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2008 Clinical Practice Guidelines - Canadian Diabetes Association

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Pharmacotherapy<br />

Pharmacotherapy for overweight people with diabetes not<br />

only improves glycemic control, but also results in a significant<br />

reduction in the doses of antihyperglycemic agents (26).<br />

Pharmacotherapy is an acceptable adjunct in the short- and<br />

long-term management of obesity when lifestyle measures<br />

fail to achieve the desired weight loss after an adequate trial<br />

of 3 to 6 months (20,35). Pharmacotherapy can be considered<br />

for people with BMI ≥30.0 kg/m 2 with no obesityrelated<br />

comorbidities or risk factors, or BMI ≥27.0 kg/m 2<br />

with obesity-related comorbidities or risk factors (20).<br />

Antiobesity drug therapy may be considered as an adjunct to<br />

nutrition therapy, physical activity and behaviour modification<br />

to achieve a target weight loss of 5 to 10% of initial body<br />

weight and for weight maintenance (20,35).<br />

Two medications, orlistat and sibutramine, have been<br />

approved in Canada for long-term management of obesity<br />

(Table 4). Drug therapy leads to even greater weight loss<br />

when coupled with lifestyle intervention and behaviour modification<br />

therapy. Both drugs have been shown to be effective<br />

in obese people with type 2 diabetes, improving glycemic and<br />

metabolic control, and resulting in favourable changes in lipid<br />

levels, BP profile and fat distribution (26,36,37). In obese<br />

people with impaired glucose tolerance (IGT), orlistat also<br />

improves glucose tolerance and reduces the progression to<br />

type 2 diabetes (38). <strong>Clinical</strong> trials with antiobesity agents<br />

have confirmed a smaller degree of weight loss in people with<br />

diabetes compared with obese people who do not have diabetes<br />

(14,26).<br />

When pharmacotherapy is being considered in the treatment<br />

of the obese or overweight person with type 2 diabetes,<br />

the choice of drug should be based on the individual’s<br />

CV risk profile, dietary habits and concomitant disease(s).<br />

People with irregular eating habits, such as those who “snack”<br />

frequently, may be better suited to sibutramine therapy<br />

because of its long-acting satiety-enhancing properties.<br />

Combining orlistat and sibutramine therapy is not advocated<br />

for clinical use. Sibutramine should be avoided in patients<br />

with ischemic heart disease, congestive heart failure or other<br />

major cardiac disease. Orlistat should be avoided in patients<br />

with inflammatory or other chronic bowel disease.<br />

Other available antiobesity drugs, such as diethylpropion<br />

and phentermine, are sympathomimetic noradrenergic<br />

appetite suppressants that are approved only for short-term<br />

use of a few weeks. They are not recommended because of<br />

modest efficacy and frequent adverse side effects.<br />

Currently, a number of new molecular entities that target<br />

receptors and metabolic processes relevant to energy<br />

metabolism are being developed for the treatment of obesity.<br />

Among these emerging strategies, cannabinoid type 1<br />

receptor antagonists currently appear to be the most promising<br />

(39).<br />

Surgery<br />

Individuals who are candidates for surgical procedures<br />

should be carefully selected after evaluation by an interdisciplinary<br />

team with medical, surgical, psychiatric and nutritional<br />

expertise. Surgery is usually reserved for people with<br />

class III obesity (BMI ≥40.0 kg/m 2 ), or class II obesity<br />

(BMI=35.0–39.9 kg/m 2 ) in the presence of comorbidities<br />

(40) and the inability to achieve weight-loss goals following<br />

an adequate trial of lifestyle intervention. Long-term, if not<br />

lifelong, medical surveillance after surgical therapy is necessary<br />

for most people. Preferred surgical options for weight<br />

loss include laparoscopic vertical banded gastroplasty and<br />

laparoscopic Roux-en-Y gastric bypass (41-43).<br />

Table 4. Medications approved for the treatment of obesity in type 2 diabetes<br />

Class Generic (trade)<br />

name<br />

Gastrointestinal lipase<br />

inhibitor<br />

Norepinephrine and<br />

serotonin reuptake<br />

inhibitor<br />

Recommended<br />

regimen<br />

orlistat (Xenical) 120 mg TID (during or<br />

up to 1 hour after each<br />

meal)<br />

sibutramine (Meridia) 10–15 mg OD<br />

(in the morning)<br />

Action Adverse<br />

effects<br />

• Nonsystemic pancreatic<br />

lipase inhibitor<br />

that exerts its therapeutic<br />

activity in the<br />

stomach and gastrointestinal<br />

tract by<br />

reducing dietary fat<br />

digestion and absorption<br />

by about 30%<br />

• Reduces food intake<br />

by enhancing satiety<br />

• May increase thermogenesis<br />

• May prevent decline<br />

in energy expenditure<br />

with weight loss<br />

• Abdominal bloating,<br />

pain and cramping<br />

• Steatorrhea<br />

• Fecal incontinence<br />

• Xerostomia<br />

• Increase heart rate<br />

and blood pressure<br />

• Constipation<br />

• Dizziness<br />

S79<br />

MANAGEMENT

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