Plasma Mannose Associated Parameter Levels in Nondiabetic Coronary Artery Disease
NCT ID: NCT04888260
Last Updated: 2021-05-17
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
240 participants
OBSERVATIONAL
2018-01-10
2020-05-15
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Methods: The plasma mannose, lipids (triglyceride, LDL, HDL, LDL, VLDL) and LDH levels were successfully will be evaluated with respect to subsequent coronary artery disease using records 120 nondiabetic patients and 120 healthy volunteers. CAD was identified from myocardial infarction and new diagnoses of angina.
The associations between mannose levels and serum lipid parameters will be investigated.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Blood Sample Measurements and Physical Activity Levels in Type II Diabetes and/or COVID-19
NCT04695158
Impact of Prediabetes on Acute Coronary Syndrome
NCT05102851
Relations Between Atherogenic Index of Plasma-Glucose Metabolism
NCT02977598
The Triglyceride/Glucose Index and SGLT-2 Inhibitors
NCT05915884
Study of Cholesterol Levels and Types in African Americans With Type 2 Diabetes
NCT01494298
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
The broad range of lipid molecular species in human plasma and their possible role in human health and disease are topics of great interest. Plasma lipidome is now progressively recognized as a potentially important marker of chronic diseases, but the exact degree of its contribution to the interindividual phenotypic variation in family studies is uncertain .
Associative evidence gathered from plasma lipidomic studies promises vital contributions to biomarker research-an important cornerstone of ongoing efforts to prevent chronic disease. The plasma lipidomic profile of humans is associated with various conditions including obesity and disorders of glucose metabolism, hypertension , cardiovascular diseases.
Plasma lipids are solubilized and distributed by associating them with different protein groups. Most free fatty acids and associated structures with carboxyl functional groups interact with albumin, while more complex lipids are transported and distributed using plasma lipoproteins.
Glycerolipids account for a high proportion of total lipids in plasma and include triacylglycerols (TAGs), diacylglycerols (DAGs), and ether-linked glycerolipids. The total plasma concentration of TAGs, allocated between chylomicrons and very-low-density lipoprotein (VLDL), depends on food intake. It is well known that various acquired or secondary risk factors (including genetic determinants, uncontrolled diabetes mellitus, obesity, and sedentary lifestyle) can cause hypertriglyceridemia, a prevalent type of dyslipidemia that is often associated with premature coronary artery disease.
D-mannose, one of the stereoisomers forms, is a structural isomer of D-glucose and commonly found in biological systems, but L-mannose is generally not found in biological systems. Mannose is transported to mammalian cells by hexose transporters primarily by glucose transporters (GLUTs) present in the plasma membrane. Studies demonstrated that plasma mannose levels in human are associated with incident type 2 diabetes mellitus and cardiocascular diseases. On the other hand, molecular mechanism by which the pathway is induced is still unclear. A recent study showed that human plasma lipidome is pleiotropically associated with the cardiovascular risk factors and death.
In mammalian cells, mannose is joined in glycolysis and gluconeogenesis pathways catalyzed by mannose phosphate isomerase. Mannose is a constituent of normal blood plasma and its concentration is generally elevated in diabetes mellitus and chronic glomerulonephritis . However, studies showed that fructose and mannose levels are significantly reduced in obese individuals . Currently, we have reported that elevated baseline mannose in plasma triggered to GLUT4 and Heksokinase-1 (HK1) associated with a progressive risk of CAD with time.
A cytoplasmic enzyme of lactate dehydrogenase (LDH) found in all body cells which transfers a hydride from one molecule to another. LDH catalyzes the reversible conversion of pyruvate to lactate as a unit of Cori cycle. A cardiac marker of LDH is expressed extensively in body cells and a marker of heart failure .
The aims of the study were to determine whether modest elevations in plasma mannose concentrations, and serum lipids \[triglyceride, low density lipoprotein (LDL), high density lipoprotein (HDL) and very-low density lipoprotein (VLDL)\] may be associated with a greater incidence of CAD among nondiabetic patients. Because hyperglycemia and/or hydrophilicity is associated with additional risk factors for CAD including hypertension, obesity, aging. Additionally, identifying the molecular and biochemical parameters in plasma associated with risk factors for CAD may have strategic importance in the treatment of these diseases.
The patient and control groups will be initially informed about the study and obtained a written consent. Patients who underwent angiography at the Department of Cardiology and newly diagnosed as coronary artery disease and who weren't on statin treatment will be included in the patient group. The control group will be consisted of healthy people with normal coronary arteries angiographically. Patients with chronic renal failure, chronic liver disease, inflammatory disease, diabetes, insulin resistance, major metabolic or endocrine disease will be also excluded. For this purpose, age and sex matched 120 patients and 120 healthy volunteers will be admitted to study.
Blood samples will be collected as described earlier into EDTA and citrate vacutainers.Total cholesterol, high-density lipoprotein and triglycerides will be measured by a commercially available enzymatic colorimetric assay (Roche, Basel,Switzerland). Glucose, creatinine and the other blood profiles will be determined by standard methods.The samples will be centrifuged at 400xg for 10 min to separate the serum.Biochemical parameters will be measured by using an Abbott ARCHITECH c800(Abbott Laboratories, USA) auto analyser and commercial kits. Serum mannose levels will be determined by enzymatic methods using in the ELISA.
Kolmogrov-Smirnov test will be used to determine whether the group was parametrically distributed. Categorical variables were given as numbers and percentages. If the parameters are parametrically distributed, continuous variables will be expressed as mean ± standard deviation; if the parameters are non-parametrically distributed, continuous variables will be expressed as median (IQR). When parametric test assumptions will be provided, the significance test of difference between two means and one-way analysis of variance will be used to compare independent group differences. When parametric test assumptions were not provided, Mann-Whitney U test will be used to compare independent group differences. The relationships between continuous variables will be analyzed using Spearman correlation analysis, chi-square test will be used for analyzing categorical variables. Furthermore, Receiver Operating Characteristic (ROC) curve analysis was used for the discriminant performance serum mannose levels under investigation. In addition, the relationships between continuous variables will be examined by Spearman correlation analysis. P \<0.05 will be considered statistically significant in all examinations.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_CONTROL
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Coronary Artery Disease Group
Patients who underwent angiography at the Department of Cardiology and newly diagnosed as coronary artery disease and who weren't on statin treatment were included in the patient group.
Laboratory parameter levels in blood samples
Mannose and lipid parameters (triglyceride, LDL, HDL, VLDL) will be analysed in blood samples by using ELISA method.
Control Group
The control group consisted of healthy people with normal coronary arteries angiographically
Laboratory parameter levels in blood samples
Mannose and lipid parameters (triglyceride, LDL, HDL, VLDL) will be analysed in blood samples by using ELISA method.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Laboratory parameter levels in blood samples
Mannose and lipid parameters (triglyceride, LDL, HDL, VLDL) will be analysed in blood samples by using ELISA method.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
For Control Group;
* To be on statin treatment. To underwent angiography at the another department or university. To have a chronic renal failure, chronic liver disease, inflammatory disease, diabetes, insulin resistance, major metabolic or endocrine disease.
18 Years
100 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Kafkas University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Ramazan Sbirli
Dr.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Aylin Koseler
Denizli, Outside of the US, Turkey (Türkiye)
Ramazan Sabirli
Kars, Outside of the US, Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
Clinical-4
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.