Psychiatry

Bipolar II Disorder

양극성장애 2형

Recurring hypomania + major depression (no full mania)

How common
Lifetime 0.5–1.5%
Typical age
Mean onset mid-20s

What is it?

Similar to Bipolar I but milder elevated phase. Mood lability + depressive predominance.

Commonly affected: Amygdala, PFC, striatum

How it develops

  1. Genetic predispositionShares some loci with BD-I
  2. Hypomanic onset≥4 days elevated/irritable mood, function preserved
  3. Depression dominance>50% of lifetime in depressive states
  4. AD-induced switchSSRI monotherapy may switch to mania

Symptoms

  • Major depressionSame as MDD
  • Suicide riskHigher attempt rate than BD-I
  • Hypomania ≥4dElevated mood, function preserved, no psychosis
  • Decreased sleep needDuring hypomania
  • Increased creativityOften perceived positively by patient

How it is examined

  • DSM-5 BD-II≥1 hypomanic (≥4d) + ≥1 MDE, never manic
  • MDQ screeningMood Disorder Questionnaire
  • AD response historyPrior switch on SSRIs

Imaging

Similar MRI changes as BD-I.

  • Amygdala changes

fMRI: altered emotion regulation circuits.

  • Emotion circuit dysregulation

Non-surgical care

  • Quetiapine (first-line BD depression)300 mg/day, proven for BD depression
  • LamotrigineDepression prevention, minimal cognitive AE
  • LithiumRelapse prevention, antisuicidal
  • CBT/psychoeducationHypomania recognition, routine management
  • Avoid AD monotherapySwitch risk; combine with stabilizer

Conservative options are generally tried first. Medications listed here can have side effects — discuss them with your prescriber.

When surgery is considered

Treatment-resistant depression

Procedures that may be discussed

  • ECT
  • rTMS
  • Ketamine (caution in BD)

Outlook

Chronic relapsing. >90% recur. Suicide attempts higher than BD-I.

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