Literature DB >> 15383188

The ORLIstat and CArdiovascular risk profile in patients with metabolic syndrome and type 2 DIAbetes (ORLICARDIA) Study.

T P Didangelos1, A K Thanopoulou, S H Bousboulas, C L Sambanis, V G Athyros, E A Spanou, K C Dimitriou, S I Pappas, B G Karamanos, D T Karamitsos.   

Abstract

BACKGROUND: Metabolic syndrome (MetSyn) is associated with a marked increase in the risk of cardiovascular disease, especially in patients with type 2 diabetes mellitus (DM). AIM: To investigate the effect of orlistat plus hypocaloric diet (HCD) vs HCD alone on the cardiovascular risk profile in patients with both MetSyn (National Cholesterol Educational Program--NCEP--Adult Treatment Panel III definition) and type 2 DM.
METHODS: This was a prospective, multicentre, open-label, randomized, controlled study. One hundred and twenty-six patients, free of cardiovascular disease at baseline, were included in the final analysis. Ninety-four (73%) patients were treated with orlistat (360 mg/day) and HCD for a 6-month period, while 34 (27%) were on HCD alone. Analysis of covariance was used to assess differences between the treatment groups over time. MAIN OUTCOME MEASURES: Components of the MetSyn criteria assessed were: waist circumference; systolic and diastolic blood pressure; fasting glucose, triglycerides; high-density lipoprotein cholesterol (HDL-C) plus body mass index; glycosylated haemoglobin (HbA1C); homeostasis model for assessment of insulin resistance (HOMA) index; and total and low-density lipoprotein cholesterol (LDL-C).
RESULTS: By protocol, all patients had MetSyn at baseline. After a 6 month treatment period there were significant differences between the orlistat plus HCD vs the HCD-alone groups in body weight (p = 0.0001), waist circumference (p < 0.0001), fasting glucose (p < 0.0001), HbA(1C) (p < 0.0001), systolic blood pressure (p = 0.024), total cholesterol (p < 0.0001), LDL-C (p = 0.034), and HOMA index (p = 0.022), while there were no significant differences in triglycerides and HDL-C. Orlistat was well tolerated. By the end of the study, 65% of the patients on orlistat plus HCD were still meeting the MetSyn criteria and 41% had four to five MetSyn components vs 91% (p < 0.0001) and 53% (p = 0.017), respectively, of those on HCD alone.
CONCLUSIONS: Orlistat plus HCD favourably modified several cardiovascular risk factors in patients with both MetSyn and type 2 DM. These effects might partly offset the excess cardiovascular risk and improve outcome in this patient population.

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Year:  2004        PMID: 15383188     DOI: 10.1185/030079904125004466

Source DB:  PubMed          Journal:  Curr Med Res Opin        ISSN: 0300-7995            Impact factor:   2.580


  14 in total

Review 1.  Orlistat: Current issues for patients with type 2 diabetes.

Authors:  Juliet M Mancino
Journal:  Curr Diab Rep       Date:  2006-11       Impact factor: 4.810

Review 2.  Orlistat-associated adverse effects and drug interactions: a critical review.

Authors:  Theodosios D Filippatos; Christos S Derdemezis; Irene F Gazi; Eleni S Nakou; Dimitri P Mikhailidis; Moses S Elisaf
Journal:  Drug Saf       Date:  2008       Impact factor: 5.606

3.  Editor's perspective on metabolic syndrome for 2008.

Authors:  I Jialal
Journal:  Metab Syndr Relat Disord       Date:  2008-06       Impact factor: 1.894

Review 4.  Management of Dyslipidemia in Patients with Hypertension, Diabetes, and Metabolic Syndrome.

Authors:  Sundararajan Srikanth; Prakash Deedwania
Journal:  Curr Hypertens Rep       Date:  2016-10       Impact factor: 5.369

Review 5.  Orlistat: a review of its use in the management of obesity.

Authors:  Sheridan Henness; Caroline M Perry
Journal:  Drugs       Date:  2006       Impact factor: 9.546

6.  Current Treatment Options for the Metabolic Syndrome.

Authors:  Prakash C Deedwania; Natalia Volkova
Journal:  Curr Treat Options Cardiovasc Med       Date:  2005-05

Review 7.  Reversal and Remission of T2DM - An Update for Practitioners.

Authors:  Lina Shibib; Mo Al-Qaisi; Ahmed Ahmed; Alexander D Miras; David Nott; Marc Pelling; Stephen E Greenwald; Nicola Guess
Journal:  Vasc Health Risk Manag       Date:  2022-06-14

Review 8.  Adiposopathy is a more rational treatment target for metabolic disease than obesity alone.

Authors:  Harold Bays; Carlos A Dujovne
Journal:  Curr Atheroscler Rep       Date:  2006-03       Impact factor: 5.113

9.  Dyslipidaemia of obesity, metabolic syndrome and type 2 diabetes mellitus: the case for residual risk reduction after statin treatment.

Authors:  Vasilios G Athyros; Konstantinos Tziomalos; Asterios Karagiannis; Dimitri P Mikhailidis
Journal:  Open Cardiovasc Med J       Date:  2011-02-24

10.  Metabolic syndrome in the Mediterranean region: Current status.

Authors:  Panagiotis Anagnostis
Journal:  Indian J Endocrinol Metab       Date:  2012-01
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