Age of Onset and Gender Issues in Bipolar Disorder
by Vivek Kusumakar, MD, FRCPC
Associate Professor, Head of the Division of Child & Adolescent Psychiatry, and Director, Mood Disorders Group, Dept of Psychiatry, Dalhousie University, Halifax, Nova Scotia.
(April 1997) - It is being
increasingly recognised that
bipolar disorder often has its onset in
adolescence or early adulthood.
First affective symptoms appear in early
teenage, and even in preadolescence. There is a growing interest, with
little consensus, in the affective and behavioural symptomatology in
childhood and adolescence preceding
the first onset of a clearly diagnosable
bipolar disorder. There is a significant time-lag between the onset of the
illness and first treatment. This may put patients at risk of increased
morbidity, including
effects on personality, school, work and social
functioning. There is growing evidence in the schizophrenia literature that
this time-lag may predict a poorer response to treatment. Although there is
no clear evidence of this in bipolar disorder, this issue should be borne in
mind.
Early onset is often defined as occurring before the age of 25. The
younger the age of onset of bipolar disorder, the more likely it is to find
a significant family history of the condition. Early onset bipolar disorder
most commonly begins with depression and there may be many episodes of
depression before the first hypomania. Depression with psychotic features
may be a predictor of future full-blown bipolar disorder in the early onset
group. Akiskal (1995) has argued that syndromal dysthymia with its onset in
childhood, particularly in the presence of a family history of bipolar
disorder, may herald a bipolar disorder. Rapid cycling, mixed states, and
psychotic features are more common in early onset conditions. The presence
of early onset substance abuse should raise one's suspicions about bipolar
disorder. Early onset bipolar disorder is more commonly associated with
response to Divalproex and a relative failure of response to Lithium not
only because rapid cycling, mixed states and substance use are common in
this group but also because adolescents and young adults are less tolerant
to the side effects of Lithium.
Gender Issues Associated with Bipolar Disorder
Female gender is more commonly associated with rapid cycling bipolar
disorder (Calabrese et al, 1995), with or without thyroid dysfunction,
perimenopausal exacerbation of the condition, the risk of exacerbation
post-partum and being diagnosed as borderline personality disorder
(especially in adolescents or young adults) when, in fact, some of these
presentations could be explained by rapid cycling bipolar disorder. Biphasic
mood dysregulation is being increasingly recognized as being more common in
subjects with borderline personality functioning and there is merit in
treating clearly established biphasic mood dysregulation even in the
presence of personality dysfunction. Postpartum psychotic and serious mood
disorders may well be part of a bipolar spectrum. There is also growing
evidence that the pharmocokinetics of many psychotropic medications,
including mood stabilizers, is altered in pregnancy, post-partum and even
around menstruation. Bipolar disorder secondary to underlying medical or
neurological conditions are associated with the condition in the elderly
(Evans et al, 1995).
Akiskal HS. Developmental Pathways to Bipolarity: Are Juvenile-Onset
Depressions PreBipolar? J Am Acad Child Adolesc Psychiatry. 1995. 34:6.
754-763
Calabrese JR, Woyshville MJ. A Medication Algorithm for Treatment of
Bipolar Rapid Cycling? J Clin Psychiatry. 1995. 56 (Suppl 3) 11-18
Egeland JA, Hostetter AM. Amish Study 1: Affective Disorders among the
Amish, 1976-1980. Am J Psychiatry. 1983. 140(1): 56-61.
Evans DL, Byerly MJ, Greer RA. Secondary Mania: Diagnosis and Treatment.
J Clin Psychiatry. 1995. 56 (Suppl 3): 31-37.
Strober M, Carlson C. Bipolar Illness in Adolescents with Major
Depression. Clinical, Genetic and Psychopharmacologic Predictors in a Three
to Four Year Prospective Follow-Up Investigation. Arch Gen Psychiatry. 1982.
39: 549-555.
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