Literature DB >> 17667215

Metabolic syndrome: treatment of hypertensive patients.

Zafar H Israili1, Badiâa Lyoussi, Rafael Hernández-Hernández, Manuel Velasco.   

Abstract

Metabolic syndrome (MetSyndr), a constellation of abnormalities [obesity, glucose intolerance, insulin resistance (IR), dyslipidemia (low HDL-cholesterol, high LDL-cholesterol and triglycerides (TG)], and elevated blood pressure (BP)], increases the risk of cardiovascular (CV) disease and premature death. From 10% to 30% of the adult population in industrialized countries has MetSyndr, which effectively predicts the development of type 2 diabetes mellitus (T2D) and CV disease. Because of the complex etiology of MetSyndr, a multi-targeted, integrated therapeutic approach is required to simultaneously treat high BP, obesity, lipid disorders and T2D (if present), to fully protect CV, cerebrovascular and renal systems. If lifestyle modification (weight control, diet, exercise, smoking cessation, moderation of alcohol intake) is ineffective, pharmaco-theraphy should be added to treat simultaneously the lipid- and non-lipid CV risk factors. Patients with HTN and MetSyndr should be started on angiotensin-converting enzyme (ACE) inhibitors, unless contraindicated. The ACE inhibitors and angiotensin receptor blockers (ARBs) reduce the odds of developing new onset T2D and also decrease albuminuria. The ACE inhibitors provide cardioprotective and renoprotective benefits beyond their effect on BP; they also improve IR. The ARBs are renoprotective in addition to being cardioprotective. Long-acting calcium channel blockers are also recommended in hypertensive patients with MetSyndr; these drugs also improve IR. Thiazides (at low doses) and selected ss-blockers can be given to patients with HTN and MetSyndr. Celiprolol in combination with diuretics has a favorable effect on glucose tolerance and IR in patients with HTN and MetSyndr, and spironolactone added to ACE inhibitor or ARB therapy provides additional reno- and CV protective benefits in patients with diabetic nephropathy. Carvedilol, a ss-blocker with vasodilating properties, added to ACE inhibitor or ARB therapy, is effective in preventing worsening of microalbuminuria in patients with HTN and MetSyndr; it also improves IR and glycemic control. Most patients eventually require two or more antihypertensive drugs to reach BP goal. It is recommended that therapy in patients whose BP is more than 20/10 mm Hg above target at diagnosis be initiated with a combination of antihypertensive drugs, administered either as individual drugs or as fixed-dose formulations. Treatment with fixed-dose combinations, such as irbesartan + hydrochlorothiazide provides good BP control in more than two-thirds of hypertensive patients with MetSyndr. Lipid and BP targets are reached in a high percent of patients with HTN and CV disease treated with a combination of amlodipine + atorvastatin. In conclusion, hypertensive patients with the MetSyndr be treated aggressively for each component of the syndrome to provide CV, cerebrovascular and renal protection.

Entities:  

Mesh:

Substances:

Year:  2007        PMID: 17667215     DOI: 10.1097/01.pap.0000249936.05650.0c

Source DB:  PubMed          Journal:  Am J Ther        ISSN: 1075-2765            Impact factor:   2.688


  12 in total

1.  Cardiovascular Consequences of Obesity and Targets for Treatment.

Authors:  Bettina Mittendorfer; Linda R Peterson
Journal:  Drug Discov Today Ther Strateg       Date:  2008

Review 2.  The metabolic syndrome.

Authors:  Marc-Andre Cornier; Dana Dabelea; Teri L Hernandez; Rachel C Lindstrom; Amy J Steig; Nicole R Stob; Rachael E Van Pelt; Hong Wang; Robert H Eckel
Journal:  Endocr Rev       Date:  2008-10-29       Impact factor: 19.871

3.  Plasma neuropeptide Y (NPY) and alpha-melanocyte stimulating hormone (a-MSH) levels in patients with or without hypertension and/or obesity: a pilot study.

Authors:  Maria Baltazi; Niki Katsiki; Christos Savopoulos; Fotios Iliadis; George Koliakos; Apostolos I Hatzitolios
Journal:  Am J Cardiovasc Dis       Date:  2011-05-20

Review 4.  Treatment of hypertension in metabolic syndrome: implications of recent clinical trials.

Authors:  Amgad N Makaryus; Philippe Akhrass; Samy I McFarlane
Journal:  Curr Diab Rep       Date:  2009-06       Impact factor: 4.810

Review 5.  The role of irbesartan in the treatment of patients with hypertension: a comprehensive and practical review.

Authors:  Claudio Borghi; Arrigo F G Cicero
Journal:  High Blood Press Cardiovasc Prev       Date:  2012-03-01

Review 6.  A comprehensive review on metabolic syndrome.

Authors:  Jaspinder Kaur
Journal:  Cardiol Res Pract       Date:  2014-03-11       Impact factor: 1.866

7.  Pharmacogenetic landscape of Metabolic Syndrome components drug response in Tunisia and comparison with worldwide populations.

Authors:  Haifa Jmel; Lilia Romdhane; Yosra Ben Halima; Meriem Hechmi; Chokri Naouali; Hamza Dallali; Yosr Hamdi; Jingxuan Shan; Abdelmajid Abid; Henda Jamoussi; Sameh Trabelsi; Lotfi Chouchane; Donata Luiselli; Sonia Abdelhak; Rym Kefi
Journal:  PLoS One       Date:  2018-04-13       Impact factor: 3.240

8.  HDL Glycoprotein Composition and Site-Specific Glycosylation Differentiates Between Clinical Groups and Affects IL-6 Secretion in Lipopolysaccharide-Stimulated Monocytes.

Authors:  Sridevi Krishnan; Michiko Shimoda; Romina Sacchi; Muchena J Kailemia; Guillaume Luxardi; George A Kaysen; Atul N Parikh; Viviane N Ngassam; Kirsten Johansen; Glenn M Chertow; Barbara Grimes; Jennifer T Smilowitz; Emanual Maverakis; Carlito B Lebrilla; Angela M Zivkovic
Journal:  Sci Rep       Date:  2017-03-13       Impact factor: 4.379

9.  Metabolic syndrome patient compliance with drug treatment.

Authors:  Nilcéia Lopes; Antonio Carlos Zanini; Antonio Casella-Filho; Antonio Carlos Palandri Chagas
Journal:  Clinics (Sao Paulo)       Date:  2008-10       Impact factor: 2.365

10.  Effect of the angiotensin receptor blocker irbesartan on metabolic parameters in clinical practice: the DO-IT prospective observational study.

Authors:  Klaus G Parhofer; Felix Münzel; Michael Krekler
Journal:  Cardiovasc Diabetol       Date:  2007-11-27       Impact factor: 9.951

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.