Victimization and Psychological Wellbeing among Sexual and Gender Minority Emerging Adults: Testing the Moderating Role of Emotional Comfort from Companion Animals

Introduction: Human-animal interaction science is a growing field, largely due to the potential psychosocial benefits companion animals provide to humans. One way companion animals may influence psychosocial outcomes is through their ability to provide emotional comfort, though few studies have examined relationships between sexual and gender minority stressors (i.e. discrimination, victimization, rejection), human-animal interaction, and psychological wellbeing. To address this gap in the literature, the current study evaluates whether, and to what extent, the association between gender-based victimization and psychological wellbeing (i.e., anxiety, depression, self-esteem) varies as a function of emotional comfort from companion animals among emerging adults. Methods: Data were collected from young people between the ages of 18 and 21 years who self-identified as a sexual and/or gender minority (N = 134; 37.3% ethnic/racial minority; 49.2% gender minority; 98.5% sexual minority). We conducted three simple moderation analyses that examined whether, and to what extent, gender-based victimization was associated with mental health (i.e., anxiety, depression, self-esteem) as a function of comfort from companion animals. Additive multiple moderation models were also conducted to examine comfort from companion animals and social support as moderators between victimization and each psychological wellbeing indicator. Results: Results of the simple moderation models suggest that the effect of gender-based victimization on self-esteem was moderated by comfort from companion animals (ΔR2 = .03, F(1, 125) = 4.66, β = .22, t(125) = 2.16, p = .03) and that the relationship is statistically significant only at low levels of comfort from companion animals (β = -0.38, t = -2.41, p = .02). Further, our additive multiple moderation model with both comfort from companion animals and social support as moderators of the relation between victimization and self-esteem found that victimization was significantly moderated by comfort from animals (ΔR2 = .03, F(1, 123) = 5.38, β = .24, t(123) = 2.32, p = .02), but not social support. The relation between victimization and self-esteem was significant and negative at low levels of comfort from companion animals, but only for those with high levels of social support (β = -0.43, t = -2.65, p \u3c .01). In contrast, when high levels of comfort from companion animals were reported, the effect of victimization on self-esteem was no longer statistically significant, regardless of whether social support was low or high. We did not find evidence of moderation in models with either anxiety or depression as the dependent variable. Conclusion: These results suggest that high levels of comfort from companion animals may be a protective factor against the harmful effects of victimization on self-esteem. However, our results suggest that comfort from companion animals may not provide the same benefits for anxiety and depression. Further research is needed to replicate our results and to elucidate whether other aspects of HAI, such as attachment to pets or caretaking for pets, may play a role in associations between victimization and anxiety and depression. Given the harmful effects of gender-based victimization and other stressful circumstances that LGBTQ+ youth are disproportionately at risk of experiencing (i.e., employment issues, housing insecurity), this study highlights the importance of exploring how, and for whom, comfort from companion animals and other aspects of HAI may provide protective benefits.https://scholarscompass.vcu.edu/gradposters/1145/thumbnail.jp

Gene expression varies within and between enzootic and epizootic lineages of Batrachochytrium dendrobatidis (Bd) in the Americas

While much research focus is paid to hypervirulent fungal lineages during emerging infectious disease outbreaks, examining enzootic pathogen isolates can be equally fruitful in delineating infection dynamics and determining pathogenesis. The fungal pathogen of amphibians, Batrachochytrium dendrobatidis (Bd), exhibits markedly different patterns of disease in natural populations, where it has caused massive amphibian declines in some regions, yet persists enzootically in others. Here we compare in vitro gene expression profiles of a panel of Bd isolates representing both the enzootic Bd-Brazil lineage, and the more recently diverged, panzootic lineage, Bd-GPL. We document significantly different lineage-specific and intralineage gene expression patterns, with Bd-Brazil upregulating genes with aspartic-type peptidase activity, and Bd-GPL upregulating CBM18 chitin-binding genes, among others. We also find pronounced intralineage variation in membrane integrity and transmembrane transport ability within our Bd-GPL isolates. Finally, we highlight unexpectedly divergent expression profiles in sympatric panzootic isolates, underscoring microgeographic functional variation in a largely clonal lineage. This variation in gene expression likely plays an important role in the relative pathogenesis and host range of Bd-Brazil and Bd-GPL isolates. Together, our results demonstrate that functional genomics approaches can provide information relevant to studies of virulence evolution within the Bd Glade12413443The authors thank Joyce Longcore for providing the Bd isolates used in this study, Miranda Gray for assistance in the laboratory, Ezra Lencer for feedback on methods, the Cornell Biotechnology Resource Center for sequencing and bioinformatics troubleshooting, and Zamudio lab members for helpful manuscript comments. This work was funded by the National Science Foundation (NSF) (grant DEB 1120249) and the Cornell Center for Vertebrate Genomic

The Moderating Effect of Comfort from Companion Animals and Social Support on the Relationship between Microaggressions and Mental Health in LGBTQ+ Emerging Adults

Introduction: Sexual and/or gender minority (SGM; e.g., lesbian, transgender, nonbinary, LGBTQ+) individuals are frequently exposed to various forms of minority stress that impact their mental health and wellbeing. Microaggressions, a form of minority stress, are defined as unconscious behaviors or statements directed at members of marginalized groups that reflect a hostile or discriminatory message. Microaggressions have been associated with several detrimental outcomes, such as depression and anxiety. Social support has been found to be an important protective factor for SGM emerging adults. Additionally, relationships with companion animals are an underexplored source of support that may be important for SGM individuals. This study aims to explore whether, and to what extent, social support from humans and comfort from companion animals moderates the relationship between SGM-related microaggressions and depressive and anxiety symptoms. Methods: We partnered with five community organizations to recruit our sample, which consisted of 134 SGM emerging adults between the ages of 18 and 21 (Mage = 19.31). Approximately 98.5% of our sample identified with a sexual minority identity, 49.5% identified with a gender minority identity, and 37.3% identified as a racial/ethnic minority. All participants had lived with a companion animal within the past year, with the majority of participants living with a dog and/or a cat. We conducted eight simple moderation analyses to explore whether, and to what extent, comfort from companion animals and human social support individually moderated the relationship between two forms of microaggressions (i.e., interpersonal, environmental) and anxiety and depressive symptoms. Further, we ran four additive moderation analyses to investigate whether comfort from companion animals and social support from humans moderated the relationship between each form of microaggressions and mental health symptoms, when the other moderator was held constant. Results: The results of our simple moderation analyses indicated that social support moderated the relationship between both forms of microaggressions and depressive symptoms (interpersonal: ΔR2 = 0.03, F(1, 125) = 4.74, ꞵ = -0.17, t(125) = -2.18, p = .03; environmental: ΔR2 = 0.02, F(1, 124) = 3.93, ꞵ = -0.19, t(124) = -1.98, p = .05). Our findings suggest that social support acted as a protective factor, because the relationship between exposure to microaggressions and depressive symptoms was not significant when participants reported high levels of social support. Comfort from companion animals also moderated the relationship between interpersonal microaggressions and depressive symptoms (ΔR2 = 0.03, F(1, 125) = 4.78, ꞵ = 0.18, t(125) = 2.19, p = .03). However, comfort from companion animals seemed to exacerbate the association between interpersonal microaggressions and depressive symptoms, as there was a positive and significant relationship between these two variables when participants reported medium or high levels of comfort from companion animals. The results of the additive moderation analyses found that the relationship between exposure to microaggressions and depressive symptoms was positive and significant when social support was low or medium and comfort from companion animals was high or medium. However, when social support was high, the relationship was no longer significant, regardless of the level of comfort from companion animals. Discussion: Our results suggest that social support from humans may be a key protective factor that buffers the relationship between microaggressions and depressive symptoms. Further, these findings also highlight the need to continue investigating the complex role of relationships with companion animals on mental health outcomes for SGM emerging adults. In particular, longitudinal studies are needed to clarify the direction of these relationships, as we are unable to make causal inferences with this cross-sectional study. The results from this study have important implications for future research in this area and practice with SGM populations.https://scholarscompass.vcu.edu/gradposters/1142/thumbnail.jp

Variants in the Mitochondrial Intermediate Peptidase (MIPEP) Gene are Associated with Gray Matter Density in the Alzheimer’s Disease Neuroimaging Initiative Cohort

poster abstractCancer and Alzheimer’s disease (AD) incidence is inversely correlated, but the genetic underpinnings of this relationship remain to be elucidated. Recent findings identified lower gray matter density in frontal regions of participants of the Alzheimer’s Disease Neuroimaging Initiative (ADNI) with cancer history compared to those without such history, across diagnostic groups (Nudelman et al., 2014). Pathways proposed to impact cancer and AD, including metabolism and survival, may play an important role in the observed difference. To test this hypothesis, a genome-wide association study (GWAS) using mean frontal gray matter cluster values was performed for all Caucasian participants in this cohort with neuroimaging and genetic data (n=1405). Analysis covaried for age, sex, AD, and cancer history. Of the two genes with the most significant SNPs (p<10-5), WD repeat domain 5B (WDR5B) and mitochondrial intermediate peptidase (MIPEP), MIPEP was selected for further analysis given the hypothesis focus on metabolism. ANOVA analysis of MIPEP top SNP rs8181878 with frontal gray matter cluster values in SPSS indicated that while this SNP is significantly associated with gray matter density (p=2x10-6), no interaction was observed with cancer history or AD diagnosis. Furthermore, whole brain gray matter voxel-wise analysis of this SNP using Statistical Parametric Mapping 8 software showed that minor allele(s) of this SNP were significantly (PFWE<0.05) associated with higher gray matter density. These results suggest that the minor allele of MIPEP SNP rs8181878 may be protective against gray matter density loss, highlighting the importance of metabolic processes in aging and disease

Association of cancer history with Alzheimer's disease onset and structural brain changes

Epidemiological studies show a reciprocal inverse association between cancer and Alzheimer's disease (AD). The common mechanistic theory for this effect posits that cells have an innate tendency toward apoptotic or survival pathways, translating to increased risk for either neurodegeneration or cancer. However, it has been shown that cancer patients experience cognitive dysfunction pre- and post-treatment as well as alterations in cerebral gray matter density (GMD) on MRI. To further investigate these issues, we analyzed the association between cancer history (CA±) and age of AD onset, and the relationship between GMD and CA± status across diagnostic groups in the Alzheimer's Disease Neuroimaging Initiative (ADNI) cohort study. Data was analyzed from 1609 participants with information on baseline cancer history and AD diagnosis, age of AD onset, and baseline MRI scans. Participants were CA+ (N = 503) and CA− (N = 1106) diagnosed with AD, mild cognitive impairment (MCI), significant memory concerns (SMC), and cognitively normal older adults. As in previous studies, CA+ was inversely associated with AD at baseline (P = 0.025); interestingly, this effect appears to be driven by non-melanoma skin cancer (NMSC), the largest cancer category in this study (P = 0.001). CA+ was also associated with later age of AD onset (P < 0.001), independent of apolipoprotein E (APOE) ε4 allele status, and individuals with two prior cancers had later mean age of AD onset than those with one or no prior cancer (P < 0.001), suggesting an additive effect. Voxel-based morphometric analysis of GMD showed CA+ had lower GMD in the right superior frontal gyrus compared to CA− across diagnostic groups (Pcrit < 0.001, uncorrected); this cluster of lower GMD appeared to be driven by history of invasive cancer types, rather than skin cancer. Thus, while cancer history is associated with a measurable delay in AD onset independent of APOE ε4, the underlying mechanism does not appear to be cancer-related preservation of GMD

Increased Iron Stores Correlate with Worse Disease Outcomes in a Mouse Model of Schistosomiasis Infection

Schistosomiasis is a significant parasitic infection creating disease burden throughout many of the world's developing nations. Iron deficiency anemia is also a significant health burden resulting from both nutritional deficit as well as parasitic infection in these countries. In this study we investigated the relationships between the disease outcomes of Schistosoma japonicum infection and iron homeostasis. We aimed to determine if host iron status has an effect on schistosome maturation or egg production, and to investigate the response of iron regulatory genes to chronic schistosomiasis infection. Wild-type C57BL/6 and Transferrin Receptor 2 null mice were infected with S. japonicum, and sacrificed at the onset of chronic disease. Transferrin Receptor 2 null mice are a model of type 3 hereditary hemochromatosis and develop significant iron overload providing increased iron stores at the onset of infection. The infectivity of schistosomes and egg production was assessed along with the subsequent development of granulomas and fibrosis. The response of the iron regulatory gene Hepcidin to infection and the changes in iron status were assessed by real-time PCR and Western blotting. Our results show that Hepcidin levels responded to the changing iron status of the animals, but were not significantly influenced by the inflammatory response. We also show that with increased iron availability at the time of infection there was greater development of fibrosis around granulomas. In conclusion, our studies indicate that chronic inflammation may not be the primary cause of the anemia seen in schistosomiasis, and suggest that increased availability of iron, such as through iron supplementation, may actually lead to increased disease severity

Longitudinal Analysis of Adolescent Girls' Activity Patterns: Understanding the Influence of the Transition to Licensure

The proportion of teens and young adults with driver's licenses has declined sharply in many industrialized countries including the United States. Explanations for this decline have ranged from the introduction of graduated driver licensing programs to the increase in online social interaction. We used a longitudinal cohort study of teenage girls in San Diego and Minneapolis to evaluate factors associated with licensure and whether teens' travel patterns become more independent as they aged. We found that licensure depended not only on age, but on race and ethnicity as well as variables that correlate with household income. Results also showed evidence that teen travel became more independent as teen's age, and that acquiring a license is an important part of this increased independence. However, we found limited evidence that teen's travel-activity patterns changed as a result of acquiring a driver's license. Rather, teen independence resulted in less parental chauffeuring, but little shift in travel patterns. For the larger debate on declining Millennial mobility, our results suggest the need for more nuanced attention to variation across demographic groups and consideration of the equity implications if declines in travel and licensure are concentrated in low-income and minority populations

Drift Macroalgal Distribution In Northern Gulf of Mexico Seagrass Meadows

Drift macroalgae, often found in clumps or mats adjacent to or within seagrass beds, can increase the value of seagrass beds as habitat for nekton via added food resources and structural complexity. But, as algal biomass increases, it can also decrease light availability, inhibit faunal movements, smother benthic communities, and contribute to hypoxia, all of which can reduce nekton abundance. We quantified the abundance and distribution of drift macroalgae within seagrass meadows dominated by turtle grass Thalassia testudinum across the northern Gulf of Mexico and compared seagrass characteristics to macroalgal biomass and distribution. Drift macroalgae were most abundant in areas with higher seagrass shoot densities and intermediate canopy heights. We did not find significant relationships between algal biomass and point measures of salinity, temperature, or depth. The macroalgal genera Laurencia and Gracilaria were present across the study region, Agardhiella and Digenia were collected in the western Gulf of Mexico, and Acanthophora was collected in the eastern Gulf of Mexico. Our survey revealed drift algae to be abundant and widespread throughout seagrass meadows in the northern Gulf of Mexico, which likely influences the habitat value of seagrass ecosystems

Analysis of the Inverse Association between Cancer and Alzheimer’s Disease: Results from the Alzheimer’s Disease Neuroimaging Initiative Cohort

poster abstractAlthough a number of studies support a reciprocal inverse association between diagnoses of cancer and Alzheimer’s disease (AD), to date there has not been any systemic investigation of the neurobiological impact of or genetic risk factors underlying this effect. To facilitate this goal, this study aimed to replicate the inverse association of cancer and AD using data from the NIA Alzheimer’s Disease Neuroimaging Initiative, which includes age-matched cases and controls with information on cancer history, AD progression, neuroimaging, and genomic data. Subjects included individuals with AD (n=234), mild cognitive impairment (MCI, n=542), and healthy controls (HC, n=293). After controlling for sex, education, race/ethnicity, smoking, and apolipoprotein E (APOE) e2/3/4 allele groups, cancer history was protective against baseline AD diagnosis (p=0.042), and was associated with later age of AD onset (p=0.001). Cancer history appears to result in a cumulative protective effect; individuals with more than one cancer had a later age of AD onset compared to those with only one cancer (p=0.001). Finally, a protective effect of AD was also observed in individuals who developed incident cancer after enrolling (post-baseline visit); 20 individuals with MCI and 9 HC developed cancer, while no AD patients had subsequent cancer diagnoses (p=0.013). This supports previous research on the inverse association of cancer and AD, and importantly provides novel evidence that this effect appears to be independent of APOE, the major known genetic risk factor for AD. Future analyses will investigate the neurobiological and genetic basis of this effect