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Hydroxy-methylglutaryl-coenzyme

The product of this reaction 3 hydroxy 3 methylglutaryl coenzyme A (HMG CoA) has the carbon skeleton of mevalonic acid and is converted to it by enzymatic reduction... [Pg.1091]

The statins lower cholesterol by inhibiting the en zyme 3 hydroxy 3 methylglutaryl coenzyme A reduc tase which is required for the biosynthesis of meva Ionic acid (see Section 26 10) Mevalonic acid is an obligatory precursor to cholesterol so less mevalonic acid translates into less cholesterol... [Pg.1096]

Statins (3-Hydroxy-3-Methylglutaryl Coenzyme A Reductase Inhibitors)... [Pg.228]

Hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase inhibitors (statins) have been shown to improve vascular outcomes due to their cholesterol-lowering effects as well as multiple pleiotropic effects. In high-risk populations, statin therapy is known to reduce the risk of vascular events such as myocardial infarction and stroke. A meta-analysis of 10 trials involving 79,494 subjects showed that statin therapy reduced the incidence of stroke by 18%, major coronary events by 27%, and all-cause mortality by 15%. The SPARCL trial recently showed that high-dose HMG-CoA reductase inhibitors prevent recurrent stroke and transient ischemic attacks. ... [Pg.101]

The NKF suggests that CKD should be classified as a coronary heart disease (CHD) risk equivalent and the goal LDL-C level should be below 100 mg/dL in all patients with CKD.22 The most frequently used agents for the treatment of dyslipidemias in patients with CKD are the 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitors ( statins ) and the fibric acid derivatives. However, other treatments have been studied in patients with CKD and should be considered if first-line therapies are contraindicated. [Pg.379]

ACE-I, angiotensin-converting enzyme inhibitors ARB, angiotensin-receptor blockers AZA, azathioprine CMV, cytomegalovirus CPK, creatinine phos-phokinase CSA, cyclosporine HMG-CoA, 3-hydroxy 3-methylglutaryl coenzyme A reductase K+, potassium LFTs, liver function tests Rl, renal insufficiency SCr, serum creatinine SRL, sirolimus TAC, tacrolimus TMP-SMX, trimethoprim-sulfamethoxazole. [Pg.847]

From the preceding sections, it is clear that chemokines are important players in atherosclerotic disease and, as such, are being considered as possible targets in the treatment of this prevalent inflammatory condition. Under consideration at this time are both traditional nonspecific therapies [e.g., 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitors, fibrates, etc.], as well as chemokine specific approaches (142). [Pg.218]

During the preparation of 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors, the benzyl ester protecting group was removed by catalytic hydrogenolysis (Scheme 4.42). [Pg.144]

Shefer, S., Tint, G. S., Jean-Guillaume, D. etal. Is there a relationship between 3-hydroxy- 3-methylglutaryl coenzyme a reductaseactivity and forebrain pathology in the PKU mouse /. Neurosci. Res. 61 549-563,2000. [Pg.682]

There is interest in the use of lipid-lowering agents, especially the 3-hydroxy-3-methylglutaryl coenzyme A-reductase inhibitors, to prevent AD. Pravastatin and lovastatin, but not simvastatin, were associated with a lower prevalence of AD. Further study is needed before these agents can be recommended for this use. [Pg.745]

Beedle, A. S., Munday, K. A., Wilton, D. C. The stereochemistry of hydrogen transfer from NADPH catalyzed by 3-hydroxy-3-methylglutaryl-coenzyme A reductase from rat liver. European J. Biochem. 28, 151—155 (1972). [Pg.67]

Fischer, V., Johanson, L., Heitz, F., Tullmann, R., Graham, E., Baldeck, J.P. and Robinson, W.T., The 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitor fluvastatin effect on human cytochrome P-450 and implications for metabolic drug interactions. Drug Metab. Dispos., 1999, 27, 410 16. [Pg.366]

Lowering LDL cholesterol is highly effective if LDL is higher than 130 mg/dl and in suspected coronary artery disease (CAD) patients. A 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitor (statin) will be the first choice, and target LDL will be less than 100 mg/dl. LDL levels between 100-129 mg/dl will also be advantageous to be treated. Other than statins, cholestylamine, forate or other types will also be used. [Pg.588]


See other pages where Hydroxy-methylglutaryl-coenzyme is mentioned: [Pg.1091]    [Pg.1091]    [Pg.1091]    [Pg.14]    [Pg.358]    [Pg.63]    [Pg.71]    [Pg.82]    [Pg.180]    [Pg.401]    [Pg.849]    [Pg.852]    [Pg.267]    [Pg.267]    [Pg.271]    [Pg.827]    [Pg.169]    [Pg.13]    [Pg.67]    [Pg.559]    [Pg.565]    [Pg.229]    [Pg.261]    [Pg.289]    [Pg.359]    [Pg.56]    [Pg.99]    [Pg.184]   


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0-Hydroxy-/3-methylglutaryl coenzyme synthase

3 -Hydroxy- 3 -methylglutaryl-coenzyme regulation

3 -Hydroxy-3 -methylglutaryl

3-Hydroxy-3-methylglutaryl coenzyme A reductase

3-Hydroxy-3-methylglutaryl coenzyme A reductase inhibitors

3-methylglutaryl

Hydroxy-3 methylglutaryl coenzyme Statin therapy

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