Multi-state models for investigating possible stages leading to bipolar disorder

• Published in: International Journal of Bipolar Disorders Vol. 3; no. 1; p. 5
• Main Authors: Keown-Stoneman, Charles DG, Horrocks, Julie, Darlington, Gerarda A, Goodday, Sarah, Grof, Paul, Duffy, Anne
• Format: Journal Article
• Language: English
• Published: Berlin/Heidelberg Springer Berlin Heidelberg 24.02.2015; Springer Nature B.V
• Subjects: Behavioral Therapy; Bipolar disorder; Clinical Psychology; Medicine; Medicine & Public Health; Neurology; Psychiatry; Psychopathology; Psychopharmacology; Psychotherapy; Risk factors; Survival analysis; Bipolar disorder; Multi-state model; High-risk
• ISSN: 2194-7511; 2194-7511
• DOI: 10.1186/s40345-014-0019-4

Background It has been proposed that bipolar disorder onsets in a predictable progressive sequence of clinical stages. However, there is some debate in regard to a statistical approach to test this hypothesis. The objective of this paper is to investigate two different analysis strategies to determine the best suited model to assess the longitudinal progression of clinical stages in the development of bipolar disorder. Methods Data previously collected on 229 subjects at high risk of developing bipolar disorder were used for the statistical analysis. We investigate two statistical approaches for analyzing the relationship between the proposed stages of bipolar disorder: 1) the early stages are considered as time-varying covariates affecting the hazard of bipolar disorder in a Cox proportional hazards model, 2) the early stages are explicitly modelled as states in a non-parametric multi-state model. Results We found from the Cox model thatthere was evidence that the hazard of bipolar disorder is increased by the onset of major depressive disorder. From the multi-state model, in high-risk offspring the probability of bipolar disorder by age 29 was estimated as 0.2321. Cumulative incidence functions representing the probability of bipolar disorder given major depressive disorder at or before age 18 were estimated using both approaches and found to be similar. Conclusions Both the Cox model and multi-state model are useful approaches to the modelling of antecedent risk syndromes. They lead to similar cumulative incidence functions but otherwise each method offers a different advantage.