- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03273738
Vascular and Metabolic Changes in Postmenopausal Diabetics
Assessment of Vascular and Metabolic Changes in Post-menopausal Women With Type 2 Diabetes Mellitus
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Introduction Complications of diabetes, such as cardiovascular disease, are associated with increased mortality among type 2 diabetes mellitus patients. The presence of type 2 diabetes mellitus (T2DM) also increases the relative risk of developing cardiovascular disease in women compared to men . Major cardiovascular disease risk factors that have been identified in T2DM patients include arterial stiffening, endothelial dysfunction, hyperglycemia , and elevated glycated haemoglobin (HbA1c) concentrations.
Cardiovascular disease is the major cause of morbidity and mortality in T2 DM, due to arterial structure and functional changes. Evaluation of vascular dysfunction in T2 DM patients include: carotid intima media thickness (IMTc), pulse wave velocity (PWV), and brachial artery flow-mediated dilation (FMD). IMTc is increased in patients with T2 DM with reductions in FMD, which have already been reported to be inversely and strongly related to the extent of hyperglycemia.
The incidence of vascular complications is multifactorial and may not be explained by hyperglycemia alone. Other presumably unrelated risk factors, such as hyperhomocysteinemia may be involved in the atherothrombotic process. High levels of homocysteine have been identified as a risk factor for cardiovascular disease in T2DM patients. Levels of plasma homocysteine increase in women after menopause, and postmenopausal diabetic women are consequently at significantly increased risk of cardiovascular disease.
High concentrations of homocysteine are associated with increased low-density lipoprotein oxidation, endothelial dysfunction, dysfunction of β-islet cells and inhibiting secretion of insulin. Also, hyperhomocysteinemia was an independent risk factor for the occurrence of diabetic peripheral neuropathy .
In newly diagnosed normotensive T2DM patients, the left ventricular mass index (LVMI), carotid intima media thickness (CIMT), and creatinine levels and 24-hr microalbuminuria were used to determine cardiac, carotid, and kidney end-organ diseases, respectively. It was found that, LVMI, CIMT, and creatinine level were positively correlated with the homocysteine level.
Moreover, determinants of hyperhomocysteinemia, such as low concentrations of folate and vitamin B12 involved in homocysteine metabolism are also associated with increased risk of vascular damage. Folic acid supplementation may improve the cardiovascular health of post-menopausal women with diabetes, reduce homocysteine levels and improve vascular health in different study populations.
Increased plasma homocysteine, triglyceride and waist circumference as well as decreased folic acid and vitamin B12 in type 2 diabetes mellitus were evaluated.
Sudchada et al. concluded that folic acid supplementation in patient with T2DM may reduce total homocysteine levels and have a trend to associate with better glycemic control compared with placebo.
in postmenopausal Korean women with type 2 diabetes mellitus, folic acid supplementation reduced serum homocysteine levels, increased serum folate and vitamin B12 levels, and lowered lipid parameters.
A case-control study showed that low intakes of folate and B12 in type 2 diabetic patients were associated with hyperhomocysteinemia. Additionally, folate has also been shown to improve glycemic control by reducing glycosylated hemoglobin fasting blood glucose, serum insulin and insulin resistance as well as homocysteinemia in type 2 diabetes patients.
Folic acid supplementation significantly reduced LDL-C levels as well as LDL-C/HDL-C and TC/HDL-C ratios. The improvements in lipid parameters might be due to the reduction of serum homocysteine levels caused by folic acid supplementation. In another study, associations between fasting plasma homocysteine concentration and age, serum creatinine, and vitamin B12. However, no association between folate and homocysteine was found.
Whether serum homocysteine levels are associated with coronary heart disease (CHD) and the metabolic syndrome (MS) needs investigation in different ethnic groups. High serum homocysteine and low folate levels are associated in Turkish men independently with coronary heart disease, which needs confirmation in a larger sample. In women, vitamin B12 concentrations are significantly associated with metabolic syndrome likelihood.
there is no support that metformin consumption increases homocysteine secondary to folate and /or B12 deficiency in patients with T2DM. Also, among adults with hypertension with no history of stroke and/or myocardial infarction, folic acid supplementation had no significant effect on the risk of new-onset diabetes.
However, clinical studies have shown that folic acid therapy is not very effective in normalizing hyperhomocysteinemia in uremic patients. Indeed, it has been demonstrated that vitamin B12 supplementation alone, or in combination with folic acid, decreases total homocysteine concentrations, but full normalization is not achieved. folate levels were comparable to controls at various chronic kidney disease stages, whereas vitamin B12 levels were lower, except at stage IV in patients with T2DM. They did not find any correlation between B-vitamins and levels of total homocysteine and cysteine, regardless of the CKD stage.
Aims of the study:
- To evaluate cardiovascular changes in type 2 diabetic postmenopausal women through measurement of vascular parameters.
- To assess the possible changes in some metabolic features in type 2 diabetic postmenopausal women.
- To relate, if found, the degree of metabolic changes to the extent in vascular parameters changes in type 2 diabetic postmenopausal women.
Type of study and its design:
Study subjects:
This study will include 50 female patients with T2DM who visited Assiut University Hospital Diabetes Clinic in Assiut, Egypt. Another 50 participants will be volunteered in the study as control.
Inclusion criteria:
For this study, 100 post-menopausal women aged 50-70 years with amenorrhea for over 24 months will be recruited. The diabetic participants will receive their treatment for T2DM (oral hypoglycemic agents or insulin).
Exclusion criteria:
- Patients receiving hormone replacement therapy.
- History of abnormal vaginal bleeding.
- Patients receiving vitamin B12, vitamin D and folic acid regularly.
- History of malignancy or neurological diseases as epilepsy, parkinsonism and Alzheimer disease.
- Antifolate medications as methotrexate are excluded from the study.
Study design:
The study will be observational study. The participants will be informed about the study and we will take their assignment on written consent. The patients included will be divided into two groups. 20 healthy participants and 100 female patients, will be subjected to clinical evaluation and blood sampling for laboratory investigations.
Evaluation of the patients:
All patients will be subjected to:
- Complete history (age, occupation, menstrual history, bleeding tendency, renal disease, therapeutic and dietary history)
- Clinical examination (weight, height, blood pressure measurement, presence of microvascular or macrovascular complications, anemia).
- ECG.
Brachial-ankle pulse wave velocity (baPWV) will be calculated further using the following equation:
baPWV = transmission distance/transmission time
- Carotid intima-media thickness (CIMT) will be done, it is noninvasive measure that uses ultrasound to detect the presence and extent of atherosclerosis.
Laboratory investigations:
- HbA1c.
- Lipid profiles (total cholesterol, LDL-C, HDL-C and triglycerides)
- Serum homocysteine will be measured using available commercial ELISA kits.
- Serum folic acid level will be measured using available commercial ELISA kits.
- Serum vitamin B12 level will be measured using available commercial ELISA kits.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Ahmed M Abd-Eldayem, MD
- Phone Number: 002 01005885676
- Email: ah_nmre@yahoo.com
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- post-menopausal women
- aged 50-70 years
- amenorrhea for over 24 months.
- The diabetic participants will receive their treatment for T2DM (oral hypoglycemic agents or insulin).
Exclusion Criteria:
- Patients receiving hormone replacement therapy.
- History of abnormal vaginal bleeding.
- Patients receiving vitamin B12, vitamin D and folic acid regularly.
- History of malignancy or neurological diseases as epilepsy, parkinsonism and Alzheimer disease.
- Antifolate medications as methotrexate are excluded from the study.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
postmenopausal diabetic women
50 female patients with T2DM who visited Assiut University Hospital Diabetes Clinic in Assiut, Egypt in these patients folate level measurement, B12 level and homocysteine are measured
|
the level of folate measured in plasma with homocysteine
B12 measurement in blood
|
postmenopausal without diabetes
Another 50 participants will be volunteered in the study as control.n
these subjects folate level measurement', B12 level and homocysteine are measured
|
the level of folate measured in plasma with homocysteine
B12 measurement in blood
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
metabolic changes in type 2 diabetes
Time Frame: baseline and 3 months
|
changes in folate level in type 2 diabetes mellitus
|
baseline and 3 months
|
metabolic changes in type 2 diabetes
Time Frame: baseline and 3 months
|
B12 level and their relation to complications
|
baseline and 3 months
|
Collaborators and Investigators
Sponsor
Investigators
- Study Chair: Lobna F Eltoony, Internal medicine
Study record dates
Study Major Dates
Study Start (Anticipated)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- Postmenopausal DM
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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