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ORIGINAL ARTICLE
Effects of sibutramine on abdominal fat mass, insulin resistance and blood pressure in obese hypertensive patients
A. N. Faria 1*, F. F. Ribeiro Filho 1 , N. E. Kohlmann 1 , S. R. Gouvea Ferreira 1 and M. T. Zanella 1
  1 Endocrinology and Nephrology Divisions, Hospital do Rim e da Hipertensão, Universidade Federal de São Paulo, São Paulo, Brazil
Correspondence to   *Alessandra Nunes Faria, Luxemburglaan 783, Heemskerk, 1966 MS, The Netherlands.
E-mail:
ale_faria@uol.com.br
Copyright Blackwell Science, 2005
KEYWORDS
hypertension • insulin resistance • sibutramine

ABSTRACT

Objective: The objective of this study is to assess the effects of sibutramine on body weight, body fat distribution, insulin resistance, plasma leptin, lipid profile and blood pressure profiles in hypertensive obese patients.

Methods: Eighty-six central obese hypertensive patients (BMI = 39 ± 5 kg/m2, 84% of women, 48 ± 8.5 years old) were placed on a hypocaloric diet and placebo therapy for 4 weeks. They were then randomized to receive sibutramine (10 mg) or placebo for 24 weeks. Both, before therapy and at the end of the study, the waist and hip circumferences were measured and the waist/hip ratio (WHR) was calculated; abdominal ultrasonography was performed in order to estimate the amount of subcutaneous fat (SF) and visceral fat (VF), and the visceral/subcutaneous ratio. Beyond HOMA-r, another insulin resistance index (IRIp) was calculated by means of the formula: peak of blood glucose after oral glucose load × plasma insulin level/104. Fasting plasma leptin and lipid levels were also determined.

Results: Sibutramine induced greater weight reduction than placebo (6.7 vs. 2.5%, p < 0.001). Reductions in WHR (0.97 ± 0.08 vs. 0.94 ± 0.07, p < 0.01), IRIp (0.11 ± 0.07 vs. 0.09 ± 0.06 mmol μ/l2) and VF (6.4 ± 2.4–6.0 ± 2.4 cm, p < 0.01) were observed only with sibutramine. Plasma leptin decreased with placebo (24 ± 15 vs. 18 ± 10 UI/l, p < 0.01), but not with sibutramine (18.8 ± 8.4 vs. 18.2 ± 13.2 UI/l). No clinically significant change in lipid profile was observed in both groups. Moreover, office and 24-h blood pressure values did not change during placebo or sibutramine therapy, whereas a significant increase in office heart rate, from 78.3 ± 7.3–82 ± 7.9 b.p.m., p = 0.02, was observed with sibutramine.

Conclusions: Sibutramine therapy induced greater body weight loss than placebo in hypertensive obese patients. This was associated with WHR reduction, decreases in VF and insulin resistance. The maintenance of leptin levels during sibutramine therapy may be important to avoid weight recovery, although this finding must be confirmed by other prospective studies.


Received 19 June 2004; returned for revision 16 September 2004; revised version accepted 6 October 2004

DIGITAL OBJECT IDENTIFIER (DOI)
10.1111/j.1463-1326.2005.00465.x About DOI

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