4.5 Article

Heterogeneous early illness courses of Korean patients with bipolar disorders: replication of the staging model

期刊

BMC PSYCHIATRY
卷 22, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s12888-022-04318-y

关键词

Bipolar disorder; Mood disorders; Staging; Staging models; Comorbidity

资金

  1. Original Technology Research Program for Brain Science through the National Research Foundation of Korea (NRF) - Ministry of Science and ICT, Republic of Korea [2019M3C7A1030624]
  2. National Research Foundation of Korea [2019M3C7A1030624] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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This study analyzed the long-term course of bipolar disorder (BD) in Korean patients using a staging model. The results found that different sub-populations had varied courses, with some progressing to higher stages at a faster rate. The study also identified associations between comorbid psychiatric disorders, age of onset, age at starting treatment, and the progression of the illness.
Background Clinical staging of bipolar disorder (BD) requires application of real-world data, as the next step in hypothesis. This study used the staging model to analyze the long-term course of BD in Korean patients based on clinical features and treatment responses to map the progression of bipolar illness from its early phase after the onset of illness. Methods A total of 136 patients diagnosed with BD-I (n = 62) or BD-II (n = 74) were recruited. Their progressive stages were retrospectively evaluated. A multi-state model was used to calculate the probability of progression to each stage. Hazard ratios of covariates expected to influence different courses of BD were calculated. Using the Alda score, long-term responses to mood stabilizers depending on the current stage were compared. Results Several sub-populations showed varied courses during the first five years after the onset of illness, with 41.5% remaining in stage 2 and 53% progressing to higher stages with shortened time for transition. Profiles of patients with BD-I and BD-II were different, suggesting biologically distinct groups. Comorbid psychiatric disorders, such as obsessive-compulsive disorder (OCD) and bulimia nervosa (BN) were associated with a recurrent course (stage 3a or 3b) or a malignant course (stage 3c or 4). Early age of onset, shorter duration of illness, older age at the start of medication, and poor response to lithium affected the illness progression. Conclusion We were able to apply the stage model based on episode recurrence patterns in early illness courses of Korean patients with BD. The stage progression pattern differed from the early phase in BD-I and BD-II patients. Psychotic comorbidity, age at onset, age at starting psychiatric treatment showed associations with the illness progression.

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