Literature DB >> 11487448

Combination lipid-altering therapy: an emerging treatment paradigm for the 21st century.

T A Jacobson1.   

Abstract

For the care of an expanding segment of the US population with multiple coronary risk factors, combination lipid-altering therapy is emerging as a treatment imperative. The most recent National Cholesterol Education Program's consensus guidelines emphasize long-term global coronary heart disease (CHD) risk status, designate patients with CHD risk equivalents (eg, diabetes, peripheral arterial disease, 20% or more 10-year absolute CHD risk) for aggressive lipid-altering therapy, and deem the metabolic syndrome (eg, obesity, insulin resistance, hypertension, elevated triglycerides, low levels of high-density lipoprotein cholesterol, small dense low-density lipoprotein particles) as a secondary target for intervention. With the advancing age of the US population and the high prevalence of diabetes, the metabolic syndrome, and CHD, increasing numbers of patients will require a more balanced metabolic attack attainable only through combination lipid-altering regimens. Many of these patients, as well as persons at heightened risk for cardiovascular disease because of a range of heritable conditions (eg, familial hypercholesterolemia, familial combined hyperlipidemia), will undoubtedly require binary or ternary regimens involving statins in concert with niacin, fibric-acid derivatives, or bile acid resins. Such approaches enable the clinician to exploit the complementary effects of these agents, allowing them to be administered at low, optimally tolerable doses that are consistent with superior efficacy and a lower risk of adverse events as compared with escalating doses of monotherapy.

Entities:  

Mesh:

Substances:

Year:  2001        PMID: 11487448     DOI: 10.1007/s11883-001-0075-y

Source DB:  PubMed          Journal:  Curr Atheroscler Rep        ISSN: 1523-3804            Impact factor:   5.113


  51 in total

Review 1.  Fluvastatin in combination with cyclosporin in renal transplant recipients: a review of clinical and safety experience.

Authors:  A Jardine; H Holdaas
Journal:  J Clin Pharm Ther       Date:  1999-12       Impact factor: 2.512

2.  Combination therapy with low-dose lovastatin and niacin is as effective as higher-dose lovastatin.

Authors:  S F Gardner; E F Schneider; M C Granberry; I R Carter
Journal:  Pharmacotherapy       Date:  1996 May-Jun       Impact factor: 4.705

3.  Pharmacokinetics and pharmacodynamics of pravastatin alone and with cholestyramine in hypercholesterolemia.

Authors:  H Y Pan; A R DeVault; B J Swites; D Whigan; E Ivashkiv; D A Willard; D Brescia
Journal:  Clin Pharmacol Ther       Date:  1990-08       Impact factor: 6.875

4.  Summary of the second report of the National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel II)

Authors: 
Journal:  JAMA       Date:  1993-06-16       Impact factor: 56.272

5.  Effect of combined fluvastatin-fenofibrate therapy compared with fenofibrate monotherapy in severe primary hypercholesterolemia. French Fluvastatin Study Group.

Authors:  M Farnier; S Dejager
Journal:  Am J Cardiol       Date:  2000-01-01       Impact factor: 2.778

6.  The lipid treatment assessment project (L-TAP): a multicenter survey to evaluate the percentages of dyslipidemic patients receiving lipid-lowering therapy and achieving low-density lipoprotein cholesterol goals.

Authors:  T A Pearson; I Laurora; H Chu; S Kafonek
Journal:  Arch Intern Med       Date:  2000-02-28

7.  Fluvastatin with and without niacin for hypercholesterolemia.

Authors:  T A Jacobson; M M Chin; G J Fromell; L A Jokubaitis; L F Amorosa
Journal:  Am J Cardiol       Date:  1994-07-15       Impact factor: 2.778

8.  Efficacy and safety of triple therapy (fluvastatin-bezafibrate-cholestyramine) for severe familial hypercholesterolemia.

Authors:  E Leitersdorf; E N Muratti; O Eliav; T K Peters
Journal:  Am J Cardiol       Date:  1995-07-13       Impact factor: 2.778

9.  Long-term efficacy with fluvastatin as monotherapy and combined with cholestyramine (a 156-week multicenter study). French-Dutch Fluvastatin Study Group.

Authors:  B Jacotot; J D Banga; R Waite; T K Peters
Journal:  Am J Cardiol       Date:  1995-07-13       Impact factor: 2.778

10.  High-dose fluvastatin and bezafibrate combination treatment for heterozygous familial hypercholesterolemia.

Authors:  O Eliav; D Schurr; P Pfister; Y Friedlander; E Leitersdorf
Journal:  Am J Cardiol       Date:  1995-07-13       Impact factor: 2.778

View more
  4 in total

1.  Atorvastatin versus Bezafibrate in Mixed Hyperlipidaemia : Randomised Clinical Trial of Efficacy and Safety (the ATOMIX Study).

Authors:  Emilio Ros; Josefina Oliván; José M Mostaza; Miquel Vilardell; Xavier Pintó; Fernando Civeira; A Hernández; Pedro Marqués da Silva; A Rodriguez-Botaro; Daniel Zambón; Joan Lima; José A Gómez-Gerique; Cristina Díaz; Rosa Arístegui; José M Sol; Gonzalo Hernández
Journal:  Clin Drug Investig       Date:  2003       Impact factor: 2.859

2.  Lipoprotein kinetics in the metabolic syndrome: pathophysiological and therapeutic lessons from stable isotope studies.

Authors:  Dick C Chan; P Hugh R Barrett; Gerald F Watts
Journal:  Clin Biochem Rev       Date:  2004-02

3.  The suppressive effect of the three-herb extract mixture on vascular and liver inflammation in atherogenic diet with high fructose-fed mice.

Authors:  Hae Seong Song; Hyun Jung Koo; Bong Kyun Park; Jeong Eun Kwon; Seon-A Jang; Hyun Jin Baek; Se Young Kim; Sung Ryul Lee; Se Chan Kang
Journal:  Pharm Biol       Date:  2018-12       Impact factor: 3.503

Review 4.  Novel Insights into the Pathogenesis and Management of the Metabolic Syndrome.

Authors:  Helen H Wang; Dong Ki Lee; Min Liu; Piero Portincasa; David Q-H Wang
Journal:  Pediatr Gastroenterol Hepatol Nutr       Date:  2020-05-08
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.