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Database analysis of children and adolescents with bipolar disorder consuming a micronutrient formula

Julia J Rucklidge1, Dermot Gately, Bonnie J Kaplan

  • 1Department of Psychology, University of Canterbury, Christchurch, New Zealand. julia.rucklidge@canterbury.ac.nz

BMC Psychiatry
|September 30, 2010
PubMed

Insights

A 36-ingredient micronutrient formula showed significant symptom reduction in children with pediatric bipolar disorder (PBD) and Attention-Deficit/Hyperactivity Disorder (ADHD). This nutritional intervention may allow for reduced psychiatric medication use.

Area of Science:

  • Nutritional Psychiatry
  • Pediatric Mental Health
  • Micronutrient Research

Background:

  • Previous studies indicated benefits of a 36-ingredient micronutrient formula (EMPowerplus) for psychiatric symptoms.
  • The current study investigated its efficacy in children aged 7-18 with pediatric bipolar disorder (PBD).
  • The impact of co-occurring Attention-Deficit/Hyperactivity Disorder (ADHD) was also assessed.

Purpose of the Study:

  • To evaluate the therapeutic potential of a specific micronutrient formula for children diagnosed with PBD.
  • To determine if the presence of ADHD influences the response to micronutrient treatment in PBD patients.
  • To assess the safety and potential for medication reduction associated with micronutrient supplementation.

Main Methods:

  • Analysis of existing database records for 120 children with reported PBD diagnoses.
  • Data included children on psychiatric medications and those with comorbid ADHD.
  • Micronutrient use data from 3 to 6 months were analyzed using Last Observation Carried Forward (LOCF).

Main Results:

  • Mean PBD symptom severity decreased by 46% (ES=0.78, p<0.001) at LOCF.
  • 46% of participants showed >50% symptom improvement; psychiatric medication use decreased by 74%.
  • Children with comorbid ADHD (n=41) also showed significant symptom reductions in both PBD (43%) and ADHD (40%).

Conclusions:

  • Micronutrient supplementation demonstrated potential therapeutic benefits for children with PBD, with or without ADHD.
  • The observed symptom improvements and reduced medication needs suggest a favorable safety profile.
  • Results support the need for randomized clinical trials to establish definitive efficacy.
Abstract

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