| Literature DB >> 18782869 |
Gilbert P August1, Sonia Caprio, Ilene Fennoy, Michael Freemark, Francine R Kaufman, Robert H Lustig, Janet H Silverstein, Phyllis W Speiser, Dennis M Styne, Victor M Montori.
Abstract
OBJECTIVE: Our objective was to formulate practice guidelines for the treatment and prevention of pediatric obesity.Entities:
Mesh:
Substances:
Year: 2008 PMID: 18782869 PMCID: PMC6048599 DOI: 10.1210/jc.2007-2458
Source DB: PubMed Journal: J Clin Endocrinol Metab ISSN: 0021-972X Impact factor: 5.958
Screening tests for the more common obesity comorbidities
| Comorbidity | Case detection tests (abnormal values) |
|---|---|
| Prediabetes | |
| Impaired fasting plasma glucose (verify fasting status) | Fasting plasma glucose (>100 mg/dl) |
| Impaired glucose tolerance (if OGTT is used) | 2-h glucose > 140 but < 200 mg/dl |
| Diabetes mellitus | Fasting plasma glucose > 126 mg/dl, or random value > 200 mg/dl (if OGTT used, 2-h glucose > 200) |
| If asymptomatic, must have repeat abnormal values on another occasion | |
| Dyslipidemia | Fasting (12–14 h) lipids |
| Triglycerides: >110 mg/dl (75th percentile); ≥160 mg/dl (90th percentile) | |
| LDL cholesterol: ≥110 mg/dl (75th percentile); ≥130 mg/dl (90th percentile) | |
| Total cholesterol: ≥180 mg/dl (75th percentile); ≥200 mg/dl (90th percentile) | |
| HDL cholesterol: ≤35 mg/dl (10th percentile); ≤40 mg/dl (25th percentile) ( | |
| Hypertension | Blood pressure > 90th percentile (standardized according to sex, age, and height percentile) ( |
| NAFLD | ALT > 2 |
OGTT, Oral glucose tolerance test.
To convert mg/dl to mmol/liter, multiply by 0.0555 for glucose, 0.0259 for cholesterol, and 0.0113 for triglycerides.
A proposed refinement of these abnormal lipid levels has the potential advantage of linking adolescents’ lipid levels to those of adults (81).
FIG. 1Diagnosis and management flow chart. *, See Section 3.2 and the Table 2 legend for criteria for the selection of candidates for pharmacotherapy. †, See Section 3.3 for criteria for the selection of candidates for bariatric surgery.
Medications proposed for the treatment of obesity1
| Drug | Dosage | Side effects | Monitoring and contraindications |
|---|---|---|---|
| Sibutramine ( | 5–15 mg PO daily | Tachycardia, hypertension, palpitations, insomnia, anxiety, nervousness, depression, diaphoresis | Monitor HR, BP. Do not use with other drugs, MAO inhibitors. |
| Orlistat ( | 120 mg PO tid | Borborygmi, flatus, abdominal cramps, fecal incontinence, oily spotting, vitamin malabsorption | Monitor 25OHD3 levels. MVI supplementation is strongly recommended. A lower dose preparation has been approved for over-the-counter sale. |
| Metformin, | 250–1000 mg PO bid | Nausea, flatulence, bloating, diarrhea; usually resolves. Lactic acidosis not yet reported in children. | Do not use in renal failure or with iv contrast. MVI supplementation is strongly recommended. |
| Octreotide, | 5–15 μg/kg/d sc divided tid | Cholelithiasis (can be prevented by concurrent ursodiol), diarrhea, edema, abdominal cramps, nausea, bloating, reduction in T4 concentrations, decreased GH but normal IGF-I. | Monitor fasting glucose, FT4, HbA1c. Useful only for hypothalamic obesity. Ursodiol coadministration is strongly recommended. |
| Leptin, | Titration of dose to serum levels, sc | Local reactions | Useful |
| Topiramate, | 96–256 mg/d PO | Paresthesias, difficulty with concentration/attention, depression, difficulty with memory, language problems, nervousness, psychomotor slowing | No pediatric data. |
| GH, | 1–3 mg/m2 sc daily | Edema, carpal tunnel syndrome, death in patients with preexisting obstructive sleep apnea |
|
MVI, Multivitamins; PO, by mouth; tid, three times daily; bid, twice daily; HR, heart rate; BP, blood pressure, MAO, monoamine oxidase; 25OHD3, 25-hydroxyvitamin D3; FT4, free T4; HbA1c, glycosylated hemoglobin.
Pharmacotherapy is not usually considered if the BMI is below the 95th percentile, but there are additional factors to consider. If we initiate pharmacotherapy early in the course of obesity, we may prevent severe weight gain and metabolic complications, but we may treat an excess of children, raise the rate of unwarranted side effects, and increase the costs to individuals and to society. Alternatively, if we begin medication late in the course of obesity, we run the risk of runaway weight gain and long-term morbidity. One approach that reconciles these difficulties is to act aggressively with lifestyle intervention in overweight and mildly obese patients to prevent severe obesity and to consider pharmacotherapy when the risk of complications is high or soon after complications emerge. The tipping point for pharmacotherapy could be if the family history is strongly positive for a major comorbidity. Lifestyle intervention should precede pharmacotherapy and should be maintained during pharmacotherapy.
The use of these non-FDA-approved agents should be restricted to large, well-controlled studies.