Doctors are watching how certain medicines affect the livers of children and adolescents. A recent look at three studies found a small connection between atypical antipsychotics and metabolic dysfunction-associated steatotic liver disease. These drugs are often used for mental health conditions. The review also noted that these medicines can raise obesity risks and cause liver toxicity in some cases. Risperidone specifically was linked to liver injury in the data. Using these drugs with more severe liver disease was also reported. The team looked at English language studies published between 1950 and 2020. They gathered data from 407 articles but only three met the strict rules for inclusion. The follow-up period covered 216 months. This long view helps understand long-term effects. However, the studies varied greatly in how they were done. Some had fair ratings while others were good. This mix makes it hard to draw firm conclusions. The results need careful interpretation because of these differences. This work serves as a foundation for future studies. It may help reform clinical guidelines for using these drugs in young people. The goal is to ensure patient safety while treating mental health issues.
Systematic review finds weak link between atypical antipsychotics and MASLD in youthAtypical antipsychotics show a small link to liver disease in young patients
AI-generated summary of the cited source, checked by automated accuracy review. How we work
This systematic review and meta-analysis, including 3 studies from English-language literature published between 1950 and 2020, investigated the association between atypical antipsychotic (AAP) use and metabolic dysfunction-associated steatotic liver disease (MASLD) in children and adolescents younger than 18 years. The review initially retrieved 407 articles, but only 3 met inclusion criteria.
The primary outcome showed a small and statistically insignificant positive association between AAP exposure and MASLD. Secondary outcomes indicated increased obesity-related risks, risperidone-induced hepatotoxicity, and more severe MASLD with psychotropic use. However, pooled effect sizes and confidence intervals were not reported.
Key limitations include significant heterogeneity among the included studies, risk of bias ratings varying from fair to good, and the small number of studies (only 3). The authors note that these results require careful interpretation due to the heterogeneity.
The authors suggest the findings may serve as a foundation for future studies, assist in devising interventions, and potentially help reform clinical guidelines for using AAP in children and adolescents to ensure patient safety. However, given the weak evidence, no changes to current practice are warranted based on this review alone.