Why are cardiovascular diseases more common among patients with severe mental illness? The potential involvement of electronegative low-density lipoprotein (LDL) L5.

Bipolar disorder Cardiovascular diseases Depression Electronegative LDL (L5) Mood disorder Schizophrenia Severe mental illness

Journal

Medical hypotheses
ISSN: 1532-2777
Titre abrégé: Med Hypotheses
Pays: United States
ID NLM: 7505668

Informations de publication

Date de publication:
Sep 2020
Historique:
received: 29 03 2020
revised: 22 04 2020
accepted: 05 05 2020
pubmed: 18 5 2020
medline: 15 5 2021
entrez: 18 5 2020
Statut: ppublish

Résumé

Despite tremendous efforts of experimental and clinical studies and knowledge, the pathophysiology of severe mental illness (SMI), including bipolar disorder (BD), unipolar depression (mood disorders, MD), and schizophrenia (SCZ), remains poorly understood. Besides their chronic course and high prevalence in society, mental and somatic comorbidities are really serious problems; patients with these disorders have increased risk of cardiovascular (CV) diseases (CVD) including coronary artery diseases (CAD, i.e. myocardial infarction and angina), stroke, sudden cardiac death, hypertension, cardiomyopathy, arrhythmia, and thromboembolic disease. Although it is determined that triglycerides, cholesterol, glucose, and low-density lipoprotein (LDL) levels are increased in MD and SCZ, the underlying reason remains unknown. Considering this, we propose that electronegative LDL (L5) is probably the main crucial element to understanding CVD induced by SMI and to discovering novel remedial approaches for these diseases. When it is hypothesized that L5 is greatly presupposed in CV system abnormalities, it follows that the anti-L5 therapies and even antioxidant treatment options may open new therapeutic opportunities to prevent CVD diseases secondary to SMI. In this review article, we tried to bring a very original subject to the attention of readers who are interested in lipoprotein metabolism in terms of experimental, clinical, and cell culture studies that corroborate the involvement of L5 in physiopathology of CVD secondary to SMI and also the new therapeutic approaches for these disorders.

Identifiants

pubmed: 32417641
pii: S0306-9877(20)30562-4
doi: 10.1016/j.mehy.2020.109821
pii:
doi:

Substances chimiques

Lipoproteins, LDL 0
oxidized low density lipoprotein 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

109821

Informations de copyright

Copyright © 2020 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Omer Akyol (O)

Michigan Math & Science Academy, Department of Science, Warren, MI, USA. Electronic address: akyol@mmsaonline.org.

Imtihan Chowdhury (I)

Michigan Math & Science Academy, High School, 11th grade, Warren, MI, USA.

Hafsa Rana Akyol (HR)

Illinois Institute of Technology, Biology, Sophomore, Chicago, IL, USA.

Kylie Tessier (K)

Michigan Math & Science Academy, High School, 11th grade, Warren, MI, USA.

Huseyin Vural (H)

Institute of Molecular Pathobiochemistry, Experimental Gene Therapy and Clinical Chemistry, RWTH University Hospital Aachen, Aachen, Germany.

Sumeyya Akyol (S)

Beaumont Health, Beaumont Research Institute, Royal Oak, MI, USA.

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Classifications MeSH