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Parental and comorbid migraine in individuals with bipolar disorder: A nationwide register study.
Sucksdorff, Dan; Brown, Alan S; Chudal, Roshan; Heinimaa, Markus; Suominen, Auli; Sourander, Andre.
Afiliación
  • Sucksdorff D; Research Centre for Child Psychiatry, University of Turku, Turku, Finland. Electronic address: dansuc@utu.fi.
  • Brown AS; Department of Psychiatry, Columbia University Medical Center, New York State Psychiatric Institute, New York, USA; Department of Epidemiology, Columbia University Mailman School of Public Health, New York, USA.
  • Chudal R; Research Centre for Child Psychiatry, University of Turku, Turku, Finland.
  • Heinimaa M; Department of Psychiatry, University of Turku, Turku, Finland.
  • Suominen A; Research Centre for Child Psychiatry, University of Turku, Turku, Finland.
  • Sourander A; Research Centre for Child Psychiatry, University of Turku, Turku, Finland; Department of Child Psychiatry, University of Turku, Turku, Finland.
J Affect Disord ; 206: 109-114, 2016 Dec.
Article en En | MEDLINE | ID: mdl-27472412
ABSTRACT

BACKGROUND:

Genetic studies imply a shared genetic etiology between bipolar disorder (BD) and migraine. Epidemiological studies have demonstrated elevated comorbidity between these disorders, but haven't controlled for parental psychopathology. No previous nationally representative studies exist on familial clustering of BD and migraine. This study examines the association between parental and comorbid migraine and BD, controlling for potential confounders.

METHODS:

We identified 1861 cases aged ≤25 years, 3643 matched controls, and their parents from Finnish national registers. Conditional logistic regression was used to calculate odds ratios (ORs) with 95% confidence intervals (CIs) and two-sided significance limits of p<0.05.

RESULTS:

Parental migraine, controlling for parental BD, was associated with offspring BD diagnosed at age ≥18 years (OR 1.52, 95%CI 1.08-2.14). Associations between BD and comorbid migraine persisted following adjustment for parental BD and parental migraine in all subjects (OR=2.46, 95% CI 1.76-3.42), both age groups of BD-diagnosis (<18 years,≥18 years) and both sexes.

LIMITATIONS:

The diagnoses were register-based, not directly ascertained.

CONCLUSIONS:

This study indicates that parental migraine, even in the absence of parental BD, is a risk factor for offspring BD. Thus, a genetic link between BD and migraine could potentially explain some of the elevated comorbidity between these disorders. However, BD shows a stronger association with comorbid migraine than with parental migraine, suggesting that much of the elevated comorbidity is related to non-genetic factors. Increased understanding of mechanisms underlying the comorbidity of BD and migraine is important since it is associated with poorer health-related outcomes compared with BD alone.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Trastorno Bipolar / Sistema de Registros / Hijo de Padres Discapacitados / Trastornos Migrañosos Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies País/Región como asunto: Europa Idioma: En Revista: J Affect Disord Año: 2016 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Trastorno Bipolar / Sistema de Registros / Hijo de Padres Discapacitados / Trastornos Migrañosos Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies País/Región como asunto: Europa Idioma: En Revista: J Affect Disord Año: 2016 Tipo del documento: Article