Final Dissertation Defense Announcement
STUDENTNAME:
Jiwandeep Kohli,M.A., M.S
COMMITTEECHAIRPERSON:
RuthCarper, Ph.D., Research Associate Professor, Department of Psychology, SDSU
COMMITTEEMEMBERS:
Martin Sereno, Ph.D., Professor, Department of Psychology,SDSU
Carrie McDonald, Ph.D., Professor in Residence, Departmentof Psychiatry, UC San Diego
Jonathan Helm, Ph.D., Associate Professor, Department ofPsychology, SDSU
Lisa Delano-Wood, Ph.D., Adjunct Professor, Department ofPsychiatry, UC San Diego
TITLE OFDISSERTATION:
Characterizing Groupwise andIdiosyncratic Anomalies of Cortical Architecture and Links to Behavior inAdults with Autism Spectrum Disorder
DATE OFDEFENSE: Friday, June 2, 2023
TIME OF DEFENSE:12:00 PM PST
LOCATIONOF DEFENSE: See Program
ABSTRACT
Rationale: Autism Spectrum Disorder (ASD) is a highlyheterogeneous condition in terms of etiology, symptomatology, and severity. Ourexisting understanding of ASD derives mainly from research in children andyoung adults, with little known about neurobiological, cognitive, andbehavioral changes later in life. This three-paper dissertation aimed tocharacterize changes in cortical architecture across middle to older age in ASDand determine how differences relate to cognition and behavior.
Design and Results: Data were drawn from an ongoing studyof adults with ASD and typical comparison (TC) participants, aged 40-70 years. Study1 (nASD=20,nTC=21;mean age=50.51 years, SD=6.35; Kohli et al., 2019) examined cortical morphology,including cortical thickness (CT), surface area (SA), and local gyrificationindex (LGI). LGI, but not CT or SA, was regionally decreased bilaterally in theASD group. LGI also showed several correlations with executive function scoresin the ASD group.
Study 2 (nASD=30, nTC=36; mean age=51.50 years, SD=7.09) aimedto identify regionally varying differences in CT and gray-white contrast (GWC) usingboth group-wise and subject-specific analyses. CT did not differ significantlybetween groups using either approach. GWC did not differ in the group-wiseanalysis, but the ASD group showed a greater spatial extent of decreased GWC thancontrols in subject-specific analyses, along with associations betweendecreased GWC and ASD symptomatology and dysexecutive symptoms.
In the same sample, Study 3 examinedintracortical myelin content (MC). Groupwise analyses showed no group differencesin average MC or its associations with age. In subject-specific analyses,neuropsychological function differed between subgroups classified by presenceor absence of aberrant MC, with poorer performance in the ASD subgroup withatypically high MC in spatially heterogeneous regions.
Conclusions: LGI was the only cortical featuredemonstrating differences in ASD when examining group level averages, butsubject-specific analyses revealed an additional decrease in GWC, along withbroad associations between both GWC and MC and neuropsychological function. These complementary approaches demonstratethe importance of accounting for increasing sources of heterogeneity whenstudying adults with ASD and provide preliminary insights into links betweenbrain structure and behavior in the second half of the lifespan in ASD.