Magnesium Sulfate Administration in Moderate Coronary Artery Disease Patients Improves Atherosclerotic Risk Factors: A Double-Blind Clinical Trial Study.


Journal

Journal of cardiovascular pharmacology
ISSN: 1533-4023
Titre abrégé: J Cardiovasc Pharmacol
Pays: United States
ID NLM: 7902492

Informations de publication

Date de publication:
09 2020
Historique:
pubmed: 4 7 2020
medline: 30 6 2021
entrez: 4 7 2020
Statut: ppublish

Résumé

Magnesium (Mg) deficiency is known to promote vascular and cardiac dysfunctions such as atherosclerosis. This study investigated the effect of oral MgSO4 therapy to improve lipid profile and serum oxidized LDL level and its receptor (LOX1) in moderate coronary atherosclerotic patients. In this randomized double-blind placebo-controlled clinical trial study, 64 patients with moderate coronary artery disease were selected according to angiography findings. Participants were divided into 2 groups including Mg-treated (n = 32) and placebo (n = 32) The patients received either placebo or MgSO4 supplement capsule, containing 300 mg MgSO4 for 6 months on a daily basis. Lipid profile, HbA1c, 2h postprandial (2hpp) blood glucose, fasting blood sugar, serum glutamate oxaloacetate transaminase (SGOT), serum glutamate pyruvate transaminase (SGPT), oxidized low-density lipoprotein, and lectin-like ox-LDL receptor 1 (LOX1) concentrations were measured at baseline and every 3 months. HbA1c, serum LOX1, and oxidized low-density lipoprotein concentrations were significantly lower in the Mg-treated group than the placebo group 3 months after MgSO4 administration. 2hpp, serum low-density lipoprotein cholesterol, SGPT, SGOT levels, and HbA1c levels significantly improved in the Mg-treated group compared with the placebo-received group. Overall, the results of this study showed that magnesium treatment improved some of the major risk factors of atherosclerosis. According to the results of liver function tests (SGOT and SGPT), magnesium therapy seems to be safe in patients with moderate atherosclerotic plaque. Therefore, it is suggested that magnesium to be used along with other atherosclerosis control drugs.

Identifiants

pubmed: 32618829
doi: 10.1097/FJC.0000000000000874
doi:

Substances chimiques

Biomarkers 0
Capsules 0
Cholesterol, LDL 0
Lipoproteins, LDL 0
OLR1 protein, human 0
Scavenger Receptors, Class E 0
oxidized low density lipoprotein 0
Magnesium Sulfate 7487-88-9
Aspartate Aminotransferases EC 2.6.1.1
Alanine Transaminase EC 2.6.1.2

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

321-328

Auteurs

Hossein Farshidi (H)

Cardiovascular Research Center, Hormozgan University of Medical Sciences, Bandar Abbas, Iran.

Ali R Sobhani (AR)

Clinical Pathology Department, Faculty of Medicine, Hormozgan University of Medical Sciences, Bandar Abbas, Iran.

Mahdiye Eslami (M)

Cardiovascular Research Center, Hormozgan University of Medical Sciences, Bandar Abbas, Iran.

Fariba Azarkish (F)

Molecular Medicine Research Center, Hormozgan Health Institute, Hormozgan University of Medical Sciences, Bandar Abbas, Iran.

Ebrahim Eftekhar (E)

Endocrinology and Metabolism Research Center, Hormozgan University of Medical Sciences, Bandar Abbas, Iran.

Mansoor Keshavarz (M)

Physiology Department, Faculty of Medicine, Tehran University of Medical Sciences, Tehran, Iran.

Nepton Soltani (N)

Physiology Department, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.

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Classifications MeSH