Parallel age‐related cognitive effects in autism: A cross‐sectional replication study. Issue 3 (4th December 2021) - Torenvliet, Carolien
Abstract: Findings on age‐related cognitive effects in autism in adulthood are inconsistent across studies. As these studies substantially differ in their methodology, replication studies are needed. In this replication study frequentist (i.e., null‐hypothesis significance testing), and Bayesian statistics were used to investigate the hypothesis that in autistic adults compared to non‐autistic adults mostly parallel, but also protective age‐related cognitive effects can be observed. Participants were 88 autistic adults, and 88 non‐autistic matched comparisons (age range: 30–89 years, mean age: 55 years). Cognitive measures were administered on the following six domains: verbal memory, visual memory, working memory, Theory of Mind (ToM), verbal fluency, and processing speed, and self‐reported cognitive failures. Non‐autistic adults outperformed autistic adults on ToM, verbal fluency, and verbal memory, but only the first two were confirmed with Bayesian replication analyses. Also, more cognitive failures were reported by autistic adults. No interactions between group and age were observed, suggesting a parallel age‐related effect on all cognitive domains. In sum, previously observed difficulties in ToM and verbal fluency were replicated which seem to persist at older age. Previously reported parallel age‐related cognitive patterns were replicated, yet no evidence for protective age‐related patterns was found. Lay summary: We investigated whether our previous findings on cognitive aging in autism could be confirmed in a new study measuring the cognitive effects of age in autistic and non‐autistic adults. As expected, tasks that younger autistic adults had difficulties with (theory of mind, fluency) were also difficult for older autistic adults, and the effect of age itself was similar in autistic and non‐autistic adults. Unexpectedly, we observed no protective effects (less cognitive aging) in autism.