Withdrawal of sibutramine for weight loss: where does this leave clinicians?

As has been well documented, the disorders of overweight and obesity currently affect more than 1.1 billion people worldwide [1]. In several developed countries more than two thirds of adults are overweight, as defined by a BMI in excess of 25 kg/m. Recent data from selected European countries and in the USA may signal a plateau in the prevalence of overweight or obesity, or even a decrease [2–5] – observations that warrant further testing in other populations as they could have very real consequences for preventative and curative health planning [6]. This notwithstanding, health practitioners still have to legislate for a considerable health burden associated with the present cohort of obese or extremely obese individuals. Thus, the present challenge is to implement preventative strategies at a population level, but also, crucially, to treat those who need to lose weight using behavioural modification, with or without pharmacological intervention or batriatric surgery. The cornerstone of non-pharmacological weight loss interventions is modification in energy intake and expenditure; however, the evidence for this approach is somewhat disappointing. A recent overview of 43 trials comprising 3,476 adult participants concluded that, when compared with no treatment, exercise resulted in some weight loss. In conjunction with dietary change, a greater weight reduction was apparent than for diet alone [7] although, again, the impact was small (weighted mean difference: –1.0 kg; 95% confidence interval (CI): –1.3 to –0.7 kg). Until quite recently, the most widely used pharmacological alternatives, or adjuncts to lifestyle change, were orlistat (a gastrointestinal lipase inhibitor) [8], rimonabant (an endocanabinoid receptor inhibitor) [9], and sibutramine (a norepinephrine and serotonin re-uptake inhibitor) [10]. Randomised trials have demonstrated that, relative to placebo, these drugs are associated with a marked weight loss in both adults and adolescents in the range of 3 to 5 kg [11–13]. Amidst some reports that sibutramine was having unfavourable effects on blood pressure and resting heart rate, the manufacturer, Abbott Laboratories, commenced SCOUT (Sibutramine Cardiovascular Outcome Trial) in 9,800 overweight or obese persons who were also at high cardiovascular disease (CVD) risk [14–16]. Although the final results are not yet published, the European Medicines Agency (EMA) was informed by the study’s Data Safety Monitoring Board of the preliminary results. The evidence was that, following 6-year follow-up of trial participants, the rate of serious CVD events was higher in trial members taking sibutramine compared to those treated with the placebo. Accordingly, following review, on January 21, 2010 the EMA reasoned that the risks of sibutramine outweighed the benefits (www.ema.europa.eu/ pdfs/human/referral/sibutramine/3940810en.pdf) and recommended the removal of sibutramine from all markets in the European Union. In detail, the EMA chose to suspend the drug because of i) the potential for raised CVD risk in obese patients, ii) a marginal weight loss compared to placebo, and iii) a lack of data on weight loss maintenance after drug cessation. This decision is somewhat debatable. Before the early results from SCOUT emerged, as described, it was already known that sibutramine had an unfavourable influence on selected CVD risk factors. Hence, while still on the market, sibutramine was contra-indicated in patients with existing CVD. The weight loss of 2–4 kg obtained with using sibutramine is similar to that seen with drugs still available (orlistat). Finally, as for other weight loss drugs, cessation of treatment is followed by weight regain. *G. David Batty is a Welcome Trust Research Fellow