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SP076 ARGININE UPTAKE IS ATTENUATED, THROUGH POST TRANSLATIONAL REGULATION, OF CATIONIC AMINO ACID TRANSPORTER-1 IN HYPERCHOLESTEROLEMIC RATS Idit Schwartz, Meirav Ingbir, Ran Reshef, Tamara Chernichovski, Doron Schwartz. Nephrology, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel SP077 ONE IMMUNOGLOBIN-BINDING PEPTIDE PLAYS A PROTECTIVE ROLE IN ANCA- ACCELERATED APOPTOSIS OF NEUTROPHILS Xiang-Ling Wang, Nan Chen, Hai-Jin Yu, Wei-Ming Wang, Li-Yan Ni. Dept Nephrology, Ruijin Hosp, Shanghai Jiaotong Univ, Shanghai, China SP078 TREATMENT WITH ROSUVASTATIN INCREASES BASAL NO ACTIVITY IN HYPERCHOLESTEROLEMIA Roland E. Schmieder, 1 Christian Ott, 1 Bernhard M.W. Schmidt, 1 Stephanie Titze, 1 Tim Schufele, 2 Markus P. Schlaich.1 1Dept Nephrology and Hypertension, Univ Erlangen-Nrnberg, Erlangen, Germany; 2Internal Medicine, Heart Inst, Lahr, Germany SP079 RENAL REDOX IMAGING AND IN VIVO ANALYSIS DURING ANTIHYPERTENSIVE TREATMENTS Aki Hirayama, 1 Takaaki Oteki, 1 Atsushi Ueda, 2 Keigyou Yoh, 1 Yoshio Shimizu, 1 Sohji Nagase.1 1Dept Nephrology, Graduate School Comprehensive Human Sciences, Univ Tsukuba, Tsukuba, Ibaraki, Japan; 2Dept Internal Medicine, Namegata District General Hosp, Namegata, Ibaraki, Japan SP080 OVEREXPRESSION OF THE RENAL Na + -INDEPENDENT LAT2 TRANSPORTER BY ALDOSTERONE Maria Joao Pinho, Patricio Soares-da-Silva. Inst Pharmacol Ther, Fac Medicine, Porto, Portugal SP081 EFFECT OF HIGH SALT INTAKE ON THE EXPRESSION OF RENAL B0AT1 AMINO ACID TRANSPORTER IN THE SPONTANEOUS HYPERTENSIVE RAT Maria Joao Pinho, Patricio Soares-da-Silva. Inst Pharmacol Ther, Fac Medicine, Porto, Portugal SP082 CARDIOPROTECTIVE EFFECT OF LOSARTAN ON SUBTOTAL NEPHRECTOMY RENAL FAILURE RATS Yongcheng He, 1 Lutan Liao, 2 Xiaoqiang Ding, 2 Shaodong Luan, 1 Tiegang Yi.3 1Dept Nephrology, Shenzhen Second People's Hosp, Shenzhen, Guangdong Province, China; 2Dept Nephrology, Zhongshan Hosp, Fudan Univ, Shanghai, China; 3Dept Nephrology, Shenzhen Chinese Traditional Medicine Hosp, Shenzhen, Guangdong Province, China SP083 VASCULAR INFLAMMATION IN END-STAGE RENAL DISEASE: THE RED BLOOD CELL CONNECTION Vittorio Sirolli, 1 Natalia Di Pietro, 2, 3 Annalisa Giardinelli, 2, 3 Sara Di Silvestre, 2, 3 Luigi Amoroso, 1 Uwe Brummer, 1 Pamela Di Tomo, 2, 3 Assunta Pandolfi, 2, 3 Mario Bonomini.1 1Dept Medicine, Inst Nephrology, 2Dept Biomorphology, G. D'Annunzio Univ, Chieti, Italy; 3Aging Research Center, Ce.S.I., G. D'Annunzio Univ Found, Chieti, Italy. May also dictate avoid the buy cheap rosuvastatin a new versionof their.

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Question: what are the herbal first aid supplies. The benefit of further alterations in lipid levels by the combined use of rosuvastatin with fibrates or niacin should be carefully weighed against the potential risks of this combination and cymbalta.
Risks were greatest at the highest dose level 40 mg ; . The FDA advises that patients should not start therapy at this dose. In addition, the FDA reported the results of a postmarketing study that found that people of Asian heritage had twice the blood levels of the drug as Caucasians who had taken the same dose. Because of this difference in drug metabolism, the FDA advises that Asian Americans should start treatment at the lowest rosuvastatin dose 5 mg ; . In general, all statin therapy should start at a lower dose and be raised incrementally until healthy cholesterol levels are maintained. Patients should immediately tell their doctor about any unusual muscle discomfort or weakness, fever, nausea or vomiting, or darkening of urine color. Statins can also affect the liver, particularly at higher doses, so patients should have periodic liver function tests. Statins should not be taken by anyone with liver problems or by women during pregnancy or breast-feeding. Similarly, high statin doses increase the risk for kidney failure, particularly for patients with other existing risk factors diabetes, hypertension, atherosclerosis, history of heart failure ; . Interactions with Drugs and Food. Statins may have some adverse interactions with other drugs, including other cholesterol-lowering medications. Among the drugs that increase the risk for adverse effects are cyclosporine, macrolide antibiotics, and certain antifungals. Patients should tell their doctors about any other medications they are taking. Grapefruit juice and Seville oranges may increase statin potency. Nicotinic Acid Niacin ; Brands. Nicotinic acid is the active compound found in niacin, or vitamin B3. It is the first choice for patients with low HDL levels. Brands include Niacor, Nicolar, and SloNiacin. An extended-release form Niaspan ; , administered at bedtime, may have fewer side effects, including headaches and flushing, than rapidly-acting niacin drugs. Although niacin is available over the counter, the active form used for cholesterol is given in much higher doses and is available only by prescription. It is important to take this medication under a doctor's direction in order to ensure its safety and effectiveness. Benefits. When used in high doses, it has the following benefits: Raises HDL levels higher than other anti-cholesterol drugs Reducing triglyceride levels very effectively Lowers LDL-cholesterol and lipoprotein a ; Costs less than other anti-cholesterol drugs Combinations with other drugs, particularly statins, may add significant benefits. Side Effects. Many patients do not like the side effects of the rapidly-absorbed form of nicotinic acid. About a quarter of patients who use rapid-acting forms of nicotinic acid stop taking them. The most common side effects are flushing of the face and neck, itching, headache, blurred vision, and dizziness. They usually occur between 5 minutes to hours after taking the drug and can last for minutes to, uncommonly, hours. The body does eventually become tolerant to these effects, and they generally subside. The following may reduce flushing and itching: Starting with low doses taken at mealtime and gradually working up to the prescribed dose. Taking low-dose aspirin about 30 minutes before taking nicotinic acid. This may help prevent flushing. Avoiding hot drinks. Choosing an extended release form. Even with this form, it is wise to gradually increase the bedtime dose over time and take a low-dose aspirin a half-hour beforehand. ; Stomach problems are common. Other side effects include dry skin and mucous membranes and darkening of the skin. About 30% of patients who take niacin experience elevated levels in blood glucose, which can be a problem for people with diabetes. Niacin's effects on HDL and triglycerides, however, are especially suited for the lipid imbalances that are common in diabetes. And, some studies report that people with diabetes who use niacin have little trouble with blood sugar control. Potentially Serious Complications. About 3 - 5% of people taking nicotinic acid develop liver problems, which disappear after the medication is discontinued. The extended form Niaspan ; appears to be safe for the liver, but people with chronic liver disease should not use any form of nicotinic acid. People with gout should also avoid nicotinic acid because it elevates uric acid. Bile-Acid Binding Resins Bile-acid binding resins work, as their name suggests, by binding to bile in the digestive tract. This reduces cholesterol in the following way: Bile is made in the liver and is used as one of the body's primary manufacturing components. Once the resins bind to bile in the digestive tract, the bile is excreted in feces. As the resins eliminate bile from the body, the liver takes more cholesterol from the bloodstream in order to produce more bile. As cholesterol is taken out of the bloodstream, LDL levels drop. When used in combination with dietary control, LDL levels are reduced by 15 - 20%. Combinations with nicotinic acid are even more effective, with reductions of 40 - 60% observed. Brands. The bile-acid binding resins and similar drugs include cholestyramine Questran, Questran Light ; . They are commonly used in a powder that is dissolved in liquid. Colesevelam Welchol ; is available in tablet form. Side Effects. None of these drugs poses major risks. Most, however, cause constipation, heartburn, gas, and other gastrointestinal problems, side effects that many people cannot tolerate. One study found that only half the standard dose of colestipol was needed when psyllium, a soluble fiber supplement found in Metamucil, Fiberall, and Perdiem ; , was added to the drink. In addition, bloating and constipation were reduced. Colesevelam, a newer resin, appears to have significantly fewer of these side effects. Bile-acting drugs may contribute to calcium loss and therefore increase the risk for osteoporosis. Over time.
Methotrexate was used in a randomized, doubleblind trial involving 29 patients with SSc. Patients received weekly injections of 15 mg of methotrexate or placebo, and the dosage was increased to 25 mg per week for poor responders. After a 24-week follow-up, significant improvement was noted in skin induration and handgrip strength.22 Additional trials involving larger numbers of patients are necessary to confirm these results. Before initiating methotrexate therapy, a thorough evaluation of the patient should be completed. Baseline laboratory tests should include complete blood cell count, platelet count, liver function tests, serum urea nitrogen, creatinine, and creatinine clearance. Cyclosporine is an immunosuppressive drug that selectively inhibits the release of IL-2 from activated T lymphocytes. There is evidence that serum levels of IL-2, its soluble receptors, or both are frequently elevated in early SSc.23, 24 An open clinical trial with cyclosporine was conducted in 10 patients with SSc.25 The starting dosage was 1 mg kg per day, which was increased progressively until toxicity appeared or when 5 mg kg per day was reached. After 48 weeks' follow-up, there was a decrease in skin induration but no improvement in pulmonary or cardiac involvement. Nephrotoxicity was frequent but usually transient and appeared mainly in patients receiving more than 3 to 4 mg kg per day.25 Because renal involvement in SSc is not uncommon, cyclosporine in the treatment of SSc should be used with great caution. Patients must be carefully monitored for the development of nephrotoxicity, hypertension, and malignant neoplasm, particularly lymphoma. Many drug interactions occur, and the patient should be questioned about concomitant medications. Extracorporeal photopheresis has been used to treat SSc. The principle of this technique is to administer oral 6-methoxypsoralen, followed by extracorporeal activation of lymphocytes by UV-A. The blood carrying covalently cross-linked DNA-psoralen lymphocytes is then transferred into the patient to elicit a specific immune response that may block proliferation of certain Tlymphocyte clones. An initial multicenter trial was encouraging and showed significant improvement in skin induration but no effect on pulmonary function.26 However, additional trials questioned the efficacy of extracorporeal photopheresis.27 Furthermore, extracorporeal photopheresis for SSc is not approved by the Food and Drug Administration. Another approach for immunosuppression in SSc was the use of antithymocyte globulin 3-5 mg kg for 5 days ; . After 6 months' follow-up, no improvement in skin score or pulmonary function was noted compared with a placebo group.28 Corticosteroids are not useful in improving or preventing the progression of skin involvement in SSc. However, they may be helpful in controlling pain caused by arthralgia or myalgia. Similar benefits can be achieved with nonsteroidal antiinflammatory agents. Antifibrotic Agents. Fibrosis consists of massive deposition of newly synthesized connective tissue, mostly collagens, which is frequently responsible for the development of organ insufficiency. Fibrosis is a prominent feature and duloxetine.

I request that you please take the time to read the attached information, as my parents are both experiencing similar reactions. My stepfather has a chronic rash and my mother gets hives at least one night a week. They receive 'Meals on Wheels' and my stepfather says it is usually after rissoles, stew or soup. Therefore I request that you read the ingredients that you are adding for flavour to these meals. Purchased chickens from Woolworths have the additive in the stuffing, Coles marinated fresh chickens contain 635, Red Rooster have in on the outside, even some chicken salt has it as well as some stocks, tinned and packet sauces and soups. Potato chips, CC's and other flavour enhanced foods are all to be avoided but there are plenty of substitutes, it just means being more vigilant as to what is served. The elderly in aged care facilities and even patients in hospitals are experiencing these reactions due to flavour enhancer 635. There are plenty of natural herbs and spices that can be added to food for flavour. A lot of suffering and possibly even death is being caused by this additive. Thanking you. Mrs E. M. R. Lloyd, Frenchville. Q4701, Ph. 49 289094 [321] 635: Life-threatening reaction to flavoured chips April 2004 ; I believe I had a very real dangerous reaction last year to chips whilst I was in early stages of pregnancy. I was admitted to emergency and due to difficulty breathing a nurse had to stay in with me. They asked me had I taken any unusual drugs etc and were baffled when the only different thing I had eaten was flavoured chips. I even took the packet with me, the reaction started almost immediately. Previously I had only ever eaten plain, but due to a craving I got a flavoured variety. I thought I was going to die. By the time I got to hospital luckily it wasn't far from home ; my mouth and throat was so swollen I couldn't talk or breath properly, of course because of this I was treated as high priority and treated straight away. Thank God I had realised straight away when I got a tingling burning sensation and felt like I had been to the dentist and had a local anaesthetic. My mother had said something about these chemicals recently in our diets I had actually dismissed this at the time ; but thank goodness she did. I think I lucky to still be here. - reader, SA. [322] 635: Rash was caused by 2 minute noodles April 2004 ; Well it hasn't even been a week yet and I'm feeling better, my rash has cured 80% best ever, the main problem was Maggi 2 minute noodles as I have been eating them at least once a week since I left home I guess mother's cooking says a lot there ; just because they were quick and easy.- from the failsafe groups. [336] 635: from school tuckshop July 2004 ; Last year one of my children had a cottage pie from the school tuckshop and when she arrived home she complained of a headache, stomach cramps and had a skin rash. The next day I read the ingredients of the cottage pies in the tuckshop. They contained preservative, MSG and flavour enhancer 635. When I read about 635 on your web site I was stunned that a tuckshop would give this stuff to children, and I realized what had caused a rash on my other daughter. After eating some cooked chicken from a supermarket, she had developed an itchy red rash which covered her whole body and I had to give her an antihistamine tablet. At the time I couldn't work out what had caused the rash. Another time she got a rash after eating some cooked chicken from the local small food store. I went to the shop to read the ingredients and sure enough the seasoning contained 635. I printed out the information from your website and gave it to the owner of the shop. They have not changed the seasoning and we have never again bought a cooked chicken from any store. - reader, Qld [339] 635: Meals on wheels disease Sept 2004 ; TO WHOM IT MAY CONCERN. Module VI Supporting self-management ; involves the principles of selfmanagement of asthma. In the IPMP study the pharmacist does not start self-management but can support patients already familiar with this kind of drug use. In the modular approach of the comprehensive intervention strategy observed problems concerning insufficient skills how to handle an inhaler and lack of knowledge about medication, dosage, disease and devices modules I, II, III and VI ; were solved before any changes in medicines or treatment were suggested to patients and their physicians modules IV and V ; . The documentation form of each pharmaceutical care module ended with a common aim agreed upon by both the health care professional and the patient or with a reference to another module. The aim was checked in a following appointment or phone call. On the basis of the literature and a pilot study carried out in four pharmacies before the start of the IPMP study these six different modules appear to be sufficient in pharmacy practice to solve existing problems with prescribed pulmonary medication and mentioned or observed insufficient treatment. The IPMP intervention provided by community pharmacists is focused on outcomes obtainable in daily Dutch pharmacy practice, i.e. well-educated patients with prescribed drug treatment according to the pulmonary guidelines. In a pilot study it appeared that Dutch pulmonary patients did not monitor their condition on a regular basis by measuring their peak-flow. Moreover, they were not generally referred to pulmonologists to do lung function tests. Therefore we decided that no clinical outcomes should be measured in the IPMP study such as PEFR or FEV1. Four weeks after the intervention was completed changes in coping behaviour or in drug use were evaluated together with the patient by telephone or in a second appointment. Insufficient improvement or unreached aims might be a reason for a new consultation or an additional counselling of the general practitioner GP ; or pulmonologist. The intervention episode was concluded when the agreed aim was reached. Follow-up After this first part the intervention was prolonged by monitoring patients' drug treatment and the refill rate of the prescriptions by reviewing the medication records during a whole year. Irregularities in the predicted refill rate could be a reason to contact the patient again and to start a new and cytotec. RISPERDAL M-TAB .25 RISPERDAL SOLN.25 risperidone .25 risperidone liquid .25 risperidone microspheres .25 risperidone orally disintegrating tab.25 RITALIN * See methylphenidate hcl .39 RITALIN SR * See methylphenidate hcl cr.39 ritonavir .27 rivastigmine tartrate.18 rizatriptan .21 RMS * SUPP.11 ROBAXIN * See methocarbamol .68 ROBINUL FORTE * See glycopyrrolate .48 ROCALTROL * See calcitriol .52 ROCEPHIN * See ceftriaxone sodium.13 ROFERON-A.58 ROMYCIN.62 ropinirole hydrochloride.25 rosiglitazone .29 rosiglitazone-glimepiride .29 rosiglitazone maleate-metformin .29 ROSULA * CLEANSER .41 orsuvastatin 40 mg .37 roshvastatin 5 mg, 10 mg, 20 mg .37 ROTATEQ.59 rotavirus vaccine.59 ROWASA * See mesalamine enema .60 ROXANOL * See morphine sulfate 20mg ml soln .12 ROXICODONE * See oxycodone hcl tablets .11 ROXICODONE * SOLN .11 RYTHMOL * See propafenone hcl .34 RYTHMOL SR .34.

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Table 2. Pharmacokinetic Parameters of Rowuvastatin tmax hr ; 3-5 Absolute Bioavailability 20% Food Effect Rate of absorption decreased by 20% Extent of absorption no effect Protein Binding 88% Metabolism Approximately 10% metabolized principally by cytochrome P450 2C9 Elimination Elimination half-life is approximately 19 hours Primarily excreted in feces 90% ; Pharmacokinetic studies show an approximate 2-fold elevation in median exposure in Japanese and Chinese subjects compared with Caucasians. While the mechanism is unknown, rozuvastatin appears to be more bioavailable in these patients. These increases should be considered when making rosuvastatin dosing decisions for patients of Japanese and Chinese ancestry.1 and misoprostol.

Drug-drug kinetic interactions are a major problem with triazole antifungal agents. Pharmacokinetic interactions commonly occur via metabolising enzymes i.e. the cytochrome CYP ; P450 isoenzymes superfamily ; or drug transporters i.e. P-glycoprotein or P-gp ; . Itraconazole as well as its metabolites ; , voriconazole, posaconazole and fluconazole, to a lesser extent, are inhibitors of the isoenzyme CYP3A4 [11-13]. Thus, they can delay the elimination of numerous drugs, since CYP3A4 is thought to be involved in the metabolism of 50% of all marketed drugs. Nevertheless, besides some hypolipidemic agents statins ; , most significant clinical interactions those leading to contraindications or dosage reductions ; will occur with drugs with a narrow therapeutic index and whose elimination predominantly involves biotransformation catalysed by CYP3A4. Given the clinical profile of inpatients receiving triazoles mainly those in oncology or intensive care units ; , major drugs of current concern are immunosuppressants cyclosporine, tacrolimus, sirolimus ; , some anticancer agents vincristine ; , some analgesics alfentanil ; and hypnotics midazolam ; . It should be remembered that ketoconazole is considered as one of the most potent CYP3A4 inhibitors. However, at the present time, it is most exclusively used as a test drug in the exploration of drug-drug interactions rather than in the treatment of invasive fungal diseases. Fluconazole and voriconazole are inhibitors of CYP2C9. As such, they can increase the anticoagulant effect of warfarin-type anticoagulants, including acenocoumarol. Itraconazole is an inhibitor of the drug transporter P-gp [14] and breast cancer resistance protein BCRP ; [15] indicating that it can increase concentrations of digoxin or the minimally metabolised statin, rosuvastatin. From the substrate point of view, antifungal activity is.
References 1. Anon, PACT Centre Pages - Cardiovascular prescribing. Prescription Pricing Authority website 2003; Feb 2. Anon, Statins. British National Formulary 2002; No.44 p128-130 3. Jones AF, The future of statin therapy. Practical Cardiovascular Risk Management 2003; Vol 1 ; p5-8 4. Kmietowicz Z, Statins are the new aspirin, Oxford researchers say. British Medical Journal 2001; Vol 323 p1145 5. Gross Z, If statins are the new aspirin what might it cost the National Health Service? Pharmaceutical Journal 2001; Vol 267 p740 6. Durrington PN, Lipid and lipoprotein disorders. Oxford Textbook of Medicine 2003; 4th Ed Vol 2 p79 7. Department of Health, National Service Framework for Coronary Heart Disease. 2000 March 8. Department of Health, Delivering better heart services. Progress report 2003 9. DeWilde S, Carey IM et al, Analysis of statin prescribing in the UK 1994-2001. Heart 2003; Vol 89 p417-21 10. Committee on Safety of Medicines. Cerivastatin Lipobay ; withdrawn. Current Problems in Pharmacovigilance 2001; Vol 27 p9 11. Schachter M, Rosuvastatin: clinical profile and key characteristics. Future Prescriber 2002; Vol 3 2 ; p19-21 12. Anon, Manufacturer claims superior action for new statin. Pharmaceutical Journal 2003; Vol 270 p427 13. Anon, Crestor falters in three Euro markets. Scrip 2003; No.2831 p19 14. Anon, AstraZeneca's new statin, CrestorR, receives first approval in Europe - Other European markets should follow in 2003. AstraZeneca press release 2002; No and calcitriol. Nature's Plus Source of Life MiniTabletten 360 MiniTabletten in der Vorratspackung VollwertMultivitamin. Der Klassiker aus den USA als leicht zu schluckende Mini Tabletten. Amerikas meistverkaufte MultivitaminMultimineralFormel. SOL enthlt alle Vitamine, Mineralstoffe und Spurenelemente eingebettet in eine hochaktive Nhrstoffbasis, angereichert mit Krutern. HypoAllergen, Vegetarisch, frei von Hefe, Weizen, Mais, Soja, Milch. Empfohlene tgliche Verzehrmenge: 26 MiniTabletten 10123 B Source of Life NoIron Eisenfrei 90 MiniTabletten NP 22, 90, for instance, what is rosuvastatin. The use of a risk index defining cardiac risk in patients going for non-cardiac surgery is low . Application of such an index would result in few tests being ordered with no change in outcome. Changes in medical management are variable and depend on the consultant and rocaltrol. Research published in the january 15th issue of the american journal of medical genetics describes the cases of two siblings with fetal valproate syndrome and their long-term follow-up.

Corresponding author: Dr Nerino Allocati Dipartimento di Scienze Biomediche, Universita' "G. d'Annunzio" Via dei Vestini, 31 I-66013 Chieti, ITALY Tel. + 39.08713555281 Fax + 39.08713555282 E-mail n.allocati dsb ch.it and carbamazepine. METHODS. Infants 4011500 g ; in the National Institute of Child Health and Human. Rosuvastatin what is rosuvastatin used for and tegretol and rosuvastatin. Table 49. Summary Service Data for Region 3: Lo-Femenal.
First launched in 2003, sales were $129 million and $908 million in 2003 and 2004, respectively, with a total patient treatment population of 4 million by the end of 200 in 2006, rosuvastatin begin a new series of commercials , under the drug's trade name of crestor and carbimazole. Health news health videos opinions forum contact statin halts build up of atherosclerosis in low risk patients featured article main category: cardiovascular cardiology news article date: 26 mar 2007 - 0: 00 pdt email to a friend printer friendly view write opinions rate article newsletters visitor ratings: healthcare professional: general public: rate this article an international study on the potent cholesterol lowering statin drug rosuvastatin has shown that it is also effective at halting the early stages of atherosclerosis in people at low risk for heart attacks and strokes.
Precautions and warnings for rosuvastatin, and rosuvastatin side effects.

Therapy with statins has been shown beyond any doubt to be beneficial in the primary and secondary prevention of coronary artery disease. The current generation of statin studies is evaluating whether intensive statin therapy, by lowering low-density lipoprotein cholesterol LDL-C ; to levels close to those we are born with and by targeting inflammation, can confer any further advantage. Recent trials such as Pravastatin or Atorvastatin Evaluation and Infection Therapy PROVE IT ; , Incremental Decrease in End Points Through Aggressive Lipid Lowering IDEAL ; , and Treating to New Targets TNT ; have indeed strongly suggested that lower LDL-C values ~70 mg dL ; are optimal in the management of the high-risk patient with coronary artery disease. However, while statins have been thought to be capable of "passivating" or "stabilizing" atherosclerotic plaques, no large multicenter studies until now have documented actual plaque regression in the coronary arteries. The Reversal of Atherosclerosis with Aggressive Lipid Lowering REVERSAL ; study, which evaluated intensive therapy with atorvastatin 80 mg compared with moderate-intensity therapy with pravastatin 40 mg did show that atorvastatin was able to prevent progression of atherosclerosis as evaluated by intravascular ultrasound IVUS ; , but statistically significant regression was not observed for either treatment group. In this setting, the same investigators designed A Study to Evaluate the Effect of Rosuvasta6in on Intravascular Ultrasound-Derived Coronary Atheroma Burden ASTEROID ; to evaluate whether intensive statin therapy with the most potent LDLC lowering statin available, rosuvastatin, can actually regress atherosclerosis assessed by IVUS.

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