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Published on: June 28, 2024
Hyperhomocysteinemia-related serum metabolome alterations not normalized by short-term folic acid treatment
A Aneesh Kumar1, Vanaja R Anusree1, Gopika Satheesh1
1Cardiovascular Diseases & Diabetes Biology, Rajiv Gandhi Centre for Biotechnology, Poojappura, Thiruvananthapuram, Kerala, 695014, India.
Insights
Folate deficiency with high homocysteine alters lipid metabolism. Short-term folic acid therapy lowers homocysteine but does not reverse these metabolic changes in individuals with folate deficiency and hyperhomocysteinemia.
Area of Science:
- Biochemistry
- Metabolomics
- Nutritional Science
Background:
- Hyperhomocysteinemia (HHCys) is a risk factor for cardiovascular diseases, Alzheimer's, and cancers.
- Folate deficiency is a primary cause of HHCys.
- The association between folate deficiency, HHCys, and serum metabolites is not well understood.
Purpose of the Study:
- Identify metabolic alterations in individuals with folate deficiency and HHCys.
- Investigate if short-term folic acid therapy can reverse these metabolic changes.
Main Methods:
- Serum metabolomics analysis was performed on 34 participants with folate deficiency/HHCys and 21 healthy controls.
- Participants with HHCys received 5 mg/day oral folic acid for 30 days.
- Statistical analyses included univariate methods and multivariable-adjusted linear regression.
Main Results:
- Individuals with folate deficiency and HHCys exhibited downregulated metabolites in lipid metabolism pathways (polyunsaturated fatty acids, glycerolipids, phospholipids).
- Folic acid therapy significantly reduced serum homocysteine levels.
- Despite homocysteine reduction, the observed alterations in lipid metabolism pathways remained unchanged.
Conclusions:
- Folate deficiency combined with HHCys is linked to altered lipid metabolism profiles.
- Short-term folic acid supplementation does not reverse these specific metabolic alterations in folate-deficient individuals with HHCys.
Introduction:
Hyperhomocysteinemia (HHCys) is an independent risk factor for various diseases such as cardiovascular diseases, Alzheimer's, and cancers. Folate deficiency is one of the significant reasons for HHCys. However, it is not known whether folate deficiency with HHCys is associated with any serum metabolites.
Objectives:
Our objective was to identify the metabolic alterations in people having folate deficiency with HHCys and check whether a short-term folic acid therapy could reverse those metabolic changes.
Methods:
The study enrolled 34 participants aged between 18 and 40 years having folate deficiency (< 4.6 ng/mL) with HHCys (> 15 μmol/L) and 21 normal healthy individuals. A short-term intervention of oral folic acid (5 mg/day) was done in the HHCys group for 30 days. Untargeted metabolomics analysis of serum was performed in all study subjects before and after the folic acid treatment. Different univariate methods and the multivariable-adjusted linear regression models were employed to determine an association between homocysteine level and metabolite profile.
Results:
Metabolomics analysis data showed that many metabolites involved in the biochemical pathways of lipid metabolisms such as polyunsaturated fatty acids, glycerolipids, and phospholipids were downregulated in the HHCys group. Short-term oral folic acid therapy significantly reduced their serum homocysteine level. However, the metabolic pathway alterations observed in folate-deficient HHCys-condition were unaltered even after the folic acid treatment.
Conclusions:
Our study revealed that people who have a folic acid deficiency with HHCys have an altered metabolite profile related to lipid metabolism, which cannot be reversed by short-term folic acid therapy.
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