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CHD Newer Risk Factors. An over view on Homocystinemia. Dr. R.V.S.N.Sarma M.D., M.Sc., (Canada). All are One. This not about the GOD There is only one disease – Over nutrition Its faces are many such as Over weight / Obesity Diabetes mellitus, IR, Syndrome X
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CHDNewer Risk Factors An over view on Homocystinemia Dr. R.V.S.N.Sarma M.D., M.Sc., (Canada)
All are One • This not about the GOD • There is only one disease – Over nutrition • Its faces are many such as • Over weight / Obesity • Diabetes mellitus, IR, Syndrome X • Atherosclerosis – HT- CHD – CVD – RVD – PVD • Hyper lipidemias – endothelial dysfunction • Wear and tear of joints …. So on • What are we to do ? - Avoid over-indulgence
How much is much ? BMI = Weight in kgs Height2 in mts 70 1.65 x 1.65 BMI = = 25.71 Underweight < 20 Over weight > 25 to 30 Normal 20 to 25 Obesity >30 Waist / Hip ratio = 35” /38” = 0.92 Normal for Males < 0.90, Females <0.80
Diets rich in Saturated Fat, Chol Sedentary Life Style Excess body weight/ Obesity Less perfect Genetic make-up Lipid abnormalities Atherosclerotic vascular disease CHD, CVD, PVD Macro-vascular Disease ROS tHcy
AVD – Clinical Manifestations For every thing the common denominator is ED
Lipid Peroxidation LDL, IDL Not normally taken up by the vessel wall ROS – Free radicals and Pro-oxidants Freely enters the vessel wall Oxidized LDL, IDL Macrophages Endothelium Scavenger pathway Foam Cells Cytokines, GF Atherosclerosis
Risk Factors for AVD • Hyperhomocyst(e)inemia • Diabetes mellitus • Hypertension • Dyslipidemia • Positive family history, Smoking, obesity and physical inactivity Oxidative Stress AVD
Free Radical Formation Homolytic fission of a covalent bond Single covalent bond A B Homolytic fission Heterolytic fission B A A B Free radicals Ions
ROS damage biological tissues- membranes Reactive Oxygen Species Lipid peroxidation Protein denaturation DNA Damage Free radicals released Cell Dysfunction and death
Classification • Preventive antioxidants -Ceruloplasmin, transferrin, lactoferrin • Enzyme antioxidants -Superoxide dismutase, catalase, glutathione peroxidase • Scavenging or ‘chain-breaking’ or ‘sacrificial’antioxidants -Vitamins A,C, and E
Reactive Oxygen Species (ROS) ROS are highly reactive….and can damage biological tissues and membranes
What is Homocysteine ? Metabolism Digestion Protein diet Methionine 1)Homocysteine Auto-oxidation Protein synthesis 2)Homocystine 3) Homocysteine thiolactone HS-CH2-CH2-CH-COOH Generation of ROS NH2 Homocysteine • 1+2+3= homocyst(e)ine • homocyst(e)ine = tHcy • Homocyst(e)inemia=hyper - tHcy • Sulfur-containing amino acid • By product of methionine metabolism
Homocysteine : Metabolic Pathways Remethylation Cycle Demethylation Cycle Diet Tetra hydrofolate Methionine Folic acid MTHFR Vitamin B6 (MS) Methyl tetrahydrofolate Homocysteine Vitamin B6 (C beta S) MS – Methionine synthase MTHFR – Methyl tetrahydro folate reductase C beta S – Cystathionine beta synthase Cystathionine Transsulfuration Pathway Cysteine Sulphate Glutathione
Hyperhomocyst(e)inemia Blood Homocyst(e)ine Levels • Moderate to severe hyper – tHcy : established risk factor for AVD 1-4 • Hyper – tHcy • - 5-7 % of the general population • - 12-47 % of patients with AVD
Causes of Hyperhomocyst(e)inemia • Nutritional : Vitamin deficiency Folic Acid Vitamin B12 Vitamin B6 • Genetic : Enzyme Abnormality • Drugs : Methotrexate, Phenytoin, Theophylline
Homocysteine & Pathogenesis of AVD Homocysteine Auto-oxidation Generation of ROS H2O2 OH/O2 Oxidizes LDL Damages endothelium Lipid peroxidation Exposure of smooth muscle, subendothelium ¯ Nitric Oxide formation Foam cells (chol) Proliferation of SM cells, Chemotaxis ¯ Vasodilation Hypertension ATHEROSCLEROSIS
Physicians Health Study • 271 male physicians who had MI and matched controls were studied • Various risk factors were analyzed • Plasma tHcy is significantly higher in those with MI compared to controls • The R.R for tHcy levels above 13 is 3.4 after adjusting for all other risk factors • 482 hyperlipedemic subjects – 72 % with ↑tHcy had atheroscleoris v/s 44 % without
Treatment of Hyperhomocyst(e)inemia • Nutritional : Vitamin Supplimentation Folic Acid – 5 mg daily (Folvite) Supplementation of Vitamin B12 Supplementation of Vitamin B6 • Drugs : Care while using drugs like Methotrexate, Phenytoin, Theophylline C. Role of anti-oxidants – no RCTs
Lp (a) or Little a • Similar to LDL molecule • a single apo-A is attached by a disulfide bond to apo-B 100 • Primary determinant is genetic • Normal value 20 mg %, > 30 high risk • It may compete with plasminogen because of structural similarity and so interfere with plasmin synthesis and thrombolytic pathway • Nicotinic acid, ? Benzafibrate, estrogens lower it