and Pr\u00E9mio Sa\u00FAde Cardiovascular na Mulher da Sociedade Portuguesa de Cardiologia; by RTP Maratona da Sa\u00FAde 2017; and by national funds through FCT\u2014Portuguese Foundation for Science and Technology, under the scope of the Cardiovascular R&D Center \u2013 UnIC (UIDB/00051/2020 and UIDP/00051/2020). European Regional Development Fund (ERDF), through the North Regional Operational Program in the framework of the project HEALTH-UNORTE: Setting-up biobanks and regenerative medicine strategies to boost research in cardiovascular, musculoskeletal, neurological, oncological, immunological and infectious diseases (reference NORTE-01-0145-FEDER-000039). Ana F. Ferreira, Maria J. Azevedo and Juliana Morais are supported by Foundation for Science and Technology (SFRH/BD/138925/2018, SFRH/BD/144982/2019 and UIBD1523062021, respectively). F\u00E1bio Trindade is supported by a post-doctoral research grant by FCT through UnIC (UIDP/00051/2020).

FundersFunder number
University of Nicosia
Horizon 2020 Framework Programme
Fundação para a Ciência e a TecnologiaUIDP/00051/2020, SFRH/BD/144982/2019, UIBD1523062021, UIDB/00051/2020, SFRH/BD/138925/2018
European Proteomics Infrastructure Consortium providing access318
European Regional Development FundNORTE-01-0145-FEDER-000039

    Keywords

    • Cardiovascular reverse remodeling
    • Cardiovascular risk factor
    • Hemodynamic overload
    • Pregnancy
    • Proteome
    • Urine

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