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Factors associated with onset-age in major affective disorders.
Miola, Alessandro; Tondo, Leonardo; Salvatore, Paola; Baldessarini, Ross J.
Affiliation
  • Miola A; International Consortium for Mood & Psychotic Disorders Research, Mailman Research Center, McLean Hospital, Belmont, Massachusetts, USA.
  • Tondo L; Department of Psychiatry, University of Padova, Padua, Italy.
  • Salvatore P; International Consortium for Mood & Psychotic Disorders Research, Mailman Research Center, McLean Hospital, Belmont, Massachusetts, USA.
  • Baldessarini RJ; Department of Psychiatry, Harvard Medical School, Boston, Massachusetts, USA.
Acta Psychiatr Scand ; 146(5): 456-467, 2022 11.
Article in En | MEDLINE | ID: mdl-36059155
BACKGROUND: Research findings on factors associated with onset-age (OA) with bipolar (BD) and major depressive disorders (MDD) have been inconsistent, but often indicate greater morbidity following early OA. METHODS: We considered factors associated with OA in 1033 carefully evaluated, systematically followed mood disorder subjects with DSM-5 BD (n = 505) or MDD (n = 528), comparing rates of descriptive and clinical characteristics following early (age <18), intermediate (18-40), or later onset (≥40 years), as well as regressing selected measures versus OA. Exposure time (years ill) was matched among these subgroups. RESULTS: As hypothesized, many features were associated with early OA: familial psychiatric illness, including BD, greater maternal age, early sexual abuse, nondepressive first episodes, co-occurring ADHD, suicide attempts and violent suicidal behavior, abuse of alcohol or drugs, smoking, and unemployment. Other features increased consistently with later OA: %-time-depressed (in BD and MDD, women and men), as well as depressions/year and intake ratings of depression, educational levels, co-occurring medical disorders, rates of marriage and number of children. CONCLUSIONS: OA averaged 7.5 years earlier in BD versus MDD (30.7 vs. 38.2). Some OA-associated measures may reflect maturation. Associations with family history and suicidal risk with earlier OA were expected; increases of time-depressed in both BD and MDD with later OA were not. We conclude that associations of OA with later morbidity are complex and not unidirectional but may be clinically useful.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bipolar Disorder / Depressive Disorder, Major Type of study: Risk_factors_studies Limits: Child / Female / Humans / Male Language: En Journal: Acta Psychiatr Scand Year: 2022 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bipolar Disorder / Depressive Disorder, Major Type of study: Risk_factors_studies Limits: Child / Female / Humans / Male Language: En Journal: Acta Psychiatr Scand Year: 2022 Type: Article Affiliation country: United States