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Dive into the research topics where Madeleine S. Goodkind is active.

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Featured researches published by Madeleine S. Goodkind.


Cognitive, Affective, & Behavioral Neuroscience | 2009

Do Tests of Executive Functioning Predict Ability to Downregulate Emotions Spontaneously and When Instructed to Suppress

Anett Gyurak; Madeleine S. Goodkind; Anita Madan; Joel H. Kramer; Bruce L. Miller; Robert W. Levenson

Behavioral regulation is a hallmark feature of executive functioning (EF). The present study investigated whether commonly used neuropsychological test measures of EF (i.e., working memory, Stroop, trail making, and verbal fluency) were related to ability to downregulate emotion both spontaneously and when instructed to suppress emotional expressions. To ensure a wide range of EF, 24 frontotemporal lobar degeneration patients, 7 Alzheimers patients, and 17 neurologically normal controls participated. Participants were exposed to an acoustic startle stimulus (single aversive noise burst) under three conditions: (1) unwarned, (2) warned with no instructions (to measure spontaneous emotion downregulation), and (3) warned with instructions to suppress (to measure instructed emotion downregulation). Results indicated that higher verbal fluency scores were related to greater emotion regulation (operationalized as reduction in body movement and emotional facial behavior when warned of the impending startle) in both regulation conditions. No relationships were found between emotion regulation in these conditions and the other EF measures. We conclude that, of four commonly used measures of EF, verbal fluency best indexes the complex processes of monitoring, evaluation, and control necessary for successful emotion regulation, both spontaneously and following instructions to suppress.


Emotion | 2012

Greater Emotional Empathy and Prosocial Behavior in Late Life

Jocelyn A. Sze; Anett Gyurak; Madeleine S. Goodkind; Robert W. Levenson

Emotional empathy and prosocial behavior were assessed in older, middle-aged, and young adults. Participants watched two films depicting individuals in need, one uplifting and the other distressing. Physiological responses were monitored during the films, and participants rated their levels of emotional empathy following each film. As a measure of prosocial behavior, participants were given an additional payment they could contribute to charities supporting the individuals in the films. Age-related linear increases were found for both emotional empathy (self-reported empathic concern and cardiac and electrodermal responding) and prosocial behavior (size of contribution) across both films and in self-reported personal distress to the distressing film. Empathic concern and cardiac reactivity to both films, along with personal distress to the distressing film only, were associated with greater prosocial behavior. Empathic concern partially mediated the age-related differences in prosocial behavior. Results are discussed in terms of our understanding both of adult development and of the nature of these vital aspects of human emotion.


Cognition & Emotion | 2012

Executive functions and the down-regulation and up-regulation of emotion

Anett Gyurak; Madeleine S. Goodkind; Joel H. Kramer; Bruce L. Miller; Robert W. Levenson

This study examined the relationship between individual differences in executive functions (EF; assessed by measures of working memory, Stroop, trail making, and verbal fluency) and ability to down-regulate and up-regulate responses to emotionally evocative film clips. To ensure a wide range of EF, 48 participants with diverse neurodegenerative disorders and 21 older neurologically normal ageing participants were included. Participants were exposed to three different movie clips that were designed to elicit a mix of disgust and amusement. While watching the films they were either instructed to watch, down-regulate, and up-regulate their visible emotional responses. Heart rate and facial behaviours were monitored throughout. Emotion regulatory ability was operationalised as changes in heart rate and facial behaviour in the down- and up-regulation conditions, controlling for responses in the watch condition. Results indicated that higher verbal fluency scores were related to greater ability to regulate emotion in both the down-regulation and up-regulation conditions. This finding remained significant even after controlling for age and general cognitive functioning. No relationships were found between emotion regulation and the other EF measures. We believe these results derive from differences among EF measures, with verbal-fluency performance best capturing the complex sequence of controlled planning, activation, and monitoring required for successful emotion regulation. These findings contribute to our understanding of emotion–cognition interaction, suggesting a link between emotion-regulatory abilities and individual differences in complex executive functions.


Psychology and Aging | 2010

Emotion Regulation Deficits in Frontotemporal Lobar Degeneration and Alzheimer's Disease

Madeleine S. Goodkind; Anett Gyurak; Megan McCarthy; Bruce L. Miller; Robert W. Levenson

We examined instructed and spontaneous emotion regulation in patients with frontotemporal lobar degeneration (FTLD, N = 32), which presents with profound emotional and personality changes; patients with Alzheimers disease (AD, N = 17), which presents with profound memory impairment; and neurologically normal controls (N = 25). Participants were exposed to an aversive acoustic startle stimulus (115 dB) under 3 different conditions: (a) unwarned without instructions to down-regulate, (b) warned without instructions to down-regulate, and (c) warned with instructions to down-regulate. In the last 2 conditions, the warning took the form of a 20-s countdown. In all conditions, visible aspects of the startle response were assessed by measuring overall somatic activity and coding emotional facial expressions. FTLD patients, AD patients, and control participants showed similar patterns of down-regulation in somatic activity across the 3 startle trials. However, differences between the 3 groups emerged in the amount of emotional facial behavior expressed in the startle trials. There were no group differences in response in the unwarned condition, indicating that the startle response was intact in the patients. In the warned with instructions condition, both FTLD and AD patients were moderately impaired in down-regulatory ability compared with controls. In the warned without instructions condition, AD patients and normal controls spontaneously down-regulated their emotional responses, but FTLD patients did not. These findings illuminate specific problems that these patients have in the emotional realm.


Emotion | 2013

The effect of the serotonin transporter polymorphism (5-HTTLPR) on empathic and self-conscious emotional reactivity.

Anett Gyurak; Claudia M. Haase; Jocelyn A. Sze; Madeleine S. Goodkind; Giovanni Coppola; Jessica Lane; Bruce L. Miller; Robert W. Levenson

We examined the relationship between a functional polymorphism of the serotonin transporter gene (5-HTTLPR) and individual differences in emotional reactivity in two laboratory studies. In Study 1, empathic responding and physiological reactivity to viewing films of others in distress were assessed in healthy adults in three age groups. In Study 2, emotional responding to watching oneself in an embarrassing situation was assessed in healthy adults and in patients with neurodegenerative diseases. In Study 1, participants with two short alleles of 5-HTTLPR reported more personal distress and showed higher levels of physiological responses in response to the films than participants with long alleles. In Study 2, participants with two short alleles reported more anger and amusement and displayed more emotional expressive behaviors in response to the embarrassing situation than participants with long alleles. These two findings from diverse samples of participants converge to indicate that individuals who are homozygous for the short allele variant of 5-HTTLPR have greater levels of emotional reactivity in two quite different socially embedded contexts.


Psychology and Aging | 2012

Aging and emotion recognition: not just a losing matter.

Jocelyn A. Sze; Madeleine S. Goodkind; Anett Gyurak; Robert W. Levenson

Past studies on emotion recognition and aging have found evidence of age-related decline when emotion recognition was assessed by having participants detect single emotions depicted in static images of full or partial (e.g., eye region) faces. These tests afford good experimental control but do not capture the dynamic nature of real-world emotion recognition, which is often characterized by continuous emotional judgments and dynamic multimodal stimuli. Research suggests that older adults often perform better under conditions that better mimic real-world social contexts. We assessed emotion recognition in young, middle-aged, and older adults using two traditional methods (single emotion judgments of static images of faces and eyes) and an additional method in which participants made continuous emotion judgments of dynamic, multimodal stimuli (videotaped interactions between young, middle-aged, and older couples). Results revealed an Age × Test interaction. Largely consistent with prior research, we found some evidence that older adults performed worse than young adults when judging single emotions from images of faces (for sad and disgust faces only) and eyes (for older eyes only), with middle-aged adults falling in between. In contrast, older adults did better than young adults on the test involving continuous emotion judgments of dyadic interactions, with middle-aged adults falling in between. In tests in which target stimuli differed in age, emotion recognition was not facilitated by an age match between participant and target. These findings are discussed in terms of theoretical and methodological implications for the study of aging and emotional processing.


Handbook of Clinical Neurology | 2008

Chapter 25 Laboratory testing of emotion and frontal cortex

Robert W. Levenson; Elizabeth A. Ascher; Madeleine S. Goodkind; Megan McCarthy; Virginia E. Sturm; Kelly Werner

Publisher Summary This chapter discusses what is considered most critical for a comprehensive assessment of emotional functioning and then describes the assessment procedures used. Since the work is primarily conducted in the laboratory, the procedures are designed for that environment. In recent years, these procedures are used with hundreds of patients with neurodegenerative diseases (frontotemporal lobar degeneration, Alzheimers, amyotrophic lateral sclerosis), congenital neurological diseases (Moebius syndrome), and focal lesions (orbitofrontal), as well as with neurologically normal controls. The laboratory is an excellent test bed for developing, refining, and evaluating assessment techniques. Those techniques that prove most useful can then be translated into forms more appropriate for use in the clinic and at the bedside. Emotions are short lived psychological–physiological phenomena that represent efficient modes of adaptation to changing environmental demands. Emotions serve important social functions, moving one toward certain people and away from others. Reflecting this view, the laboratory assessment of emotional functioning focuses on brief emotional phenomena (not on longer moods) and on the activation of multiple response systems (not on a single system such as verbal report of emotional experience). The chapter describes a number of tests that can be used in the laboratory to obtain differentiated, comprehensive assessment of emotional functioning.


Brain | 2011

Behaviour, physiology and experience of pathological laughing and crying in amyotrophic lateral sclerosis

Nicholas Olney; Madeleine S. Goodkind; Catherine Lomen-Hoerth; Patrick K. Whalen; Craig Williamson; Deborah E. Holley; Alice Verstaen; Laurel M. Brown; Bruce L. Miller; John Kornak; Robert W. Levenson; Howard J. Rosen

Pathological laughing and crying is a disorder of emotional expression seen in a number of neurological diseases. The aetiology is poorly understood, but clinical descriptions suggest a disorder of emotion regulation. The goals of this study were: (i) to characterize the subjective, behavioural and physiological emotional reactions that occur during episodes of pathological laughing and crying; (ii) to compare responses during these episodes to those that occur when emotions are elicited under standard conditions (watching sad and amusing emotional films, being startled); and (iii) to examine the ability of patients with this disorder to regulate their emotions under standardized conditions. Twenty-one patients with pathological laughing and crying due to amyotrophic lateral sclerosis and 14 with amyotrophic lateral sclerosis but no pathological laughing and crying were studied. Emotional measures included self-reported emotional experience, video recordings of facial reactivity and peripheral physiological responses (skin conductance, heart rate and somatic activity). Nineteen of the 21 patients with histories of pathological laughing and crying had at least one episode in the laboratory that they agreed constituted pathological laughing or crying (a total of 56 episodes were documented). Compared with viewing sad and amusing films, the episodes were associated with greater facial and physiological activation. Contrary to many clinical descriptions, episodes were often induced by contextually appropriate stimuli and associated with strong experiences of emotion that were consistent with the display. When instructed to regulate their facial responses to emotion-eliciting films, patients with pathological laughing and crying showed impairments compared with patients who did not have a history of this disorder. These findings support the idea that pathological laughing and crying represents activation of all channels of emotional responding (i.e. behavioural, physiological and subjective). Furthermore, they support previously advanced theories that, rather than being associated with general emotional hyperreactivity, this disorder may be due to dysfunction in frontal neural systems that support voluntary regulation of emotion.


Human Brain Mapping | 2012

Tracking emotional valence: The role of the orbitofrontal cortex

Madeleine S. Goodkind; Marc Sollberger; Anett Gyurak; Howard J. Rosen; Katherine P. Rankin; Bruce L. Miller; Robert W. Levenson


Emotion | 2015

Emotion recognition in frontotemporal dementia and Alzheimer's disease: A new film-based assessment.

Madeleine S. Goodkind; Virginia E. Sturm; Elizabeth A. Ascher; Suzanne M. Shdo; Bruce L. Miller; Katherine P. Rankin; Robert W. Levenson

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Bruce L. Miller

University of British Columbia

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Jocelyn A. Sze

University of California

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Joel H. Kramer

University of California

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Megan McCarthy

University of California

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