Reaching C-Reactive Protein and Low-Density Lipoprotein Cholesterol Goals in Dyslipidemic Patients (from the Lipid Treatment Assessment Project [L-TAP] 2)


Autoria(s): CHIANG, Cheng-Wen; SANTOS, Raul D.; WATERS, David D.; MESSIG, Michael; TARASENKO, Lisa; JUKEMA, J. Wouter; FERRIERES, Jean; FOODY, JoAnne; SEUNG, Ki-Bae; Lipid Treatment Assessment Project
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

19/10/2012

19/10/2012

2011

Resumo

The purpose of the present substudy of the Lipid Treatment Assessment Project 2 was to assess dual C-reactive protein (CRP) and low-density lipoprotein (LDL) cholesterol goal attainment across a spectrum of low-, moderate-, and high-risk patients with dyslipidemia in 8 countries in North America, Latin America, Europe, and Asia. Of the 9,518 patients studied overall, 45% were women, 64% had hypertension, 31% had diabetes, 14% were current smokers, 60% were high risk, and 79% were taking a statin. The median CRP level was 1.5 mg/L (interquartile range 0.2 to 2.8). On multivariate analysis, higher CRP levels were associated with older age, female gender, hypertension, current smoking, greater body mass index, larger waist circumference, LDL cholesterol level, and triglyceride/high-density lipoprotein cholesterol ratio. In contrast, being from Asia or taking a statin was associated with lower levels. Across all risk groups, 59% of patients attained the CRP target of <2 mg/L, and 33% had <1 mg/L. Overall, 44% of patients attained both their National Cholesterol Education Program Adult Treatment Panel III LDL cholesterol target and a CRP level of <2 mg/L, but only 26% attained their LDL cholesterol target and a CRP level of <1 mg/L. In the very high-risk group with coronary heart disease and >= 2 risk factors, only 19% attained both their LDL cholesterol goal and a CRP level of <2 mg/L and 12% their LDL cholesterol goal and a CRP level of <1 mg/L. In conclusion, with current treatment, most dyslipidemic patients do not reach the dual CRP and LDL cholesterol goals. Smoking cessation, weight reduction, and the greater use of more potent statins at higher doses might be able to improve these outcomes. (C) 2011 Elsevier Inc. All rights reserved. (Am J Cardiol 2011;107:1639-1643)

Pfizer, Inc., New York, New York

Identificador

AMERICAN JOURNAL OF CARDIOLOGY, v.107, n.11, p.1639-1643, 2011

0002-9149

http://producao.usp.br/handle/BDPI/21274

10.1016/j.amjcard.2011.01.050

http://dx.doi.org/10.1016/j.amjcard.2011.01.050

Idioma(s)

eng

Publicador

EXCERPTA MEDICA INC-ELSEVIER SCIENCE INC

Relação

American Journal of Cardiology

Direitos

restrictedAccess

Copyright EXCERPTA MEDICA INC-ELSEVIER SCIENCE INC

Palavras-Chave #CARDIOVASCULAR-DISEASE #METABOLIC SYNDROME #HEART-DISEASE #INFLAMMATION #ATORVASTATIN #ASSOCIATION #JAPANESE #Cardiac & Cardiovascular Systems
Tipo

article

original article

publishedVersion