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Updated: Sep 3, 2026

A Computer-Based Platform for Aiding Clinicians in Eating Disorder Analysis and Diagnosis
Published on: May 10, 2022
Characteristics of Monozygotic Twins Discordant for Anorexia Nervosa: Comprehensive Risk Evaluation for Anorexia
Hunna J Watson1,2, Elisabeth Welch3,4, Elin Monell5,6
1Department of Psychiatry, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
Objective:
To characterise the clinical and phenotypic profile of the Comprehensive Risk Evaluation for Anorexia nervosa in Twins (CREAT) cohort, identify candidate risk and illness-related correlates of AN, and establish a foundation for forthcoming biological, neuroimaging, endocrinological, and microbiota studies.
Methods:
MZ twins discordant for lifetime AN (44 individuals) and control MZ twin pairs (42 individuals) were recruited. Analyses included total-sample associations with AN, between-group comparisons (affected, unaffected co-twins, controls), and within-pair analyses of discordant twins.
Results:
Affected twins, most of whom were weight-restored and non-acute, differed markedly from unaffected co-twins and controls. Lifetime AN was associated with higher perfectionism, goal-directed drive, neuroticism, behavioural inhibition, impulsivity, broader psychiatric symptoms, teasing history, autism symptoms, and lower quality of life. Within-pair analyses implicated perfectionism, goal-directed drive, and competency-related teasing as candidate individual-specific risk factors for AN, with evidence of additional associations with impulsivity, behavioural inhibition, neuroticism, broader psychiatric symptoms, and autism symptoms.
Conclusion:
Findings support a multifactorial model of AN involving individual-specific influences and shared familial liability. Perfectionism, goal-directed drive, and competency-related teasing emerged as candidate individual-specific risk factors, while the pattern of elevations, with unaffected co-twins often falling between affected twins and healthy controls, suggests that several clinical and phenotypic features may reflect familial liability for AN.

