AI Article Synopsis

  • * The review investigates various molecular changes in comorbidities linked to heart failure through extensive searches of multiple electronic databases.
  • * Insights gained from these molecular pathways can lead to the development of targeted therapies and personalized medicine approaches, ultimately improving treatment outcomes for patients with heart failure and related conditions.

Article Abstract

Recent advances in genomics and proteomics have helped in understanding the molecular mechanisms and pathways of comorbidities and heart failure. In this narrative review, we reviewed molecular alterations in common comorbidities associated with heart failure such as obesity, diabetes mellitus, systemic hypertension, pulmonary hypertension, coronary artery disease, hypercholesteremia and lipoprotein abnormalities, chronic kidney disease, and atrial fibrillation. We searched the electronic databases, PubMed, Ovid, EMBASE, Google Scholar, CINAHL, and PhysioNet for articles without time restriction. Although the association between comorbidities and heart failure is already well established, recent studies have explored the molecular pathways in much detail. These molecular pathways demonstrate how novels drugs for heart failure works with respect to the pathways associated with comorbidities. Understanding the altered molecular milieu in heart failure and associated comorbidities could help to develop newer medications and targeted therapies that incorporate these molecular alterations as well as key molecular variations across individuals to improve therapeutic outcomes. The molecular alterations described in this study could be targeted for novel and personalized therapeutic approaches in the future. This knowledge is also critical for developing precision medicine strategies to improve the outcomes for patients living with these conditions.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11512903PMC
http://dx.doi.org/10.1007/s11033-024-10024-7DOI Listing

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