We are proud to announce that JDP student Elizabeth Rangel (entering class of 2020) has been selected to participate in one of the Robert Wood […]
Congratulations to JDP student Zanjbeel Mahmood (entering class of 2017) for being awarded a 2021-22 American Association of University Women Dissertation Fellowship! “The purpose of […]
Congratulations to JDP student Chelsea Rapoport (entering class of 2020) for being chosen as the recipient of an APAGS/Psi Chi Junior Scientist Fellowship! This Fellowship […]
Congratulations to JDP student Laura Campbell (entering class of 2017) on receiving the 2021 Diana Jacobs Kalman/AFAR Scholarship for Research on the Biology of Aging! […]
The two recipients of 2021-2022 P.E.O. Scholar Awards, who were nominated by P.E.O. International’s local chapter in Rancho Santa Fe, are both from our clinical […]
We are proud to announce that JDP student Elizabeth Rangel (entering class of 2020)...
Congratulations to JDP student Zanjbeel Mahmood (entering class of 2017) for being...
Congratulations to JDP student Chelsea Rapoport (entering class of 2020) for being...
Congratulations to JDP student Laura Campbell (entering class of 2017) on receiving...
The two recipients of 2021-2022 P.E.O. Scholar Awards, who were nominated by P.E.O....
Final Dissertation Defense - Jiwandeep Kohli, M.A., M.S
June 2, 2023 12:00 pm - 1:00 pm
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.
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Final Dissertation Defense - Lily Kamalyan
June 8, 2023 12:00 pm - 1:00 pm See Program
STUDENT NAME: Lily Kamalyan
COMMITTEE CHAIRPERSON:
Igor Grant, M.D., Distinguished Professor, Department of Psychiatry, University of California San Diego
COMMITTEE MEMBERS:
Linda Gallo, Ph.D., Professor, Department of Psychology, San Diego State University
Jonathan Helm, Ph.D., Associate Professor, Department of Psychology, San Diego State University
Mariana Cherner, Ph.D., Professor, Department of Psychiatry, University of California San Diego
Tarik Benmarhnia, Ph.D., Associate Professor, Department of Family Medicine & Public Health, University of California San Diego
María Marquine, Ph.D., Associate Professor, Department of Medicine, Duke University
TITLE OF DISSERTATION: Associations between neighborhood vulnerabilities and neuropsychiatric outcomes during the COVID-19 pandemic among a diverse cohort of people aging with HIV
DATE OF DEFENSE: June 8th, 2023
TIME OF DEFENSE: 12pm PST
LOCATION OF DEFENSE: See Program
Rationale: Neighborhood factors adversely impact neurocognitive impairment and depression among older adults without HIV. These associations are unknown among diverse older people with HIV (PWH), who have higher rates of negative neuropsychiatric outcomes. COVID-19 repercussions disproportionally impacted vulnerable communities. We aimed to 1) examine associations between neighborhood characteristics and neurocognitive decline and worsened mood during the COVID-19 pandemic among older PWH, and 2) determine if the neighborhood impact of COVID- 19, as a severe community stressor, moderated these relationships.
Design: Participants were 180 PWH (60% non-Hispanic White, 24% Latino, 16% Black) 50+ years, enrolled in observational studies at the HIV Neurobehavioral Research Center. Seventy-nine PWH completed neuropsychiatric assessments at two time-points: (1) pre-COVID-19, March 2019-March 2020; and (2) March 2021-June 2022. Negative change in global mean scaled scores (GSS) reflected neurocognitive decline. Negative change in Medical Outcomes Study HIV Health Survey Mental Health Summary T- scores (MSS) indicated worsened mood. Exploratory factor analyses of publicly available census and satellite data created ‘Sociodemographic,’ ‘Economic,’ and ‘Undeveloped’ neighborhood factors. Cumulative COVID-19 cases rates per zip code reflected the neighborhood impact of COVID-19. Participants’ home addresses were geocoded and linked to neighborhood data. Multivariable linear regression models investigated relationships between neighborhood factors and changes in GSS and MSS, and the moderating effect of COVID-19 case rates.
Results: Average GSS change was 0.05 (SD=0.99) scaled score. Average MSS change was -1.76 (SD=6.91) T-score. Average COVID-19 case rate was 23%. ‘Sociodemographic,’ ‘Economic,’ and ‘Undeveloped’ factors were not significantly related to neurocognitive decline or worsened mood (ps > .05). COVID-19 cases did not significantly moderate neighborhood relationships with cognitive or emotional decline (ps>.05). Exploratory analyses suggested that living in neighborhoods with more crowded households was significantly related to decline in MSS (b = -0.45, p = .04), though not upheld after multiple imputation (b = -0.12, p = .49).
Conclusions: Neighborhood features did not relate to neurocognitive or emotional decline among older diverse PWH during a historically stressful time. Lack of substantial neuropsychiatric change may have contributed to null findings. Larger samples may elucidate how heterogenous environmental exposures relate to health outcomes for those vulnerable to neuropsychiatric decline.
Final Dissertation Defense - Joseph Happer, M.S.
June 12, 2023 12:00 pm - 2:00 pm See Program
STUDENT NAME: Joseph Happer, M.S.
Ksenija Marinkovic, Ph.D., Associate Professor, Department of Psychology, SDSU
Joanna Jacobus, Ph.D., Associate Adjunct Professor, Department of Psychiatry, UCSD Carrie McDonald, Ph.D., Professor in Residence, Department of Psychiatry, UCSD Marc Schuckit, Ph.D., Distinguished Professor, Department of Psychiatry, UCSD Martin Sereno, Ph.D., Professor Emeritus, Department of Psychology, SDSU
TITLE OF DISSERTATION: Examining the Spatio-Temporal Dynamics of Inhibitory Control in the Context of Attentional Processing, Genetic Variability, Risk for Alcohol Misuse, and Alcohol Challenge
DATE OF DEFENSE: Monday, June 12, 2023 TIME OF DEFENSE: 12:00PM
Rationale: Inhibitory control is an executive function essential for flexible and adaptive behavior. This 3-paper dissertation examined its spatio- (“where”) temporal (“when”) neural dynamics with inhibitory Go/NoGo paradigms. A multimodal anatomically- constrained magnetoencephalography (aMEG) method combined the temporal precision and distributed source modeling of MEG with structural MRI and provided insight into the anatomical distribution of the engaged areas and their functional interdependence.
Study 1 examined the relative contributions of attentional and inhibition-related processes using a modified Go/NoGo task in a cohort of healthy participants (N=26). Attentional capture was subserved by early activity within right-lateralized temporoparietal areas followed by activation of a “braking” network comprised of ventrolateral prefrontal areas responding specifically to inhibitory demands. Medial prefrontal areas supported integrative processing of inhibitory and attentional stimulus properties.
Study 2 explored how genetically-determined cortical dopamine availability in individuals genotyped for the COMT Val158Met polymorphism (Met/Met: N=21; Val/Val: N=21) modulated neural activity of response preparation, inhibition, and execution. Met homozygotes (high dopamine) exhibited an increase in beta power during early motor preparation suggestive of a transient “pause,” which could underlie the tendency of Met homozygotes to be more cautious and inhibited. In contrast, Val homozygotes (low dopamine) commonly endorse higher impulsivity. They exhibited greater beta decrease during early motor preparation, indicative of high response readiness.
Study 3 evaluated the effects of alcohol intoxication on the neurocircuitry of inhibitory control in social drinkers with (FHP) or without (FHN) a family history of alcoholism (N=19 per group), a heritable, multifaceted risk factor for the development of alcohol use disorder (AUD). In FHP, lower inhibition-induced oscillatory power was associated with extraversion. Converging evidence across behavioral and neural indices supports low responsivity of FHP to alcohol intoxication, which may mediate the development of AUD.
The multimodal aMEG method can provide high-resolution insight into the neural underpinnings of inhibitory control with implications for healthy behavior and genetically- determined interindividual differences in impulsivity. Because of their sensitivity to synaptic signaling, these indices can reveal neural signature of the acute and persistent impact of alcohol on self-regulatory functions, and may serve as endophenotypes of disinhibitory disorders, including the vulnerability to AUD.
Final Dissertation Announcement - Jack Brady
June 15, 2023 8:45 am - 10:15 am See Program
JackBrady
Aaron J. Blashill, Professor,Psychology, San Diego State University
Kristen Wells, Professor, Psychology, San Diego StateUniversity
Scott Roesch, Professor, Psychology, San Diego StateUniversity
David J. Moore, Professor in Residence, Psychiatry,University of California San Diego
Jessica Montoya, Assistant Professor, Psychiatry,University of California San Diego
TITLEOF DISSERTATION:
TheEffect of Patient Navigation for PrEP-related Health Care on Mental Healthamong Latinx Sexual Minority Men: Mediation through Social Support
DATEOF DEFENSE: 06/15/2023
TIMEOF DEFENSE: 8:45AM – 10:15AM
Rationale: Sexual minority men (SMM; e.g., men whoidentify as gay/bisexual and/or report same-gender attraction/sexual behavior)are disproportionately affected by internalizing disorders and symptoms (e.g.,anxiety and depressive disorders/symptoms) in comparison to their heterosexualmale peers. Hispanic/Latinx SMM may be especially burdened by internalizingdisorders/symptoms due to decreased access to culturally competent health care,stigma surrounding mental disorders, and stress from within the SMM community. Patientnavigation (PN) is a partnership-based, individualized intervention thatfocuses on decreasing barriers to health care. Patient navigation forpre-exposure prophylaxis (PrEP)—a medication taken to prevent HIV infection—couldreduce internalizing symptoms of anxiety and depression among Hispanic/LatinxSMM by providing social support.
Design: This study used secondary data analysisto examine the impact of PN on internalizing symptom outcomes through six-monthfollow-up (6MFU) among a sample of Hispanic/Latinx SMM between the ages of 18and 29 (N = 57). Data analyzed were from a randomized controlled trialinvestigating the efficacy of a PN intervention (versus usual care) to assistHispanic/Latinx SMM at high risk for HIV infection with accessing PrEP. Hispanic/LatinxSMM peer patient navigators were utilized to provide culturally competent careand decrease social stigma. Usual care consisted of written information aboutPrEP, sexual health and HIV prevention services, and how to access care. It washypothesized that the PN condition would be associated with decreasedinternalizing symptoms and that the effect would be mediated by two socialsupport constructs at three-month follow-up: emotional support and informationalsupport. Data were analyzed using two analytic approaches: 1) cross-laggedpanel models and 2) latent difference scores.
Results: The PN condition was not associatedwith a significant decrease in internalizing symptoms at 6MFU and the effectwas not mediated through social support.
Conclusions: Results may be related to the flooreffect of internalizing symptoms at baseline, analyses that assumed changes insocial support were occurring within the first three months of the study, andvariability in the frequency of using PN services. Future studies would benefitfrom gathering data at additional time points and selecting participants withhigher internalizing symptoms and/or lower social support.
SDSU/UC San Diego Joint Doctoral Program in Clinical Psychology 6363 Alvarado Court, Suite 103 San Diego, CA 92120 Phone: 619-594-2246 Fax: 619-594-6780 Email: psycjdp@sdsu.edu
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