<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" article-type="Research Article" dtd-version="1.0"><front><journal-meta><journal-id journal-id-type="pmc">srjm</journal-id><journal-id journal-id-type="pubmed">SRJM</journal-id><journal-id journal-id-type="publisher">SRJM</journal-id><issn>2788-9440</issn></journal-meta><article-meta><article-id pub-id-type="doi">https://doi.org/10.47310/srjm.2021.v01i01.013</article-id><title-group><article-title>A Study of Pathophysiology of Homocysteine in Causing Acute Myocardial Infarction: A Study in a Rural Medical College of Himachal Pradesh</article-title></title-group><contrib-group><contrib contrib-type="author"><name><given-names>Aman</given-names><surname>Sharma</surname></name></contrib></contrib-group><contrib-group><contrib contrib-type="author"><name><given-names>Shilpa</given-names><surname>Sharma</surname></name></contrib></contrib-group><aff-id id="aff-a" /><abstract>Homocysteine, sulfhydryl group containing amino acid, is intermediate product during metabolism of the amino acids methionine and cysteine. Homocysteine is nonprotein amino acid which behaves as both a substrate and product of methionine. Homocysteine has key role in methylation cycle, within which a methyl group is transferred to a different substrate Formed homocysteine can be utilized in two ways: 1) homocysteine can be remethylated to methionine by catalytic activity of the enzyme N5, N10-methylenetetrahydrofolate reductase; 2) homocysteine can be converted to cysteine in a reaction that is catalyzed by Cystathionine β-Synthase (CBS). In this article, we tend to describe the pathophysiology of homocysteine in causing acute myocardial infarction.</abstract></article-meta></front><body /><back /></article>