Global cardiovascular disease risk management in Italian patients with metabolic syndrome in the clinical practice setting

被引:1
|
作者
Ambrosioni E. [1 ]
Cicero A.F.G. [1 ,4 ]
Parretti D. [2 ]
Filippi A. [2 ]
Rossi A. [2 ]
Peruzzi E. [3 ]
Borghi C. [1 ]
机构
[1] Internal Medicine, Aging and Kidney Diseases Department, University of Bologna, Bologna
[2] Italian Society of General Medicine (SIMG), Florence
[3] Medical Department, Novartis Farma, Origgio
[4] Internal Medicine, Aging and Kidney Diseases Department, Sant'Orsola-Malpighi Hospital, University of Bologna, 40138 Bologna
关键词
Fluvastatin; Metabolic syndrome; Risk management; Risk stratification; SCORE; Valsartan;
D O I
10.2165/00151642-200815020-00001
中图分类号
学科分类号
摘要
Background: Metabolic syndrome is a highly prevalent condition in the Italian population. This study assesses the feasibility and efficacy of a multifactorial approach for primary prevention of cardiovascular disease risk assessment in patients with metabolic syndrome in the daily clinical practice setting. Methods: 726 patients were enrolled (males : females = 7 : 3), their ages ranging from 26 to 70 years, with metabolic syndrome and cardiovascular death risk ≥5%, computed by means of the European Systematic COronary Risk Evaluation (SCORE) algorithm. The first phase (3 months) consisted of an improvement in lifestyle and, if necessary, the initial administration of an antihypertensive therapy (valsartan 160 mg/day for patients with blood pressure ≥140/90 mmHg and ≥130/80 mmHg for diabetic patients). During phase 2 (6 months), patients with systolic blood pressure (SBP) ≥140 mmHg and/or diastolic blood pressure (DBP) ≥90 mmHg (≥130/80 mmHg for diabetic patients) were administered valsartan 160 mg/day + hydrochlorothiazide 12.5 mg/day combined; those with total cholesterol levels ≥190 mg/dL (≥175 mg/dL for diabetic patients) started treatment with fluvastatin 80 mg prolonged release (XL), as prescribed in the guidelines. A control group was approached with another conventional treatment. Results: After 9 months of monitoring, the SBP dropped by 27 mmHg in the valsartan-treated patients and by 11 mmHg in the control group, while the DBP dropped by 12 mmHg in the former group and 2 mmHg in the latter. Total cholesterolaemia was reduced by 47 mg/dL in patients undergoing fluvastatin and valsartan therapy, by 19 mg/dL in those treated with valsartan only and by 33 mg/dL in those administered another conventional treatment. Relative risk reduction observed after 9 months, compared with the beginning of the study, was almost 48% in the valsartan/valsartan + fluvastatin group, versus 28% observed with the other conventional treatment. The reduction of risk at 60 years of age was an average of 39% at 3 months and 48% at 9 months, compared with the beginning of the study. Therapeutic success was accomplished with 78% of the patients treated with valsartan/valsartan + fluvastatin, compared with 47% of patients in the conventional therapy group. Conclusion: The present study demonstrated that the normalization of the main cardiovascular risk factors in patients with metabolic syndrome may be easily achieved in standard clinical practice settings, by leading an adequate lifestyle and, if necessary, the administration of antihypertensive and/or lipid-lowering monotherapy at the usual doses. © 2008 Adis Data Information BV. All rights reserved.
引用
收藏
页码:37 / 45
页数:8
相关论文
共 50 条
  • [21] The Impact of Disease Activity in Patients with Rheumatoid Arthritis on Metabolic Syndrome and Cardiovascular Risk Assessment
    Aleksic, Ivana
    Stojanovic, Sonja
    Tasic, Ivan
    Stamenkovic, Bojana
    ACTA FACULTATIS MEDICAE NAISSENSIS, 2019, 36 (03) : 177 - 187
  • [22] Hypogonadism in testicular cancer patients is associated with risk factors of cardiovascular disease and the metabolic syndrome
    Bogefors, C.
    Isaksson, S.
    Bobjer, J.
    Kitlinski, M.
    Leijonhufvud, I.
    Link, K.
    Giwercman, A.
    ANDROLOGY, 2017, 5 (04) : 711 - 717
  • [23] Angiographic severity of coronary artery disease and cardiovascular risk in acute coronary syndrome in patients with metabolic syndrome
    Widecka, Katarzyna
    Safranow, Krzysztof
    Lewandowski, Maciej
    Przybycien, Krzysztof
    Goracy, Jaroslaw
    Kornacewicz-Jach, Zdzislawa
    KARDIOLOGIA POLSKA, 2018, 76 (03) : 662 - 668
  • [24] Analysis and Clinical Applications of Metabolic Syndrome Risk Factors for Cardiovascular
    Wu, Li
    Zhang, Xiaochun
    2014 2ND INTERNATIONAL CONFERENCE ON SOCIAL SCIENCE AND HEALTH (ICSSH 2014), PT 4, 2014, 58 : 159 - 163
  • [25] INFLAMMATION MARKERS IN PATIENTS WITH CARDIOVASCULAR DISEASE AND METABOLIC SYNDROME
    Korita, Irena
    Bulo, Anyla
    Langlois, Michel
    Blaton, Victor
    JOURNAL OF MEDICAL BIOCHEMISTRY, 2013, 32 (03) : 214 - 219
  • [26] Metabolic syndrome and estimates of cardiovascular disease in cirrhotic patients
    Chavez-Tapia, Norberto C.
    Tellez-Avila, Felix I.
    Valdes-Escarcega, Marisol
    Montano-Reyes, Maria A.
    Ramos, Martha H.
    Lizardi-Cervera, Javier
    Uribe, Misael
    JOURNAL OF DIGESTIVE DISEASES, 2008, 9 (03) : 149 - 155
  • [27] The clinical significance of metabolic syndrome in hypertension: Metabolic syndrome increases cardiovascular risk: The pro position
    De La Sierra A.
    High Blood Pressure & Cardiovascular Prevention, 2008, 15 (2) : 53 - 57
  • [28] New approaches in the intensive management of cardiovascular risk in the metabolic syndrome
    Rosenson, RS
    Alpert, JS
    CURRENT PROBLEMS IN CARDIOLOGY, 2005, 30 (05) : 241 - 279
  • [29] A CLINICAL STUDY ON ASSOCIATION OF METABOLIC SYNDROME AND CARDIOVASCULAR RISK IN PSORIASIS
    Babu, Venna Ashok
    Venkateswaran, K. Sri
    Rajasekar, R. M.
    JOURNAL OF EVOLUTION OF MEDICAL AND DENTAL SCIENCES-JEMDS, 2016, 5 (93): : 6859 - 6868
  • [30] Incidence of cardiovascular disease and validity of equations of coronary risk in diabetic patients with metabolic syndrome
    Canon Barroso, Lourdes
    Diaz Herrera, Natalio
    Calvo Hueros, Juan Ignacio
    Cruces Muro, Eloisa
    Nieto Hernandez, Teresa
    Buitrago Ramirez, Francisco
    MEDICINA CLINICA, 2007, 128 (14): : 529 - 535