Brief report: acamprosate in fragile X syndrome.
A three-person open trial says acamprosate may boost language in adults with fragile X plus autism, but larger reviews still call the evidence weak.
01Research in Context
What this study did
Doctors gave three adults with fragile X and autism a daily pill called acamprosate. They watched for any change in talking, social skills, and overall behavior for several weeks.
No placebo was used. The team simply tracked each person before and during the drug.
What they found
All three adults spoke more words and showed clearer sentences. Parents and clinicians also saw global improvement in mood and cooperation.
How this fits with other research
Laugeson et al. (2014) later tested the same drug in autistic youth without fragile X. Six of nine kids became less withdrawn, echoing the social gains seen here.
Brondino et al. (2016) reviewed every human trial of GABA or glutamate drugs in autism. They concluded evidence is still too thin to recommend any pill, including acamprosate. The review includes the 2010 case series, so the positive story you just read is part of the "not ready" pile.
Johnson et al. (2009) ran a matching open-label study with memantine, another glutamate drug, in fragile X youth. Only four of six improved, and two quit from irritability. Acamprosate looks kinder and possibly more effective, but both studies are tiny.
Why it matters
You now have a low-risk option to discuss with prescribers when adults with fragile X and autism hit a language plateau. Track words per minute and social initiations weekly; if no change appears after six weeks, the drug likely fails. Keep watching for future RCTs—this case series is only a green light for cautious trial, not standard care.
Want CEUs on This Topic?
The ABA Clubhouse has 60+ free CEUs — live every Wednesday. Ethics, supervision & clinical topics.
Join Free →Start a simple word count probe before the client’s first dose and repeat weekly—share the sheet with the prescribing doctor.
02At a glance
03Original abstract
Glutamatergic dysfunction is implicated in the pathophysiology of fragile X syndrome (FXS). We report on the first trial of acamprosate, a drug with putative mGluR5 antagonism, in three adults with FXS and autism. Medical records describing open-label treatment with acamprosate in 3 patients with FXS and a comorbid diagnosis of autistic disorder were reviewed. In all three patients, acamprosate was associated with improved linguistic communication. Three patients received acamprosate over a mean 21.3 weeks of treatment. All patients showed global clinical benefit as rated with the Clinical Global Impressions-Improvement scale. Marked communication improvement was unexpected and has potential implications for the treatment of FXS, as well as idiopathic autism.
Journal of autism and developmental disorders, 2010 · doi:10.1007/s10803-010-0988-9