Psychosocial Resources and Physiological Dysregulation

Author(s):  
Joshua F. Wiley ◽  
Tara L. Gruenewald ◽  
Teresa E. Seeman

Psychosocial resources refer to individual personality and social relationship factors that tend to cluster together and contribute to psychological and physical health and well-being. Growing evidence demonstrates robust relations between psychosocial resources and health. Physiological dysregulation represents one key mechanism that may help to explain the link between psychosocial resources and health. The current chapter focuses on the relations of psychosocial resources with physiology, drawing on findings from the Midlife in the United States (MIDUS) study and other large, epidemiological studies. The focus is on the relations of psychosocial resources with allostatic load, a composite index of multisystem physiological dysregulation, while also highlighting select findings for individual biomarkers. The summary of evidence examines psychosocial resources as both a direct and a moderating factor on biological outcomes. The chapter concludes with suggestions for future research.

2019 ◽  
Vol 3 (Supplement_1) ◽  
pp. S434-S434
Author(s):  
Konstantinos Mantantzis ◽  
Denis Gerstorf ◽  
Thomas M Hess

Abstract Research into peripheral physiology and its association with cognition, emotionality, and social/physical functioning has received considerable attention over the years. However, many of the underlying mechanisms are not well understood. In this symposium, we have compiled a set of four empirical projects that showcase current and future endeavors to address some of the long-standing questions about when, how, and why physiology shapes and is shaped by key psychosocial resources. Hawkley et al. make use of data from the NSHAP and HRS longitudinal studies to investigate whether social relationships such as number of friends predicts risk of diabetes among older adults. Wilson et al. use dyadic data from young and middle-aged couples to examine cardiometabolic similarity among spouses, and how such concordance is shaped by key relationship factors such as emotional closeness. Pauly et al. use data from two daily-life studies of older couples to investigate how physiological synchrony in cortisol is modulated by partner interactions, empathy, and empathic accuracy. Finally, Mantantzis et al. make use of multi-year longitudinal data from the Berlin Aging Study II to examine the role of glucose regulation capacity for trajectories of subjective well-being among older adults. Thomas Hess will discuss the importance of these papers, discuss strengths and weaknesses of the approaches chosen, and consider implications for future research.


2020 ◽  
Vol 4 (Supplement_1) ◽  
pp. 410-410
Author(s):  
Xin Yao Lin ◽  
Margie Lachman

Abstract Social media platforms allow people to connect and share content online (e.g., Facebook, Twitter). Although older adults are becoming more frequent users of social media, there continue to be mixed views on whether social media positively or negatively impacts well-being. Past studies have mainly focused on cross-sectional analyses for individual differences. However, both the time spent on social media and one’s affect can fluctuate on a daily basis. Thus, it is important to understand how the relationship between daily social media usage and affect varies within individuals from day to day. The current study adds to the literature by examining whether daily variations in time spent with social media are related to daily positive and negative affect and whether there are age differences in these relationships. The current study used an eight-day daily diary from the Midlife in the United States (MIDUS) Refresher dataset for 782 participants (ages 25-75). Multilevel modeling results revealed that age moderated the relationship between daily time spent on social media and negative affect: for younger adults, on days when they spent more time on social media, they had more negative affect. For older adults, on days when they spent more time on social media, they had less negative affect. Surprisingly, daily time spent on social media was not related to daily positive affect, nor did this relationship differ by age. Implications for future research are discussed with a focus on how social media usage can contribute to daily well-being for adults of different ages.


2021 ◽  
pp. 026540752110435
Author(s):  
Heidi L. Fritz

Prior research links adaptive humor styles (affiliative and self-enhancing) with enhanced psychological well-being and maladaptive humor styles (aggressive and self-defeating) with worse psychological well-being, primarily through humor styles’ influence on individuals’ social interactions and efforts to positively reframe stressors. The present study examined the unique relation of each humor style with psychological well-being with a focus on understanding mechanisms of adjustment under highly stressful conditions. Ninety-nine parents of children with disabilities were surveyed at the beginning of the COVID-19 pandemic in the United States in March 2020, and 79 parents completed follow-up surveys in July 2020. As predicted, at T1, self-enhancing humor was associated with less psychological distress and greater family satisfaction, self-defeating humor was associated with greater distress, and aggressive humor was associated with lower family satisfaction. Moreover, affiliative humor predicted decreased psychological distress over time, whereas self-defeating humor predicted increased psychological distress and decreased family satisfaction over time. Relations were largely mediated by caregiver positive reappraisal, family efforts to reframe daily disability-related challenges, and negative social interactions. Future research should further examine the influence of caregiver humor styles on family dynamics, family reframing norms, and caregiving efficacy.


2021 ◽  
pp. 026921632110458
Author(s):  
Jenny Baxley Lee ◽  
Sonja McIlfatrick ◽  
Lisa Fitzpatrick

Background: Living with life-limiting illness significantly impacts quality of life. A growing body of evidence suggests that arts engagement facilitated by artists promotes well-being. However, no synthesis of the literature exists to describe arts engagement delivered by artists with individuals receiving palliative care. Aim: To systematically review and synthesize evidence to identify outcomes and key knowledge gaps to inform future research and practice. Design: A systematic integrative literature review was conducted using a pre-defined search strategy and reported using PRISMA guidelines. Analysis was conducted iteratively and synthesis achieved using constant comparison to generate themes. Data sources: PubMed/MEDLINE, CINAHL, PsycINFO, Scopus, Web of Science, and Embase were searched for studies published between database inception and August 2020. Search terms included variations on arts/artists; patients/service users; and palliative or end-of-life care. Eligibility criteria was applied and study quality assessed. Results: Seven reviewed studies explored literary, performing, and visual arts engagement in hospitals, hospice and community settings in England, the United States, France, and Canada. Study designs, interventions and findings were discussed. Themes identified across studies associated arts engagement with (1) a sense of well-being, (2) a newly discovered, or re-framed, sense of self, (3) connection with others, and (4) challenges associated with practice. Conclusion: Recommendations for future research were offered in order to maximize benefits, minimize risks and address complexity of artists’ engagement in palliative care including: (1) consistency in methods and reporting; (2) inclusion of wider perspectives; and (3) key considerations for adapting the arts by health condition and art form.


2021 ◽  
Vol 5 (Supplement_1) ◽  
pp. 876-876
Author(s):  
Setarreh Massihzadegan ◽  
Jan Mutchler

Abstract Utilizing the first set of 5-year American Community Survey data available since the United States’ legalization of same-sex marriage in mid-2015, this poster investigates the economic security of older adults (age 50+) in same-sex marriages compared to those in same-sex partnerships who are cohabiting but not married. Viewed through the lens of cumulative disadvantage theory, we consider differences in the economic circumstances of same-sex couples by gender and by geographic location. Findings point to gender differences in economic well-being, but relatively few differences based on marital status. For example, rates of low income are somewhat higher among female couples than among their male counterparts, but marital status differences are not substantial. These findings suggest that the benefits of being married that have long been recognized among older adults may not extend equally to same-sex couples. Findings are discussed with respect to the emerging salience of marriage within the LGBTQ older community, future research opportunities, and important policy implications.


Author(s):  
Patricia Crittenden ◽  
Susan J. Spieker ◽  
Steve Farnfield

Attachment may have reached a turning point in which two sometimes incompatible approaches to individual differences in attachment are being compared. The outcome could influence future work in attachment. This article focuses on individual differences because applications of attachment are predicated on the consequences of individual differences for adaptation and well-being. The issue is which model is better suited to future research and clinical applications. Both models augment the original Ainsworth ABC model that everyone agrees is not sufficiently differentiated to cover the range of human behavior. The two models are “ABC+D” (the model that has disorganization (D) as its fourth category) and “DMM” (the model that expands the A and C categories from two subcategories each to a total of eight each, plus A/C combinations). The current disagreement has two sources: (a) the increasing acceptance outside the United States of the DMM, particularly in clinical and forensic settings, while the US remains largely unaware of the DMM; and (b) the recent announcement by prominent ABC+D researchers from Europe and the US that D is not a suitable category for clinical or forensic use. ABC+D researchers have not proposed an alternative, and some US funding sources and courts eschew attachment altogether, believing the theory itself lacks validity and utility, thus weakening attachment’s potential to inform clinical research and decision-making. This article proposes DMM as a viable alternative to both ABC+D and psychiatric diagnoses and examines the development and contributions of each model for the purpose of creating a model of individual differences in attachment that is scientifically robust, open to change as new evidence becomes available, and applicable to troubled individuals and families. Notably, attachment theory has engendered controversy from its beginnings. When John Bowlby offered attachment as a universal human characteristic that promoted species and individual survival, he was criticized by others in his field. When Mary Ainsworth identified the ABC categories of individual differences in attachment, her ideas were attacked from outside attachment theory. While the “first generation” issue around the existence of attachment has largely died away, a second generation of attachment theorists is disputing the nature of individual differences, their focus on individuals (ABC+D) or interpersonal systems (DMM Family Functional Formulations), and their relevance to clinical work. The ABC+D and DMM models that expand Ainsworth’s work were developed by two of her students, Mary Main (ABC+D) and Patricia Crittenden (DMM). They and their colleagues have worked separately for half a century producing two large and sometimes discrepant bodies of work, which have now become the topic of open debate. This bibliography focuses on the conceptual and empirical bases for that exchange. Part I outlines the roots of the ABC+D and DMM models, together with comparative validating information. Part II presents the central research findings on individual differences in attachment from four decades of research with each model. The authors wish to thank Robbie Duschinsky, Udita Iyengar, and Andrea Landini for their helpful comments on this bibliography.


2021 ◽  
pp. 073346482110482
Author(s):  
Takashi Yamashita ◽  
Wonmai Punksungka ◽  
Samuel Van Vleet ◽  
Abigail Helsinger ◽  
Phyllis Cummins

Little is known about the overall experiences and feelings of diverse older populations during the 2020 COVID-19 pandemic. To provide the baseline information for future research and policy, this study analyzed the 2020 Health and Retirement Study COVID-19 project data ( n = 1782). More than 70% of older adults reported the following activities: watching TV (98%), reading (90%), using a computer and the internet (83%), gardening (82%), walking (75%), baking and cooking (73%), and praying (73%). Volunteering and attending community groups, which are known to benefit well-being, were unpopular (less than 8%). During the pandemic, older adults were generally satisfied with their lives, but more than half of them were concerned about their own health, family’s health, and future prospects. Our study also showed the differences in the experiences and feelings by gender and race as well as the intersection of gender and race in the United States.


Author(s):  
Jennifer Morozink Boylan ◽  
Christopher L. Coe ◽  
Carol D. Ryff

Epidemiological evidence from the Midlife in the United States and other studies shows robust socioeconomic disparities in mental and physical health outcomes. Considerable heterogeneity exists in health within socioeconomic strata; not all socioeconomically disadvantaged individuals exhibit poor health. Evidence is presented supporting an integrative conceptual framework wherein psychological factors moderate the association between socioeconomic status and health, illuminating unique risk and resilience profiles. Regarding protective factors, distinctions between hedonic well-being and eudaimonic well-being are highlighted. Regarding psychological risk factors, the focus is on the experience and expression of anger. Several pathways through which socioeconomic and psychological factors may affect health, including health behaviors, emotion regulation, and physiological responses to stress are considered. The chapter concludes with directions for future research, including efforts to integrate psychological strengths and risk factors and the need for longitudinal and intervention approaches to address the public health issue of health disparities from a biopsychosocial perspective.


Plant Disease ◽  
2020 ◽  
Vol 104 (10) ◽  
pp. 2541-2550
Author(s):  
J. Valle-Torres ◽  
T. J. Ross ◽  
D. Plewa ◽  
M. C. Avellaneda ◽  
J. Check ◽  
...  

Tar spot of corn has been a major foliar disease in several Latin American countries since 1904. In 2015, tar spot was first documented in the United States and has led to significant yield losses of approximately 4.5 million t. Tar spot is caused by an obligate pathogen, Phyllachora maydis, and thus requires a living host to grow and reproduce. Due to its obligate nature, biological and epidemiological studies are limited and impact of disease in corn production has been understudied. Here we present the current literature and gaps in knowledge of tar spot of corn in the Americas, its etiology, distribution, impact and known management strategies as a resource for understanding the pathosystem. This will in turn guide current and future research and aid in the development of effective management strategies for this disease.


2018 ◽  
Vol 36 (30_suppl) ◽  
pp. 118-118
Author(s):  
Matthew F. Hudson ◽  
Mark Allen O'Rourke ◽  
Dawn W. Blackhurst ◽  
Jennifer Caldwell ◽  
Regina A. Franco ◽  
...  

118 Background: Oncology faces workforce shortages and increasing stress. Oncology provider well-being and resilience are mediated by organizational factors through clinical work intensity. Clinical work intensity (CWI) is the level of requisite technical skill, physical and mental effort and clinical judgement necessary, plus care provision-associated stress. Suboptimal clinical work intensity may result from unfavorable practice organizational factors preceding burnout. This pilot study assess CWI experienced by medical oncologists and oncologic advanced practice registered nurses (APRNs)/nurse practitioners as a prelude to a study of provider resilience. Methods: Investigators solicited seventeen medical oncologists-12 physicians and 5 nurse practitioners-from five oncology clinics in the Northwest, Midwest, and Southern regions of the United States Providers reported on level of work intensity associated with 339 patient visits occurring over an 8 week period where for each provider 5 visits were randomly selected from each of 4 randomly selected clinic days. Intensity was measured by the NASA-Task Load Index that assesses 6 dimensions (subscales) with additional questions measuring stress and visit satisfaction. Results: Compared to medical oncologists, APRNs reported a higher work intensity score on average (38.6 vs. 32.9; p < 0.0064), and higher scores on the frustration subscale (36.5 vs. 21.5; p < 0.0001). APRNs also scored higher on stress (27.8 vs. 22.2; p < 0.048), and scored lower on provider-perceived satisfaction with the visit (73.0 vs. 81.1; p < 0.0001). There was no difference between oncologists and nurse practitioners on the other dimensions, including mental, time, and physical demand, and effort. Conclusions: Oncologic APRNs may experience greater work intensity than medical oncologists. Future research will consider whether APRN work intensity scores reflect different or disproportionate challenges owing to scope of practice, workload, or administrative responsibilities, and determine those dimensions of higher work intensity that portend provider burnout. The goal is to identify strategies optimizing work intensity among oncology providers, mitigating provider burnout and enhancing the practice environment.


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