At, with and beyond risk
Expectations of Living With the Possibility of Future Dementia
Datos Bibliográficos
| ID | 2249390 |
|---|---|
| Autores | Richard Milne (0000-0002-8770-2384, Institute of Public Health University of Cambridge UK, autor de correspondencia), Ana Díaz (0000-0003-4339-7485, Alzheimer Europe, Luxembourg), Shirlene Badger (0009-0009-3696-8578, Institute of Public Health University of Cambridge UK), Eline Bunnik (Erasmus MC Rotterdam The Netherlands), Eline M Bunnik (0000-0003-1481-6222, Erasmus MC), Karine Fauria (0000-0003-1506-4405, Pasqual Maragall Foundation Barcelona Spain), Katie Wells (0000-0002-4168-1493, Imperial College London UK) |
| Año | 2018 |
| Volumen | 40 |
| Número | 6 |
| Páginas | 969-987 |
| Fecha de publicación | 2018-07-01 |
| Peer Reviewed | Sí |
| Open Access | Sí |
| Tipo | ARTICLE |
| Revista | Sociology of Health & Illness (JOURNAL) |
| Identificadores de la revista | ISSN: 0141-9889 • E-ISSN: 1467-9566 |
| Editorial | Wiley (PUBLISHER • GB) |
| DOI | 10.1111/1467-9566.12731 |
| PMID | 29659032 |
| OpenAlex | W2803004736 |
| Idioma | EN |
| Citas recibidas | 12 |
| Referencias citadas | 75 |
Biomedical research aimed at the development of therapies for chronic and late-onset conditions increasingly concentrates on the early treatment of symptom-less disease. This broad trend is evidenced in prominent shifts in contemporary dementia research. Revised diagnostic criteria and new approaches to clinical trials propose a focus on earlier stages of disease and prompt concerns about the implications of communicating test results associated with the risk of developing dementia when no effective treatments are available. This article examines expectations of the implications of learning test results related to dementia risk, based on focus group research conducted in the UK and Spain. It points to the extended social and temporal aspects of the dementia risk experience. Three key dimensions of this risk experience are elaborated: living 'at risk', represented in efforts to reduce risk and plan for the future; 'with risk', through vigilance towards cognitive health and earlier or prolonged contact with healthcare services; and finally, 'beyond risk' through a cessation of the self in its current social, legal and financial form. A virtual abstract of this paper can be viewed at: https://www.youtube.com/channel/UC_979cmCmR9rLrKuD7z0ycA
Cognition · Cognitive psychology · Dementia · Disease · Pathology · Psychiatry · Test (biology) · Vigilance (psychology) · Dementia and Cognitive Impairment Research · Medicine · Mental Health and Patient Involvement · Mental Health and Psychiatry · Psychology
Representations of dementia and their role in social expectations regarding ageing
Detecting value(s)
People's interest in brain health testing
The familial canopy as thought space for meaning making, emotional calibration and planful action around inherited cancer risk
Alzheimer’s disease and the development of a post-genomic science
Biomarkers and brains
The turn towards prevention – moral narratives and the vascularization of Alzheimer’s disease
Soccer, CTE, and the Cultural Representation of Dementia
Technologies of Ascription
What matters to people with memory problems, healthy volunteers and health and social care professionals in the context of developing treatment to prevent Alzheimer's dementia? A qualitative study
Digital phenotyping and the (data) shadow of Alzheimer's disease
Circularity, psychiatry & biomarkers
Biocapital
The Alzheimer Conundrum
Reconsidering Successful Aging
The diagnosis of mild cognitive impairment due to Alzheimer's disease
Dementia As a Cultural Metaphor
Toward defining the preclinical stages of Alzheimer's disease
Aging without agency
The Converged Experience of Risk and Disease
Dementia screening and early diagnosis
Time-framing and health risks
Families' Roles in Advance Directives
Disrupted Lives
The Earlier the Better
Diagnosing dementia
Bedsides healthcare rationing dilemmas
Being at risk of dementia
The experience of risk as ‘measured vulnerability
The practical ethics of genetic responsibility
Repositioning the patient
The relative contributions of disease label and disease prognosis to Alzheimer's stigma
Postgenomics, uncertain futures, and the familiarization of susceptibility genes
Bodies at Risk
The Politics of Life Itself
Patients-in-Waiting
The Body, Identity, and Self
Making sense of nonsense
Managing Courtesy Stigma
The rise of surveillance medicine
Ageing, dementia and the social mind
The risk experience
The pursuit of preventive care for chronic illness
Doing the right thing
Dementia and the phenomenon of social death
Genetic risk and the birth of the somatic individual
| Obras citantes distintas | 12 |
|---|---|
| Citas por año | 1,71 |
| Intervalo de citas | 2019 - 2024 (6) |
| Velocidad de citación | recent |
| Altamente citado | No |
| Tipos de cita | Neutras: 10 |