Sociodemographic and clinical characteristics of treated and untreated adults with bulimia nervosa or binge-eating disorder recruited for a large-scale research study.

Autor: Carrino EA; Department of Psychology and Neuroscience, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA., Flatt RE; Department of Psychology and Neuroscience, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.; Department of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA., Pawar PS; Department of Biotechnology, Dr D. Y. Patil Biotechnology and Bioinformatics Institute, Dr. D. Y. Patil Vidyapeeth, Pune, India., Sanzari CM; Department of Psychology, State University of New York at Albany, Albany, NY, USA., Tregarthen JP; Recovery Record, Inc, Palo Alto, CA, USA., Argue S; Recovery Record, Inc, Palo Alto, CA, USA., Thornton LM; Department of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA., Bulik CM; Department of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA. cynthia.bulik@ki.se.; Department of Nutrition, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA. cynthia.bulik@ki.se.; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Nobels Väg 12A, 171 65, Solna, Stockholm, Sweden. cynthia.bulik@ki.se., Watson HJ; Department of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.; Discipline of Psychology, School of Population Health, Curtin University, Perth, Australia.; Division of Paediatrics, School of Medicine, The University of Western Australia, Perth, Australia.
Jazyk: angličtina
Zdroj: Journal of eating disorders [J Eat Disord] 2023 Jul 31; Vol. 11 (1), pp. 126. Date of Electronic Publication: 2023 Jul 31.
DOI: 10.1186/s40337-023-00846-4
Abstrakt: Background: Eating disorders affect millions of people worldwide, but most never receive treatment. The majority of clinical research on eating disorders has focused on individuals recruited from treatment settings, which may not represent the broader population of people with eating disorders. This study aimed to identify potential differences in the characteristics of individuals with eating disorders based on whether they self-reported accessing treatment or not, in order to contribute to a better understanding of their diverse needs and experiences.
Methods: The study population included 762 community-recruited individuals (85% female, M ± SD age = 30 ± 7 years) with bulimia nervosa or binge-eating disorder (BN/BED) enrolled in the Binge Eating Genetics Initiative (BEGIN) United States study arm. Participants completed self-report surveys on demographics, treatment history, past and current eating disorder symptoms, weight history, and their current mental health and gastrointestinal symptoms. Untreated participants (n = 291, 38%) were compared with treated participants (n = 471, 62%) who self-reported accessing BN/BED treatment at some point in their lives.
Results: Untreated participants disproportionately self-identified as male and as a racial or ethnic minority compared with treated participants. Treated participants reported a more severe illness history, specifically, an earlier age at onset, more longstanding and frequent eating disorder symptoms over their lifetime, and greater body dissatisfaction and comorbid mental health symptoms (i.e., depression, anxiety, ADHD) at the time of the study. A history of anorexia nervosa was positively associated with treatment engagement. Individuals self-reporting a history of inpatient or residential treatment exhibited the most severe illness history, those with outpatient treatment had a less severe illness history, and untreated individuals had the mildest illness history.
Conclusions: Historically overlooked and marginalized populations self-reported lower treatment access rates, while those who accessed treatment reported more severe eating disorder and comorbid mental health symptoms, which may have motivated them to seek treatment. Clinic-based recruitment samples may not represent individuals with milder symptoms or racial and ethnic diversity, and males. Community-based recruitment is crucial for improving the ability to apply research findings to broader populations and reducing disparities in medical research. Trial Registration ClinicalTrials.gov NCT04162574 ( https://clinicaltrials.gov/ct2/show/NCT04162574 ).
(© 2023. The Author(s).)
Databáze: MEDLINE
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