Electrophysiological Endophenotypes and the Error-Related Negativity (ERN) in Autism Spectrum Disorder: A Family Study.
The error-related negativity is not a reliable family marker for autism, so stick with cheaper, proven screeners.
01Research in Context
What this study did
Ann et al. (2017) wired up kids and adults with and without autism. They measured the error-related negativity, a tiny brain wave that pops up right after a mistake. The goal was to see if this wave could serve as a family marker for autism.
What they found
The wave looked the same in both groups. No bigger, no smaller, no delayed timing. Because relatives also showed no special pattern, the team concluded the ERN is not a useful autism endophenotype.
How this fits with other research
Stevens et al. (2018) found a five-item checklist that does work for cheap screening. Their OERA gave 93 % sensitivity and 91 % specificity in kids aged 3–10. The ERN study used expensive EEG yet came up empty; the OERA used simple questions and succeeded.
Villa et al. (2010) already showed the PEP-R has solid reliability for kids under 12. Like the ERN paper, they asked “does this tool hold up?” The PEP-R passed; the ERN did not.
Nadwodny et al. (2025) and Dudley et al. (2019) tell the same story for LENA. One day of recording gives stable toddler data, but the algorithm fails in older kids. Together these papers warn: a fancy metric is only helpful if it survives real-world use.
Why it matters
Before you buy new EEG gear or add a neural marker to reports, pause. Quick rating scales like OERA or play-based tools like PEP-R already give actionable data for less money and time. Save the lab budget for clients who truly need neuro-assessment, not for routine screening.
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02At a glance
03Original abstract
We examined the error-related negativity (ERN) as an endophenotype of ASD by comparing the ERN in families of ASD probands to control families. We hypothesized that ASD probands and families would display reduced-amplitude ERN relative to controls. Participants included 148 individuals within 39 families consisting of a mother, father, sibling, and proband. Robust ANOVAs revealed non-significant differences in ERN amplitude and behavioral performance among ASD probands relative to control youth. In subsequent multiple regression analyses group and kinship (proband, sibling, mother, father) did not significantly predict ΔERN (error minus correct ERN) or behavioral performance. Results do not provide evidence for the ERN as an endophenotype of ASD. Future research is needed to examine state- or trait-related factors influencing ERN amplitudes in ASD.
Journal of autism and developmental disorders, 2017 · doi:10.1007/s10803-017-3066-8