4.5 Article

Metformin add-on vs. antipsychotic switch vs. continued antipsychotic treatment plus healthy lifestyle education in overweight or obese youth with severe mental illness: results from the IMPACT trial

Journal

WORLD PSYCHIATRY
Volume 19, Issue 1, Pages 69-80

Publisher

WILEY
DOI: 10.1002/wps.20714

Keywords

Antipsychotics; weight gain; youth; obesity; metformin; antipsychotic switch; healthy lifestyle education; IMPACT

Categories

Funding

  1. NIMH [R01 MH080270, R01 MH080274, RR118535, R01 MH080325]
  2. Johns Hopkins Institute for Clinical and Translational Research [NIH UL1TR001079]
  3. National Institute of Health Clinical and Translational Science Award (CTSA) program at University of North Carolina [RR0046, UL1TR001111]
  4. Mid-Atlantic Nutrition Obesity Research Center [2P30DK072488-11]

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Antipsychotics are used for many psychiatric conditions in youth. Although developmentally inappropriate weight gain and metabolic abnormalities, which are risk factors for premature cardiovascular mortality, are especially frequent in youth, optimal strategies to reduce pediatric antipsychotic-induced overweight/obesity are unclear. The Improving Metabolic Parameters in Antipsychotic Child Treatment (IMPACT) was a randomized, parallel group, 24-week clinical trial which enrolled overweight/obese, psychiatrically stable youth, aged 8-19 years, with a DSM-IV diagnosis of severe mental illness (schizophrenia spectrum disorder, bipolar spectrum disorder or psychotic depression), at four US universities. All of them had developed substantial weight gain following treatment with a second-generation antipsychotic. The centralized, computer-based randomization system assigned participants to unmasked treatment groups: metformin (MET); antipsychotic switch (aripiprazole or, if already exposed to that drug, perphenazine or molindone; SWITCH); or continued baseline antipsychotic (CONTROL). All participants received healthy lifestyle education. The primary outcome was body mass index (BMI) z-score change from baseline, analyzed using estimated least squares means. Altogether, 127 participants were randomized: 49 to MET, 31 to SWITCH, and 47 to CONTROL. BMI z-score decreased significantly with MET (week 24: -0.09 +/- 0.03, p=0.002) and SWITCH (week 24: -0.11 +/- 0.04, p=0.003), while it increased non-significantly with CONTROL (week 24: +0.04 +/- 0.03). On 3-way comparison, BMI z-score changes differed significantly (p=0.001). MET and SWITCH were each superior to CONTROL (p=0.002), with effect sizes of 0.68 and 0.81 respectively, while MET and SWITCH did not differ. More gastrointestinal problems occurred in MET than in SWITCH or CONTROL. The data safety monitoring board closed the perphenazine-SWITCH arm because 35.2% of subjects discontinued treatment due to psychiatric worsening. These data suggest that pediatric antipsychotic-related overweight/obesity can be reduced by adding metformin or switching to a lower risk antipsychotic. Healthy lifestyle education is not sufficient to prevent ongoing BMI z-score increase.

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