Target intelligence / Profile preview

null

Target
null
Molecular classification
Other (Metabolic pathway)
01

Overview

The homocysteine pathway encompasses the biochemical reactions whereby the amino acid homocysteine is generated from methionine and then either converted back to methionine by remethylation or irreversibly catabolized to cysteine by transsulfuration. Key enzymes include methionine synthase (remethylation) and cystathionine β-synthase (transsulfuration), which rely on cofactors such as folate, vitamin B12, and vitamin B6. Disruptions in these pathways, resulting in elevated homocysteine (hyperhomocysteinemia), have been strongly associated with an increased risk of cardiovascular disease, neurodegenerative disorders, pregnancy complications, and other systemic conditions.

Other names
Homocysteine metabolismMethionine cycleRemethylation pathwayTranssulfuration pathway
02

Mechanism of action

Lower homocysteine level via enzyme cofactor supplementation (B vitamins)\nEnhance remethylation (folate/B12)\nEnhance transsulfuration (B6)\nMethyl donor supplementation (betaine)

03

Biological functions

Amino acid metabolismMethyl group transferRedox homeostasisEpigenetic regulation
04

Disease associations

Cardiovascular diseaseStrokeNeurodegenerative diseaseCancerPregancy-related complicationsOsteoporosis
05

Safety considerations

Even after vitamin therapy, lowering homocysteine does not always reduce cardiovascular riskHigh-level B vitamin supplementation may have adverse effects in some contextsPotential pro-inflammatory/pro-proliferative consequences in advanced disease
06

Interacting drugs

Folic acid (vitamin B9)

3 more in the full profile.

07

Biomarkers

Plasma total homocysteine (tHcy) levelGenetic variants in MTHFR, CBS, MTR, GNMT genes

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