Topic Editors

School of Health and Kinesiology, University of Nebraska-Omaha, 6001 Dodge St, Omaha, NE 68182, USA
Dr. Gwenael Layec
School of Health and Kinesiology, University of Nebraska, Omaha, NE 68182, USA

Cardiovascular Disease in Special Populations: From Basic Science to Clinical Practice

Abstract submission deadline
31 October 2025
Manuscript submission deadline
31 December 2025
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Topic Information

Dear Colleagues,

Research on cardiovascular diseases (CVDs) has experienced significant growth in recent years, increasing our understanding and fueling the discovery of prominent therapeutic options. Despite these advancements, there are still many unknowns regarding the manifestation and treatment of CVDs in special populations. Special populations can encompass a wide range of physical, sensory, cognitive, and metabolic factors, each influencing cardiovascular health differently. As such, there is a significantly greater health concern in special populations, as recent studies have found that factors specific to special populations contribute to heightened CVD risk factors and early mortality. In addition, it is unclear as to whether common CVD treatment options are effective in CVD patients from special populations. Therefore, the goal of this research topic is to provide a scientific platform that fosters our clinical understanding of the manifestation as well as the effectiveness of therapeutic interventions in special populations with CVD. Both research and review articles are welcome.

Dr. Song-Young Park
Dr. Gwenael Layec
Topic Editors

Keywords

  • cardiovascular disease
  • cardiovascular medicine
  • cardiovascular interventions
  • diabetes
  • coronary artery disease
  • multiple sclerosis
  • neuropathy
  • spinal cord injury
  • peripheral artery disease
  • cerebral vascular disease

Participating Journals

Journal Name Impact Factor CiteScore Launched Year First Decision (median) APC
Antioxidants
antioxidants
6.0 10.6 2012 15.5 Days CHF 2900 Submit
Biomedicines
biomedicines
3.9 5.2 2013 15.3 Days CHF 2600 Submit
Disabilities
disabilities
- 1.1 2021 39.9 Days CHF 1000 Submit
Journal of Cardiovascular Development and Disease
jcdd
2.4 2.6 2014 22.9 Days CHF 2700 Submit

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Published Papers (1 paper)

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13 pages, 2706 KiB  
Article
Changes in Mitochondrial Function and Cell Death Patterns in Peripheral Blood Mononuclear Cells during Trastuzumab Treatment Following Doxorubicin Chemotherapy
by Krit Leemasawat, Nichanan Osataphan, Nattayaporn Apaijai, Panat Yanpiset, Arintaya Phrommintikul, Areewan Somwangprasert, Siriporn C. Chattipakorn and Nipon Chattipakorn
Biomedicines 2024, 12(9), 1970; https://doi.org/10.3390/biomedicines12091970 - 1 Sep 2024
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Abstract
Trastuzumab, a monoclonal antibody which works against human epidermal growth factor receptor 2 (HER2), possibly causes cardiotoxicity through mitochondrial dysfunction. The usefulness of isolated peripheral blood mononuclear cells (PBMCs) in the assessment of trastuzumab-induced cardiotoxicity remains uncertain. This study aimed to determine the [...] Read more.
Trastuzumab, a monoclonal antibody which works against human epidermal growth factor receptor 2 (HER2), possibly causes cardiotoxicity through mitochondrial dysfunction. The usefulness of isolated peripheral blood mononuclear cells (PBMCs) in the assessment of trastuzumab-induced cardiotoxicity remains uncertain. This study aimed to determine the temporal changes in mitochondrial function, oxidative stress, and cell death in the isolated PBMCs of HER2-positive breast cancer patients during breast cancer treatment and to compare the changes with HER2-negative breast cancer patients who did not receive trastuzumab therapy. Eighteen newly diagnosed HER2-positive breast cancer women who received sequential doxorubicin and trastuzumab were consecutively recruited. Age- and gender-matched controls with HER2-negative breast cancer were selected. Echocardiography was carried out, and blood samples for the study of cardiac biomarkers and PBMCs were collected periodically during treatment. Only one patient in our cohort developed asymptomatic left ventricular dysfunction during trastuzumab treatment. However, trastuzumab following doxorubicin aggravated subclinical cardiac injury, determined by cardiac troponin and echocardiography. Cellular and mitochondrial oxidative stress in isolated PBMCs remained unchanged throughout breast cancer treatment. Regarding mitochondrial respiration, the maximal respiration and spare respiration capacity was significantly increased in controls after doxorubicin treatment but not in patients who received trastuzumab therapy. Moreover, the percentage of apoptosis and necroptosis in isolated PBMCs was dramatically decreased in the control, compared to patients with trastuzumab treatment. In conclusion, trastuzumab caused subtle myocardial injury and impaired mitochondrial respiration and cell viability in isolated PBMCs. Full article
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