Abstract

BackgroundGenetically determined Intellectual Disability (ID) is an intractable condition that involves severe impairment of mental abilities such as learning, reasoning and predicting the future. As of today, little is known about the placebo response in patients with ID.ObjectiveTo determine if placebo response exists in patients with genetically determined ID.Data sources and Study selectionWe searched Medline/PubMed, EMBASE, CENTRAL and PsycINFO to find all placebo-controlled double-blind randomized clinical trials (RCTs) in patients with genetically determined ID, published up to April 2013, focusing on core ID symptoms.Data extraction and synthesisTwo investigators extracted outcome data independently.Main outcomes and measuresBias-corrected standardized mean difference (Hedge’s g) was computed for each outcome measure, using the Comprehensive Meta-Analysis software. A priori defined patient sub-groups were analyzed using a mixed-effect model. The relationship between pre-defined continuous variable moderators (age, IQ, year of publication and trial duration) and effect size was analyzed using meta-regressionResultsTwenty-two placebo-controlled double-blind RCTs met the inclusion criteria (n = 721, mean age = 17.1 years, 62% men, mean trial duration = 35 weeks). There was a significant overall placebo response from pre- to post-treatment in patients with ID (g = 0.468, p = 0.002), both for “subjective outcomes” (a third-person’s evaluation of the patient) (g = 0.563, p = 0.022) and “objective outcomes” (direct evaluation of the patient’s abilities) (g = 0.434, p = 0.036). Individuals with higher IQ had higher response to placebo (p = 0.02) and no placebo response was observed in ID patients with comorbid dementia. A significant effect of age (p = 0.02) was found, indicating higher placebo responses in treatment of younger patients.Conclusions and relevanceResults suggest that patients with genetically determined ID improve in the placebo arm of RCTs. Several mechanisms may contribute to placebo effects in ID, including expectancy, implicit learning and “placebo-by-proxy” induced by clinicians/family members. As the condition is refractory, there is little risk that improvements are explained by spontaneous remission. While new avenues for treatment of genetically determined ID are emerging, our results demonstrate how contextual factors can affect clinical outcomes and emphasize the importance of being vigilant on the role of placebos when testing novel treatments in ID.

Highlights

  • Intellectual Disability (ID) is characterized by deficits in intellectual functions, such as reasoning, abstract thinking, judgment and learning from experience

  • Individuals with higher IQ had higher response to placebo (p = 0.02) and no placebo response was observed in ID patients with comorbid dementia

  • Results suggest that patients with genetically determined ID improve in the placebo arm of randomised controlled trials (RCTs)

Read more

Summary

Introduction

Intellectual Disability (ID) is characterized by deficits in intellectual functions, such as reasoning, abstract thinking, judgment and learning from experience. Genetic causes of ID include visible chromosomal anomalies (such as Down’s syndrome, which is the most frequent aneuploidy), chromosomal microdeletion (including Prader-Willi and Williams’ syndrome) and monogenic diseases (such as mutation of the gene FMR1 leading to Fragile X syndrome). None of these disorders improve spontaneously over time. In spite of the emerging interest in cognitive improvement in ID, little is known about patients’ ability to improve core ID symptoms as a response to placebo treatment. Little is known about the placebo response in patients with ID

Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call