Dyslipidemias Clinical Trial
Official title:
Effect of Adding Folic Acid on Lipid Parameters in Population With Dyslipidemias
Background: Homocysteinemia is associated with increased risk of stroke, dyslipidemias,
dementia, peripheral vascular disease and coronary artery disease. folic acid is involved in
the metabolism of homocysteine. Folic acid supplementation helps to reduce homocysteine
levels and lowering of homocysteine may cause improvement in serum lipid profile. In this
study we will assess the effect of folic acid supplementation for 6 weeks, on lipid parameter
in patients who have dyslipidemia.
Methods: It is a placebo controlled randomized trial, consisting of two groups, Group A
(n=34) and Group B (n=34). Group A (intervention group) will be given Folic acid supplements
and the second group will be given a placebo. After 6 weeks changes in lipid parameters, will
be measured in both groups.
Discussion: Folic acid is water soluble vitamin also known as vitamin B-9. Folic acid works
as co-factor in many biochemical enzymatic reactions. Homocysteine metabolism also requires
folic acid, homocysteinemia may worsen renal function, lipid parameter, accelerate
atherosclerosis, angiopathies, and progression of dementia, also increase the risk of stroke
and coronary artery disease. In this study, Group A (treatment Group) will be given folic
acid supplementation while the Group B (Placebo Group) will be given placebo and at the end
of 6 weeks, HDL, LDL, Triglycerides and serum cholesterol levels will be measured and
compared with the pre-treatment levels. If Post-treatment group shows significant decrease in
serum LDL, total cholesterol, triglycerides and increase in HDL then Folic acid
supplementation may be routinely recommended for patient with dyslipidemias.
Status | Not yet recruiting |
Enrollment | 68 |
Est. completion date | March 15, 2019 |
Est. primary completion date | February 28, 2019 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: - 1. Otherwise, healthy individuals of either sex with any of the following characteristics will be including in the study. 1. Serum cholesterol >200mg/dl 2. Serum triglyceride > 150mg/dl 3. Serum LDL >100mg/dl 4. Serum HDL < 40mg/dl Exclusion Criteria: 1. Patients who have any clinically significant or unstable medical or psychiatric illnesses. 2. Patients with CKD, diabetes mellitus, coronary artery disease, with history of stroke, myocardial infarction or any chronic illnesses. 3. Substance abuse such as alcoholism excluded by taking history. 4. Patients who are pregnant are excluded by taking history and urine dipstick test where applicable. 5. Patient who are treated with any investigational drug within last 60 days. 6. Patients who are taking a statin or any other lipid lowering drug. |
Country | Name | City | State |
---|---|---|---|
Pakistan | Shaheed Zulfiqar Ali Bhutto Medical University, Pakistan Institute of Medical Sciences Hospital | Islamabad |
Lead Sponsor | Collaborator |
---|---|
Shaheed Zulfiqar Ali Bhutto Medical University |
Pakistan,
Baszczuk A, Thielemann A, Musialik K, Kopczynski J, Bielawska L, Dzumak A, Kopczynski Z, Wysocka E. The Impact of Supplementation with Folic Acid on Homocysteine Concentration and Selected Lipoprotein Parameters in Patients with Primary Hypertension. J Nutr Sci Vitaminol (Tokyo). 2017;63(2):96-103. doi: 10.3177/jnsv.63.96. — View Citation
Blom HJ, Smulders Y. Overview of homocysteine and folate metabolism. With special references to cardiovascular disease and neural tube defects. J Inherit Metab Dis. 2011 Feb;34(1):75-81. doi: 10.1007/s10545-010-9177-4. Epub 2010 Sep 4. Review. — View Citation
Mierzecki A, Kloda K, Bukowska H, Chelstowski K, Makarewicz-Wujec M, Kozlowska-Wojciechowska M. Association between low-dose folic acid supplementation and blood lipids concentrations in male and female subjects with atherosclerosis risk factors. Med Sci Monit. 2013 Sep 4;19:733-9. doi: 10.12659/MSM.889087. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | LDL | mg/dL | 6 weeks | |
Primary | HDL | mg/dL | 6 weeks | |
Primary | Triglycerides | mg/dL | 6 weeks | |
Primary | Total Cholesterol | mg/dL | 6 weeks |
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